Cancer is a group of diseases where abnormal cells grow and spread. Cancer can affect almost any organ and may cause tiredness, weight change, pain, or a new lump. Many people first hear about cancer when a test or scan finds something during a routine checkup. It can be short term if found early and treated, but some cancers can be long term or come back. Treatment often includes surgery, chemotherapy, radiation, targeted drugs, or immunotherapy, and survival varies by cancer type and stage.

Short Overview

Symptoms

Cancer symptoms vary by type and where it starts. Common symptoms include a new lump, unexplained weight loss, fatigue, pain that doesn’t fade, persistent cough, unusual bleeding, or changes in bowel, bladder, or skin. Seek care for symptoms that persist.

Outlook and Prognosis

Cancer outcomes vary widely by type, stage, tumor biology, and overall health. Many cancers are highly treatable, especially when found early; others need longer, combined treatments and close follow-up. Advances in targeted drugs, immunotherapy, and precision surgery keep improving survival and quality of life.

Causes and Risk Factors

Cancer develops from accumulated genetic changes influenced by age and chance. Risk factors for cancer include tobacco, alcohol, excess weight, inactivity, certain infections, UV or radiation, environmental or occupational chemicals, hormone exposure, immune suppression, and inherited mutations or family history.

Genetic influences

Genetics matter in cancer, but not all cancers are inherited. Most cancers arise from acquired DNA changes over time; a smaller share comes from inherited variants like BRCA1/2. Family history, ancestry, and tumor testing can guide screening, prevention, and treatment.

Diagnosis

Doctors diagnose Cancer using your history, exam, and imaging. The diagnosis of cancer is confirmed by a biopsy, where a small tissue sample is examined under a microscope. Further tests, including scans and tumor genetic testing, help stage the disease and guide treatment.

Treatment and Drugs

Cancer care is personalized. Treatment often combines surgery, medicines like chemotherapy, targeted or immunotherapy, and radiation, chosen by cancer type and stage. Many also benefit from supportive care for pain, fatigue, nutrition, and emotional well‑being during cancer treatment.

Symptoms

Cancer can be hard to spot early because symptoms depend on where it starts and how fast it grows. Symptoms vary from person to person and can change over time. Early symptoms of cancer may look like everyday issues—tiredness, small lumps, or changes in weight—so noticing what sticks around is key. If a new symptom lasts more than a couple of weeks or disrupts daily life, talk with a healthcare professional.

  • Weight loss: Losing weight without trying can be an early sign of some cancers. If your clothes fit looser over weeks or months without diet or exercise changes, it’s worth checking.

  • Lasting fatigue: Tiredness that doesn’t improve with rest or sleep and lingers for weeks can be a red flag. It can stem from hidden bleeding, inflammation, or body-wide changes.

  • Persistent pain: Ongoing or worsening pain, especially at night or in one spot, should be assessed. Common causes include strains and arthritis, but pain without a clear trigger that keeps returning deserves attention.

  • New lump or swelling: A firm, growing lump under the skin—in a breast, testicle, neck, or armpit—can be related to cancer. Lumps that are painless and don’t go away after a few weeks should be checked.

  • Skin or mole changes: A new spot or a mole that changes size, shape, or color can point to skin cancer. Itching, bleeding, or a sore that won’t heal on sun-exposed areas are other clues.

  • Persistent cough or hoarseness: A cough lasting longer than three weeks or a voice that stays hoarse may be linked to lung or throat cancer. Shortness of breath, chest pain, or coughing up blood needs prompt medical care.

  • Bowel habit changes: Ongoing constipation, diarrhea, narrower stools, or blood in the stool can signal colon or rectal cancer. Symptoms that persist beyond a few weeks should be evaluated.

  • Bladder changes: Needing to urinate more often, burning with urination, or urine that looks pink or red can show up. Infections, stones, or medications are common causes, but persistent blood or pain merits a check.

  • Trouble swallowing: Food sticking, frequent choking, or persistent heartburn can make meals harder to finish. If swallowing problems continue or worsen, an evaluation can look for narrowing or other causes.

  • Unusual bleeding: Bleeding between periods, after sex, from the rectum, or in urine can sometimes be due to cancer. Nosebleeds, gum bleeding, or easy bruising that appears without injury also deserve attention.

  • Non-healing sores: A sore in the mouth, on the skin, or on the genitals that doesn’t heal within three weeks should be checked. Dentures that newly rub or a white or red patch in the mouth are worth mentioning at your visit.

  • Frequent fevers or infections: Repeated infections or fevers without a clear source can signal a problem with the immune or blood system. Pale skin, easy bruising, or feeling wiped out may occur alongside these.

How people usually first notice

Many people first notice cancer through a new or changing feature in their body that doesn’t go away, like a lump, unusual bleeding, a sore that won’t heal, or a persistent cough or hoarseness. Others sense more general, lingering changes—unexplained weight loss, fatigue that feels different from everyday tiredness, night sweats, or pain that’s new and progressive—prompting a visit to a clinician. Sometimes the first signs of cancer are found incidentally on routine screening tests or imaging, which is why recommended screenings (like mammograms, Pap tests, colonoscopies, and low-dose CT scans for eligible smokers) are so important even when you feel well.

Dr. Wallerstorfer Dr. Wallerstorfer

Types of Cancer

Cancer isn’t a single disease; it’s a large group of conditions that behave differently depending on where they start and how the cells look and grow. When people ask about types of Cancer, they’re usually talking about broad categories based on the original cell type, which helps guide testing and treatment. Clinicians often describe them in these categories: carcinomas, sarcomas, leukemias, lymphomas, myelomas, and certain rare types. Not everyone will experience every type.

