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. 2023 Jun 15;9(8):1147–1150. doi: 10.1001/jamaoncol.2023.1723

An Updated Report on the Prevalence of Prior Cancer Among Persons Newly Diagnosed With Cancer in the Surveillance, Epidemiology, and End Results Program

Caitlin C Murphy 1,, Guillermo A Tortolero 1, David E Gerber 2,3,4, Sandi L Pruitt 3,4
PMCID: PMC10273127  PMID: 37318821

Abstract

This cohort study uses population-based data from the National Cancer Institute Surveillance, Epidemiology, and End Results program of cancer registries to estimate prevalence of prior cancer among adults diagnosed with an incident cancer in 2019.


The population of cancer survivors in the US continues to increase.1 Three authors of the present study reported in 2018 that 18.4% of adults newly diagnosed with cancer (2009-2013) survived a previous cancer and may therefore be excluded from cancer clinical trials.2 Many organizations3 have since recommended considering cancer survivors who are newly diagnosed with cancer for enrollment in trials. We provide an update on the prevalence of prior cancer, including differences by age, sex, and race and ethnicity.

Methods

We used population-based data from the National Cancer Institute Surveillance, Epidemiology, and End Results (SEER) program of cancer registries to estimate prevalence of prior cancer among adults (age ≥18 years) diagnosed with an incident cancer in 2019. Demographic information, including race and ethnicity, was abstracted from SEER registry data. Details are in eMethods in Supplement 1. The institutional review board at the University of Texas Southwestern Medical Center approved this study with a waiver of informed patient consent because the research involved no more than minimal risk and could not practicably be carried out without a waiver; data are deidentified and publicly available. All analyses were conducted using SAS, version 9.4 (SAS Institute Inc) between August and October 2022.

Results

There were 135 117 persons diagnosed with an incident cancer in 2019, of whom 1.9% had a prior cancer of the same type, 8.6% of a different type, and 8.9% of an unknown type (19.4% with any prior cancer). Prior cancer of a different type was more common for age 65 years or older (14.1%; 95% CI, 13.8%-14.4%) vs ages 18 to 49 years (1.6%; 95% CI, 1.4%-1.8%), men (10.3%; 95% CI, 10.1%-10.6%) vs women (8.9%; 95% CI, 8.7%-9.2%), and non-Hispanic White (11.0%; 95% CI, 10.8%-11.2%) vs non-Hispanic Black (5.7%; 95% CI, 5.2%-6.1%) persons (Table 1). Prevalence also differed by incident cancer type.

Table 1. Prevalence of Prior Cancer of a Different Type by Incident Cancer Type, Age, Sex, Race and Ethnicity, and Stage at Diagnosis.

