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成人原发性难治性或复发性急性髓系白血病的序贯化疗:II期Gemia方案的结果

Time sequential chemotherapy for primary refractory or relapsed adult acute myeloid leukemia: results of the phase II Gemia protocol.

作者信息

Martino R, Guardia R, Altés A, Sureda A, Brunet S, Sierra J

机构信息

Servei d'Hematologia Clínica, Hospital de la Santa Creu i Sant Pau, Av. Sant Antoni M Claret, 167, 08025 Barcelona, Spain. 5059@hsp. santpau.es.

出版信息

Haematologica. 1999 Mar;84(3):226-30.

Abstract

BACKGROUND AND OBJECTIVE

High-dose cytarabine (HDAra-C), mitoxantrone and etoposide are the mainstay of several active regimens against relapsed or refractory acute myelogenous leukemia (AML). We designed a phase II study to assess the efficacy and side effects of a time sequential application of mitoxantrone plus intermediate-dose Ara-C followed by HDAra-C plus etoposide (GEMIA) in adult patients with refractory or relapsed AML.

DESIGN AND METHODS

Patients with refractory or relapsed AML were eligible for GEMIA salvage therapy, which comprised mitoxantrone 12 mg/m2/day on days 1-3, Ara-C 500 mg/m2/day as a 24-hour continuous infusion on days 1-3, followed by HDAra-C 2 g/m2/12-hourly on days 6-8 and etoposide 100 mg/m2/12-hourly on days 6-8. Granulocyte colony-stimulating factor was started on day 14. In patients above the age of 55 the dose of Ara-C in the first sequence (days 1-3) was reduced to 250 mg/m2.

RESULTS

Twenty patients were included, of whom 12 achieved complete remission after GEMIA (60%, 95% CI 40-80%), one was refractory and five died early from infection. Two additional patients achieved partial remission after GEMIA and complete remission after consolidation chemotherapy, for a final CR rate of 70% (95% CI 48-88%). Neutrophils recovered at a median of 27 days (range, 22-43) and platelets 46 days (range, 25-59) after the start of treatment. The median duration of remission was 133 days (range, 36-417+) whereas overall survival time lasted for a median of 153 days (range, 13-554+). Treatment-associated toxicity was comprised predominantly of infection, mucositis and diarrhea that reached World Health Organization grades III-V in 40%, 40% and 30% of patients, respectively. Despite the intention to rapidly proceed to a hematopoietic stem cell transplant in patients in remission, only five patients reached the transplant.

INTERPRETATION AND CONCLUSIONS

The GEMIA time sequential chemotherapy regimen appears effective in obtaining remissions in refractory and relapsed adult AML. The high toxicity seen, however, suggests that its design is amenable to further improvements, especially in more elderly patients. Since remissions are short-lived, more innovative post-remission strategies are needed.

摘要

背景与目的

大剂量阿糖胞苷(HDAra-C)、米托蒽醌和依托泊苷是几种针对复发或难治性急性髓系白血病(AML)的有效方案的主要药物。我们设计了一项II期研究,以评估米托蒽醌加中剂量阿糖胞苷序贯应用,随后使用HDAra-C加依托泊苷(GEMIA)方案在难治性或复发性成年AML患者中的疗效和副作用。

设计与方法

难治性或复发性AML患者 eligible for GEMIA挽救治疗,该方案包括第1 - 3天米托蒽醌12 mg/m²/天,第1 - 3天阿糖胞苷500 mg/m²/天持续24小时静脉输注,随后第6 - 8天HDAra-C 2 g/m²每12小时一次,第6 - 8天依托泊苷100 mg/m²每12小时一次。第14天开始使用粒细胞集落刺激因子。55岁以上患者第一个疗程(第1 - 3天)阿糖胞苷剂量减至250 mg/m²。

结果

纳入20例患者,其中12例在GEMIA治疗后达到完全缓解(60%,95%CI 40 - 80%),1例难治,5例早期死于感染。另外2例患者在GEMIA治疗后达到部分缓解,巩固化疗后达到完全缓解,最终完全缓解率为70%(95%CI 48 - 88%)。治疗开始后中性粒细胞中位恢复时间为27天(范围22 - 43天),血小板为46天(范围25 - 59天)。缓解期中位持续时间为133天(范围36 - 417 +天),而总生存时间中位持续153天(范围13 - 554 +天)。治疗相关毒性主要包括感染、粘膜炎和腹泻,分别有40%、40%和30%的患者达到世界卫生组织III - V级。尽管计划在缓解患者中迅速进行造血干细胞移植,但只有5例患者进行了移植。

解读与结论

GEMIA序贯化疗方案在难治性和复发性成年AML患者中诱导缓解似乎有效。然而,观察到的高毒性表明其设计有待进一步改进,尤其是在老年患者中。由于缓解期短暂,需要更具创新性的缓解后策略。

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