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
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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
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