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Risk of Secondary Malignancies After Multiple Myeloma: A Nationwide Case-Control Cohort Study.
Ko, Heejoo; Han, Seunghoon; Park, Sung-Soo; Choi, Suein; Byun, Ja Min; Min, Chang-Ki.
Afiliación
  • Ko H; Department of Pharmacology, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea. Electronic address: kohjoo7@catholic.ac.kr.
  • Han S; Department of Pharmacology, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea. Electronic address: waystolove@catholic.ac.kr.
  • Park SS; Department of Hematology, Seoul St. Mary's Hematology Hospital, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea.
  • Choi S; Department of Pharmacology, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea.
  • Byun JM; Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Jongro-gu, Seoul, Republic of Korea.
  • Min CK; Department of Hematology, Seoul St. Mary's Hematology Hospital, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea.
Article en En | MEDLINE | ID: mdl-38849282
ABSTRACT

INTRODUCTION:

In light of improved survival rates among multiple myeloma (MM) survivors, we sought to assess their risk of secondary malignancies compared to the general population. MATERIALS AND

METHODS:

This nationwide population-based case-control cohort study utilized the Korea National Health Insurance Service (KNHIS) database incorporating data from 2009 to 2020. We analyzed a total of 7348 patients diagnosed with MM in the case cohort. We selected a control group of 29,351 individuals from the general population without MM, employing a 14 propensity score matching approach. Matching criteria included age, sex, and comorbidities to ensure a balanced and reliable comparison.

RESULTS:

The cumulative incidence of any secondary malignancy was significantly higher in the case cohort than the control cohort (Hazard ratio [HR] 1.576, 95% confidence interval [CI], [1.381-1.798]). Hematologic malignancy risk was notably higher in the case cohort (HR 8.026, 95% CI, [5.402-11.924]), especially therapy-related myeloid neoplasms (t-MN) (HR 12.063, 95% CI, [6.839-21.278]). No significant difference was shown in nonhematologic malignancy incidence. In subgroup analysis, transplant-eligible MM patients had a significantly higher incidence of any secondary malignancy (HR 1.104, 95% CI, [1.003-1.214]) than transplant-ineligible patients. The incidence of secondary malignancy in MM patients in the lenalidomide-available era was not significantly increased compared to the prelenalidomide era.

CONCLUSION:

While hematologic malignancies, particularly t-MN, are significantly elevated in MM patients compared to general population, nonhematologic malignancies do not appear to be significantly elevated.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Clin Lymphoma Myeloma Leuk Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Clin Lymphoma Myeloma Leuk Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article