新辅助免疫治疗联合夹心放化疗治疗局部晚期鼻咽癌的疗效和安全性:回顾性研究。

IF 2.7 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
OncoTargets and therapy Pub Date : 2024-11-29 eCollection Date: 2024-01-01 DOI:10.2147/OTT.S489714
Huimin Fu, Zetan Chen, Jiawei Chen, Shuai Zhang
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引用次数: 0

摘要

目的:探讨新辅助免疫治疗联合夹心放化疗治疗局部晚期鼻咽癌(NPC)的安全性和可行性。患者和方法:本回顾性研究纳入37例局部晚期鼻咽癌患者,采用上述方案治疗。所有患者接受4个周期的新辅助免疫治疗和化疗,间隔3周,包括给药PD-1抑制剂,即辛替单抗(固定剂量200mg,第1天)或托利单抗(240 mg,第1天)。化疗方案包括nab-紫杉醇(260 mg/m2,第1天)加奈达铂(85 mg/m2,第1天)。与调强放疗(IMRT)同时,患者接受尼莫妥珠单抗(200 mg)靶向药物治疗,为期6个周期。最后进行4个周期的S-1辅助化疗。结果:本研究中,新辅助免疫治疗联合化疗有效率为94.6%,CR率为67.6%,IMRT后3个月有效率为100%。全组2年总生存率(OS)、局部区域控制率(LCR)、远端无转移生存率(DMFS)和无进展生存率(PFS)分别为97.3%、94.6%、97.3%和91.9%。中性粒细胞减少是最常见的血液学毒性(100%),≥3级中性粒细胞减少发生率为40.5%。未发生3级贫血和血小板减少症。全组未发生甲状腺功能减退、免疫性肺炎、心肌炎等不良反应。然而,皮疹、肌肉骨骼疼痛和肝毒性的发生率较高(分别为45.9%、54.1%和37.8%)。结论:局部晚期鼻咽癌患者采用新辅助免疫治疗联合夹心放化疗的生存效益好,毒副作用可耐受。本研究为局部晚期鼻咽癌免疫治疗的应用提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and Safety of Neoadjuvant Immunotherapy Combined with Sandwich Chemoradiotherapy in Locally Advanced Nasopharyngeal Carcinoma: A Retrospective Study.

Purpose: We aimed to determine the safety and feasibility of neoadjuvant immunotherapy combined with sandwich chemoradiotherapy in patients with locally advanced nasopharyngeal carcinoma (NPC).

Patients and methods: This retrospective study involved 37 patients with locally advanced NPC treated with the above regimen. All patients received four cycles of neoadjuvant immunotherapy and chemotherapy at three-week intervals, including the administration of PD-1 inhibitors, namely, sintilimab (a fixed dose of 200 mg on Day 1) or toripalimab (240 mg on Day 1). The chemotherapy program consisted of nab-paclitaxel (260 mg/m2, Day 1) plus nedaplatin (85 mg/m2, Day 1). Concurrent with intensity-modulated radiation therapy (IMRT), the patients received targeted drug therapy with nimotuzumab (200 mg) across six cycles. Finally, 4 cycles of S-1 adjuvant chemotherapy were administered.

Results: In this study, the efficiency of neoadjuvant immunotherapy combined with chemotherapy was 94.6%, the CR rate was 67.6%, and the efficiency 3 months after IMRT was 100%. The 2-year overall survival (OS), locoregional control (LCR), distant metastasis-free survival (DMFS), and progression-free survival (PFS) rates of the whole group were 97.3%, 94.6%, 97.3% and 91.9%, respectively. Neutropenia was the most common hematological toxicity (100%), and the incidence of grade ≥ 3 neutropenia was 40.5%. Grade 3 anemia and thrombocytopenia did not occur. Additionally, no adverse reactions, such as hypothyroidism, immune pneumonia, or myocarditis, occurred in the whole group. However, the incidences of rash, musculoskeletal pain, and hepatotoxicity were high (45.9%, 54.1% and 37.8%, respectively).

Conclusion: The survival benefit of neoadjuvant immunotherapy combined with sandwich chemoradiotherapy is excellent, with tolerable toxicity, in patients with locally advanced NPC. This study provides new insight into the application of immunotherapy in locally advanced NPC.

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来源期刊
OncoTargets and therapy
OncoTargets and therapy BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ONCOLOGY
CiteScore
9.70
自引率
0.00%
发文量
221
审稿时长
1 months
期刊介绍: OncoTargets and Therapy is an international, peer-reviewed journal focusing on molecular aspects of cancer research, that is, the molecular diagnosis of and targeted molecular or precision therapy for all types of cancer. The journal is characterized by the rapid reporting of high-quality original research, basic science, reviews and evaluations, expert opinion and commentary that shed novel insight on a cancer or cancer subtype. Specific topics covered by the journal include: -Novel therapeutic targets and innovative agents -Novel therapeutic regimens for improved benefit and/or decreased side effects -Early stage clinical trials Further considerations when submitting to OncoTargets and Therapy: -Studies containing in vivo animal model data will be considered favorably. -Tissue microarray analyses will not be considered except in cases where they are supported by comprehensive biological studies involving multiple cell lines. -Biomarker association studies will be considered only when validated by comprehensive in vitro data and analysis of human tissue samples. -Studies utilizing publicly available data (e.g. GWAS/TCGA/GEO etc.) should add to the body of knowledge about a specific disease or relevant phenotype and must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Bioinformatics studies must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Single nucleotide polymorphism (SNP) studies will not be considered.
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