Artigo Revisado por pares

Combined differentiating therapy for myelodysplastic syndromes: A phase II study

1996; Elsevier BV; Volume: 20; Issue: 10 Linguagem: Inglês

10.1016/0145-2126(95)00156-5

ISSN

1873-5835

Autores

Dario Ferrero, Benedetto Bruno, Patrizia Pregno, Silvia De Stefani, E Larizza, G Ciravegna, Annalisa Luraschi, Guido Vietti-Ramus, Piercarla Schinco, Mario Bazzan, E Gallo, Alessandro Pileri,

Tópico(s)

Hematopoietic Stem Cell Transplantation

Resumo

An in vitro synergism between different inducers of AML cell differentiation has been previously observed. Therefore, we treated 53 myelodysplastic (MDS) patients with a low dose combination of cis-retinoic acid (cRA, 20–40 mg/day) and 1,25 α(OH)2 cholecalciferol [(OH)2D3, 1–1.5μg/day] ± intermittent 6-thioguanine (30 mg/m2/day). The latter was reserved for patients with bone marrow (BM) blast excess (⩾5%). The treatment was well tolerated, without major toxicity. Among 25 patients with BM blasts less than 5%, we observed one complete, eight partial and four minor responses (response rate 52%) with a median response duration of 8 months (2+−24). Median survival, which did not correlate with response, is projected at 76 months. Thirty-one patients with BM blast excess (⩾ 5%), including three of the previous group who progressed to refractory anemia with excess of blasts (RAEB), were treated with the three-drug protocol. One complete, 12 partial and six minor responses were obtained (response rate 61%) with a median response duration of 6 months (2−29+). A significant difference in survival (P < 0.005) was observed between the 19 responders (median 25 months) and the 12 non-responders (median 9 months). A reduction in the transfusion need was observed in 41% of the transfusion-dependent patients with blast excess and in 53% of those without blast excess. Therefore, combined differentiating therapy seems more effective than previously reported single agent treatments and should be considered for a larger randomized study to assess its actual impact on survival of MDS patients.

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