1. Low-dose melphalan in elderly patients with relapsed or refractory acute myeloid leukemia: A well-tolerated and effective treatment after hypomethylating-agent failure
- Author
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Jan Stratmann, Sebastian Koschade, Aaron Becker von Rose, Shabnam Shaid, Stefani Parmentier, Christian Brandts, Joerg Chromik, Markus Schaich, Hubert Serve, Christoph Rummelt, Christoph Röllig, Elisabeth van Kann, Björn Steffen, Michael Lübbert, Olivier Ballo, and Martin Sebastian
- Subjects
Male ,Melphalan ,Cancer Research ,medicine.medical_specialty ,Kaplan-Meier Estimate ,Disease ,Gastroenterology ,03 medical and health sciences ,0302 clinical medicine ,Refractory ,Recurrence ,hemic and lymphatic diseases ,Internal medicine ,medicine ,Humans ,Effective treatment ,Treatment Failure ,Antineoplastic Agents, Alkylating ,Aged ,Proportional Hazards Models ,Aged, 80 and over ,business.industry ,Low dose ,Age Factors ,Myeloid leukemia ,Hematology ,Leukemia, Myeloid, Acute ,Treatment Outcome ,medicine.anatomical_structure ,Oncology ,Hypomethylating agent ,Drug Resistance, Neoplasm ,030220 oncology & carcinogenesis ,Retreatment ,Female ,Bone marrow ,business ,030215 immunology ,medicine.drug - Abstract
Relapsed or refractory (R/R) disease remains challenging in acute myeloid leukemia (AML), especially in elderly patients not considered eligible for intensive treatment options. We retrospectively evaluated the safety and efficacy of low-dose melphalan (LD-Mel) in a multicenter analysis in patients over 65 years with R/R AML, who previously had received ≥1 non-curative treatment line. The study included 31 patients (median age 77 years) with 1-4 previous treatment lines. Three patients (9.7%) achieved a complete remission. Two patients (6.5%) achieved a partial remission, nine patients (29.0%) had disease stabilization with reduction of peripheral or bone marrow blast burden, resulting in an overall response rate of 16.1% and 45.2% achieved clinical benefit. Responders showed a significantly longer median overall survival than non-responders (16.3 vs. 2.3 months, p 0.001). Multivariate analysis identified complex karyotype as the only risk factor associated with inferior survival (p 0.001), whereas prior treatment with hypomethylating agents (HMAs) in 25 of 31 patients was associated with superior OS, regardless of prior response to HMAs (p = 0.03). LD-Mel was well tolerated, with mild myelosuppressive side effects. Conclusively, LD-Mel is an effective treatment option in elderly patients with R/R AML, particularly after HMA therapy and in the absence of a complex karyotype.
- Published
- 2019
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