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JNCI Journal of the National Cancer Institute logoLink to JNCI Journal of the National Cancer Institute
. 2024 Jul 13;116(11):1784–1790. doi: 10.1093/jnci/djae135

Prevalence of cancer survivors in the United States

Emily Tonorezos 1,, Theresa Devasia 2, Angela B Mariotto 3, Michelle A Mollica 4, Lisa Gallicchio 5, Paige Green 6, Michelle Doose 7, Rachelle Brick 8, Brennan Streck 9, Crystal Reed 10, Janet S de Moor 11
PMCID: PMC11542986  PMID: 39002121

Abstract

Background

With aging of the population and improvements in diagnosis, treatment, and supportive care, the number of cancer survivors in the United States has increased; updated prevalence estimates are needed.

Methods

Cancer prevalence on January 1, 2022, was estimated using the Prevalence Incidence Approach Model, utilizing incidence, survival, and mortality. Prevalence by age decade, sex, and time from diagnosis was calculated. The percentage of cancer survivors in the projected US population by age and sex was calculated as the ratio of the sex-specific projected prevalence to the sex-specific projected US population.

Results

There were an estimated 18.1 million US cancer survivors as of January 1, 2022. From 2022 to 2030, the number of US cancer survivors is projected to increase to 21.6 million; by 2040, the number is projected to be 26 million. Long-term survivors are highly prevalent; in 2022, 70% of cancer survivors had lived 5 years or more after diagnosis, and 11% of cancer survivors had lived 25 years or more after diagnosis. Among all US females aged 40-54 years, 3.6% were cancer survivors; among females aged 65-74 years, 14.5% were cancer survivors; among females aged 85 years and older, 36.4% were cancer survivors. Among all US males aged 40-54 years, 2.1% were cancer survivors; among males aged 65-74 years, 16% were cancer survivors; and among those aged 85 years and older, 48.3% were cancer survivors.

Conclusions

Cancer survivors are growing in number. In the United States, most cancer survivors are long-term and very long-term survivors, representing a substantial proportion of the US population.


In the United States, more than 1 in 3 people will be diagnosed with cancer in their lifetime (1). This population, known as cancer survivors (2), is growing, in part because the underlying population is older now than in prior decades. The probability of developing invasive cancer is nearly 10 times higher for adults aged 70 years and older compared with those aged 49 years and younger (1). At the same time, improvements in screening, diagnosis, treatment, and supportive care have led to longer survival (3-5). As a result, the number of cancer survivors has been increasing steadily over the past 50 years—a trend that has been well documented and is expected to continue (6-8).

Cancer survivors represent a heterogeneous population with a variety of health-care needs. Cancer site, stage, and treatment inform the risks for long-term and late effects from treatment, while ongoing screening, surveillance, and follow-up care are necessary (8,9). Some of the most common late effects include fatigue, frailty, cognitive impairment, chemotherapy-induced peripheral neuropathy, ovarian failure or infertility, psychological distress, cardiotoxicity, and second cancers (10,11). In addition, the majority of cancer survivors are older adults for whom the ongoing need for survivorship care intersects with the demands of aging (8,12). Simultaneously, the oncology workforce is shrinking (13), and many regions of the United States represent health-care deserts (14). Several federal agencies are leading an effort to write survivorship standards, intended to represent expected or required elements of survivorship care. Yet, attainment of this type of care is difficult, inadequate, or incomplete (15-17). The survivor population is aging, growing in complexity, and living without access to risk-based follow-up care (6,18,19).

More than 10 years ago, a detailed description of the overall population of US cancer survivors was published, with updates since then emphasizing the proportion of survivors who are older adults. Therefore, an updated, detailed description of the population of cancer survivors living in the United States, including the estimated number of individuals and the expected trends in these statistics, is critically needed (7). In addition, the proportion of the US population represented by cancer survivors has not previously been calculated. The emphasis of this work is on the trends in long-term cancer survivorship and the public health implications of a proportion of the US population with a history of a diagnosis of cancer.

Methods

Statistical analysis

Cancer prevalence as of January 1, 2022, was estimated using the Prevalence Incidence Approach Model (PIAMOD). PIAMOD calculates prevalence from cancer survival, cancer incidence, and all-cause mortality data (20). Incidence and survival data from the Surveillance, Epidemiology, and End Results (SEER) Program, all-cause mortality data from the National Center for Health Statistics, and US Census Bureau population estimates were obtained from the SEER*Stat software (SEER*Stat Software v 8.3.9, version 8.3.5) and used in the calculation of prevalence estimates.

