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Impact of Second Primary Malignancy Post-Autologous Transplantation on Outcomes of Multiple Myeloma: A CIBMTR Analysis

Authors :
Brittany Knick Ragon
Mithun Vinod Shah
Anita D'Souza
Noel Estrada-Merly
Lohith Gowda
Gemlyn George
marcos DeLima
Shahrukh Hashmi
Mohamed A Kharfan-Dabaja
Navneet S Majhail
Rahul Banerjee
Ayman Saad
Gerhard C. Hildebrandt
Hira Mian
Muhammad Bilal Abid
Minoo Battiwalla
Lazaros J. Lekakis
Sagar S. Patel
Hemant S. Murthy
Yago Nieto
Christopher S Strouse
Sherif M. Badawy
Samer AI Al Hadidi
Bhagirathbhai Dholaria
Mahmoud Aljurf
David H Vesole
Cindy H Lee
Attaphol Pawarode
Usama Gergis
Kevin Charles Miller
Leona A Holmberg
Aimaz Afrough
Melhem M Solh
Pashna Munshi
Taiga Nishihori
Larry D. Anderson
Baldeep Wirk
Gurbakhash Kaur
Muzaffar H Qazilbash
Nina Shah
Shaji K Kumar
Saad Z. Usmani
Source :
Blood Advances.
Publication Year :
2023
Publisher :
American Society of Hematology, 2023.

Abstract

The overall survival (OS) has improved significantly in multiple myeloma (MM) over the last decade with use of proteasome inhibitor and immunomodulatory drug-based combinations, followed by high-dose melphalan and autologous hematopoietic stem cell transplantation (auto-HSCT) and subsequent maintenance therapies in eligible newly diagnosed patients. However, clinical trials employing auto-HSCT followed by lenalidomide maintenance have shown an increased risk of second primary malignancies (SPM), including second hematological malignancies (SHM). We evaluated the impact of SPM and SHM on progression-free survival (PFS) and OS in MM patients following auto-HSCT using CIBMTR registry data. Adult MM patients who underwent first auto-HSCT in the United States with melphalan conditioning regimen from 2011 to 2018 and received maintenance therapy were included (n=3,948). At a median follow up of 37 months, 175 (4%) patients developed SPM, including 112 (64%) solid, 36 (20%) myeloid, 24 (14%) SHM, not otherwise specified, and 3 (2%) lymphoid malignancies. Multivariate analysis demonstrated that SPM and SHM were associated with an inferior PFS (HR 2.62, P

Subjects

Subjects :
Hematology

Details

ISSN :
24739537 and 24739529
Database :
OpenAIRE
Journal :
Blood Advances
Accession number :
edsair.doi...........7f8a2d8b50b1819f401bd7620962bbde