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米托蒽醌、长春新碱和泼尼松用于复发或原发难治性急性淋巴细胞白血病及末端脱氧核苷酸转移酶阳性原始细胞期慢性粒细胞白血病的成人患者。

Mitoxantrone, vincristine, and prednisone in adults with relapsed or primarily refractory acute lymphocytic leukemia and terminal deoxynucleotidyl transferase positive blastic phase chronic myelocytic leukemia.

作者信息

Paciucci P A, Keaveney C, Cuttner J, Holland J F

出版信息

Cancer Res. 1987 Oct 1;47(19):5234-7.

PMID:3476201
Abstract

A combination of mitoxantrone, vincristine, and prednisone was used to treat 19 patients with acute lymphocytic leukemia. Of these, 12 were patients with acute lymphoblastic leukemia (ALL) (9 in first relapse and 5 primarily refractory to standard induction therapy with daunorubicin, vincristine, and prednisone), 2 had a phenotypic ALL relapse after an initial diagnosis of acute myelocytic leukemia and 5 had terminal deoxynucleotidyl transferase positive blastic phase chronic myelogenous leukemia (BCML). Eight patients with ALL (and of these, four with primarily anthracycline resistant disease), and two with BCML achieved complete remission. Five patients died in induction (three ALL from sepsis and two BCML from bleeding), and five had progressive disease. Median duration of response was 5 months, with two primarily refractory ALL patients remaining in continuing complete remission at 28 and 31 months. Treatment was well tolerated, with minimal nausea and vomiting, and oral mucositis. Posttreatment transient hepatic dysfunction was seen in 80% of patients. Mitoxantrone, vincristine, and prednisone are an active combination for the treatment of relapsed or refractory ALL and of terminal deoxynucleotidyl transferase positive BCML. The finding that four of five primarily refractory ALL patients were induced in complete remission supports the contention that mitoxantrone and anthracyclines are not cross-resistant.

摘要

采用米托蒽醌、长春新碱和泼尼松联合治疗19例急性淋巴细胞白血病患者。其中,12例为急性淋巴细胞白血病(ALL)患者(9例首次复发,5例对柔红霉素、长春新碱和泼尼松标准诱导治疗原发性耐药),2例在急性髓细胞白血病初始诊断后出现ALL表型复发,5例为末端脱氧核苷酸转移酶阳性的慢性粒细胞白血病急变期(BCML)。8例ALL患者(其中4例对蒽环类药物原发性耐药)和2例BCML患者获得完全缓解。5例患者在诱导期死亡(3例ALL死于败血症,2例BCML死于出血),5例病情进展。中位缓解持续时间为5个月,2例原发性耐药ALL患者分别在28个月和31个月时仍持续完全缓解。治疗耐受性良好,恶心、呕吐和口腔黏膜炎轻微。80%的患者治疗后出现短暂性肝功能障碍。米托蒽醌、长春新碱和泼尼松联合用药对复发或难治性ALL以及末端脱氧核苷酸转移酶阳性的BCML治疗有效。5例原发性耐药ALL患者中有4例诱导获得完全缓解,这一发现支持米托蒽醌和蒽环类药物不存在交叉耐药的观点。

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