Carcinomas

These start in the lining cells of organs like the breast, colon, lung, prostate, or skin. They are the most common types of Cancer and often form solid tumors. Symptoms vary by organ, such as a new lump, bleeding, or changes in bowel habits.

Sarcomas

These arise from connective tissues such as muscle, fat, bone, or cartilage. They tend to form solid masses in limbs, the abdomen, or chest. Pain, swelling, or a growing lump are common early symptoms of Cancer in this group.

Leukemias

These begin in blood-forming cells in the bone marrow and flow through the bloodstream rather than forming solid tumors. People may notice fatigue, frequent infections, or easy bruising and bleeding. Blood tests often show abnormal white blood cells.

Lymphomas

These start in the lymphatic system, which includes lymph nodes and immune cells. Swollen, painless lymph nodes in the neck, armpit, or groin are common, sometimes with fever, night sweats, or weight loss. Imaging and a lymph node biopsy are usually needed to confirm the type.

Myelomas

These develop from plasma cells in the bone marrow. Bone pain, anemia, frequent infections, or high calcium levels may occur. Back or rib pain and fractures can be early signs.

Central nervous system

These include brain and spinal cord tumors that start in nerve tissue. Headaches, seizures, balance problems, or vision changes may appear depending on the tumor’s location. Some grow slowly, while others can progress quickly.

Neuroendocrine tumors

These start in hormone-producing cells found in organs like the pancreas, lungs, or intestines. Symptoms can include flushing, diarrhea, or low blood sugar if hormones are released, or pressure symptoms from a mass. Many are slow-growing but can still spread.

Germ cell tumors

These arise from reproductive cells in the ovaries or testes, and can also appear in the chest or abdomen. A painless testicular lump, pelvic pain, or swelling are common clues. Blood markers and imaging help guide diagnosis and treatment.

Did you know?

Some inherited changes, like BRCA1 or BRCA2 variants, raise the chance of early breast or ovarian cancer and can mean cancers appear at younger ages or in both breasts. Lynch syndrome variants (MLH1, MSH2, MSH6, PMS2) often lead to early colorectal or uterine cancer.

Dr. Wallerstorfer Dr. Wallerstorfer

Causes and Risk Factors

Cancer often begins when cells collect DNA damage over many years. Risk rises with age and is higher with smoking, heavy alcohol use, unhealthy diet, obesity, and low activity. Sunlight and UV, some infections like HPV or hepatitis, radiation, and certain workplace or air exposures can add risk. Some people inherit gene changes or a strong family history that raises their chance, while others develop new gene changes during life. Having risk factors doesn’t mean you’ll definitely develop the condition, and early symptoms of cancer may not be obvious.

Environmental and Biological Risk Factors

Cancer develops over time when cells pick up changes that let them grow when they shouldn’t. Both what’s inside the body and what we meet in our surroundings can raise risk. Doctors often group risks into internal (biological) and external (environmental). Knowing these can be as important as watching for early symptoms of cancer.

  • Older age: Cancer risk rises as years pass because cell-repair systems slow and damage accumulates. Most cancers are diagnosed later in life, though some appear in children and young adults.

  • Hormone exposure: Long or high exposure to hormones like estrogen or androgens can raise risk for cancers such as breast, uterus, and prostate. Natural timing of first periods, pregnancies, and menopause shapes lifetime hormone exposure.

  • Chronic inflammation: Ongoing inflammation can drive repeated cell turnover and DNA damage, increasing cancer risk. Conditions like long-standing reflux or inflammatory bowel disease raise risk in the affected tissues.

  • Immune suppression: A weakened immune system makes it harder to clear virus-infected or abnormal cells, raising cancer risk. Higher risks are seen after organ transplant, with long-term immune-suppressing medicines, or with advanced HIV infection.

  • Ionizing radiation: High or repeated exposure to X-rays, CT scans, or past radiation therapy can damage DNA and increase later cancer risk. Environmental sources from nuclear accidents also contribute, though these exposures are uncommon.

  • UV radiation: Ultraviolet light from the sun damages skin cell DNA and increases the risk of skin cancer. Risk builds with cumulative exposure over the years.

  • Air pollution: Fine particles and diesel exhaust are linked to lung cancer and may affect other organs. Urban or industrial air pollution can add to lifetime cancer risk.

  • Occupational exposures: Workplace carcinogens such as asbestos, benzene, formaldehyde, vinyl chloride, and silica increase cancer risk in exposed workers. Risk often depends on the intensity and duration of exposure.

  • Radon gas: This natural radioactive gas can accumulate indoors and is a leading environmental cause of lung cancer. Risk rises with higher indoor levels and longer time spent in affected buildings.

  • Infections: Certain infections raise cancer risk, including HPV, hepatitis B and C, Epstein–Barr virus, HTLV-1, and Helicobacter pylori. They can trigger chronic inflammation or direct changes in cells that lead to cancer.

  • Chemical contaminants: Arsenic in drinking water and aflatoxins from moldy grains or nuts are well-established cancer risks in some regions. Some industrial solvents and byproducts can also contribute when exposure is high or prolonged.

  • Prior cancer therapy: Some chemotherapy drugs and earlier radiation therapy can increase the chance of a second cancer years later. Risk depends on the specific medicines, total dose, and age at treatment.

  • Precancerous changes: Abnormal tissue changes like colon polyps, Barrett’s esophagus, or cervical dysplasia signal higher local cancer risk. These changes reflect early steps toward cancer in those tissues.

