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利妥昔单抗联合三个周期CHOP方案及受累野放疗用于局限期侵袭性B细胞淋巴瘤患者的II期研究:西南肿瘤协作组研究0014

Phase II study of rituximab plus three cycles of CHOP and involved-field radiotherapy for patients with limited-stage aggressive B-cell lymphoma: Southwest Oncology Group study 0014.

作者信息

Persky Daniel O, Unger Joseph M, Spier Catherine M, Stea Baldassarre, LeBlanc Michael, McCarty Matthew J, Rimsza Lisa M, Fisher Richard I, Miller Thomas P

机构信息

Arizona Cancer Center, University of Arizona, Tucson, AZ, USA.

出版信息

J Clin Oncol. 2008 May 10;26(14):2258-63. doi: 10.1200/JCO.2007.13.6929. Epub 2008 Apr 14.

DOI:10.1200/JCO.2007.13.6929
PMID:18413640
Abstract

PURPOSE

To evaluate the effect of rituximab in limited-stage diffuse large B-cell lymphoma (DLBCL), we conducted a multicenter phase II trial combining rituximab with three cycles of CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone; R-CHOP) followed by involved-field radiation therapy (IFRT).

PATIENTS AND METHODS

Southwest Oncology Group (SWOG) study S0014 enrolled patients with newly diagnosed, aggressive, CD20-expressing non-Hodgkin's lymphoma (NHL). Patients had limited-stage disease and at least one adverse risk factor as defined by the stage-modified International Prognostic Index (nonbulky stage II disease, age > 60 years, WHO performance status of 2, or elevated serum lactate dehydrogenase). Four doses of rituximab were infused on days -7, 1, 22, and 43, and CHOP was administered on days 3, 24, and 45, followed 3 weeks later by 40 to 46 Gy of IFRT.

RESULTS

Sixty patients with aggressive NHL were eligible. With the median follow-up of 5.3 years, treatment resulted in a progression-free survival (PFS) of 93% at 2 years and 88% at 4 years. Overall survival (OS) was 95% at 2 years and 92% at 4 years. These results were compared with those from a historic group of patients treated without rituximab on S8736, demonstrating PFS of 78% and OS of 88% at 4 years.

CONCLUSION

In limited-stage DLBCL, the addition of rituximab to three cycles of CHOP plus IFRT met prespecified study criteria of efficacy, with 2-year PFS of at least 84%, meriting further investigation. There is a pattern of continuing relapse with modest survival gains. We hypothesize that such a pattern may be the result of biologic differences between limited- and advanced-stage lymphoma.

摘要

目的

为评估利妥昔单抗在局限期弥漫性大B细胞淋巴瘤(DLBCL)中的疗效,我们开展了一项多中心II期试验,将利妥昔单抗与三个周期的CHOP方案(环磷酰胺、多柔比星、长春新碱和泼尼松;R-CHOP)联合使用,随后进行受累野放射治疗(IFRT)。

患者与方法

西南肿瘤协作组(SWOG)的S0014研究纳入了新诊断的、侵袭性的、表达CD20的非霍奇金淋巴瘤(NHL)患者。患者患有局限期疾病,且至少有一项根据分期修正的国际预后指数定义的不良风险因素(非大包块II期疾病、年龄>60岁、世界卫生组织体能状态为2或血清乳酸脱氢酶升高)。在第-7、1、22和43天静脉输注四剂利妥昔单抗,在第3、24和45天给予CHOP方案,3周后给予40至46 Gy的IFRT。

结果

60例侵袭性NHL患者符合条件。中位随访5.3年,治疗导致2年无进展生存率(PFS)为93%,4年为88%。总生存率(OS)2年时为95%,4年时为92%。这些结果与S8736研究中一组未使用利妥昔单抗治疗的历史患者的结果进行了比较,该组患者4年时的PFS为78%,OS为88%。

结论

在局限期DLBCL中,在三个周期的CHOP方案加IFRT基础上加用利妥昔单抗符合预设的疗效研究标准,2年PFS至少为84%,值得进一步研究。存在持续复发且生存获益有限的模式。我们推测这种模式可能是局限期和晚期淋巴瘤生物学差异的结果。

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