HIV相关结外NK/T细胞淋巴瘤,鼻型:一例病例报告及文献复习
HIV-associated extranodal NK/T cell lymphoma, nasal type: a case report and literature review.
文献信息
| PMID | 42909113 |
|---|---|
| 原文 | 在 PubMed 查看原文 ↗ |
| 发表日期 | 2026 |
| 作者 | Junjie Wang |
| 作者单位 | Center of Infectious Diseases, West China Hospital of Sichuan University, Chengdu, China. |
| 期刊 | Frontiers in immunology |
| SCI 分区 | Q1 |
| IF | 7.4 |
| 研究类型 | 临床研究 · 临床 |
| 所属专科 | 鼻科 |
中文摘要
结外NK/T细胞淋巴瘤(ENKTCL)是一种罕见的侵袭性淋巴瘤,其治疗因HIV-1合并感染而变得复杂,原因在于药物-药物相互作用和重叠毒性,特别是化疗方案与ART同时使用所致的肝肾和血液学毒性汇聚。我们报告一名中年HIV-1阳性男性(CD4+ T细胞:198/μL,HIV-1 RNA:9.70×10³拷贝/mL),患有IE期ENKTCL鼻型,其最初的鼻塞被反复误诊为鼻窦炎。基于整合酶链转移抑制剂(INSTIs)的ART无法负担,且依非韦伦因既往过敏而禁忌,因此不得不继续使用基于洛匹那韦/利托那韦的ART,尽管其具有CYP3A4抑制作用。多学科团队指导同步治疗,给予两个全剂量周期的P-GemOxD(吉西他滨、培门冬酶、奥沙利铂、地塞米松),随后进行巩固性放疗(20次)。患者耐受治疗,未发生≥3级不良事件。治疗后PET-CT证实完全代谢缓解,HIV-1 RNA检测不到。在9个月随访时,缓解持续存在,CD4+ T细胞升至255/μL。本病例表明,在无法获得基于INSTI的方案时,MDT模式为使用非INSTI类药物给予全剂量P-GemOxD化疗提供了一个实用的管理框架。我们的经验为管理HIV与恶性肿瘤并发的治疗复杂性提供了参考策略。
英文摘要
Extranodal NK/T-cell lymphoma (ENKTCL) is a rare aggressive lymphoma whose management is complicated by HIV-1 co-infection due to drug-drug interactions and overlapping toxicities, specifically the convergent hepatorenal and hematological toxicities resulting from the concurrent use of chemotherapeutic regimens and ART. We report a middle-aged HIV-1 positive man (CD4+ T cells:198/μL, HIV-1 RNA:9.70×10³ copies/mL) with stage IE ENKTCL nasal type, whose initial nasal congestion was repeatedly misdiagnosed as sinusitis. An integrase strand transfer inhibitor-based (INSTIs) ART was unaffordable, and efavirenz was contraindicated by prior allergy, necessitating continuation of lopinavir/ritonavir-based ART despite its CYP3A4 inhibition. A multidisciplinary team guided concurrent therapy with two full-dose cycles of P-GemOxD (gemcitabine, pegaspargase, oxaliplatin, dexamethasone) followed by consolidative radiotherapy (20 fractions). The patient tolerated treatment without grade ≥ 3 adverse events. Post-therapy PET-CT confirmed complete metabolic response, with HIV-1 RNA undetectable. At 9-month follow-up, remission persisted and CD4+ T cells rose to 255/μL. This case illustrates that an MDT model offers a practical management framework for delivering full-dose P-GemOxD chemotherapy with non-INSTIs when INSTI-based regimens are not accessible. Our experience provides a reference strategy for managing the therapeutic complexities of concurrent HIV and malignancy.