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喷司他丁治疗毛细胞白血病患者缓解期、死亡率及第二原发性恶性肿瘤的长期随访

Long-term follow-up of remission duration, mortality, and second malignancies in hairy cell leukemia patients treated with pentostatin.

作者信息

Flinn I W, Kopecky K J, Foucar M K, Head D, Bennett J M, Hutchison R, Corbett W, Cassileth P, Habermann T, Golomb H, Rai K, Eisenhauer E, Appelbaum F, Cheson B, Grever M R

机构信息

Johns Hopkins University, Baltimore, MD, USA.

出版信息

Blood. 2000 Nov 1;96(9):2981-6.

Abstract

The nucleoside analogue, pentostatin, has demonstrated high complete response rates and long relapse-free survival times in patients with hairy cell leukemia, a disease that historically had been unresponsive to treatment. Long-term data on duration of overall survival and relapse-free survival and incidence of subsequent malignancies with this agent are lacking. Patients completing the treatment phase of a randomized, intergroup study who received pentostatin as an initial treatment or who crossed over after failure of interferon alpha were followed for survival, relapse, and diagnosis of subsequent malignancies. Two hundred forty-one patients treated with pentostatin as initial therapy (n = 154) or who crossed over after failure of interferon alpha (n = 87) were followed for a median duration of 9.3 years. Estimated 5- and 10-year survival rates (95% confidence interval) for all patients combined were 90% (87%-94%) and 81% (75%-86%), respectively. In the 173 patients with a confirmed complete response to pentostatin treatment, 5- and 10-year relapse-free survival rates were 85% (80%-91%) and 67% (58%-76%), respectively. Survival curves for patients initially treated with pentostatin and those crossed over were similar. Only 2 of 40 deaths were attributed to hairy cell leukemia. The mortality rate and incidence of subsequent malignancies were not higher than expected in the general population. Pentostatin is a highly effective regimen for hairy cell leukemia that produces durable complete responses. Subsequent malignancies do not appear to be increased with pentostatin treatment.

摘要

核苷类似物喷司他丁已在毛细胞白血病患者中显示出高完全缓解率和长无复发生存时间,而毛细胞白血病这种疾病在历史上一直对治疗无反应。目前缺乏关于该药物总体生存时间、无复发生存时间以及后续恶性肿瘤发生率的长期数据。对完成一项随机、组间研究治疗阶段的患者进行随访,这些患者最初接受喷司他丁治疗或在α干扰素治疗失败后交叉使用喷司他丁,以观察其生存、复发及后续恶性肿瘤的诊断情况。241例接受喷司他丁作为初始治疗(n = 154)或在α干扰素治疗失败后交叉使用喷司他丁(n = 87)的患者,中位随访时间为9.3年。所有患者合并后的估计5年和10年生存率(95%置信区间)分别为90%(87% - 94%)和81%(75% - 86%)。在173例对喷司他丁治疗有确诊完全缓解的患者中,5年和10年无复发生存率分别为85%(80% - 91%)和67%(58% - 76%)。最初接受喷司他丁治疗的患者和交叉使用喷司他丁的患者的生存曲线相似。40例死亡患者中只有2例归因于毛细胞白血病。死亡率和后续恶性肿瘤的发生率不高于一般人群的预期。喷司他丁是治疗毛细胞白血病的一种高效方案,可产生持久的完全缓解。喷司他丁治疗似乎不会增加后续恶性肿瘤的发生。

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