  • Organ scarring: Long-standing scarring in organs, such as liver cirrhosis, raises cancer risk in that tissue. Scarring creates cycles of injury and repair that can cause DNA damage over time.

Genetic Risk Factors

Some cancers run strongly in families because of inherited changes in single genes. These genetic risk factors for cancer don’t cause every case, but when present they can raise lifetime risk for certain tumor types and may show up across generations. Carrying a genetic change doesn’t guarantee the condition will appear.

  • BRCA1/BRCA2 variants: Inherited changes in BRCA1 or BRCA2 can greatly raise the chance of breast and ovarian cancer. They can also increase risks for prostate and pancreatic cancer, and male breast cancer.

  • Lynch syndrome genes: Inherited changes in DNA repair genes linked to Lynch syndrome raise the risk of colorectal and endometrial cancer. Ovarian, stomach, small bowel, and urinary tract cancers may also occur more often.

  • TP53 (Li-Fraumeni): Changes in TP53 can lead to a very high lifetime risk for many cancers, often at young ages. Common tumors include sarcomas, brain tumors, breast cancer, leukemia, and adrenal cancers.

  • APC (FAP): Harmful APC variants cause familial adenomatous polyposis with hundreds to thousands of colon polyps. Without early management, colorectal cancer is very likely, sometimes in the teens or early adulthood.

  • PTEN (Cowden): PTEN changes increase risks for breast, thyroid, endometrial, and kidney cancers. Many people also develop noncancerous growths that signal the condition.

  • STK11 (Peutz-Jeghers): STK11 variants cause digestive tract polyps and characteristic darker spots on the lips or mouth. Cancer risks rise for pancreas, stomach and intestines, breast, ovary, and cervix.

  • CDH1 variants: Inherited CDH1 changes raise the risk of diffuse stomach cancer and lobular breast cancer. Risk may appear at younger ages than in the general population.

  • RET (MEN2): Harmful RET variants cause a high risk of medullary thyroid cancer. Adrenal tumors called pheochromocytomas and parathyroid overactivity can also occur.

  • VHL syndrome: Variants in the VHL gene raise the risk of clear cell kidney cancer and multiple benign and malignant tumors. People may develop tumors in the brain, spinal cord, eyes, or adrenal glands over time.

  • Moderate-risk genes: Changes in genes such as PALB2, CHEK2, and ATM can moderately increase the chance of breast or other cancers. The overall impact often depends on the exact variant and family history.

  • Polygenic risk: Many common DNA changes with small effects can add up and shift overall cancer risk. Polygenic risk scores are increasingly used in research and some clinics to refine who may benefit from earlier checks.

  • Ancestry-specific variants: Certain inherited changes are more common in specific groups, such as some BRCA1/BRCA2 variants in people with Ashkenazi Jewish ancestry. Knowing ancestry can help tailor the most informative genetic testing.

  • Family history patterns: Multiple relatives with the same or related cancers, diagnoses at young ages, or cancers on one side of the family suggest an inherited predisposition. This pattern can guide whether genetic testing is appropriate.

  • De novo or mosaic: A genetic change can arise for the first time in an individual, so there may be no clear family history. Mosaic changes present in only some cells can also affect personal risk and what is passed to children.

Dr. Wallerstorfer Dr. Wallerstorfer

Lifestyle Risk Factors

Many common habits influence cancer risk over time. The strongest lifestyle risk factors for cancer include tobacco, alcohol, diet, body weight, and physical activity. Understanding how lifestyle affects cancer can guide practical changes with real impact. Below are key lifestyle risk factors for cancer and how they work.

  • Tobacco use: Cigarette smoking and other tobacco products cause many cancers, including lung, head and neck, bladder, and pancreatic. Quitting at any age lowers future risk and improves treatment outcomes.

  • Alcohol intake: Regular drinking raises the risk of breast, colorectal, liver, esophageal, and head and neck cancers. Cutting down or avoiding alcohol reduces cumulative risk.

  • Excess body weight: Overweight and obesity increase risk of at least 13 cancers, including breast (postmenopausal), colorectal, uterine, kidney, and pancreatic. Sustained weight loss can lower hormone and inflammation signals that drive tumor growth.

  • Physical inactivity: Too little moderate or vigorous activity raises risk of breast, colorectal, and endometrial cancers. Regular exercise helps regulate insulin, sex hormones, and inflammation that influence tumor development.

  • Sedentary time: Long periods of sitting are linked to higher risks of colon, endometrial, and lung cancers independent of exercise. Breaking up sitting with short movement breaks may reduce these effects.

  • Diet quality: Diets high in ultra-processed foods, added sugars, and low in whole foods are associated with higher overall cancer risk. Emphasizing minimally processed foods supports healthier hormone and metabolic profiles.

  • Red and processed meats: Frequent intake of processed meats and high amounts of red meat raise colorectal cancer risk. Limiting processed meats and keeping red meat to modest portions lowers exposure to carcinogenic compounds.

  • Cooking methods: Charring or high-temperature frying/grilling of meats forms carcinogens like HCAs and PAHs. Using lower-heat methods, marinating, and avoiding charring can reduce these exposures.

  • Fiber and plants: Higher fiber, whole grains, legumes, fruits, and vegetables are linked to lower colorectal and overall cancer risk. These foods support a healthier microbiome and reduce harmful byproducts in the gut.

  • Hormone therapy: Prolonged use of combined estrogen-progestin therapy increases breast cancer risk, while estrogen-only therapy can raise uterine cancer risk. Using the lowest effective dose for the shortest time and regular review with a clinician can reduce risk.