Variable Prior cancer of a different type (n = 11 629)a No prior cancer (n = 108 940) Total (N = 120 569)
No. % (95% CI)
Incident cancer typeb
Myeloid and monocytic leukemia 323 21.1 (19.1-23.1) 1208 1531
Mesothelioma 35 18.0 (12.6-23.5) 159 194
Penis and other male genital organs 24 17.4 (11.1-23.7) 114 138
Urinary bladder and other urinary organs 892 17.0 (16.0-18.1) 4344 5236
Lung and other respiratory 1812 14.7 (14.1-15.3) 10 532 12 344
Pancreas 520 14.1 (13.0-15.2) 3169 3689
Bone and joints, including soft tissue 135 13.6 (11.4-15.7) 861 996
Esophagus 155 13.1 (11.2-15.0) 1030 1185
Eye and orbit 27 12.7 (8.2-17.1) 186 213
Miscellaneous 490 12.5 (11.5-13.6) 3425 3915
Melanoma 875 12.2 (11.4-12.9) 6323 7198
Anus, anal canal, anorectum 65 12.1 (9.3-14.8) 474 539
Stomach 234 11.8 (10.4-13.3) 1741 1975
Lymphoma 621 11.0 (10.2-11.9) 5007 5628
Oral cavity and pharynx 439 10.9 (10.0-11.9) 3574 4013
Liver and intrahepatic bile duct 379 10.7 (9.7-11.7) 3165 3544
Kidney and renal pelvis 437 10.3 (9.3-11.2) 3822 4259
Myeloma 201 9.8 (8.5-11.1) 1843 2044
Colon and rectum 948 9.4 (8.8-10.0) 9123 10 071
Lymphocytic leukemia 144 8.8 (7.4-10.2) 1488 1632
Cervix and other female genital organs 131 7.9 (6.6-9.1) 1537 1668
Brain and other nervous system 117 7.8 (6.5-9.2) 1380 1497
Ovary 104 7.6 (6.2-9.0) 1259 1363
Corpus and uterus 334 7.3 (6.6-8.1) 4216 4550
Thyroid and other endocrine 210 5.6 (4.9-6.4) 3518 3728
Prostate 955 5.4 (5.0-5.7) 16 796 17 751
Breast (female only) 958 5.2 (4.9-5.5) 17 517 18 475
Kaposi sarcoma 5 4.7 (0.7-8.7) 102 107
Testis 9 1.2 (0.4-2.0) 750 759
Age at incident cancer, y
18-49 255 1.6 (1.4-1.8) 15 748 16 003
50-64 1922 5.1 (4.9-5.3) 35 622 37 544
≥65 9452 14.1 (13.8-14.4) 57 570 67 022
Sex
Female 5267 8.9 (8.7-9.2) 53 735 59 002
Male 6362 10.3 (10.1-10.6) 55 205 6362
Race and ethnicityc
Hispanic (any race) 690 6.6 (6.2-7.1) 9700 10 390
Non-Hispanic Asian or Pacific Islander 1024 8.2 (7.7-8.7) 11 419 12 443
Non-Hispanic Black 598 5.7 (5.2-6.1) 9970 10 568
Non-Hispanic White 9235 11.0 (10.8-11.2) 74 892 84 127
Otherd 82 2.7 (2.1-3.3) 2959 3041
Stage of incident cancere
Local 5471 9.2 (9.0-9.5) 53 697 59 168
Regional 2057 8.3 (8.0-8.7) 22 582 24 639
Distant 3244 11.1 (10.8-11.5) 25 856 29 100
a

Of 135 117 persons diagnosed with an incident cancer in 2019, 108 940 (80.6%) had no prior cancer and 26 177 (19.4%) had any prior cancer. Those with any prior cancer included 2539 (1.9%) with a prior cancer of the same type, 11 629 (8.6%) with a prior cancer of a different type, and 12 009 (8.9%) with a prior cancer of an unknown type. Only those with no prior cancer or a prior cancer of a different type are displayed in the table.

b

Incident cancer type is listed in order of prevalence of prior cancer of a different type.

c

Race and ethnicity information was abstracted from Surveillance, Epidemiology, and End Results registry data.

d

Other includes American Indian or Alaska Native and “some other race” as coded according to the North American Association of Central Cancer Registries item 160 (described in detail at http://datadictionary.naaccr.org/).

e

Does not include missing, not staged, or not applicable (n = 7662).

Findings were generally similar for female breast, colorectal, lung, and prostate cancers and melanoma (Table 2), the 5 most common incident cancers. For example, persons diagnosed with local (vs distant) stage colorectal (adjusted odds ratio [AOR], 1.33; 95% CI, 1.11-1.60) or lung (AOR, 1.59; 95% CI, 1.41-1.79) cancer were more likely to have prior cancer of a different type.

Table 2. Adjusted Associations of Prior Cancer of a Different Type and Age, Sex, Race and Ethnicity, and Stage at Diagnosis for Persons Diagnosed With 1 of the 5 Most Common Cancers in 2019a,b.

