含氟达拉滨的化疗用于先前未治疗的低级别非霍奇金淋巴瘤患者。

The Korean Journal of Hematology Pub Date : 2011-09-01 Epub Date: 2011-09-30 DOI:10.5045/kjh.2011.46.3.180
Jae-Sook Ahn, Deok-Hwan Yang, Sung-Hoon Jung, Soo-Young Bae, Huong Thi Thanh Tran, Hyung Chul Park, Ha-Na Kim, Yeo-Kyeoung Kim, Hyeoung-Joon Kim, Je-Jung Lee
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引用次数: 3

摘要

背景:研究氟达拉滨联合化疗治疗既往未治疗的低级别(NHL)患者的临床疗效和安全性。方法:对25例新诊断为低级别非霍尼赫淋巴瘤的患者采用氟达拉滨联合化疗。氟达拉滨联合方案由氟达拉滨、米托蒽醌和地塞米松或氟达拉滨、环磷酰胺和米托蒽醌联合或不联合利妥昔单抗组成,每4周重复一次。结果:中位年龄为60岁(范围35 ~ 77岁),25例患者中有13例(52%)年龄≥60岁。25例中危滤泡性淋巴瘤国际预后指数(FLIPI)患者中有7例(28%)和25例高危FLIPI患者中有9例(36%)纳入本研究。化疗的中位数为6次(范围,2-9个周期)。氟达拉滨治疗的总缓解率为88%,包括52%的完全缓解和36%的部分缓解。在中位随访19个月期间,估计2年无事件生存率为63±10% (95% CI, 43-83), 2年总生存率为78±9% (95% CI, 60-96)。氟达拉滨联合化疗在84%的患者中经常伴有3级或4级中性粒细胞减少。然而,只有1例(4%)患者出现中性粒细胞减少感染。4例患者(16%)出现3级或以上的非血液学毒性,如急性冠状动脉综合征、颅内出血、过敏反应和胃癌。结论:氟达拉滨联合治疗对未治疗的低度非霍奇金淋巴瘤是一种高度有效且耐受性良好的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Fludarabine-containing chemotherapy for patients with previously untreated low-grade non-Hodgkin's lymphoma.

Background: The clinical efficacy and safety of fludarabine combination chemotherapy was investigated for the treatment of previously untreated patients with low-grade (NHL).

Methods: Twenty-five patients who were newly diagnosed as low-grade NHL were treated with fludarabine combination chemotherapy. Fludarabine combination regimens consisted of fludarabine, mitoxantrone and dexamethasone or fludarabine, cyclophosphamide and mitoxantrone with or without rituximab and repeated every 4 weeks.

Results: The median age was 60 years (range, 35-77 years), with 13 of 25 patients (52%) ≥60 years of age. Seven of 25 patients (28%) with an intermediate risk follicular lymphoma international prognostic index (FLIPI) and 9 of 25 patients (36%) with a high risk FLIPI were enrolled in this study. The delivered median number of chemotherapy was six (range, 2-9 cycles). The overall response rate with fludarabine-based treatment was 88%, including 52% complete remission and 36% partial remission. During the median follow-up of 19 months, the estimated 2-year event-free survival was 63±10% (95% CI, 43-83) and the 2-year overall survival was 78±9% (95% CI, 60-96). Fludarabine combination chemotherapy was frequently associated with grade 3 or 4 neutropenia in 84% patients. However, neutropenic infection was observed in only one (4%) patient. Four patients (16%) showed grade 3 or more non-hematologic toxicities, such as acute coronary syndrome, intracranial hemorrhage, anaphylaxis and gastric cancer.

Conclusion: Fludarabine-combination treatment was a highly active regimen with well toleration in untreated low-grade NHL.

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