SEER-9 incidence rates from 1975 to 1999 and SEER-18 incidence rates from 2000 to 2018 were applied to US population estimates to obtain US incidence counts by calendar year, age (single-year and age 90 years and older), and cancer type. For each cancer site, counts were restricted to the first primary invasive case diagnosed in a person, except urinary bladder, which included in situ cases. Relative survival from 1975 to 2017 was obtained from SEER-9 registries by sex, age group (0-54, 55-64, 65-74, 75-84, 85-99 years), and year of diagnosis (1975-1984, 1985-1989, …, 2005-2009, 2010-2017). Survival estimates excluded cancers diagnosed through death certificate or autopsy and cases that were lost to follow-up at the month of diagnosis. Prevalence proportions for ages 85-89 years were used to estimate prevalence counts for the population aged 90 years and older. To ensure that PIAMOD estimates were consistent with other published prevalence figures (such as those in SEER*Explorer), which employ a simpler methodology with fewer assumptions and are more closely aligned with observed data, adjustment factors were applied to the PIAMOD estimates. These adjustment factors were calculated by comparing the 2018 prevalence estimates from SEER*Explorer and PIAMOD, broken down by cancer type and sex (21).

The 2017 US Census Bureau National Population Projections (22), which are based on the 2010 Census, were used to project US incidence and mortality for 2019-2040 by applying the 2016-2018 average rates by age, sex, and cancer site to the US population projections (8). Using PIAMOD, prevalence for each cancer site was projected from 2019 to 2040 using projected incidence and mortality, survival for the period 2010-2017 (future survival was assumed to remain constant), and US Census population projections. Prevalence projections for 2019 through 2040 were calibrated to 2018 complete prevalence by applying the cancer- and sex-specific adjustment factors.

Prevalence was quantified by age group (0-9, 10-19, …, 70-79, 80 years and older) and sex for each cancer site. PIAMOD also provides estimates of prevalence by years since diagnosis for each calendar year of diagnosis. In our analysis, we focused on survivors living 0 to less than 1 year, 1 to less than 5 years, 5 to less than 10 years, 10 to less than 15 years, 15 to less than 20 years, 20 to less than 25 years, and 25 years or more postdiagnosis. The percentage of cancer survivors in the projected US population by sex was calculated as the ratio of the sex-specific projected prevalence to the sex-specific projected US population.

Results

Current survivorship prevalence and projections through 2040

There were an estimated 18.1 million people in the United States diagnosed with cancer as of January 1, 2022. This represents a nearly fourfold increase compared with the mid-1970s. From 2022 to the end of the decade (2030), the number of survivors is projected to increase to 21.6 million; by 2040, the number of cancer survivors living in the United States is projected to be 26 million, representing a 43.6% increase compared with 2022 (Figure 1).

Figure 1.

Figure 1.

Number of cancer survivors living in the United States by year and time since diagnosis in years (duration). M = million.

Among the current population of cancer survivors, 70% of cancer survivors have survived 5 years or more after diagnosis, 48% of cancer survivors have survived 10 years or more after diagnosis, 19% of cancer survivors have survived 20 years or more after diagnosis, and 11% of cancer survivors have survived 25 years or more after diagnosis.

These trends are estimated to continue. From 2022 to 2040, the number of survivors who are fewer than 5 years from diagnosis will increase from 5.5 million to 6.8 million (24%). During this same period, the number of survivors who are 5 or more years from diagnosis will increase from 12.6 million to 19.2 million (53%). From 2022 to 2040, survivors who are 5 or more years from diagnosis will grow to represent 74% of all survivors, with a corresponding decrease in relative proportion of survivors who are fewer than 5 years from diagnosis. The largest relative increase in number of cancer survivors by time since diagnosis is among people who are 15 or more years from diagnosis. Among this group, prevalence is expected to increase from 5.6 million (31%) of all survivors in 2022 to 10.4 million (40%) of all survivors in 2040.

