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CHOP±利妥昔单抗样疗法联合放射治疗对Ⅰ期弥漫性大B细胞淋巴瘤患者的疗效

[Efficacy of CHOP+/-Rituximab-like therapy plus radiation therapy for patients with diffuse large B-cell lymphoma stage I].

作者信息

Ueda Kyoko, Yokoyama Masahiro, Asai Hiroaki, Koudaira Makoto, Yamada Syuhei, Katsube Atsushi, Mishima Yuko, Sakajiri Sakura, Takeuchi Kengo, Saotome Takashi, Terui Yasuhito, Takahashi Syunji, Hatake Kiyohiko

机构信息

Dept. of Medical Oncology and Hematology, Cancer Institute Hospital.

出版信息

Gan To Kagaku Ryoho. 2010 May;37(5):853-7.

Abstract

Clinically, R-CHOP-like therapy plus radiation therapy is commonly performed for patients with limited stage diffuse large B-cell lymphoma. However, the efficacy and the safety of the management have not been evaluated properly. In particular, we have few definitive reports about patients with stage I DLBCL. This time we evaluated the effect of CHOP+/-R-like therapy plus radiation therapy, by analyzing 28 patients with stage I DLBCL, retrospectively. 15 patients were treated with the RCHOP-like therapy, and 13 received CHOP-like therapy combined with radiation therapy. A complete response was observed in all of the patients. With a median follow-up time of 14 months, 1-year progression-free survival (PFS) was 100%, and the 1-year overall survival (OS) was 100% for the patients receiving the R-CHOP-like therapy. With a median follow-up time of 68 months, 5-year PFS was 84. 6%, and 5-year OS was 100% for patients receiving the CHOP-like therapy. Since the followup time was not enough and the patient numbers were too few, the benefit of the addition of Rituximab to the CHOP therapy could not be clarified. We need to assess the safety and the efficacy of the combined modality therapy for patients with limited-stage DLBCL by a larger prospective study.

摘要

临床上,对于局限期弥漫性大B细胞淋巴瘤患者,通常采用类似R-CHOP方案的治疗加放射治疗。然而,这种治疗方式的疗效和安全性尚未得到恰当评估。特别是,关于Ⅰ期弥漫性大B细胞淋巴瘤(DLBCL)患者,我们几乎没有确切的报道。此次我们通过回顾性分析28例Ⅰ期DLBCL患者,评估了类似CHOP±R方案的治疗加放射治疗的效果。15例患者接受了类似RCHOP方案的治疗,13例接受了类似CHOP方案的治疗并联合放射治疗。所有患者均观察到完全缓解。接受类似R-CHOP方案治疗的患者,中位随访时间为14个月,1年无进展生存率(PFS)为100%,1年总生存率(OS)为100%。接受类似CHOP方案治疗的患者,中位随访时间为68个月,5年PFS为84.6%,5年OS为100%。由于随访时间不足且患者数量过少,CHOP方案加用利妥昔单抗的益处尚无法明确。我们需要通过更大规模的前瞻性研究来评估局限期DLBCL患者联合治疗模式的安全性和疗效。

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