  • Reproductive choices: Having children earlier, having more children, and breastfeeding are associated with lower lifetime breast and ovarian cancer risk. Choosing to breastfeed when possible can confer modest protection.

Risk Prevention

You can’t remove every risk for cancer, but you can lower it with steady, doable habits and smart medical care. Prevention can mean both medical steps, like vaccines, and lifestyle steps, like exercise. Screening tests also help catch problems early—sometimes before you notice early symptoms of cancer—when treatment tends to work best.

  • Tobacco-free living: Avoid smoking and vaping, and stay away from secondhand smoke. Tobacco is linked to many cancers, including lung, throat, bladder, and pancreatic cancer.

  • HPV and Hep B vaccines: Get vaccinated against human papillomavirus (HPV) and hepatitis B if you’re eligible. These vaccines lower the risk of cervical, anal, throat, and liver cancers.

  • Sun and UV safety: Use broad‑spectrum sunscreen, wear protective clothing, and seek shade, especially at midday. This helps prevent skin cancer, including melanoma.

  • Limit alcohol: If you drink, keep it light—fewer drinks per week lowers risk. Alcohol raises the chance of breast, colorectal, mouth, throat, and liver cancers.

  • Healthy body weight: Aim for a weight that’s right for your body over the long term. Keeping weight steady can reduce risk for several cancers, including breast and colorectal cancer.

  • Move most days: Build regular activity into your week with walking, cycling, or sports. Physical activity helps lower risk for colon, breast, and other cancers.

  • Plant‑forward eating: Fill most meals with vegetables, fruit, beans, and whole grains, and limit processed and red meats. This pattern is linked with lower colorectal and overall cancer risk.

  • Screening and check‑ups: Stay up to date on age‑ and risk‑based tests like mammograms, colonoscopy or stool tests, Pap/HPV tests, and low‑dose CT for heavy smokers. Screening can find cancer early or catch precancerous changes.

  • Home radon testing: Test your home for radon and fix high levels with ventilation or sealing. Radon exposure raises lung cancer risk, even in non‑smokers.

  • Safer work practices: Use protective gear and follow safety rules if you work around dusts, fumes, solvents, or other chemicals. Reducing exposure can lower occupational cancer risks.

  • Sexual health steps: Use condoms or dental dams and consider HPV vaccination to reduce infection risks. Safer sex lowers the chance of HPV‑related cancers.

  • Family risk planning: If close relatives had cancers—especially at younger ages—ask about genetic counseling and testing. High‑risk families may benefit from earlier screening, extra monitoring, or risk‑reducing medicines.

How effective is prevention?

Prevention for cancer lowers risk, but it can’t erase it. Not smoking, limiting alcohol, staying active, maintaining a healthy weight, sun protection, and vaccines (HPV, hepatitis B) can prevent many cancers or their precursors. Screening tests like Pap tests, colonoscopy, mammography, and low-dose CT in high-risk smokers catch cancer early, when treatment is more effective. For hereditary risks, options like earlier screening and risk-reducing surgery can cut risk substantially, but benefits depend on your genes, age, and consistent follow-through.

Dr. Wallerstorfer Dr. Wallerstorfer

Transmission

Cancer isn’t contagious: you can’t “catch” cancer from hugging, kissing, sex, sharing food or cups, coughing, or donating blood. Very rarely, a cancer cell can be transferred through an organ or tissue transplant, which is why donors are screened and recipients take anti-rejection medicines with close monitoring.

What can spread are some infections that raise cancer risk—most notably human papillomavirus (HPV) and hepatitis B or C—so vaccines, safer sex, and not sharing needles help. Most cancers aren’t inherited, but some families pass down gene changes that increase risk; this is how cancer is inherited in a minority of people and reflects genetic transmission of cancer risk, not the disease itself.

When to test your genes

Consider genetic testing if cancer runs strongly in your family, you were diagnosed at a young age, or you have multiple or rare cancers. Testing can guide tailored screening, prevention, and treatment choices, including targeted therapies. Ask a genetics professional to review your personal and family history to time testing well.

Dr. Wallerstorfer Dr. Wallerstorfer

Diagnosis

You might notice small changes in daily routines, like feeling unusually tired, a lingering cough, or a lump that wasn’t there before. These clues often lead to a visit with your healthcare team, where the focus is on how cancer is diagnosed and what the next steps look like. The diagnosis of cancer usually relies on a combination of exams, scans, and a tissue sample called a biopsy to confirm it. Many people feel relief just knowing what’s really going on.

  • Medical history and exam: Your provider asks about symptoms, timing, and risk factors, then examines the area of concern. Patterns in weight change, pain, bleeding, or swelling can guide which tests come next.

  • Blood tests: General tests can look for anemia, signs of inflammation, or how organs are working. Some cancers release markers, but these are usually not enough to diagnose on their own.

  • Imaging scans: X‑ray, CT, MRI, or PET create pictures of the body to spot unusual masses or enlarged nodes. Imaging helps show size and location, and it guides whether a biopsy is needed.

  • Ultrasound: Sound waves create real-time images of soft tissues, breast, thyroid, or abdomen. It can help tell if a lump is solid or fluid-filled and can guide a needle during biopsy.

  • Endoscopy: A thin, flexible camera is used to look inside areas like the colon, stomach, lungs, or bladder. If something looks abnormal, small samples can be taken during the same procedure.

  • Biopsy: A small piece of tissue is removed with a needle, scope, or minor surgery. Under the microscope, pathologists confirm whether cells are cancer and what type they are.