Characteristics of cancer survivors in the United States

Table 1 describes survivorship prevalence by cancer site for the top 10 most common cancers among males and females, stratified by age and sex. The most prevalent cancer sites are breast (4 million survivors), prostate (3.5 million survivors), melanoma (1.5 million survivors), colorectal (1.4 million survivors), and thyroid (1.1 million survivors). For all sites, the number of survivors is higher with older age, while more than 78% of survivors currently living in the United States are age 60 years or older. Across cancer sites, a higher proportion of cancer survivors are females than males, except for adults ages 70-79 years among whom male survivors outnumber female survivors.

Table 1.

Estimated number of cancer survivors by age, gender, and cancer site for the 10 most common cancers as of January 1, 2022

Age, y
Site Sex All ages 0-9 10-19 20-29 30-39 40-49 50-59 60-69 70-79 80 and older
All sites Male 8 321 203 17 190 41 193 91 550 180 186 327 067 876 204 2 071 665 2 613 319 2 102 829
Female 9 738 892 17 046 40 885 97 221 253 238 581 775 1 360 802 2 398 887 2 529 966 2 459 072
Total 18 060 095 34 236 82 078 188 771 433 424 908 842 2 237 006 4 470 552 5 143 285 4 561 901
Bladder Male 597 877 50 135 573 2293 8166 35 985 117 770 203 091 229 814
Female 191 854 22 60 280 927 2879 11 371 35 213 58 369 82 733
Total 789 731 72 195 853 3220 11 045 47 356 152 983 261 460 312 547
Breast Male a
Female 4 055 775 2 20 3271 44 053 204 968 570 793 1 030 059 1 109 526 1 093 083
Total 4 055 775 2 20 3271 44 053 204 968 570 793 1 030 059 1 109  526 1 093  083
Colorectal Male 729 071 8 306 2060 7923 26 177 85 075 179 741 216 975 210 806
Female 710 673 23 452 2381 7645 23 300 70 652 145 691 190 395 270 134
Total 1 439 744 31 758 4441 15 568 49 477 155 727 325 432 407 370 480 940
Kidney Male 376 273 1531 2274 2425 5675 18 321 54 481 105 790 110 491 75 285
Female 230 956 1571 2656 2969 5238 12 010 29 802 56 527 62 350 57 833
Total 607 229 3102 4930 5394 10 913 30 331 84 283 162 317 172 841 133 118
Lung Male 287 058 6 22 104 618 3956 23 565 74 534 107 424 76 829
Female 367 568 24 55 225 990 5422 29 799 90 341 129 239 111 473
Total 654 626 30 77 329 1608 9378 53 364 164 875 236 663 188 302
Melanoma Male 760 638 53 483 4251 18 027 42 871 98 176 186 546 217 662 192 569
Female 713 794 99 772 8277 33 089 65 618 118 187 174 323 162 267 150 802
Total 1 474 432 152 1255 12 528 51 116 108 489 216 363 360 869 380 289 343 371
Prostate Male 3 523 238 21 97 217 454 11 489 182 558 835 157 1 322 743 1 170 502
Female
Total 3 523 238 21 97 217 454 11 489 182 558 835 157 1 322 743 1 170 502
Corpus uteri Male
Female 891 553 1 15 585 6645 27 423 102 027 242 777 265 117 246 963
Total 891 553 1 15 585 6645 27 423 102 027 242 777 265 117 246 963
Non-Hodgkin lymphoma Male 451 366 797 3480 7905 16 304 30 382 63 903 112 610 122 736 93 249
Female 394 185 400 1751 4998 10 997 20 455 46 279 89 502 107 042 112 761
Total 845 551 1197 5231 12 903 27 301 50 837 110 182 202 112 229 778 206 010
Thyroid Male 238 831 56 857 5511 16 604 29 683 48 207 63 286 49 612 25 015
Female 823 801 65 2842 25 231 78 153 127 307 178 794 198 050 134 209 79 150
Total 1 062 632 121 3699 30 742 94 757 156 990 227 001 261 336 183 821 104 165
a

not applicable.

Survivors as a proportion of the US population

With increasing age, the proportion of the US population represented by cancer survivors increases (Figure 2). For example, among US females aged 40-54 years, cancer survivors represent 3.6% of the population. Among females aged 65-74 years, survivors represent 14.5% of the population. Among females aged 85 years and older, more than one-third (36.4%) of the population is cancer survivors.

Figure 2.

Figure 2.

Proportion of the population represented by cancer survivors living in the United States by age and calendar year for females (A) and males (B).

