Fu Huimin, Chen Zetan, Chen Jiawei, Zhang Shuai
Department of Radiation Oncology, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 570311, People's Republic of China.
Department of Radiation Oncology, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 570311, People's Republic of China.
Onco Targets Ther. 2024 Nov 29;17:1145-1155. doi: 10.2147/OTT.S489714. eCollection 2024.
We aimed to determine the safety and feasibility of neoadjuvant immunotherapy combined with sandwich chemoradiotherapy in patients with locally advanced nasopharyngeal carcinoma (NPC).
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.
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).
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.
我们旨在确定新辅助免疫治疗联合夹心放化疗在局部晚期鼻咽癌(NPC)患者中的安全性和可行性。
这项回顾性研究纳入了37例接受上述治疗方案的局部晚期NPC患者。所有患者每三周接受四个周期的新辅助免疫治疗和化疗,包括给予PD-1抑制剂,即信迪利单抗(第1天固定剂量200mg)或特瑞普利单抗(第1天240mg)。化疗方案包括白蛋白结合型紫杉醇(260mg/m²,第1天)加奈达铂(85mg/m²,第1天)。在调强放射治疗(IMRT)的同时,患者接受六个周期的尼妥珠单抗(200mg)靶向药物治疗。最后,给予4个周期的S-1辅助化疗。
在本研究中,新辅助免疫治疗联合化疗的有效率为94.6%,完全缓解(CR)率为67.6%,IMRT后3个月的有效率为100%。全组2年总生存(OS)、局部区域控制(LCR)、无远处转移生存(DMFS)和无进展生存(PFS)率分别为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级中性粒细胞减少的发生率为40.5%。未发生3级贫血和血小板减少。此外,全组未发生甲状腺功能减退、免疫性肺炎或心肌炎等不良反应。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%)。
新辅助免疫治疗联合夹心放化疗在局部晚期NPC患者中生存获益良好,毒性可耐受。本研究为免疫治疗在局部晚期NPC中的应用提供了新的见解。