A national overview covering the 26 most common adult cancers, the leading pediatric cancers, and the prevention pillars that shape outcomes. This is the umbrella page over the entire FFH Cancer Dashboard Family — start here, drill down to the cancer that matters most to you or your community.
When most sources (CDC, ACS, NCI) say "rates" they mean incidence — new diagnoses per 100,000 people per year. That's NOT the same as deaths. A high-incidence cancer can be highly survivable; a lower-incidence cancer can be much deadlier. Always check which number is being shown.
📍 On this page: numbers are INCIDENCE (new cases/yr) unless the column or label explicitly says "deaths" or "mortality." Survival rates are 5-year relative survival.
Cancer starts at the DNA level. Three categories of genes go wrong: oncogenes (promote growth — when broken, they're stuck "on"), tumor-suppressor genes (apply brakes — when damaged, no brakes), and DNA-repair genes (fix copy errors — when broken, errors accumulate exponentially).
Most adult cancers need 5-7 different gene mutations to fully form. That's why cancer takes years to develop — and why prevention works: every year you avoid carcinogens is a year of mutations you don't accumulate.
📊 Data sources NCI — Cancer Biology Hallmarks of Cancer (Hanahan & Weinberg) NIH — How Cancer StartsCancer is a disease of cellular control failure. Every cell in the body follows a set of rules: when to grow, when to divide, when to repair, when to die. Cancer happens when those rules break. Damaged DNA accumulates, normal control systems fail, and cells start growing where they shouldn't, dividing when they shouldn't, and surviving long past when they should have died.
The result is a tumor (a mass of abnormal cells) that can stay local (benign), invade nearby tissue (malignant), or spread through blood or lymph to distant organs (metastatic). Cancer is named by where it starts — breast cancer that spreads to bone is still breast cancer, not bone cancer. There is no single disease called "cancer." There are more than 200 distinct types, each with its own biology, risk factors, screening tests, and treatments.
Mutations in genes that control growth (oncogenes), repair (tumor suppressors), and death (apoptosis) accumulate over time.
Most adult cancers develop over 10-20+ years before becoming detectable. This is why prevention + early screening work.
A risk factor raises the odds, but doesn't guarantee cancer. Most people with risk factors never develop cancer; some with no risk factors do.
The American Cancer Society estimates ~40% of cancer cases and ~50% of cancer deaths in the US are linked to modifiable risks (smoking, weight, alcohol, sun, infection, screening).
Each FFH Cancer Dashboard surfaces national + state + county data, screening guidance, and the prevention plays that move the needle for that specific cancer. Live dashboards have full data + Reality Health Games tied in. Upcoming dashboards will follow the same template — usually 4-6 weeks build per cancer.
If you don't see your cancer dashboard yet, use the 26-cancers grid below for the data, then come back when the full dashboard launches. Want to sponsor a specific cancer dashboard build? Reach out to Coach Lucy.
FFH builds cancer-specific dashboards on a rolling schedule. Each dashboard covers incidence, mortality, screening, survival, prevention plays, and Reality Health Games tied to that cancer. Live dashboards are linked. Upcoming dashboards show the build window.
FFH × Larry Fitzgerald Foundation
LIVENational + state + county data wired in
LIVEAdjacent — blood disorder umbrella
#1 cancer killer · highest preventability via tobacco cessation
Most common in men · PSA screening 50-70
Silent killer · BRCA-linked · My Girl Power™ Series
HPV-driven · highly preventable via vaccine + screen
UV-driven · sun-protection prevention plays
Adult + pediatric crossover · blood-cancer umbrella
Umbrella dashboard for childhood cancers
Bladder, kidney, thyroid, NHL, pancreatic, liver, etc.
New cases (incidence) tells you how common a cancer is. 5-year relative survival tells you how survivable it is when caught + treated. Read them together.
High-incidence + high-survival cancers (breast, prostate, thyroid, melanoma) → screening saves lives at scale. Lower-incidence + low-survival cancers (pancreatic, liver, esophageal) → prevention & risk-factor modification are more impactful than screening because we don't yet have great early-detection tests.
