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利妥昔单抗时代弥漫性大 B 细胞淋巴瘤自体干细胞移植后累及野放疗。

Involved field radiation after autologous stem cell transplant for diffuse large B-cell lymphoma in the rituximab era.

机构信息

Department of Radiation Oncology, University of Rochester Medical Center, Rochester, New York 14642, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2010 May 1;77(1):79-85. doi: 10.1016/j.ijrobp.2009.04.036. Epub 2009 Aug 3.

DOI:10.1016/j.ijrobp.2009.04.036
PMID:19647953
Abstract

PURPOSE

For patients with recurrent or refractory large B-cell non-Hodgkin's lymphoma, high-dose chemotherapy and autologous stem cell transplant (ASCT) is the treatment of choice. We evaluated the role of involved field radiation therapy (IFRT) post-ASCT for patients initially induced with cyclophosphamide, adriamycin, vincristine, and prednisone (CHOP) or, more recently, rituximab-CHOP (R-CHOP).

MATERIALS AND METHODS

Between May 1992 and April 2005, 176 patients underwent ASCT for recurrent or refractory large B-cell non-Hodgkin's lymphoma; 164 patients were evaluable for endpoint analysis. Fifty percent of the CHOP group (n = 131), and 39% of the R-CHOP group (n = 33), received IFRT. Follow-up from the time of transplant was a median/mean of 1.7/3 years (range, 0.03-13 years).

RESULTS

The 5-year overall survival (OS) and disease-specific survival (DSS) improved with IFRT in both the R-CHOP (p = 0.006 and 0.02, respectively) and CHOP (p = 0.02 and p = 0.04, respectively) groups. IFRT was associated with a 10% (p = 0.17) reduction in local failure, alone or with a distant site. On univariate analysis, IFRT was associated with superior OS (hazard ratio [HR] = 0.50 [95% CI 0.32, 0.78]; p = 0.002) and DSS (HR = 0.53 [95% CI 0.33, 0.86]; p = 0.009). Presence of B symptoms was adverse (p = 0.03). On multivariate analysis, only IFRT was associated with significant improvement in OS (HR = 0.35 [0.18, 0.68]; p = 0.002) and DSS (HR = 0.39 [95% CI 0.18, 0.84]; p = 0.01).

CONCLUSIONS

Recognizing that positive and negative patient selection bias exists for the use of IFRT post-ASCT, patients initially treated with CHOP or R-CHOP and who undergo ASCT for recurrent or refractory disease may benefit from subsequent IFRT presumably due to enhanced local control that can translate into a survival advantage.

摘要

目的

对于复发或难治性大 B 细胞非霍奇金淋巴瘤患者,大剂量化疗和自体干细胞移植(ASCT)是首选治疗方法。我们评估了 ASCT 后受累野放疗(IFRT)在最初接受环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)诱导或最近接受利妥昔单抗-CHOP(R-CHOP)诱导的患者中的作用。

材料和方法

1992 年 5 月至 2005 年 4 月,176 例患者因复发或难治性大 B 细胞非霍奇金淋巴瘤接受 ASCT;164 例患者可进行终点分析。CHOP 组的 50%(n=131)和 R-CHOP 组的 39%(n=33)接受了 IFRT。从移植时起的中位/平均随访时间为 1.7/3 年(范围,0.03-13 年)。

结果

R-CHOP 组(p=0.006 和 0.02)和 CHOP 组(p=0.02 和 p=0.04)中,IFRT 可改善 5 年总生存率(OS)和疾病特异性生存率(DSS)。IFRT 可单独或联合远处部位降低局部失败率 10%(p=0.17)。单因素分析显示,IFRT 与 OS 改善相关(风险比[HR]为 0.50[95%CI 0.32, 0.78];p=0.002)和 DSS(HR 为 0.53[95%CI 0.33, 0.86];p=0.009)。存在 B 症状是不利的(p=0.03)。多因素分析显示,只有 IFRT 与 OS(HR=0.35[0.18, 0.68];p=0.002)和 DSS(HR=0.39[95%CI 0.18, 0.84];p=0.01)的显著改善相关。

结论

鉴于在 ASCT 后使用 IFRT 存在阳性和阴性患者选择偏倚,最初接受 CHOP 或 R-CHOP 治疗且因复发或难治性疾病接受 ASCT 的患者可能受益于随后的 IFRT,可能是因为增强局部控制可转化为生存优势。

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