Variable Five most common incident cancers, AOR (95% CI)
Female breast (n = 18 475) Colorectal (n = 10 071) Lung (n = 12 344) Prostate (n = 17 751) Melanoma (n = 7198)
Age at incident cancer, y
18-49 1 [Reference] 1 [Reference] 1 [Reference] 1 [Reference] 1 [Reference]
50-64 2.79 (2.06-3.79) 2.07 (1.34-3.20) 1.92 (1.11-3.34) 4.09 (1.01-16.59) 5.43 (3.15-9.38)
≥65 5.94 (4.44-7.94) 8.93 (5.69-13.38) 4.64 (2.70-7.95) 9.17 (2.28-36.98) 23.52 (14.01-39.49)
Sex
Female NA 1 [Reference] 1 [Reference] NA 1 [Reference]
Male NA 0.99 (0.86-1.14) 1.08 (0.97-1.20) NA 1.12 (0.96-1.32)
Race and ethnicityc
Hispanic (any race) 0.89 (0.69-1.14) 0.85 (0.65-1.12) 0.86 (0.68-1.09) 0.66 (0.48-0.89) 1.03 (0.62-1.73)
Non-Hispanic Asian or Pacific Islander 0.82 (0.66-1.02) 0.84 (0.66-1.06) 0.74 (0.61-0.88) 1.04 (0.82-1.33) 1.11 (0.58-2.11)
Non-Hispanic Black 0.41 (0.29-0.58) 0.63 (0.48-0.84) 0.65 (0.52-0.80) 0.40 (0.30-0.53) NA
Non-Hispanic White 1 [Reference] 1 [Reference] 1 [Reference] 1 [Reference] 1 [Reference]
Otherd 0.71 (0.38-1.30) 0.11 (0.03-0.43) 0.56 (0.28-1.11) 0.14 (0.06-0.34) NA
Stage of incident cancer
Local 1.17 (0.85-1.60) 1.33 (1.11-1.60) 1.59 (1.41-1.79) 0.75 (0.61-0.92) 1.16 (0.78-1.70)
Regional 0.96 (0.69-1.35) 0.97 (0.80-1.17) 1.27 (1.11-1.46) 0.53 (0.40-0.70) 1.25 (0.80-1.96)
Distant 1 [Reference] 1 [Reference] 1 [Reference] 1 [Reference] 1 [Reference]

Abbreviations: AOR, adjusted odds ratio; NA, not applicable.

a

Observations missing stage not included in adjusted models; by incident cancer type, the analytic sample size was 18 148 (female breast); 9467 (colorectal); 11 619 (lung); 16 888 (prostate); and 6773 (melanoma).

b

By incident cancer type, Akaike information criteria was 7012.8 (female breast); 5402.6 (colorectal); 9472.7.9 (lung); 6835.5 (prostate); and 4333.3 (melanoma).

c

Race and ethnicity information was abstracted from Surveillance, Epidemiology, and End Results registry data.

d

Other includes American Indian or Alaska Native and “some other race” as coded according to the North American Association of Central Cancer Registries item 160 (described in detail at http://datadictionary.naaccr.org/).

Discussion

The increase in number of persons newly diagnosed with cancer in the US (from 1 618 263 in 2013 to 1 737 969 in 2019), combined with the increasing prevalence of prior cancer (from 18.4% in a previous study to 19.4%), show an approximately 15% increase in the number of cancer survivors diagnosed with a new cancer in 6 years.

Recommendations against excluding patients from clinical trials solely on the basis of prior cancer are supported by growing evidence that persons newly diagnosed with cancer who have survived a prior cancer of a different type have equivalent survival compared with those without prior cancer.3,4 Yet implementation of these recommendations has been slow. Two-thirds of NCI-supported trials from 2018 to 2020 exclude patients with prior or concurrent cancers.5

White persons were more likely to have prior cancers of a different type compared with Black persons, perhaps associated with survival long enough to be diagnosed with multiple cancers. Understanding multiple cancer diagnoses by race and ethnicity may help achieve equity in cancer care.6

In addition, our findings point to unique needs of cancer survivors. The American Cancer Society, American Society of Clinical Oncology, and National Comprehensive Cancer Network provide care guidelines for survivors, but only for a few specific cancers. Developing evidence-based guidelines for long-term care of this population is critical to improving outcomes and mitigating risk of multiple cancers. Limitations include that nearly 10% of persons newly diagnosed with cancer had a prior cancer of an unknown type, likely representing prior cancers diagnosed outside of SEER-defined regions and for which information on tumor site and histology was not available.

Conclusions

Increasing prevalence of prior cancer underscores the continued importance of evaluating exclusion criteria of clinical trials, improving equity in cancer care, and addressing the unique needs of this large and growing population.

Supplement 1.

eMethods

Supplement 2.

Data Sharing Statement

References

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Associated Data

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

Supplementary Materials

Supplement 1.

eMethods

Supplement 2.

Data Sharing Statement


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