The grid is sorted by incidence (most common first). Stars (⭐) mark cancers with a live FFH dashboard. Click any card to drill in.
📊 Data sources ACS Cancer Facts & Figures 2026 NCI SEER Cancer Stat Facts CDC US Cancer Statistics (USCS) CDC USCS At A GlanceEstimated 2026 new cases (incidence) + 5-year relative survival rates from American Cancer Society + NCI SEER. Sorted by incidence — most common first. ⭐ marks cancers with a live FFH dashboard.
Estimated annual new cases per ACS Cancer Facts & Figures 2026 (projected) + NCI SEER. Survival rates are 5-year relative survival, all stages combined, SEER 2014-2020. Numbers are estimates and update annually.
The biggest cancer story of the last 25 years isn't just incidence — it's direction. Cancers that respond to prevention plays (lung from tobacco cessation, cervical from HPV vaccine + Pap, stomach from H. pylori treatment, colorectal in age 50+ from screening) have plummeted. Cancers driven by obesity, alcohol, infections, environmental exposure, and overdiagnosis from imaging have surged.
The most concerning recent shift is young-onset cancer: colorectal, breast, pancreatic, and kidney cancers are rising in adults under 50 for reasons researchers are still investigating. Diet, microbiome, environmental exposure, obesity, and antibiotics are all under study.
📊 Data sources NCI SEER Cancer Statistics Review NCI Cancer Trends Progress Report CDC MMWR — Cancer Trends ACS — Annual Report to the Nation 2024 Lancet Public Health — Young-Onset Cancer TrendsUS age-adjusted incidence trends from NCI SEER + ACS Annual Report to the Nation. Approximate cumulative % change over each window. Toggle the period to see how the picture shifts.
Even as overall cancer rates fall in adults 50+, cancers in adults under 50 are rising sharply. Researchers don't yet have a complete answer for why — leading candidates: obesity, dietary changes, microbiome shifts, environmental exposures, antibiotic use in childhood, and sedentary lifestyle from earlier ages.
Cancer is now the global #2 cause of death (after cardiovascular disease) — and projected to be #1 in low + middle income countries by 2030 as infectious diseases come under control and populations age. Today: ~20M new cases / yr · ~9.7M deaths / yr globally. By 2050: projected ~35M cases / yr, with the steepest rise in Africa, Asia, and Latin America.
The disparity is brutal: high-income countries have ~2× the incidence of low-income countries — but low-income countries have higher mortality because diagnosis comes later and treatment access is limited. The same cervical cancer that's nearly eliminated in Australia (HPV vaccine + screening) still kills women routinely in sub-Saharan Africa.
📊 Data sources WHO IARC GLOBOCAN 2022 IARC World Cancer Day Statistics WHO Cancer Fact Sheet Lancet Global Burden of Disease — CancerThe world has roughly 20 million new cancer cases each year and 9.7 million cancer deaths. The most common globally: lung, breast, colorectal, prostate, stomach. Trends and disparities vary sharply by region.
Click a region to see top cancers + what's driving the trend.
Childhood cancer is biologically different from adult cancer. Adult cancers are mostly driven by accumulated lifestyle exposures over decades — smoking, sun, weight, alcohol. Childhood cancers don't have time for that. They tend to be driven by random genetic mistakes during rapid early-life cell division, plus rare inherited conditions.
What makes pediatric oncology hopeful: survival rates have transformed since 1975, when 5-year survival was ~58%. Today it's ~85%. That's one of the biggest medical achievements of the past 50 years — driven by clinical trials, multidisciplinary care, and pediatric oncology centers.
The hard reality: survivors face long-term side effects (heart, fertility, secondary cancers, learning challenges) that play out over decades. Survivorship care is part of the cancer fight, not the end of it.
📊 Data sources ACS — Cancer in Children + Adolescents NCI SEER Cancer Statistics Review St. Jude Children's Research Hospital CureSearch — Pediatric Cancer ResearchCancer in children + adolescents (ages 0-19) is rare compared to adult cancer — but it's the leading cause of disease-related death in children past infancy. The biology is different, the treatments are different, and the FFH approach treats pediatric cancer as its own dashboard family.