Among males, the proportion of the US population that is represented by cancer survivors is higher with older age (Figure 2, B). Among males aged 40-54 years, survivors represent 2.1% of the population, while among males aged 65-74 years, 16% were cancer survivors. In the oldest group, those aged 85 years and older, nearly half (48.3%) the population is cancer survivors.

When comparing estimates for 2022 to estimates for 2040, the percent of projected US population that are cancer survivors is very similar for males in every age group. However, among females, cancer survivors will make up a higher percentage of the US population in 2040 than in 2022—particularly among those aged 65 years and older (Figure 2, A). For example, in 2022, approximately 19.7% of females aged 75-84 years were cancer survivors. In 2040, this proportion is expected to increase to 22.5%.

Discussion

The prevalence of cancer survivors in the United States now reaches more than 18 million and is expected to continue to increase; in particular, survivors who are more than 25 years from diagnosis and survivors who are older adults are growing in number. Overall, cancer survivors represent a substantial proportion of the US population. These survivors represent a range of diagnosis and treatment histories, as well as a variety of life experiences and comorbid conditions, with a large number of poorly understood or unmet needs (23,24). Importantly, this population also includes those who are living with metastatic or advanced cancer (5,25).

The increasing number of survivors and the increasing proportion of the population that has a history of a diagnosis of cancer will continue to exert pressure on the US health-care system. Prior analysis of SEER-Medicare data showed that, compared with 2020 levels, the total number of survivors receiving care by medical oncologists is expected to increase 24% by 2030 and 42% by 2040, with the highest increase in use projected to occur among cancer survivors who survive 10 or more years following diagnosis between 2020 and 2030 (13). Yet, this model of oncologist-led survivorship care is unlikely to be sustainable—and may lead to harms (26).

At the same time, primary care providers often do not have access to cancer diagnosis and treatment information, or it may not be organized in a way that represents actionable data. Primary care providers’ lack of exposure to cancer treatment algorithms and limited involvement in care during the active treatment phase may limit their comfort level with managing posttreatment sequela in survivors (26,27). Electronic health records are not designed to fill these gaps, which likely worsen as time from treatment increases. Models that are designed to overcome these barriers are still lacking evidence, which has slowed our progress toward optimal survivorship care delivery (26). The result is fragmented care, which may contribute to undertreatment or oversight of surveillance, treatment-related late effects, and other survivorship needs (26,28). As the number of survivors in the United States continues to grow, especially those populations of older adults and long-term cancer survivors, better survivorship care delivery is urgently needed (29). Ideally, survivorship care should be implemented at diagnosis and tailored to survivors’ needs, some of which are not well described. In addition, given the substantial increases in the number of survivors more than 10 years from diagnosis, evaluating and revisiting or reassessing the needs of very long-term survivors is critical.

Our findings further emphasize the growing population of older adult cancer survivors. These survivors remain at risk of long-term adverse effects, including cognitive impairment, cardiovascular disease, and premature and accelerated aging resulting from their cancer treatments, yet are not well represented in research (10,12,30). Oncology continues to be underprepared for this demographic shift because of the historic exclusion of older adults from treatment trials (31). Despite the US Food and Drug Administration’s efforts to increase inclusion of older adults in clinical trials (32), the underrepresentation of this population has led to a paucity of data for establishing efficacy and safety of new therapies (31), which may lead to continued use of expensive treatments that confer higher toxicity and smaller benefit. Care for older adults with cancer is complex and multifaceted. Before older adults are diagnosed with cancer, many will have had major health challenges requiring informal caregiving (33). Older adults are more likely to experience cancer treatment–related toxicities (34) due to a loss of physiologic resilience and capacity with age (34,35) and are less likely to be offered chemotherapy because of concerns of tolerability (36). Although the field of geriatric oncology has been around for decades (37,38), the specialty, practice, and principals of caring for older adults with cancer need be routinely adopted, given the large and growing population. Thus, it will become important for oncology to become more multidisciplinary to strengthen the evidence base, address systemic biases, and adequately address the complex care needs of older adults (37).

