Your new experience awaits. Try the new design now and help us make it even better

ORIGINAL RESEARCH article

Front. Med.

Sec. Hematology

Volume 12 - 2025 | doi: 10.3389/fmed.2025.1666601

This article is part of the Research TopicNovel anti-cancer drugs combination radio-immunotherapy strategy: new frontiers in cancer immunotherapyView all 8 articles

P3-GemOx as a novel immunochemotherapy candidate in NK/T-cell lymphoma management

Provisionally accepted
  • Huazhong University of Science and Technology Tongji Medical College Union Hospital, Wuhan, China

The final, formatted version of the article will be published soon.

Given the rarity of natural killer/T-cell lymphoma (NKTL), this study represents a relatively large-scale clinical investigation into this disease, which exhibits suboptimal responses to existing therapeutic protocols. In this study, we report the efficacy of the P3-GemOx regimen (mitoxantrone hydrochloride liposome [Plm60] combined with the PP-GemOx [anti-Programmed death-1 antibody, Pegaspargase, GEMcitabine, and OXaliplatin] regimen) compared to the traditional PP-GemOx regimen in advanced NKTL. Eleven patients received a median of 3 cycles (range, 1-4) of the P3-GemOx regimen every 3-4 weeks, while another eleven patients received a median of 4 cycles (range, 2-6) of the PP-GemOx regimen, also every 3-4 weeks. Treatment responses were primarily assessed using 18F-fluorodeoxyglucose positron emission tomography (18FDG-PET) and computed tomography or magnetic resonance imaging. All patients treated with the P3-GemOx regimen exhibited significant responses, with nine complete remissions (CR) and two partial remissions (PR), resulting in an overall response rate (ORR) of 100%. Moreover, seven of these patients successfully underwent hematopoietic stem cell transplantation (HSCT). In contrast, the ORR for patients receiving the PP-GemOx regimen was 63.6%, with none undergoing HSCT. All adverse events were manageable and resolved. In conclusion, the P3-GemOx regimen demonstrates superior efficacy in advanced NKTL.

Keywords: NK/T-cell lymphoma, immunochemotherapy, prognosis, Hematopoieticstem cell transplantation, Retrospective Studies

Received: 15 Jul 2025; Accepted: 13 Oct 2025.

Copyright: © 2025 Zhang, Kou, Cheng, Lu, HU and Tang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Liang Tang, lancet.tang@qq.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.