Cumulative exposure to melphalan chemotherapy and subsequent risk of developing acute myeloid leukemia and myelodysplastic syndromes in patients with multiple myeloma

被引:11
|
作者
Jonsdottir, Gudbjorg [1 ,2 ]
Bjorkholm, Magnus [3 ,4 ]
Turesson, Ingemar [5 ]
Hultcrantz, Malin [3 ,4 ,6 ]
Diamond, Benjamin [6 ]
Porwit, Anna [7 ]
Landgren, Ola [8 ]
Kristinsson, Sigurdur Y. [1 ,3 ,4 ]
机构
[1] Univ Iceland, Fac Med, Reykjavik, Iceland
[2] Univ Iowa Hosp & Clin, Dept Hematol Oncol Blood & Marrow Transplantat, Iowa City, IA 52242 USA
[3] Karolinska Univ Hosp, Div Hematol, Dept Med, Stockholm, Sweden
[4] Karolinska Inst, Stockholm, Sweden
[5] Skane Univ Hosp, Dept Hematol, Malmo, Sweden
[6] Mem Sloan Kettering Ctr, Myeloma Serv, New York, NY USA
[7] Lund Univ, Div Pathol, Dept Clin Sci, Lund, Sweden
[8] Univ Miami, Myeloma Program, Sylvester Comprehens Canc Ctr, Miami, FL USA
关键词
acute myeloid leukemia; myelodysplastic syndromes; alkylating therapy; melphalan; multiple myeloma; second malignancies; STEM-CELL TRANSPLANTATION; HIGH-DOSE MELPHALAN; BONE-MARROW-TRANSPLANTATION; 2ND PRIMARY MALIGNANCIES; RANDOMIZED-TRIAL; THERAPY; SURVIVAL; LENALIDOMIDE; NEOPLASMS; SINGLE;
D O I
10.1111/ejh.13650
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The aim of this study was to determine risk factors for development of acute myeloid leukemia/myelodysplastic syndromes (AML/MDS) in patients with multiple myeloma (MM). Methods We identified all patients diagnosed with MM in Sweden from January 1st, 1958 to December 31, 2011. A total of 26 627 patients were diagnosed with MM with during the study period. Of these, 124 patients (0.5%) developed subsequent AML/MDS. For each patient with MM and a subsequent AML/MDS diagnosis, we randomly selected a matched (age, sex, and date of MM diagnosis) MM patient without a subsequent second malignancy diagnosis. Results The cumulative melphalan exposure was significantly higher (OR = 2.8, 95% CI 1.7-5.2; P < .001) among cases (median 988 mg; IQR 644-1640) compared with controls (median 578 mg; IQR 360-967). Median time to AML/MDS development was 3.8 years (IQR 2.8-5.8). Risk of AML/MDS was not statistically altered by M protein isotype, anemia, renal failure, hypercalcemia, lytic bone lesions, or radiation therapy. Conclusion In this nationwide population-based study, we show that increased cumulative doses of alkylating therapy with melphalan increases the subsequent risk of developing AML/MDS in patients with MM. Given improved survival in MM patients over the last decade future studies will be important to better define long-term risks.
引用
收藏
页码:275 / 282
页数:8
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