These findings demonstrate that nearly half of US cancer survivors have lived 10 or more years after diagnosis, while 19% have lived 20 or more years. A recent publication of the prevalence of cancer survivors in Europe reflects similar patterns of diagnosis and survivorship, although the incidence rates for some cancers, such as melanoma, vary widely between countries. As in the United States, the number of very long-term survivors (20 or more years after diagnosis) in Europe is growing (39). This long-term survivorship population has not been well characterized (40). A recent portfolio analysis of the National Institutes of Health funded studies reflects the low number of studies representing long-term survivorship (41). In addition, a report from the 2019 National Cancer Institute Cancer Survivorship Workshop that explored survivorship care called out research on long-term survivors an evidence gap (29). Lack of research can be attributed to limited inclusion or documentation of this population in clinical trials, minimal epidemiological studies capturing 10 or more years of cancer-related outcomes data, and fragmentation within medical care delivery systems. To adequately serve this population, it will be critical to study the characteristics and needs and examine clinician knowledge and treatment patterns for and understand health-care access and utilization of this growing population. Existing data resources that may support preliminary characterization, needs assessment, and health-care utilization of long-term survivorship populations include SEER-Medicare linked data resource (21) and large population-based surveys (eg, National Health and Aging Trends Survey) (42), as well as electronic medical record systems within established health networks. As existing clinical settings develop and implement learning health-care systems for cancer, additional documentation of treatment exposures, time-varying diagnoses, and patient-reported outcomes will be necessary to further characterize the needs of this population (43). Careful methodological approaches must be considered to capture the intersection of the development and progression of long-term and late effects of cancer with survivors’ precancer health profiles (44). The outcomes of this foundational research can support the development of long-term survivorship care planning, prepare workforce needs in terms of survivorship care delivery, and assess potential policy-related changes that support long-term survivors, their health-care providers, and related health systems (44).

Some limitations of this work should be acknowledged. These estimates utilize cancer incidence and survival data from the SEER registries, which do not include the entire United States. Prevalence projections are based on incidence and survival trends while reflecting the dynamic aging effect on the prevalence estimates. Although prevalence estimates are robust, they do not account for new cancer control policies or interventions that may arise during the study period. In addition, these findings do not include information on stage at diagnosis or the prevalence of cancer survivors living with advanced or metastatic cancer (5).

Finally, it is important to acknowledge a group of people who are not accounted for in this work. The growth in the number of cancer survivors, including those living beyond and those living with their cancer, means that there is also an increased number of people serving as informal cancer caregivers. There are currently an estimated 3 million cancer caregivers in the United States (45). Cancer caregivers provide unpaid support to their family, friends, or loved ones with cancer, including instrumental, emotional, and medical task support (46). Research has demonstrated that cancer caregivers experience substantial burden and have substantial needs for psychosocial support, financial assistance, and medical or nursing skills training to support their loved ones (2). Given the critical role that caregivers play, and the changing landscape of survivorship, future research should aim to examine and mitigate the trajectory of needs for cancer caregivers.

As the population of long-term survivors continues to grow so will the need to design health-care delivery to meet the needs of this population. A strong research and practice agenda, informed by survivorship science, is needed to continue to optimize survivorship care and patient outcomes.

Contributor Information

Emily Tonorezos, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Theresa Devasia, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Angela B Mariotto, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Michelle A Mollica, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Lisa Gallicchio, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Paige Green, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Michelle Doose, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Rachelle Brick, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Brennan Streck, Division of Cancer Prevention, National Cancer Institute, Rockville, MD, USA.

Crystal Reed, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Janet S de Moor, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD, USA.

Data availability

These data and software, along with detailed tutorials, are publicly available at https://seer.cancer.gov/seerstat/.

Author contributions

Emily S. Tonorezos, MD, MPH (Conceptualization; Data curation; Investigation; Methodology; Supervision; Visualization; Writing—original draft; Writing—review & editing), Theresa Devasia, PhD (Formal analysis; Investigation; Methodology; Software; Writing—original draft; Writing—review & editing), Angela B Mariotto, PhD (Data curation; Formal analysis; Investigation; Methodology; Resources; Software; Supervision; Validation; Writing—original draft; Writing—review & editing), Michelle A Mollica, PhD, MPH, RN, OCN (Conceptualization; Investigation; Writing—original draft; Writing—review & editing), Lisa Gallicchio, PhD (Conceptualization; Investigation; Writing—original draft; Writing—review & editing), Paige Green, PhD (Conceptualization; Investigation; Visualization; Writing—original draft; Writing—review & editing), Michelle Doose, PhD, MPH (Conceptualization; Investigation; Visualization; Writing—original draft; Writing—review & editing), Rachelle Brick, PhD, MSPH, OTR/L (Conceptualization; Investigation; Writing—original draft; Writing—review & editing), Brennan Streck, PhD, RN, MPH (Conceptualization; Investigation; Writing—original draft; Writing—review & editing), Crystal Reed, MHA (Investigation; Writing—original draft; Writing—review & editing), and Janet S de Moor, PhD, MPH (Conceptualization; Data curation; Investigation; Methodology; Supervision; Visualization; Writing—original draft; Writing—review & editing).

