Clinical Outcomes of Cetuximab and Paclitaxel after Progression on Immune Checkpoint Inhibitors in Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

被引:9
|
作者
Suzuki, Shinsuke [1 ]
Toyoma, Satoshi [1 ]
Kawasaki, Yohei [1 ]
Koizumi, Koh [1 ]
Iikawa, Nobuko [1 ]
Shiina, Kazuhiro [1 ]
Endo, Tentaro [1 ]
Abe, Tomoe [1 ]
Kouga, Teppei [1 ]
Yamada, Takechiyo [1 ]
机构
[1] Akita Univ, Grad Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Akita 0108543, Japan
来源
MEDICINA-LITHUANIA | 2021年 / 57卷 / 11期
关键词
head and neck squamous cell carcinoma; cetuximab; paclitaxel; immune checkpoint inhibitor; chemotherapy; SALVAGE CHEMOTHERAPY; COMBINATION;
D O I
10.3390/medicina57111151
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives: In recent years, the effectiveness of chemotherapy after immune checkpoint inhibitor administration has attracted attention in various cancers, including head and neck cancers. However, individual assessments of the administered chemotherapy regimens are insufficient. This study aimed to evaluate the efficacy and safety of chemotherapy after immune checkpoint inhibitor administration in recurrent metastatic head and neck cancer by focusing on a single regimen. Materials and Methods: We retrospectively reviewed clinical and radiological data from the medical records of 18 patients with recurrent or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) who received systemic chemotherapy with weekly cetuximab and paclitaxel (Cmab + PTX) after progression following immune checkpoint inhibitor (ICI) therapy. The objective response rate (ORR) and disease control rate (DCR) were assessed using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. Progression-free survival (PFS) and overall survival (OS) were estimated using the Kaplan-Meier method. Adverse events (AEs) were recorded using National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.0. Results: In all patients, the ORR, DCR, median PFS, and median OS were 44.4%, 72.2%, 3.8 months, and 9.6 months, respectively. Regarding AEs, three patients developed grade 3 neutropenia. Grade 3 anemia, paronychia, asthenia, and peripheral neuropathy were observed in one patient each. There were no treatment-related deaths. Conclusions: Cmab + PTX was shown to maintain high efficacy and acceptable safety for R/M HNSCC that progressed after ICI therapy. Further research is needed to establish optimal treatment sequences and drug combinations for recurrent R/M HNSCC.
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页数:8
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