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- W2037829609 abstract "Objectives In vitro studies have shown synergistic anti-myeloma effects of bortezomib combined with alkylating agents or anthracycline. We tested safety and efficacy of the combination of bortezomib, doxorubicin cyclophosphamide, and dexamethasone (ABCD) in the treatment of relapsed/refractory myeloma. Methods ABCD consisted of bortezomib given intravenous (IV) at dosage 1.3 mg/m2, dexamethasone 40 mg IV on days 1, 4, 8, and 15, pegylated liposomal doxorubicin (PLD) 20 mg IV on days 1 and 15, plus cyclophosphamide 100 mg/d per os for 15 d. Between January 2008 and February 2009, 24 patients received a median of four 28-d ABCD cycles (range 1–6). All patients had been already treated with a median of two previous lines of treatment (range 1–6): 38% were resistant to previous therapies and 62% were relapsed. Results Clinical response was observed in 12 patients (50%), including 29% of very good partial remissions or better. Side effects included hematological toxicity (31% any grade), grades 3–4 thrombocytopenia (9%), grades 3–4 anemia (17%). Non-hematological toxicity affected 32% of administered cycles and included gastrointestinal disturbances (54%), peripheral neuropathy (8%), and infections (8%). After a median follow-up of 21.5 months (range 2–44 months), median of progression-free survival (PFS) was 8.7 months and median overall survival was 22.5 months. Achieving at least partial response within the second cycle was associated with a better PFS (19.5 months vs. 3.5 months), P = 0.03, HR 0.35 (CI 95% 0.13–0.90). Conclusion ABCD is safe and effective for relapsed/refractory MM subjects previously treated with novel agents." @default.
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- W2037829609 date "2014-04-18" @default.
- W2037829609 modified "2023-09-25" @default.
- W2037829609 title "Salvage therapy with pegylated liposomal doxorubicin, bortezomib, cyclophosphamide, and dexamethasone in relapsed/refractory myeloma patients" @default.
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- W2037829609 doi "https://doi.org/10.1111/ejh.12325" @default.
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