Response to salvage chemotherapy after progression on immune checkpoint inhibitors in patients with recurrent and/or metastatic squamous cell carcinoma of the head and neck

被引:114
|
作者
Saleh, Khalil [1 ]
Daste, Amaury [2 ]
Martin, Nicolas [3 ]
Pons-Tostivint, Elvire [4 ]
Auperin, Anne [5 ]
Herrera-Gomez, Ruth Gabriela [1 ]
Baste-Rotllan, Neus [1 ]
Bidault, Francois [6 ]
Guigay, Joel [3 ]
Le Tourneau, Christophe [4 ,7 ,8 ]
Saada-Bouzid, Esma [3 ,9 ]
Even, Caroline [1 ]
机构
[1] Gustave Roussy Canc Campus, Dept Head & Neck Oncol, 114 Rue Edouard Vaillant, F-94800 Villejuif, France
[2] CHU Bordeaux, Bordeaux Univ Hosp, Hop St Andre, Dept Med Oncol, Bordeaux, France
[3] Ctr Antoine Lacassagne, Dept Med Oncol, Auperin, Nice, France
[4] Inst Curie, Dept Drug Dev & Innovat, St Cloud, France
[5] Gustave Roussy Canc Campus, Dept Biostat & Epidemiol, Villejuif, France
[6] Inst Gustave Roussy, Dept Radiol, Villejuif, France
[7] INSERM, U900, Res Unit, St Cloud, France
[8] Paris Saclay Univ, Paris, France
[9] Unit Cote Azur, Nice, France
关键词
Salvage chemotherapy; Immune checkpoint inhibitor; PD-1; PD-L1; CTLA-4; Squamous cell carcinoma of head and neck; OPEN-LABEL; NIVOLUMAB; CANCER; DOCETAXEL; THERAPY; PHASE-3; RATES;
D O I
10.1016/j.ejca.2019.08.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Immune checkpoint inhibitors (ICI) are active in patients with recurrent/metastatic squamous cell carcinoma of the head and neck (R/M SCCHN). Recent data suggest that exposure to ICI improves response to salvage chemotherapy (SCT) in advanced non-small-cell lung cancer. We evaluated response to chemotherapy in patients who had progressed on ICI in patients with R/M SCCHN. Patients and methods: A retrospective study was conducted at 4 French centres. Eligibility criteria were patients who progressed after treatment with ICI for R/M SCCHN and received SCT and for whom efficacy data were available between September 2014 and January 2018. Results: Of 232 patients treated with ICI, 82 met eligibility criteria: 84% were male. ICI was given as monotherapy in 45% of patients or as combination in 55%. SCT included taxanes 56.1%), cetuximab in combination with taxanes or platinum (50%), platinum-based regimen (36.6%). The median number of treatment lines before SCT was 2 (range 1-6). The objective response rate (ORR) to SCT was 30%. Three patients (4%) presented complete response and 22 patients (27%) had partial response. Median progression-free survival was 3.6 months and median overall survival was 7.8 months. The age at SCT, initial tumour location, number of prior chemotherapy regimens, type of chemotherapy before ICI, best response to ICI, site of relapse and Eastern Cooperative Oncology Group at SCT were not associated with response to SCT on univariate analysis. Conclusion: In R/M SCCHN, the ORR to SCT was high (30%) suggesting that exposure to ICI may increase tumour sensitivity to chemotherapy. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:123 / 129
页数:7
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