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苯达莫司汀联合利妥昔单抗治疗初治慢性淋巴细胞白血病患者:德国慢性淋巴细胞白血病研究组的一项多中心 II 期试验。

Bendamustine in combination with rituximab for previously untreated patients with chronic lymphocytic leukemia: a multicenter phase II trial of the German Chronic Lymphocytic Leukemia Study Group.

机构信息

Clemens-Martin Wendtner, University of Cologne, Cologne, Germany.

出版信息

J Clin Oncol. 2012 Sep 10;30(26):3209-16. doi: 10.1200/JCO.2011.39.2688. Epub 2012 Aug 6.

Abstract

PURPOSE

We investigated the safety and efficacy of bendamustine and rituximab (BR) in previously untreated patients with chronic lymphocytic leukemia (CLL).

PATIENTS AND METHODS

In all, 117 patients, age 34 to 78 years, 46.2% of patients at Binet stage C, and 25.6% of patients age 70 years or older received BR chemoimmunotherapy for first-line treatment of CLL. Bendamustine was administered at a dose of 90 mg/m(2) on days 1 and 2 combined with 375 mg/m(2) rituximab on day 0 of the first course and 500 mg/m(2) on day 1 during subsequent courses for up to six courses.

RESULTS

Overall response rate was 88.0% (95% CI, 80.7% to 100.0%) with a complete response rate of 23.1% and a partial response rate of 64.9%. Ninety percent of patients with del(11q), 94.7% with trisomy 12, 37.5% with del(17p), and 89.4% with unmutated IGHV status responded to treatment. After a median observation time of 27.0 months, median event-free survival was 33.9 months, and 90.5% of patients were alive. Grade 3 or 4 severe infections occurred in 7.7% of patients. Grade 3 or 4 adverse events for neutropenia, thrombocytopenia, and anemia were documented in 19.7%, 22.2%, and 19.7% of patients, respectively.

CONCLUSION

Chemoimmunotherapy with BR is effective and safe in patients with previously untreated CLL.

摘要

目的

我们研究了苯达莫司汀和利妥昔单抗(BR)在未经治疗的慢性淋巴细胞白血病(CLL)患者中的安全性和疗效。

患者和方法

共有 117 例年龄在 34 至 78 岁的患者,46.2%的患者处于 Binet 期 C,25.6%的患者年龄在 70 岁或以上,接受 BR 化疗免疫治疗作为 CLL 的一线治疗。苯达莫司汀剂量为 90mg/m2,在第 1 天和第 2 天给药,第 0 天第 1 疗程给予 375mg/m2利妥昔单抗,第 1 疗程给予 500mg/m2,最多 6 个疗程。

结果

总缓解率为 88.0%(95%CI,80.7%至 100.0%),完全缓解率为 23.1%,部分缓解率为 64.9%。90%的 del(11q)患者、94.7%的 trisomy 12 患者、37.5%的 del(17p)患者和 89.4%的 IGHV 未突变患者对治疗有反应。在 27.0 个月的中位观察时间后,中位无事件生存时间为 33.9 个月,90.5%的患者存活。7.7%的患者发生 3 级或 4 级严重感染。中性粒细胞减少、血小板减少和贫血的 3 级或 4 级不良事件分别在 19.7%、22.2%和 19.7%的患者中发生。

结论

BR 化疗免疫治疗对未经治疗的 CLL 患者有效且安全。

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