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全反式维甲酸治疗急性早幼粒细胞白血病:纽约经验的最新进展。

Treatment of acute promyelocytic leukemia with all-trans retinoic acid: an update of the New York experience.

作者信息

Warrell R P, Maslak P, Eardley A, Heller G, Miller W H, Frankel S R

机构信息

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10021.

出版信息

Leukemia. 1994 Jun;8(6):929-33.

PMID:8207986
Abstract

In an ongoing study, we treated 79 patients with a molecular diagnosis of acute promyelocytic leukemia (APL) using all-trans retinoic acid (RA) for remission induction. Newly diagnosed patients received cytotoxic chemotherapy for consolidation, and previously treated patients received extended all-trans RA therapy, or a radionuclide-conjugated monoclonal antibody as post-remission treatment. Unlike studies in Europe, full-dose chemotherapy was not given during induction for patients who developed leukocytosis. Overall, 43 of 49 newly diagnosed patients (88%) and 25 of 30 previously treated patients (83%) achieved complete remission. We did not encounter de novo resistance to all-trans RA in any patient who was positive for PML/RAR-alpha rearrangements by reverse transcription polymerase chain reaction analysis. Ten patients died during induction from intracranial or pulmonary hemorrhage (six patients) or the 'retinoic acid syndrome' (four patients). The use of leukapheresis or low-dose chemotherapy (hydroxyurea or cytosine arabinoside) for drug-induced leukocytosis did not decrease early mortality. Compared to historical controls, early mortality was not affected by treatment with all-trans RA; however, both relapse-free and overall survival were significantly increased. Maintenance therapy with all-trans RA was associated with short remission duration, and relapses while taking the drug were universally associated with resistance to further retinoid treatment. We conclude that the use of all-trans RA for remission induction, with or without full-dose chemotherapy, has significantly increased the survival of patients with APL. While early mortality has not yet been reduced, the avoidance of full-dose chemotherapy during induction has significantly reduced early morbidity. The major outstanding clinical issue is the development of strategies that maximize safety in high-risk patients for whom intracranial hemorrhage remains the major cause of death.

摘要

在一项正在进行的研究中,我们使用全反式维甲酸(RA)对79例分子诊断为急性早幼粒细胞白血病(APL)的患者进行缓解诱导治疗。新诊断的患者接受细胞毒性化疗进行巩固治疗,既往接受过治疗的患者接受延长的全反式RA治疗,或接受放射性核素偶联单克隆抗体作为缓解后治疗。与欧洲的研究不同,对于发生白细胞增多症的患者,诱导治疗期间未给予全剂量化疗。总体而言,49例新诊断患者中有43例(88%)、30例既往接受过治疗的患者中有25例(83%)实现了完全缓解。通过逆转录聚合酶链反应分析,在任何PML/RAR-α重排呈阳性的患者中,我们均未遇到对全反式RA的原发性耐药。10例患者在诱导治疗期间死于颅内或肺出血(6例患者)或“维甲酸综合征”(4例患者)。对于药物诱导的白细胞增多症,使用白细胞去除术或低剂量化疗(羟基脲或阿糖胞苷)并未降低早期死亡率。与历史对照相比,全反式RA治疗对早期死亡率没有影响;然而,无复发生存期和总生存期均显著延长。全反式RA维持治疗与缓解期持续时间短相关,在服用该药物期间复发普遍与对进一步的维甲酸治疗耐药有关。我们得出结论,使用全反式RA进行缓解诱导治疗,无论是否联合全剂量化疗,均显著提高了APL患者的生存率。虽然早期死亡率尚未降低,但诱导治疗期间避免使用全剂量化疗显著降低了早期发病率。主要的突出临床问题是制定策略,以最大限度地提高高危患者的安全性,对于这些患者,颅内出血仍然是主要的死亡原因。

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