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PEG 方案(培门冬酶、依托泊苷、吉西他滨)诱导化疗联合累及野放疗治疗早期结外鼻型自然杀伤/T 细胞淋巴瘤的Ⅱ期临床研究。

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

机构信息

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.

Department of Hematology, the First Affiliated Hospital of Gannan Medical College, Ganzhou, People's Republic of China.

出版信息

Hematology. 2024 Dec;29(1):2402102. doi: 10.1080/16078454.2024.2402102. Epub 2024 Sep 13.

Abstract

OBJECTIVE

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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). ClinicalTrials.gov identifier: NCT02705508.

摘要

目的

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

方法

对初诊的早期 ENKTL 患者进行培门冬酶、依托泊苷和吉西他滨(PEG)联合累及野放疗(IFRT)的 2 期研究。患者接受 4 个周期的 PEG 治疗,然后进行 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。

结果

共纳入 34 例 Ann Arbor 分期 I/II 期患者。3 例患者在 PEG 治疗时进展,其余 31 例患者接受 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(IQR,36.0-66.9 个月),5 年 PFS 和 OS 估计分别为 87.4%(95%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,易于处理。

结论

PEG 联合 IFRT 是早期 ENKTL 的一种安全有效的初始治疗方法,显示出令人印象深刻的 PFS 和 OS 率。这种有前途的方法值得在随机对照试验(ClinicalTrials.gov 注册号:NCT02705508)中进一步验证。

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