Roughly 16,000 children and adolescents (ages 0-19) are diagnosed with cancer each year in the US. About 1,800 die annually. Survival has dramatically improved over 50 years — but treatment side effects can persist into adulthood, making survivorship care critical.
FFH dashboard build target: Q2 2027 · The Pediatric Cancers umbrella will integrate with the My Girl Power™ Series and FFH Foundation's pediatric scholarship pathway. Sponsored builds welcomed earlier.
Per Dr. Rob's classification system used across all FFH dashboards: only family history, age, biological sex, race/ancestry, and congenital conditions are non-modifiable. Everything else is on the modifiable list — and that's where prevention lives.
Obesity, diabetes, smoking, sedentary lifestyle, alcohol, sun exposure, and infection (HPV, Hepatitis, H. pylori) — all modifiable. Get them right and you knock out a meaningful percentage of your lifetime cancer risk before it starts.
The American Cancer Society estimates roughly 40% of cancer cases and 50% of cancer deaths in the US are linked to modifiable risk factors. Prevention isn't theoretical — it's quantified. Here's the full split.
The table below shows guidelines for average-risk adults. If you have family history, BRCA mutation, Lynch syndrome, prior radiation, or any other elevated-risk condition, screening starts earlier and happens more often. Always discuss with your doctor.
The 5 cancers with screening that demonstrably reduces mortality: breast, cervical, colorectal, lung (in smokers), and prostate (with shared decision-making). Other cancers (ovarian, pancreatic, etc.) don't yet have effective population-wide screening — that's where prevention + symptom awareness matter most.
📊 Data sources USPSTF Recommendations ACS Screening by Age CDC Cancer ScreeningScreening guidelines for average-risk adults · per USPSTF (US Preventive Services Task Force) + ACS (American Cancer Society). High-risk individuals start earlier + screen more often.
| Cancer | Test | Start Age | Frequency |
|---|---|---|---|
| 🎀 Breast (women) | Mammography | 40 | Every 2 yrs (USPSTF 2024) · annual under ACS |
| 💙 Colorectal | Colonoscopy / FIT / Cologuard | 45 | Colonoscopy every 10 yrs · FIT yearly |
| 💗 Cervical | Pap smear / HPV test | 21 | Pap every 3 yrs (21-29) · HPV co-test every 5 yrs (30-65) |
| 🫁 Lung (smokers) | Low-dose CT | 50 | Annual · 50-80, 20+ pack-year smoking history |
| 💜 Prostate (men) | PSA blood test | 50 | Discuss with doctor · 45 if Black or family history |
| ⬛ Skin / Melanoma | Self-exam (ABCDE) · clinical exam | Any age | Self-exam monthly · clinical annual if higher risk |
| 🩸 Oral | Visual exam during dental visit | Any age | Annual dental exam includes oral cancer screen |
| 🟢 Liver (high risk) | Ultrasound + AFP | Variable | Every 6 months for cirrhosis or chronic Hep B |
| 🩺 Gynecologic (women) | Pelvic exam · symptom awareness | Any age | Annual well-woman visit · know ovarian/endometrial symptoms |
Guidelines for average-risk adults. ACS and USPSTF recommendations occasionally differ — discuss with your physician. If you have family history, known mutations, or prior cancer, your screening schedule will be different.
Treatment is decided by a multidisciplinary tumor board — surgeon, medical oncologist, radiation oncologist, pathologist, often radiology + palliative care all in the room. They look at: cancer type, stage (I-IV), tumor biology + biomarkers (HER2, EGFR, BRCA, PD-L1, MSI, KRAS, etc.), patient age + fitness, comorbidities, and patient preferences.
The shift over the past 15 years: from "one-size-fits-all" chemo to biomarker-driven precision treatment. A breast cancer patient today gets a different drug regimen based on whether her tumor is HER2+/-, hormone+/-, or triple-negative. Same for lung (EGFR/ALK/ROS1) and many others.
Always ask about clinical trials. Many of today's standard-of-care drugs were trials 5-10 years ago.
📊 Data sources NCCN Treatment Guidelines ASCO — American Society of Clinical Oncology ClinicalTrials.govMost cancer treatment plans combine more than one of these. The right combination depends on cancer type, stage, biology, age, and patient preferences.
