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培门冬酶、依托泊苷、吉西他滨(PEG)序贯受累野放疗治疗早期结外 NK/T 细胞淋巴瘤的 II 期研究

英文原题:Phase II study of pegaspargase, etoposide, gemcitabine (PEG) followed by involved-field radiation therapy in early-stage extranodal natural killer/T-cell lymphoma.

查看英文原题

Phase II study of pegaspargase, etoposide, gemcitabine (PEG) followed by involved-field radiation therapy in early-stage extranodal natural killer/T-cell lymphoma.

PubMed 2024/09/13(内容时间) Hematology Q3 · IF 2(JCR 2025)

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研究概要

PEG 后接 IFRT 是早期 ENKTL 安全有效的初始治疗,显示出令人印象深刻的 PFS 和 OS 率。这一有前景的方法值得在随机对照试验中进一步验证(注册于 ClinicalTrials.gov NCT02705508)。试验注册:ClinicalTrials.gov 标识符:NCT02705508。

研究思路结论见上方概要

结外NK/T细胞淋巴瘤(ENKTL)的预后较差,最佳治疗方案仍存在争议。本研究旨在评估一种新的联合治疗方案的安全性和有效性。

培门冬酶、依托泊苷和吉西他滨(PEG)联合受累野放疗(IFRT)治疗新诊断早期ENKTL患者的2期研究。患者接受4个疗程PEG后行IFRT。主要终点为IFRT后的完全缓解(CR)、部分缓解(PR)和客观缓解率(ORR)。次要终点包括无进展生存期(PFS)、总生存期(OS)和不良事件。

共纳入34例Ann Arbor I/II期连续患者。3例患者在PEG治疗期间出现疾病进展,其余31例接受了IFRT。ORR为88.2%(30/34),包括28例(82.4%)完全缓解和2例(5.8%)部分缓解。中位随访时间为56.0个月(四分位距[IQR],36.0-66.9个月),估计5年PFS和OS分别为87.4%(95%置信区间[CI],69.5%-94.8%)和97.1%(95%CI,80.1%-99.6%)。大多数不良事件为血液学毒性,且易于管理。

展开英文摘要原文

The prognosis of extra-nodal NK/T cell lymphoma (ENKTL) is poor, and the optimal therapy remains controversial. This study aims to evaluate the safety and efficacy of a new combined modality therapy.

Phase-2 study of pegaspargase, etoposide and gemcitabine (PEG) combined with involved field radiation therapy (IFRT) in newly-diagnosed patients with early-stage ENKTL. Patients received 4 course of PEG followed by IFRT. The primary endpoints were complete response (CR), partial response (PR), and objective response rate (ORR) after IFRT. Secondary endpoints included progression-free survival (PFS), overall survival (OS) and adverse events.

34 consecutive patients with Ann Arbor stage I/II were enrolled. 3 patients progressed on PEG, while the remaining 31 received IFRT. The ORR was 88.2% (30/34), included 28 (82.4%) complete and 2 (5.8%) partial responses. With a median follow-up of 56.0 months (Interquartile Range [IQR], 36.0-66.9 months), the estimated 5-year PFS and OS were 87.4% (95% Confidence Interval [CI],69.5%-94.8%) and 97.1% (95%CI, 80.1%-99.6%), respectively. Most adverse events were hematological and easily managed.

PEG followed by IFRT is a safe and effective initial therapy for early-stage ENKTL, demonstrating impressive PFS and OS rates. This promising approach warrants further validation in a randomized controlled trial (Registered at Clinicaltrials.gov NCT02705508). Trial registration: ClinicalTrials.gov identifier: NCT02705508.

论文信息

作者
Feng D、Yan Z、Fu B、Bai S、Zhu L、Gale RP、Xia Z、Liang Y
单位
State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.China
文献类型
II 期临床试验
期刊
Hematology (Amsterdam, Netherlands)2024 Dec
原文标识
PubMed 39268981 · DOI 10.1080/16078454.2024.2402102