| Literature DB >> 30874851 |
Sabrina Trudel1, Benoît Tessoulin1,2, Maxime Jullien1, Nicolas Blin1, Thomas Gastinne1, Béatrice Mahé1, Viviane Dubruille1, Antoine Bonnet1, Anne Lok1, Patrice Chevallier1, Pierre Peterlin1, Alice Garnier1, Thierry Guillaume1, Amandine Le Bourgeois1, Steven Le Gouill1,2,3, Philippe Moreau1,2,3, Cyrille Touzeau4,5,6,7.
Abstract
Pomalidomide dexamethasone is a standard of care for relapsed multiple myeloma (MM) patients who received at least two prior lines of therapy, including both lenalidomide and proteasome inhibitors (PI). We report here a real-life single-center series of 49 consecutive patients with relapsed and refractory MM treated with the triplet pomalidomide cyclophosphamide dexamethasone (PCD) combination. The median of prior lines of therapy was 3 and all patients were previously exposed to proteasome inhibitors and lenalidomide. The overall response rate was 76%, including 27% very good partial response or better. With a median follow-up of 16 months, the median progression-free survival (PFS) was 7.3 months and the median overall survival was not reached. Regarding safety, most frequent toxicity was hematologic, including 37% grade 3-4 cytopenias. Nine patients (18%) discontinued therapy due to adverse event. Our study confirms that PCD combination is feasible and results in favorable response rate and PFS in comparison with pomalidomide dexamethasone alone.Entities:
Keywords: Cyclophosphamide; Dexamethasone; Multiple myelomas; PCD; Pomalidomide; Relapse
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Year: 2019 PMID: 30874851 DOI: 10.1007/s00277-019-03649-3
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673