  • Cytology: Cells collected from fluids or surface swabs, such as a Pap test or sputum sample, are examined. This can detect abnormal or cancerous cells without a full tissue sample.

  • Molecular testing: If cancer is confirmed, the tumor sample may be tested for genetic changes. Results can help match treatments to the cancer’s specific features.

  • Staging tests: Additional scans and sometimes bone marrow or lymph node sampling check how far cancer has spread. Staging helps plan treatment and estimate outlook.

  • Screening programs: Tests like mammograms, colonoscopy, Pap tests, or low‑dose CT for high‑risk smokers look for cancer before symptoms appear. Abnormal screening results lead to follow‑up testing to confirm a diagnosis.

Stages of Cancer

Staging describes how far Cancer has grown or spread and helps guide treatment choices and outlook. Different tests may be suggested to help determine stage, such as imaging scans, biopsies, and checks of nearby lymph nodes. While stage doesn’t always match early symptoms of cancer, most solid tumors use a similar 0–IV system, with details that vary by cancer type.

Stage 0

In situ: Abnormal cells are limited to the layer where they started and have not invaded deeper tissue. Often found through screening; treatment aims to remove or closely monitor the area.

Stage I

Localized tumor: A small cancer is confined to one area and hasn’t reached lymph nodes. Surgery or focused local therapy is often effective, and the outlook is generally favorable.

Stage II

Larger or deeper: The tumor is bigger or has grown further into nearby tissue; lymph node involvement depends on the cancer type. Care often combines surgery with radiation or chemotherapy.

Stage III

Regional spread: Cancer has reached nearby structures or regional lymph nodes. Treatment usually involves multiple therapies together, and cure may still be possible in some cancers.

Stage IV

Distant spread: Cancer has metastasized to organs farther from where it started. Treatment focuses on control and symptom relief while aiming to extend life; targeted or immune therapies may be options.

Did you know about genetic testing?

Did you know genetic testing can help show whether you carry inherited changes that raise your risk for certain cancers, so you can start screening earlier and catch problems when they’re most treatable? It can also guide tailored care if you’re already diagnosed, helping your team choose medicines that target your tumor’s specific traits. For many families, results help loved ones decide if they should be tested too, turning knowledge into a plan for prevention.

Dr. Wallerstorfer Dr. Wallerstorfer

Outlook and Prognosis

Looking ahead can feel daunting, but most people want a clear picture of what to expect with cancer. Outlook depends on the cancer type, stage at diagnosis, how fast the cells are growing, and your overall health. Treatments have improved survival for many cancers over the past two decades, and some cancers now have five‑year survival rates above 90% when found early. Early symptoms of cancer can be subtle, so screening and prompt evaluation of changes—like a new lump, unexplained weight loss, or persistent cough—often lead to better outcomes.

Prognosis refers to how a condition tends to change or stabilize over time. For localized cancers caught early, surgery or focused radiation may be curative; once cancer has spread, combinations of chemotherapy, targeted drugs, immunotherapy, and radiation can still control disease for years. Mortality varies widely: some aggressive cancers carry higher short‑term risks, while others progress slowly and may never become life‑limiting. With ongoing care, many people maintain good quality of life through and after treatment, managing side effects with supportive therapies and lifestyle adjustments.

Talk with your doctor about what your personal outlook might look like. Your team can explain stage‑specific statistics, how your tumor’s features affect response to treatment, and whether clinical trials or genetic testing might refine predictions. Not everyone with the same gene change will have the same outlook, so numbers are guides, not guarantees. Understanding the prognosis can guide planning and help you focus on treatments and habits that support both length and quality of life.

Long Term Effects

Cancer can leave lasting effects that show up months or years after treatment, affecting energy, thinking, mood, and specific organs. Long-term effects vary widely, and they depend on the type of cancer, the treatments used, and your overall health. This is different from early symptoms of cancer, which often improve with treatment. Doctors often describe these as long-term effects or chronic outcomes.

  • Lasting fatigue: Tiredness may linger even after treatment ends. It can wax and wane and may not fully match how active you are.

  • Nerve changes: Tingling, numbness, or burning in hands or feet can follow certain drugs. These sensations may slowly improve, stay the same, or rarely progress.

  • Cognitive changes: Many notice forgetfulness, slower thinking, or trouble focusing after therapy. These changes often ease over time but can persist for some.

  • Heart strain: Some treatments can weaken the heart muscle or affect rhythms. Your care team may monitor heart function for years.

  • Lymphedema: Swelling of an arm, leg, or chest can occur when lymph nodes are removed or damaged during cancer care. It can appear months or years later and may need ongoing management.

  • Bone thinning: Therapies that lower hormones can speed bone loss. This raises fracture risk in the spine, hip, or wrist.

  • Fertility changes: Some treatments reduce sperm count or affect egg supply. Periods may become irregular or stop, and pregnancy planning may need specialist input.

  • Sexual health: People may experience pain, dryness, erectile changes, or lower desire. Body image shifts after cancer can also affect intimacy.

  • Chronic pain: Scars, joint stiffness, or nerve injury can cause ongoing pain. Gentle movement, medications, or procedures may help.

  • Secondary cancers: A small number develop a new, different cancer years after certain treatments. Lifelong screening plans aim to catch problems early.

  • Digestive issues: Bowel urgency, diarrhea, constipation, or reflux can follow surgery or radiation. Some notice food triggers and benefit from tailored nutrition plans.

  • Emotional health: Worry, low mood, or post-treatment anxiety can surface after cancer ends. Support from counseling, peers, or medication can make a real difference.