Removing the tumor + nearby tissue. Often first-line for solid tumors caught early. Curative when cancer is localized.
Oldest pillarDrugs that kill rapidly dividing cells. Used systemically for cancers that have spread or to shrink tumors before/after surgery.
SystemicHigh-energy beams that damage cancer cell DNA. Local treatment for tumors that can't be surgically removed or to clean up margins.
LocalDrugs designed to attack specific genetic mutations or proteins in cancer cells (e.g., HER2 in breast, EGFR in lung, BRAF in melanoma). Less collateral damage than chemo.
PrecisionDrugs that unleash or train the patient's own immune system to attack cancer (checkpoint inhibitors, CAR-T, monoclonal antibodies). Transforming melanoma, lung, kidney, lymphoma outcomes.
Newest pillarHormone-blocking drugs for hormone-sensitive cancers (breast, prostate, endometrial). Plus stem-cell transplant, photodynamic, ablation, and emerging modalities.
Cancer-specificBlack Americans have the highest cancer mortality rate of any racial/ethnic group in the US across most cancers — even when incidence is lower (as in breast). Drivers are mostly access + screening + treatment delays, not biology.
Hispanic + Asian populations have lower overall cancer rates but higher rates for specific cancers (liver, stomach, gallbladder, cervical) often tied to infection patterns + immigration history.
The disparity story is the story of access: who gets screened, who gets diagnosed early, who gets to a high-quality cancer center, who can afford treatment. Move those, and the numbers move.
All-cancer-combined incidence rates per 100,000 (age-adjusted) by race/ethnicity. Mortality rates tell a sharper disparity story than incidence.
SEER 2017-2021. White and Black incidence are similar overall — but specific cancer types vary widely.
⚠️ Black Americans have the highest cancer mortality of any racial/ethnic group despite similar incidence to white Americans. That's the disparity story in one chart.
The PHIT cancer sub-score weights 8 inputs because each one independently predicts outcomes: incidence + mortality (the headline numbers), screening adherence (catches cancer early), early-stage diagnosis rate (best stage-shift indicator), the disparity gap (equity floor), HPV vaccination + tobacco + obesity rates (the three biggest preventable drivers).
What's not in the score: alcohol consumption, environmental exposures, family-history density. Those move slowly and don't have reliable county-level data. If a county wants to move its PHIT score, the fastest levers are screening adherence + tobacco + obesity — not changing the underlying disease biology.
📊 Data sources County Health Rankings CDC PLACES Data ACS — Cancer Action Network State ReportsFFH's Public Health Improvement Tool (PHIT) Score rolls cancer-specific outcomes into the county + state composite. Cancer sub-indicators include incidence, mortality, screening adherence, early-stage diagnosis rate, and the Black:White mortality gap. PHIT lets you compare any county against state + national benchmarks in one glance.
Each individual cancer dashboard surfaces its own PHIT sub-score so a county can see, for example, "we're average overall but our breast cancer screening rate is in the bottom 20% — that's where to invest." Cancer ZIP-code lookup launches in the breast cancer + colon cancer dashboards now.
The four authoritative cancer-statistics sources in the US are: ACS Cancer Facts & Figures (annual, projected estimates), NCI SEER (gold-standard registry data, 2-3 year lag), CDC USCS (covers ~98% of US population), and the Annual Report to the Nation (NCI + CDC + ACS + NAACCR consensus, published yearly).
Numbers don't always match across sources because they use different reference periods, different age-adjustment standards, and different statistical models. Don't worry about ±5% differences — focus on direction and magnitude.
Be cautious of: blog/social-media "statistics" without primary sources, projections more than 5 years out (uncertainty grows fast), and any number that doesn't specify incidence vs mortality vs survival.
📊 Data sources ACS Cancer Facts & Figures NCI SEER CDC US Cancer Statistics Annual Report to the NationUse this overview to understand the landscape — then drill into the dashboard for the cancer that matters most to you, your family, or your community. The Force for Health Network builds dashboard-by-dashboard because each cancer has its own story, its own data, and its own prevention plays. Start where you are.