Funding

Not applicable. This manuscript was prepared as part of the authors’ official duties as employees of the US federal government. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the National Cancer Institute.

Conflicts of interest

None.

References

  • 1. Siegel RL, Miller KD, Wagle NS, Jemal A.. Cancer statistics, 2023. CA Cancer J Clin. Jan 2023;73(1):17-48. doi: 10.3322/caac.21763 [DOI] [PubMed] [Google Scholar]
  • 2. Caplan ZUS. Older Population Grew From 2010 to 2020 at Fastest Rate Since 1880 to 1890. 2023. https://www.census.gov/library/stories/2023/05/2020-census-united-states-older-population-grew.html. Accessed June 23, 2023.
  • 3. Schilsky RL, Nass S, Le Beau MM, Benz EJ.. Progress in cancer research, prevention, and care. New Engl J Med. 2020;383(10):897-900. doi: 10.1056/NEJMp2007839 [DOI] [PubMed] [Google Scholar]
  • 4. Cronin KA, Scott S, Firth AU, et al. Annual report to the nation on the status of cancer, part 1: national cancer statistics. Cancer. 2022;128(24):4251-4284. doi: 10.1002/cncr.34479 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Gallicchio L, Devasia TP, Tonorezos E, Mollica MA, Mariotto A.. Estimation of the number of individuals living with metastatic cancer in the United States. J Natl Cancer Inst. 2022;114(11):1476-1483. doi: 10.1093/jnci/djac158 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Bluethmann SM, Mariotto AB, Rowland JH.. Anticipating the “Silver Tsunami”: prevalence trajectories and comorbidity burden among older cancer survivors in the United States. Cancer Epidemiol Biomarkers Prev. 2016;25(7):1029-1036. doi: 10.1158/1055-9965.Epi-16-0133 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. de Moor JS, Mariotto AB, Parry C, et al. Cancer survivors in the United States: Prevalence across the survivorship trajectory and implications for care. Cancer Epidemiol Biomarkers Prev. 2013;22(4):561-570. doi: 10.1158/1055-9965.Epi-12-1356 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Miller KD, Nogueira L, Devasia T, et al. Cancer treatment and survivorship statistics, 2022. CA Cancer J Clin. 2022;72(5):409-436. doi: 10.3322/caac.21731 [DOI] [PubMed] [Google Scholar]
  • 9. Mollica MA, Smith AW, Tonorezos E, et al. Survivorship for Individuals Living With Advanced and Metastatic Cancers: National Cancer Institute Meeting Report. J Natl Cancer Inst. 2022;114(4):489-495. doi: 10.1093/jnci/djab223 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Lustberg MB, Kuderer NM, Desai A, Bergerot C, Lyman GH.. Mitigating long-term and delayed adverse events associated with cancer treatment: implications for survivorship. Nat Rev Clin Oncol. 2023;20(8):527-542. doi: 10.1038/s41571-023-00776-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Ness KK, Wogksch MD.. Frailty and aging in cancer survivors. Transl Res. 2020;221:65-82. doi: 10.1016/j.trsl.2020.03.013 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Guida JL, Ahles TA, Belsky D, et al. Measuring aging and identifying aging phenotypes in cancer survivors. J Natl Cancer Inst. 2019;111(12):1245-1254. doi: 10.1093/jnci/djz136 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Mariotto AB, Enewold L, Parsons H, Zeruto CA, Yabroff KR, Mayer DK.. Workforce caring for cancer survivors in the United States: estimates and projections of use. J Natl Cancer Inst. 2022;114(6):837-844. doi: 10.1093/jnci/djac036 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Finster LJ, Salvy SJ, Haile RW.. A cancer care desert: Living in between the urban and rural and the case for defining semirural regions. Front Oncol. 