How is it to live with Cancer?

Living with cancer often means your days are organized around treatment cycles, energy levels, and checkups, with good stretches where you feel nearly yourself and tougher days when fatigue, pain, nausea, or “chemo brain” slow you down. Many people become masters of planning: pacing activity, protecting infection risk, managing symptoms, and carving out time for joy and normal routines. Loved ones may take on new roles—driving to appointments, helping with meals, or simply keeping company—and they feel the emotional weight too, which makes open communication and shared support important. With a care team, symptom control, and practical help at home and work, many find a steady rhythm that keeps life meaningful even during treatment.

Dr. Wallerstorfer Dr. Wallerstorfer

Treatment and Drugs

Cancer treatment aims to remove or control the tumor, stop it from spreading, and ease symptoms so daily life feels more manageable. Options often include surgery, chemotherapy, radiation therapy, targeted drugs, immunotherapy, and hormone therapy; the exact plan depends on the cancer type, stage, location, tumor genetics, and your overall health. Treatment plans often combine several approaches, and may be given before surgery (to shrink a tumor), after surgery (to lower the chance of return), or as long-term care to keep cancer in check. When treatment is tailored to your genes, it’s often called personalized medicine, and it can help match you with targeted or immune-based therapies that are more likely to work for your specific cancer. Side effects vary, and many are manageable—ask your doctor about the best starting point for you.

Non-Drug Treatment

Living with cancer often involves more than medicines alone. Alongside medicines, non-drug therapies can ease symptoms, protect function, and support everyday life at home and work. These options vary by cancer type, stage, and your goals, and your plan may change over time. If new issues arise—like fatigue, pain, or eating problems—ask early so support can be built in quickly.

  • Surgery: Removing a tumor can relieve pain, prevent blockages, or improve how a body part works. For some cancers, surgery aims to cure; for others, it reduces symptoms and improves comfort.

  • Radiation therapy: Focused beams target cancer areas to shrink tumors and ease pain or bleeding. It can be used alone or with other treatments, often in short daily sessions over several weeks.

  • Physical therapy: Targeted exercises help rebuild strength, balance, and endurance after treatment. Therapists teach safe ways to move and manage fatigue so daily tasks feel more doable.

  • Occupational therapy: Practical strategies make bathing, dressing, cooking, and work tasks safer and easier. Adaptive tools and energy-conservation tips help you save strength for what matters most.

  • Nutrition counseling: A dietitian helps with appetite loss, nausea, weight changes, or swallowing issues. Plans focus on foods you enjoy and can tolerate, plus supplements if needed.

  • Exercise programs: Gentle, regular activity can reduce fatigue, preserve muscle, and lift mood. Plans are tailored to your energy level, treatment schedule, and any movement limits.

  • Psychological counseling: Counseling can reduce anxiety, low mood, and sleep problems, and build coping skills. Options include one-on-one therapy, group support, or family sessions.

  • Pain procedures: Nerve blocks, spinal treatments, or targeted injections can relieve hard-to-control pain. These can lower the need for pain pills and improve activity and sleep.

  • Palliative care: A supportive team focuses on comfort, symptom relief, and quality of life at any stage. They help align care with your goals and support caregivers too.

  • Lymphedema therapy: Specialized massage, compression, and exercises help manage swelling after lymph node removal or radiation. Early care can prevent worsening and protect skin health.

  • Speech therapy: Therapists help with speech, voice, and swallowing changes after head, neck, or brain treatments. Strategies and exercises can make eating and communication safer and clearer.

  • Fertility counseling: Before treatment, specialists discuss options like egg, sperm, or embryo freezing. They also address timing, pregnancy safety, and family-building after therapy.

  • Smoking cessation: Quitting tobacco can improve healing, reduce treatment side effects, and lower recurrence risk. Support includes counseling, quit plans, and nicotine-replacement options.

  • Acupuncture: Fine needles placed at specific points may help with nausea, hot flashes, pain, or nerve symptoms. Ask your care team which issues it may help and how many sessions are typical.

  • Massage therapy: Gentle massage can ease muscle tension, anxiety, and sleep problems. Oncology-trained therapists adjust techniques for ports, surgical areas, and lymphedema risk.

  • Sleep support: A steady sleep routine, light exposure in the morning, and relaxing wind-down habits can improve rest. Better sleep often boosts energy and thinking during the day.

  • Symptom tracking: Keeping notes on pain, nausea, bowel habits, or early symptoms of cancer helps your team act quickly. Simple logs or apps can reveal patterns and triggers you might miss.

  • Social work support: Social workers help with transportation, work or school accommodations, insurance, and financial aid. They can connect you with local resources and support groups.

  • Sexual health therapy: Specialists address pain with sex, body-image changes, low desire, and intimacy concerns. Options may include lubricants, pelvic floor therapy, and communication strategies.

Did you know that drugs are influenced by genes?

Think of cancer drugs as tools that fit differently depending on a tumor’s genetic locks. Tumor and patient DNA can change how well a medicine works or how it’s processed, guiding choices about drug type, dose, and targeted or immunotherapy options.

Dr. Wallerstorfer Dr. Wallerstorfer

Pharmacological Treatments

Medicines for cancer include chemotherapy, targeted therapies, immunotherapies, and hormone blockers, often used alone or in combination. Treatment is tailored to the cancer type, stage, biomarker results, your health, and how you handled earlier care and even early symptoms of cancer. Not everyone responds to the same medication in the same way. Your oncology team also uses supportive drugs to prevent or ease side effects so you can stay on treatment.

