Cumulative incidence estimates for solid tumors after HCT in the CIBMTR and California Cancer Registry

Author:

Schonfeld Sara J.1ORCID,Valcarcel Bryan1ORCID,Meyer Christa L.2ORCID,Shaw Bronwen E.3,Phelan Rachel34,Rizzo J. Douglas3ORCID,Brunson Ann5ORCID,Cooley Julianne J. P.6ORCID,Abrahão Renata5ORCID,Wun Ted56ORCID,Gadalla Shahinaz M.1ORCID,Engels Eric1ORCID,Albert Paul S.1,Yusuf Rafeek2ORCID,Spellman Stephen R.2ORCID,Curtis Rochelle E.1ORCID,Auletta Jeffery J.27ORCID,Muffly Lori8ORCID,Keegan Theresa H. M.56ORCID,Morton Lindsay M.1ORCID

Affiliation:

1. 1Division of Cancer Epidemiology and Genetics, National Institutes of Health, Department of Health and Human Services, National Cancer Institute, Bethesda, MD

2. 2Center for International Blood and Marrow Transplant Research, National Marrow Donor Program/Be The Match, Minneapolis, MN

3. 3Department of Medicine, Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI

4. 4Division of Pediatric Hematology/Oncology/Blood and Marrow Transplant, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI

5. 5Division of Hematology and Oncology, Center for Oncology and Hematology Outcomes Research and Training, University of California Davis Comprehensive Cancer Center, Sacramento, CA

6. 6California Cancer Reporting and Epidemiologic Surveillance Program, University of California Davis Comprehensive Cancer Center, Sacramento, CA

7. 7Divisions of Hematology, Oncology & Blood and Marrow Transplant and Infectious Diseases, Nationwide Children’s Hospital, Columbus, OH

8. 8Division of Blood and Marrow Transplantation & Cellular Therapy, Stanford University, Stanford, CA

Abstract

Abstract Compared with the general population, hematopoietic cell transplantation (HCT) survivors are at elevated risk for developing solid subsequent neoplasms (SNs). The Center for International Blood and Marrow Transplant Research (CIBMTR) is a key resource for quantifying solid SN incidence following HCT, but the completeness of SN ascertainment is uncertain. Within a cohort of 18 450 CIBMTR patients linked to the California Cancer Registry (CCR), we evaluated the completeness of solid SN data reported to the CIBMTR from 1991 to 2018 to understand the implications of using CIBMTR data alone or combined with CCR data to quantify the burden of solid SNs after HCT. We estimated the cumulative incidence of developing a solid SN, accounting for the competing risk of death. Within the cohort, solid SNs were reported among 724 patients; 15.6% of these patients had an SN reported by CIBMTR only, 36.9% by CCR only, and 47.5% by both. The corresponding cumulative incidence of developing a solid SN at 10 years following a first HCT was 4.0% (95% confidence interval [CI], 3.5-4.4) according to CIBMTR data only, 5.3% (95% CI, 4.9-5.9) according to CCR data only, and 6.3% (95% CI, 5.7-6.8) according to both sources combined. The patterns were similar for allogeneic and autologous HCT recipients. Linking detailed HCT information from CIBMTR with comprehensive SN data from cancer registries provides an opportunity to optimize SN ascertainment for informing follow-up care practices and evaluating risk factors in the growing population of HCT survivors.

Publisher

American Society of Hematology

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