Second primary malignancies in multiple myeloma: An overview and IMWG consensus Journal Article


Authors: Musto, P.; Anderson, K. C.; Attal, M.; Richardson, P. G.; Badros, A.; Hou, J.; Comenzo, R.; Du, J.; Durie, B. G. M.; San Miguel, J.; Einsele, H.; Chen, W. M.; Garderet, L.; Pietrantuono, G.; Hillengass, J.; Kyle, R. A.; Moreau, P.; Lahuerta, J. J.; Landgren, O.; Ludwig, H.; Larocca, A.; Mahindra, A.; Cavo, M.; Mazumder, A.; McCarthy, P. L.; Nouel, A.; Rajkumar, S. V.; Reiman, A.; Serra, E. R.; Sezer, O.; Terpos, E.; Turesson, I.; Usmani, S.; Weiss, B. M.; Palumbo, A.
Article Title: Second primary malignancies in multiple myeloma: An overview and IMWG consensus
Abstract: Background: Therapeutic advancements following the introduction of autologous stem cell transplantation and ` novel' agents have significantly improved clinical outcomes for patients with multiple myeloma (MM). Increased life expectancy, however, has led to renewed concerns about the long-term risk of second primary malignancies (SPMs). This review outlines the most up-to-date knowledge of possible host-, disease-, and treatment-related risk factors for the development of SPMs in patients with MM, and provides practical recommendations to assist physicians. Design: A Panel of International Myeloma Working Group members reviewed the most relevant data published in the literature as full papers, or presented at meetings of the American Society of Clinical Oncology, American Society of Hematology, European Hematology Association, or International Myeloma Workshops, up to June 2016. Here, we present the recommendations of the Panel, based on this literature review. Results: Overall, the risk of SPMs in MM is low, multifactorial, and partially related to the length of patients' survival and MM intrinsic susceptibility. Studies suggest a significantly increased incidence of SPMs when lenalidomide is administered either following, or concurrently with, oral melphalan. Increased SPM incidence has also been reported with lenalidomide maintenance following high-dose melphalan, albeit to a lesser degree. In both cases, the risk of death from MM was significantly higher than the risk of death from SPMs, with lenalidomide possibly providing a survival benefit. No increase in SPM incidence was reported with lenalidomide plus dexamethasone (without melphalan), or with bortezomib plus oral melphalan, dexamethasone, or thalidomide. Conclusion: In general, the risk of SPMs should not alter the current therapeutic decision- making process in MM. However, regimens such as lenalidomide plus dexamethasone should be preferred to prolonged exposure to lenalidomide plus oral melphalan. SPM risk should be carefully discussed with the patient in the context of benefits and risks of different treatment options.
Keywords: lenalidomide; multiple myeloma; risk factors; myelodysplastic syndrome; stem-cell transplantation; maintenance; autologous transplantation; myelomonocytic leukemia; international myeloma working group; second primary malignancy; low-dose dexamethasone; spm; bortezomib-melphalan-prednisone; secondary primary malignancies; daratumumab monotherapy; ineligible patients
Journal Title: Annals of Oncology
Volume: 28
Issue: 2
ISSN: 0923-7534
Publisher: Oxford University Press  
Date Published: 2017-02-01
Start Page: 228
End Page: 245
Language: English
ACCESSION: WOS:000397278300009
DOI: 10.1093/annonc/mdw606
PROVIDER: wos
PUBMED: 27864218
Notes: Review -- Source: Wos
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  1. Carl Ola Landgren
    336 Landgren