  • Platinum drugs: Cisplatin, carboplatin, and oxaliplatin damage cancer cell DNA so the cells can’t divide. They’re used in many solid tumors, sometimes with other drugs.

  • Taxanes: Paclitaxel, docetaxel, and nab‑paclitaxel stop cancer cells from dividing by freezing their internal “skeleton.” Common uses include breast, lung, and ovarian cancers.

  • Anthracyclines: Doxorubicin and epirubicin block enzymes cancer cells need to copy DNA. Doctors monitor heart health during treatment and may limit lifetime dose.

  • Antimetabolites: 5‑fluorouracil, capecitabine, gemcitabine, and pemetrexed disrupt DNA building blocks. They’re common in colorectal, pancreatic, and lung cancer care.

  • Topoisomerase inhibitors: Irinotecan and etoposide interfere with DNA unwinding in tumor cells. These drugs often pair with others in multi‑drug regimens.

  • Alkylating agents: Cyclophosphamide, ifosfamide, bendamustine, and temozolomide damage DNA so cancer cells die. They’re used across blood cancers and some solid tumors.

  • EGFR inhibitors: Erlotinib, gefitinib, afatinib, and osimertinib target tumor cells driven by EGFR signals. Testing guides who is most likely to benefit.

  • HER2‑targeted therapy: Trastuzumab, pertuzumab, trastuzumab deruxtecan, and T‑DM1 focus on HER2‑positive cancers. They can shrink tumors and lower the chance of recurrence.

  • VEGF pathway blockers: Bevacizumab and ramucirumab cut off tumor blood supply. These drugs are often added to chemotherapy for several advanced cancers.

  • BRAF/MEK inhibitors: Dabrafenib plus trametinib or encorafenib plus binimetinib target BRAF‑mutated tumors. Matching the drug to the mutation is essential.

  • ALK and ROS1 inhibitors: Alectinib, lorlatinib, and crizotinib block growth signals in certain lung cancers. These tablets can control disease for extended periods.

  • PARP inhibitors: Olaparib, niraparib, rucaparib, and talazoparib exploit DNA‑repair weaknesses in some ovarian, breast, pancreatic, and prostate cancers. They’re often used as maintenance therapy after chemotherapy.

  • CDK4/6 inhibitors: Palbociclib, ribociclib, and abemaciclib slow cell‑cycle engines in hormone receptor–positive breast cancer. They’re usually combined with endocrine therapy.

  • BTK inhibitors: Ibrutinib, acalabrutinib, and zanubrutinib target B‑cell signaling in CLL and some lymphomas. Many take these as daily pills over months to years.

  • PD‑1/PD‑L1 immunotherapy: Pembrolizumab, nivolumab, atezolizumab, and durvalumab help the immune system recognize cancer. They can work for a long time, though immune‑related side effects need prompt attention.

  • CTLA‑4 inhibitor: Ipilimumab removes a brake on immune cells so they can attack tumors. It may be combined with PD‑1 drugs in melanoma and other cancers.

  • CAR‑T cell therapy: Tisagenlecleucel and axicabtagene ciloleucel re‑engineer your own immune cells to fight blood cancers. These are given in specialized centers with close monitoring.

  • Breast hormone therapy: Tamoxifen, anastrozole, letrozole, and exemestane lower or block estrogen in hormone receptor–positive breast cancer. They reduce recurrence risk and are often taken for 5–10 years.

  • Prostate hormone therapy: Leuprolide, goserelin, degarelix, abiraterone, and enzalutamide lower or block testosterone signals. These drugs can control advanced prostate cancer and ease symptoms.

  • Antinausea medicines: Ondansetron, aprepitant, and olanzapine help prevent chemotherapy‑related nausea. Good control allows many to continue treatment comfortably.

  • White‑cell boosters: Filgrastim and pegfilgrastim lower the risk of infection by raising neutrophil counts after chemotherapy. This support can keep cancer care on schedule.

  • Bone‑strengthening drugs: Zoledronic acid and denosumab protect bones when cancer has spread or when hormone therapy thins bone. They also lower the risk of painful fractures.

Genetic Influences

Genes can influence how likely someone is to develop cancer, but they’re only part of the picture. Most cancer happens because of gene changes that build up over a lifetime, while a smaller share—about 5 to 10 percent—comes from gene changes you inherit at birth. When inherited, certain well-known genes, such as BRCA1/BRCA2 or those linked to Lynch syndrome, can raise the risk for specific cancers in a family. Family history is one of the strongest clues to a genetic influence. If several relatives developed cancer at younger-than-usual ages, or the same kind of cancer appears across generations, that pattern may point to an inherited risk. Genetic counseling and, when appropriate, genetic testing for cancer risk can clarify your personal risk and guide screening or prevention plans, and many people with an inherited change never develop cancer.

How genes can cause diseases

Humans have more than 20 000 genes, each carrying out one or a few specific functiosn in the body. One gene instructs the body to digest lactose from milk, another tells the body how to build strong bones and another prevents the bodies cells to begin lultiplying uncontrollably and develop into cancer. As all of these genes combined are the building instructions for our body, a defect in one of these genes can have severe health consequences.

Through decades of genetic research, we know the genetic code of any healthy/functional human gene. We have also identified, that in certain positions on a gene, some individuals may have a different genetic letter from the one you have. We call this hotspots “Genetic Variations” or “Variants” in short. In many cases, studies have been able to show, that having the genetic Letter “G” in the position makes you healthy, but heaving the Letter “A” in the same position disrupts the gene function and causes a disease. Genopedia allows you to view these variants in genes and summarizes all that we know from scientific research, which genetic letters (Genotype) have good or bad consequences on your health or on your traits.

