Therapy-related myeloid leukemias are observed in patients with chronic lymphocytic leukemia after treatment with fludarabine and chlorambucil: Results of an intergroup study, cancer and leukemia group B 9011

被引:147
作者
Morrison, VA
Rai, KR
Peterson, BL
Kolitz, JE
Elias, L
Appelbaum, FR
Hines, JD
Shepherd, L
Larson, RA
Schiffer, CA
机构
[1] Vet Affairs Med Ctr, Sect Hematol, Minneapolis, MN 55417 USA
[2] Vet Affairs Med Ctr, Sect Infect Dis, Minneapolis, MN 55417 USA
[3] Long Isl Jewish Med Ctr, New Hyde Pk, NY 11042 USA
[4] N Shore Univ Hosp, Manhasset, NY USA
[5] Canc & Leukemia Grp Stat Ctr B, Durham, NC USA
[6] Univ New Mexico, Hlth Sci Ctr, Albuquerque, NM USA
[7] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[8] Case Western Reserve Univ, Sch Med, Cleveland, OH USA
[9] Natl Canc Inst Canada Clin Trials Grp, Kingston, ON, Canada
[10] Univ Chicago, Ctr Med, Chicago, IL USA
[11] Wayne State Univ, Sch Med, Detroit, MI USA
关键词
D O I
10.1200/JCO.2002.08.128
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Patients with chronic lymphocytic leukemia (CLL) may have disease transformation to non-Hodgkin's lymphoma or prolymphocytic leukemia; however, development of therapy-related acute myeloid leukemia (t-AML) is unusual. A series of patients enrolled onto an intergroup CLL trial were examined for this complication. Patients and Methods: A total of 544 previously untreated B-cell CLL patients were enrolled onto a randomized intergroup study comparing treatment with chlorambucil, fludarabine, or fludarabine plus chlorambucil. Case report forms from 521 patients were reviewed for t-AML. Results: With a median follow-up of 4.2 years, six patients (1.2%) to date have developed therapy-related myelodysplastic syndrome (t-MDS; n = 3), t-AML (n = 2), or t-MDS evolving to t-AML (n = 1), from 27 to 53 months (median, 34 months) after study entry. This included five (3.5%) of 142 patients treated with fludarabine plus chlorambucil and one (0.5%) of 188 receiving fludarabine; no chlorambucil-treated patients developed t-MDS or t-AML (P = .007). At study entry, the median age among these six patients was 56 years (range, 44 to 72 years); three were male; the CLL Rai stage was I/II (n = 4) or III/IV (n = 2). Response to CLL therapy was complete (n = 4) or partial remission (n = 1) and stable disease (n = 1). Marrow cytogenetics, obtained in three of six cases at diagnosis of t-MDS or t-AML, were complex, with abnormalities in either or both chromosomes 5 and 7. Other abnormalities involved chromosomes X, 1, 8, 12, 17, and 19. Median survival after diagnosis of t-MDS/AML was 3.5 months (range, 0.5 to 10.1 months). Conclusion: Our findings raise the possibility that alkylator-purine analog combination therapy may increase the risk of therapy-related myeloid malignancies, which is of particular relevance with regard to ongoing trials using these combination therapies. (C) 2002 by American Society of Clinical Oncology.
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页码:3878 / 3884
页数:7
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