联合度伐利尤单抗和曲美木单抗与质子治疗用于复发性或转移性头颈部鳞状细胞癌的 II 期临床试验。

Phase II Trial of Combined Durvalumab Plus Tremelimumab with Proton Therapy for Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma.

机构信息

Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Division of Radiation-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Cancer Res Treat. 2023 Oct;55(4):1104-1112. doi: 10.4143/crt.2023.502. Epub 2023 May 17.

Abstract

PURPOSE

This phase II study investigated whether durvalumab/tremelimumab with proton therapy improves the objective response rate (ORR), overall survival (OS), and progression-free survival (PFS) in heavily treated recurrent or metastatic head and neck squamous cell carcinoma (HNSCC) patients.

MATERIALS AND METHODS

Patients who previously received more than one chemotherapy, including at least one platinum-based regimen, and who had at least two measurable lesions were enrolled. Patients received 1,500 mg durvalumab intravenously combined with 75 mg tremelimumab intravenously every 4 weeks for four cycles followed by 1,500 mg durvalumab every 4 weeks. After one cycle of the durvalumab/tremelimumab treatment, proton therapy was given with a total dose of 25 Gy in 5 Gy daily fractions to one of the measurable lesions. We also assessed the ORR in the target lesion outside the radiation field to evaluate the abscopal effect.

RESULTS

Thirty-one patients were enrolled between March 2018 and July 2020. With 8.6 months of follow-up, the ORR was 22.6% (7/31), including one complete response and six partial responses. The median OS was 8.4 months (95% confidence interval [CI], 2.5 to 14.3) and the median PFS was 2.4 months (95% CI, 0.6 to 4.2). Among the 23 evaluable patients who completed proton therapy, the ORR was 30.4% (7/23). The median OS was 11.1 months (95% CI, 6.5 to 15.8), and the median PFS was 3.7 months (95% CI, 1.6 to 5.7). Grade 3 or higher adverse events were observed in six patients (19.4%) as follows: anemia (n=1), constipation (n=1), electrolyte imbalances (n=2), hyperglycemia (n=1), and pneumonia (n=1).

CONCLUSION

The combination of durvalumab/tremelimuab with proton therapy was tolerated well and had encouraging anti-tumor efficacy in non-irradiated tumor lesions of heavily treated HNSCC patients.

摘要

目的

本 II 期研究旨在探讨 durvalumab/tremelimumab 联合质子治疗能否提高经多线治疗的复发或转移性头颈部鳞状细胞癌(HNSCC)患者的客观缓解率(ORR)、总生存期(OS)和无进展生存期(PFS)。

材料与方法

入组患者为既往接受过一种以上化疗,包括至少一种含铂方案,且至少有两个可测量病灶的患者。患者接受 durvalumab 1500 mg 静脉输注联合 tremelimumab 75 mg 静脉输注,每 4 周 1 次,共 4 个周期,随后每 4 周接受 durvalumab 1500 mg 静脉输注。durvalumab/tremelimumab 治疗 1 个周期后,对可测量病灶之一给予总剂量 25 Gy、5 Gy/次的 5 次分割质子治疗。我们还评估了放射野外靶病灶的 ORR,以评估远隔效应。

结果

2018 年 3 月至 2020 年 7 月共入组 31 例患者。截至 8.6 个月的随访时,ORR 为 22.6%(7/31),包括 1 例完全缓解和 6 例部分缓解。中位 OS 为 8.4 个月(95%CI,2.5 至 14.3),中位 PFS 为 2.4 个月(95%CI,0.6 至 4.2)。在 23 例完成质子治疗的可评估患者中,ORR 为 30.4%(7/23)。中位 OS 为 11.1 个月(95%CI,6.5 至 15.8),中位 PFS 为 3.7 个月(95%CI,1.6 至 5.7)。6 例(19.4%)患者出现 3 级或以上不良事件,包括贫血(n=1)、便秘(n=1)、电解质失衡(n=2)、高血糖(n=1)和肺炎(n=1)。

结论

durvalumab/tremelimumab 联合质子治疗对经多线治疗的 HNSCC 患者的非照射肿瘤病灶具有良好的耐受性和令人鼓舞的抗肿瘤疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba03/10582547/cc47f9c2fd8c/crt-2023-502f1.jpg

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