Increase in platelet count in older, poor-risk patients with acute myeloid leukemia or myelodysplastic syndrome treated with valproic acid and all-trans retinoic acid

被引:75
|
作者
Pilatrino, C
Cilloni, D
Messa, E
Morotti, A
Giugliano, E
Pautasso, M
Familiari, U
Cappia, S
Pelicci, PG
Lo Coco, F
Saglio, G
Guerrasio, A
机构
[1] Osped San Luigi Orbassano, Clin Pathol Lab, I-10043 Orbassano, Turin, Italy
[2] Osped San Luigi Orbassano, Dept Pathol, I-10043 Orbassano, Turin, Italy
[3] Univ Turin, Dept Clin & Biol Sci, Turin, Italy
[4] European Inst Oncol, Milan, Italy
[5] Univ Roma La Sapienza, Dept Cellular Biotechnol & Hematol, Rome, Italy
关键词
differentiation therapy; histone deacetylase inhibitors; valproic acid; acute myeloid leukemia; myelodysplasia; poor-risk patients;
D O I
10.1002/cncr.21132
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The authors investigated the efficacy and safety of the histone deacetylase inhibitors valproic acid (VPA) and all-trans retinoic acid (ATRA) as differentiation agents in a cohort of older, poor-risk patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). METHODS. Twenty older patients with recurrent or refractory AML or MDS were treated in a Phase 11 protocol with sequential VPA and ATRA therapy. VPA was started at a dose of 10 mg/kg per day and then escalated to achieve the serum concentration of 45-100 mu g/mL. ATRA was added at 45 mg/square meters (sm) per day when VPA reached the target serum concentration. Only patients treated continuously for 2 months were considered evaluable. RESULTS. Hematologic improvement, according to World Health Organization criteria, was observed in 6 of 20 patients enrolled in the protocol but in 6 of 11 considered evaluable. In five patients, a major platelet response was observed, achieving platelet transfusion independence. Three of these five patients also exhibited a minor erythroid response. A sixth patient showed both a minor erythroid response and a platelet response. The median duration of response was 189 days (range, 63-550 days). No significant reduction in the blast count was observed. Grade 3 neurocortical toxicity was observed in four patients. Severe bone pain was experienced by 4 patients (2 Grade 4 and 2 Grade 3) and was associated with an increase in the peripheral blast cell count. Treatment with ATRA did not modify the response observed with VPA alone. CONCLUSIONS: Differentiation therapy with VPA was of clinical benefit in approximately 30% of elderly patients with AML and MDS of the refractory anemia with excess of blast type with unfavorable prognostic features. A striking platelet transfusion independence lasting several months may be obtained in some patients, reducing the burden of palliative care and improving the quality of life. (c) 2005 American Cancer Society.
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收藏
页码:101 / 109
页数:9
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