2023;13:1204821. doi: 10.3389/fonc.2023.1204821 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Ohlsen TJD, Chen Y, Baldwin LM, et al. Primary care utilization and cardiovascular screening in adult survivors of childhood cancer. JAMA Netw Open. 2023;6(12):e2347449. doi: 10.1001/jamanetworkopen.2023.47449 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Lax H, Baum J, Lehmann N, et al. Patterns of follow-up care in adult blood cancer survivors-prospective evaluation of health-related outcomes, resource use, and quality of life. Cancer Med. 2024;13(7):e7095. doi: 10.1002/cam4.7095 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Rodriguez SA, Lee SC, Higashi RT, et al. Factors influencing implementation of a care coordination intervention for cancer survivors with multiple comorbidities in a safety-net system: an application of the Implementation Research Logic Model. Implement Sci. 2023;18(1):68. doi: 10.1186/s13012-023-01326-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Verhoeven D, Doose M, Chollette V, Weaver SJ.. Team complexity and care coordination for cancer survivors with multiple chronic conditions: a mixed methods study. J Cancer Surviv 2024. doi: 10.1007/s11764-023-01488-w [DOI] [PubMed] [Google Scholar]
  • 19. Simons BCR, Hillen MA, Aarts JWM, Tromp JM, de Heus E, Duijts SFA.. Disentangling trust of patients with rare cancer in their healthcare professionals and the healthcare system: a qualitative interview study. J Cancer Surviv. 2024. doi: 10.1007/s11764-023-01531-w [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Verdecchia A, De Angelis G, Capocaccia R.. Estimation and projections of cancer prevalence from cancer registry data. Stat Med. 2002;21(22):3511-3526. doi: 10.1002/sim.1304 [DOI] [PubMed] [Google Scholar]
  • 21. SEER. SEERExplorer: An interactive Website for SEER Statistics. https://seer.cancer.gov/statistics-network/explorer/application.htm. Accessed November 29, 2023.
  • 22. U.S. Census Bureau. 2017 National Population Projections Datasets.https://www.census.gov/data/datasets/2017/demo/popproj/2017-popproj.html. Accessed November 29, 2023.
  • 23. Jiang C, Deng L, Karr MA, et al. Chronic comorbid conditions among adult cancer survivors in the United States: results from the National Health Interview Survey, 2002-2018. Cancer. 2022;128(4):828-838. doi: 10.1002/cncr.33981 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Rees-Punia E, Masters M, Teras LR, et al. Long-term multimorbidity trajectories in older adults: the role of cancer, demographics, and health behaviors. Cancer. 2024;130(2):312-321. doi: 10.1002/cncr.35047 [DOI] [PubMed] [Google Scholar]
  • 25. Hudock NL, Mani K, Khunsriraksakul C, et al. Future trends in incidence and long-term survival of metastatic cancer in the United States. Commun Med (Lond). 2023;3(1):76. doi: 10.1038/s43856-023-00304-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Alfano CM, Oeffinger K, Sanft T, Tortorella B.. Engaging TEAM medicine in patient care: redefining cancer survivorship from diagnosis. Am Soc Clin Oncol Educ Book. 2022;42:1-11. doi: 10.1200/edbk_349391 [DOI] [PubMed] [Google Scholar]
  • 27. Nekhlyudov L, O’Malley DM, Hudson SV.. Integrating primary care providers in the care of cancer survivors: gaps in evidence and future opportunities. Lancet Oncol. 2017;18(1):e30-e38. doi: 10.1016/s1470-2045(16)30570-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Jefford M, Howell D, Li Q, et al. Improved models of care for cancer survivors. Lancet. 2022;399(10334):1551-1560. doi: 10.1016/s0140-6736(22)00306-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Gallicchio L, Tonorezos E, de Moor JS, et al. Evidence gaps in cancer survivorship care: a report from the 2019 national cancer institute cancer survivorship workshop. J Natl Cancer Inst. 2021;113(9):1136-1142. doi: 10.1093/jnci/djab049 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Schuitema I, Alexander T, Hudson MM, Krull KR, Edelstein K.. Aging in adult survivors of childhood cancer: implications for future care. J Clin Oncol. 2021;39(16):1741-1751. doi: 10.1200/jco.20.02534 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Hutchins LF, Unger JM, Crowley JJ, Coltman CA Jr, Albain KS.. Underrepresentation of patients 65 years of age or older in cancer-treatment trials. N Engl J Med. 1999;341(27):2061-2067. doi: 10.1056/nejm199912303412706 [DOI] [PubMed] [Google Scholar]