Pharmacogenetics — how genetics influence drug effects

Cancer treatment today is increasingly tailored to the genes found in the tumor and, in some cases, to your own inherited genes. If the cancer carries certain changes—such as EGFR or ALK in some lung cancers, HER2 in some breast cancers, or BRAF in melanoma—targeted medicines are chosen because they act on those specific changes. Your genes can also affect how your body handles chemotherapy, which can influence dose and side effects. For example, variants in the DPYD gene can make it harder to break down 5-fluorouracil or capecitabine, and changes in UGT1A1 can raise the risk of side effects with irinotecan; testing can guide safer starting doses. In many European centers, DPYD testing before 5-FU is common, and it is increasingly used in the United States as well. Genetics is only one factor, though—age, liver and kidney health, and other medicines matter too. Used with the rest of your medical history, pharmacogenetic testing for cancer treatment can help doctors match the drug and dose more precisely.

Interactions with other diseases

Cancer often occurs alongside other health conditions, which can change how symptoms feel and how treatments work. Doctors call it a “comorbidity” when two conditions occur together, and this pairing can affect safety, side effects, and recovery. For example, diabetes can raise infection risk and slow wound healing during cancer surgery, while steroids used to control chemotherapy side effects may spike blood sugar. Heart or lung disease can complicate cancer care too, since some chemotherapy and radiation treatments stress the heart or make breathlessness worse, and the higher risk of blood clots in cancer may interact with blood thinners. Long-term kidney or liver problems may limit which cancer medicines are safe, and chronic infections like HIV or hepatitis can both increase the chance of certain cancers and heighten infection risks when the immune system is suppressed. Autoimmune conditions may flare with modern immunotherapy, so teams often adjust dosing, add preventive medicines, or choose alternative treatments. These overlaps can also blur early symptoms of cancer, so coordinated care and clear communication between your cancer team and other specialists helps tailor a plan that fits your whole health.

Special life conditions

Cancer can affect daily life differently at various stages and life events. During pregnancy, some cancers can still be safely treated with carefully chosen medicines or surgery, while imaging and certain drugs are timed to protect the baby; a team that includes obstetrics and oncology helps balance both needs. Children with cancer often have faster-growing tumors but also respond well to tailored treatments; families may notice school routines shift, and growth, learning, and fertility protection are part of long-term planning. Older adults with cancer may have other health conditions or take several medicines, so doctors weigh benefits and side effects closely and sometimes choose gentler options to keep independence and quality of life. Active athletes and highly active people with cancer can usually stay moving, but intensity often needs to be adjusted around fatigue, anemia, or low immunity; working with the care team helps set safe targets. Not everyone experiences changes the same way, and early symptoms of cancer may be subtle across all ages, so new, persistent changes—like unexplained weight loss, a lump, or unusual bleeding—warrant timely medical advice. Talk with your doctor before major life events, travel, or training changes, as planning ahead can help treatments fit more smoothly into your routine.

History

Throughout history, people have described stubborn swellings that did not heal, deep aches that worsened at night, or an unexpected lump that slowly grew despite poultices and rest. A trader might have noticed a hard node in the neck after a winter cough; a farmer might have found blood in the stool and growing fatigue during harvest. Families quietly compared notes: an aunt with a breast mass in midlife, a grandfather with a sore on his lip that would not close. These everyday details, passed down in letters and clinic notes, formed the earliest map of what we now call cancer.

Ancient surgeons in Egypt, Greece, India, and China recorded tumors they could see or feel and sometimes cut away with knives or hot irons. Some described growths as “crab-like,” a term that echoed the way the disease seemed to cling to nearby tissues. Without microscopes, they relied on the pattern of symptoms and what happened after surgery. Many people did well after a small lump was removed; others returned months later with pain, weight loss, or new lumps nearby, hinting that the illness could spread beyond the first spot.

In the 17th and 18th centuries, autopsies revealed hidden growths in organs like the liver, brain, and lungs. Doctors began to recognize that cancer could travel from a starting point to distant sites. The 19th century brought the microscope, and with it the ability to see disordered cells. Pathologists learned to tell one tumor from another by cell shape and arrangement, which helped explain why cancers behave differently depending on where they begin and how fast their cells divide. Surgery became safer as anesthesia and infection control improved, allowing wider, more precise operations.

By the early 20th century, X-rays and then radium introduced radiation therapy, offering a way to treat tumors that could not be reached by a scalpel. Chemotherapy emerged mid-century after observations that certain chemicals slowed fast-dividing cells. Screening programs followed: the Pap test reduced deaths from cervical cancer; mammography found breast cancers earlier; colonoscopy allowed removal of precancerous polyps. Public health efforts linked tobacco to lung cancer and workplace exposures to specific tumors, shaping prevention.

Late in the 20th century and into the 21st, genetics and molecular biology reframed cancer as a disease of altered cell signals—genes acting more like stuck accelerators or failed brakes. Advances in genetics clarified why cancers run in some families and why tumors in the same organ can behave very differently. Targeted drugs began to home in on specific changes inside cancer cells, and immunotherapies taught the immune system to better recognize and attack them. Today, pathologists often pair what they see under the microscope with genetic testing of the tumor to guide treatment.

Looking back helps explain why cancer care now blends prevention, early detection, and increasingly tailored treatments. The story stretches from careful bedside notes to modern lab tools, and each step has pushed survival higher for many cancers while reminding us that progress comes from combining human observation with science.

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