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CHOP化疗后序贯托西莫单抗/碘I-131托西莫单抗用于初治滤泡性非霍奇金淋巴瘤的II期试验:西南肿瘤协作组S9911方案的五年随访

Phase II trial of CHOP chemotherapy followed by tositumomab/iodine I-131 tositumomab for previously untreated follicular non-Hodgkin's lymphoma: five-year follow-up of Southwest Oncology Group Protocol S9911.

作者信息

Press Oliver W, Unger Joseph M, Braziel Rita M, Maloney David G, Miller Thomas P, Leblanc Michael, Fisher Richard I

机构信息

Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

出版信息

J Clin Oncol. 2006 Sep 1;24(25):4143-9. doi: 10.1200/JCO.2006.05.8198. Epub 2006 Aug 8.

Abstract

PURPOSE

Advanced follicular lymphoma (FL) is incurable with conventional chemotherapy and radiotherapy, and optimal front-line management is controversial. This study was performed to determine the efficacy of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy followed by tositumomab/iodine I-131 tositumomab.

PATIENTS AND METHODS

From 1999 to 2000, the Southwest Oncology Group (SWOG) conducted a phase II trial (S9911) to test a novel new regimen consisting of six cycles of CHOP chemotherapy followed 4 to 8 weeks later by tositumomab/iodine I-131 tositumomab in 90 eligible patients with previously untreated, advanced-stage FL.

RESULTS

The overall response rate was 91%, including a 69% complete remission (CR) rate. After a median follow-up time of 5.1 years, the estimated 5-year overall survival (OS) rate was 87%, and the progression-free survival (PFS) rate was 67%. The 5-year estimates of OS and PFS were each 23% better (absolute difference) than the corresponding figures for patients treated on previous SWOG protocols with CHOP alone. An analysis according to the Follicular Lymphoma International Prognostic Index showed that 21% of patients had high-risk features, 44% had intermediate-risk features, and 34% had low-risk features. High-risk patients had worse OS than lower risk patients (P = .05), but differences in PFS were not statistically significant (P = .21). Serial monitoring of the t(14;18) translocation in bone marrow by polymerase chain reaction demonstrated that 32 of 38 informative patients obtained molecular CRs, including seven patients (18%) after CHOP and 24 additional patients (63%) after tositumomab/iodine I-131 tositumomab. (The timing of conversion of one patient was unclear.)

CONCLUSION

A prospective, phase III, randomized Intergroup Trial is currently underway comparing the efficacy of the promising CHOP + tositumomab/iodine I-131 tositumomab regimen with the efficacy of CHOP + rituximab.

摘要

目的

晚期滤泡性淋巴瘤(FL)无法通过传统化疗和放疗治愈,最佳一线治疗方案存在争议。本研究旨在确定环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)化疗后使用托西莫单抗/碘I - 131托西莫单抗的疗效。

患者与方法

1999年至2000年,西南肿瘤协作组(SWOG)开展了一项II期试验(S9911),以测试一种新的方案,该方案包括六个周期的CHOP化疗,4至8周后对90例符合条件的先前未接受治疗的晚期FL患者使用托西莫单抗/碘I - 131托西莫单抗。

结果

总缓解率为91%,其中完全缓解(CR)率为69%。中位随访时间为5.1年后,估计5年总生存率(OS)为87%,无进展生存率(PFS)为67%。OS和PFS的5年估计值分别比之前SWOG仅使用CHOP方案治疗的患者的相应数值高出23%(绝对差异)。根据滤泡性淋巴瘤国际预后指数进行的分析显示,21%的患者具有高危特征,44%具有中危特征,34%具有低危特征。高危患者的OS比低危患者差(P = 0.05),但PFS差异无统计学意义(P = 0.21)。通过聚合酶链反应对骨髓中t(14;18)易位进行连续监测表明,38例可提供信息的患者中有32例获得了分子CR,其中包括7例(18%)在CHOP治疗后和另外24例(63%)在托西莫单抗/碘I - 131托西莫单抗治疗后。(1例患者的转化时间不明。)

结论

目前正在进行一项前瞻性III期随机组间试验,比较有前景的CHOP + 托西莫单抗/碘I - 131托西莫单抗方案与CHOP + 利妥昔单抗方案的疗效。

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