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Smitherman, Andrew B

0000-0002-1059-3853

Mayo Clinic

Division of Pediatric Hematology-Oncology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.

Citations 3

Incidence of chronic medical conditions among survivors of adolescent and young adult cancer compared to a population without cancer
Keegan, Theresa H.M. , Abrahão, Renata , Chubak, Jessica , Sauder, Candice A. M. , Ruddy, Kathryn J. , Li, Qian , Haupt, Eric C. , Laurent, Cecile A. , Casperson, Mallory, Chao, Chun , Smitherman, Andrew B. , Nichols, Hazel B. , Chao, Chun , Smitherman, Andrew B , Nichols, Hazel B , Hahn, Erin E , Chubak, Jessica , Quesenberry, Charles P. , Li, Qian , Brunson, Ann , Kirchhoff, Anne C. , Kushi, Lawrence H.

Cancer | October 10, 2025 | Volume: 131 | Issue: 20 | Pages: No page available

10.1002/cncr.70125 Get It

Abstract Background Few studies have assessed the burden of chronic medical conditions in adolescent and young adult (AYA) cancer survivors. This study estimated the risk of these conditions among AYA survivors compared to a matched cohort without cancer. Methods This retrospective cohort study included 2‐year survivors ( n = 14,917) of 11 common AYA (15–39 years) cancers diagnosed at the integrated health care organizations of Kaiser Permanente (KP) Southern and Northern California during 2006–2020. A comparison cohort ( n = 149,164) without cancer (matched 10:1 by age, sex, calendar year, and KP site) was included. Cumulative incidence (CMI) accounting for death as a competing risk was calculated. Poisson regression estimated the incidence rate ratio (IRR) of each condition in cancer survivors versus the matched cohort, adjusting for age, sex, and race/ethnicity. Results The 5‐year CMI was highest for thyroid (17.4%), respiratory (6.6%), cardiovascular (5.0%), and liver (4.8%) diseases. At 10 years, the CMI of any condition was 39% in survivors versus 26% in the matched cohort. Survivors had a 2‐fold increased risk of being diagnosed with any medical condition (IRR, 2.0; 95% confidence interval [CI], 1.9–2.0) as well as two or more conditions (IRR, 2.3; 95% CI, 2.2–2.5). Risk was highest among survivors of hematologic cancers and those diagnosed with distant stage disease. Elevated risks were observed within all sociodemographic groups of this insured population. Conclusion AYAs with cancer had a higher risk of chronic medical conditions compared to those without cancer. Long‐term surveillance, risk mitigation through lifestyle modifications and effective disease management are crucial to reduce premature mortality.
Time to cancer treatment and reproductive outcomes after fertility preservation among adolescent and young adult women with cancer
Meernik, Clare , Engel, Stephanie M. , Baggett, Christopher D. , Wardell, Ally, Zhou, Xi , Ruddy, Kathryn J. , Wantman, Ethan, Baker, Valerie L. , Mersereau, Jennifer E. , Smitherman, Andrew B. , Nichols, Hazel B. , Smitherman, Andrew B , Nichols, Hazel B , Wardell, Ally, Luke, Barbara , Cai, Jianwen , Olshan, Andrew F.

Cancer | November 1, 2022 | Volume: 129 | Issue: 2 | Pages: 307-319

10.1002/cncr.34520 Get It

AbstractBackgroundFertility preservation (FP) may be underused after cancer diagnosis because of uncertainty around delays to cancer treatment and subsequent reproductive success.MethodsWomen aged 15 to 39 years diagnosed with cancer between 2004 and 2015 were identified from the North Carolina Central Cancer Registry. Use of assisted reproductive technology (ART) after cancer diagnosis between 2004 and 2018 (including FP) was assessed through linkage to the Society for Assisted Reproductive Technology. Linear regression was used to examine time to cancer treatment among women who did (n = 95) or did not (n = 469) use FP. Modified Poisson regression was used to estimate risk ratios (RRs) and 95% CIs for pregnancy and birth based on timing of ART initiation relative to cancer treatment (n = 18 initiated before treatment for FP vs n = 26 initiated after treatment without FP).ResultsThe median time to cancer treatment was 9 to 33 days longer among women who used FP compared with women who did not, matched on clinical factors. Women who initiated ART before cancer treatment may be more likely to have a live birth given pregnancy compared with women who initiated ART after cancer treatment (age‐adjusted RR, 1.47; 95% CI, 0.98‐2.23), though this may be affected by the more frequent use of gestational carriers in the former group (47% vs 20% of transfer cycles, respectively).ConclusionsFP delayed gonadotoxic cancer treatment by up to 4.5 weeks, a delay that would not be expected to alter prognosis for many women. Further study of the use of gestational carriers in cancer populations is warranted to better understand its effect on reproductive outcomes.