  • 32. Food and Drug Administration. Inclusion of Older Adults in Cancer Clinical Trials: Guidance for Industry. 2022. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/inclusion-older-adults-cancer-clinical-trials. Accessed June 28, 2024.
  • 33. Ornstein KA, Liu B, Schwartz RM, Smith CB, Alpert N, Taioli E.. Cancer in the context of aging: health characteristics, function and caregiving needs prior to a new cancer diagnosis in a national sample of older adults. J Geriatr Oncol. 2020;11(1):75-81. doi: 10.1016/j.jgo.2019.03.019 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Hurria A, Togawa K, Mohile SG, et al. Predicting chemotherapy toxicity in older adults with cancer: a prospective multicenter study. J Clin Oncol. 2011;29(25):3457-3465. doi: 10.1200/jco.2011.34.7625 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Boss GR, Seegmiller JE.. Age-related physiological changes and their clinical significance. West J Med. 1981;135(6):434-440. [PMC free article] [PubMed] [Google Scholar]
  • 36. Hurria A, Wong FL, Villaluna D, et al. Role of age and health in treatment recommendations for older adults with breast cancer: the perspective of oncologists and primary care providers. J Clin Oncol. 2008;26(33):5386-5392. doi: 10.1200/jco.2008.17.6891 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Dale W, Jacobsen PB, Mohile SG.. Geriatric oncology comes of age: advancing the science of caring for older adults with cancer. J Clin Oncol. 2021;39(19):2055-2057. doi: 10.1200/jco.21.00887 [DOI] [PubMed] [Google Scholar]
  • 38. Lichtman SM, Balducci L, Aapro M.. Geriatric oncology: a field coming of age. J Clin Oncol. 2007;25(14):1821-1823. doi: 10.1200/jco.2007.10.6567 [DOI] [PubMed] [Google Scholar]
  • 39. De Angelis R, Demuru E, Baili P, et al. ; EUROCARE-6 Working Group. Complete cancer prevalence in Europe in 2020 by disease duration and country (EUROCARE-6): a population-based study. Lancet Oncol. 2024;25(3):293-307. doi: 10.1016/s1470-2045(23)00646-0 [DOI] [PubMed] [Google Scholar]
  • 40. León-Salas B, Álvarez-Pérez Y, Ramos-García V, et al. Information needs and research priorities in long-term survivorship of breast cancer: patients and health professionals’ perspectives. Eur J Cancer Care (Engl). 2022;31(6):e13730. doi: 10.1111/ecc.13730 [DOI] [PubMed] [Google Scholar]
  • 41. Mollica MA, Tesauro G, Gallicchio L, Guida J, Maher ME, Tonorezos E.. Survivorship science at the National Institutes of Health 2017-2021. J Cancer Surviv 2023. doi: 10.1007/s11764-023-01414-0 [DOI] [PubMed] [Google Scholar]
  • 42. Freedman VA, Kasper JD.. Cohort Profile: The National Health and Aging Trends Study (NHATS). Int J Epidemiol. 2019;48(4):1044-1045g. doi: 10.1093/ije/dyz109 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Hsu ER, Klemm JD, Kerlavage AR, Kusnezov D, Kibbe WA.. Cancer moonshot data and technology team: enabling a national learning healthcare system for cancer to unleash the power of data. Clin Pharmacol Ther. 2017;101(5):613-615. doi: 10.1002/cpt.636 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44. Leach CR, Weaver KE, Aziz NM, et al. The complex health profile of long-term cancer survivors: prevalence and predictors of comorbid conditions. J Cancer Surviv. 2015;9(2):239-251. doi: 10.1007/s11764-014-0403-1 [DOI] [PubMed] [Google Scholar]
  • 45. Kent EE, Mollica MA, Buckenmaier S, Wilder Smith A.. The characteristics of informal cancer caregivers in the United States. Semin Oncol Nurs. 2019;35(4):328-332. doi: 10.1016/j.soncn.2019.06.002 [DOI] [PubMed] [Google Scholar]
  • 46. Mollica MA, Smith AW, Kent EE.. Caregiving tasks and unmet supportive care needs of family caregivers: a U.S. population-based study. Patient Educ Couns. 2020;103(3):626-634. doi: 10.1016/j.pec.2019.10.015 [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

These data and software, along with detailed tutorials, are publicly available at https://seer.cancer.gov/seerstat/.


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