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一项在初治局限期 I/IE 期鼻型结外 NK/T 细胞淋巴瘤,上呼吸消化道患者中比较 CEOP 方案联合或不联合司莫司汀作为诱导化疗的随机 II 期研究。

A randomized phase II study of CEOP with or without semustine as induction chemotherapy in patients with stage IE/IIE extranodal NK/T-cell lymphoma, nasal type in the upper aerodigestive tract.

机构信息

Department of Radiation Oncology, Fudan University, Shanghai, China.

出版信息

Radiother Oncol. 2009 Dec;93(3):492-7. doi: 10.1016/j.radonc.2009.08.045. Epub 2009 Sep 24.

Abstract

PURPOSE

In this randomized phase II study, we evaluated the efficacy of semustine added to CEOP regimen as induction chemotherapy in patients with stage I(E)/II(E) extranodal NK/T-cell lymphoma, nasal type in the upper aerodigestive tract.

PATIENTS AND METHODS

Seventy-five eligible patients were randomized to receive either CEOP or CEOP plus semustine followed by involved-field radiotherapy.

RESULTS

The overall response rate of induction chemotherapy was 57.9% in CEOP arm compared with 62.2% in CEOP plus semustine arm (P=0.71). With a median follow-up of 30.1 months, 2-year overall survival was 73.3% and 62.2%, respectively (P=0.37). Toxicities in both arms were comparable and manageable. Through univariate and multivariate analysis, PS of 2, Stage II(E) and elevated LDH level were identified to be adverse prognostic factors. A new prognostic index categorized three groups of patients (low risk, no adverse factors; intermediate risk, one factor; and high risk, 2 or 3 factors) with highly significant difference of prognosis. Two-year overall survival was 87.5%, 60.6% and 30%, respectively (P=0.0002).

CONCLUSIONS

The addition of semustine to CEOP regimen was not associated with improved efficacy. More effective treatment needs to be explored in patients with intermediate or high risk.

摘要

目的

在这项随机的 II 期研究中,我们评估了司莫司汀联合 CEOP 方案作为诱导化疗方案在治疗上呼吸消化道结外 NK/T 细胞淋巴瘤,鼻型(ⅠE/ⅡE 期)患者中的疗效。

方法

75 例合格患者被随机分为 CEOP 组或 CEOP 加司莫司汀组,随后接受累及野放疗。

结果

CEOP 组诱导化疗的总缓解率为 57.9%,CEOP 加司莫司汀组为 62.2%(P=0.71)。中位随访 30.1 个月后,2 年总生存率分别为 73.3%和 62.2%(P=0.37)。两组的毒性反应相当且可管理。通过单因素和多因素分析,PS 为 2、ⅡE 期和升高的 LDH 水平被确定为不良预后因素。一个新的预后指数将患者分为三组(低危,无不良因素;中危,有一个因素;高危,有 2 或 3 个因素),三组患者的预后有显著差异。2 年总生存率分别为 87.5%、60.6%和 30%(P=0.0002)。

结论

司莫司汀联合 CEOP 方案并未提高疗效。需要探索更有效的治疗方法来治疗中高危患者。

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