Response rates and survival to systemic therapy after immune checkpoint inhibitor failure in recurrent/metastatic head and neck squamous cell carcinoma.
Antineoplastic Agents, Immunological
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Combined Modality Therapy
Female
Humans
Male
Neoplasm Metastasis
Neoplasm Recurrence, Local
Neoplasm Staging
Retreatment
Retrospective Studies
Squamous Cell Carcinoma of Head and Neck
/ diagnosis
Survival Analysis
Treatment Failure
Treatment Outcome
HNSCC
Head and neck squamous cell carcinoma
Immune checkpoint inhibitors
Immunotherapy
Journal
Oral oncology
ISSN: 1879-0593
Titre abrégé: Oral Oncol
Pays: England
ID NLM: 9709118
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
received:
17
07
2019
revised:
05
10
2019
accepted:
11
12
2019
pubmed:
23
12
2019
medline:
24
9
2020
entrez:
23
12
2019
Statut:
ppublish
Résumé
Prior reports have demonstrated a potential enhancement in overall response rate (ORR) to chemotherapy after exposure to immunotherapy. The goal of this study was to evaluate the ORR and survival to chemotherapy and/or targeted therapy in head and neck squamous cell carcinoma (HNSCC) patients who progressed on immune checkpoint inhibitors (ICI). We retrospectively collected clinical and pathologic data from patients with recurrent/metastatic HNSCC who progressed on ICI and subsequently received chemotherapy or targeted therapy. ORR was assessed by RECIST version 1.1. Progression-free survival (PFS) and overall survival (OS) were estimated using the Kaplan-Meier method. A total of 43 patients met criteria for inclusion. The majority were male (91%) and former smokers (60%). Most patients received ICI as first-line (58.14%); the vast majority was platinum exposed (90.7%). The ORR to ICI was 21%. The ORR to systemic therapy before ICI was 47%, and the ORR after ICI failure was 42%. After progression on ICI, the median PFS and OS on the subsequent line of therapy were 4.2 and 8.4 months respectively. In our cohort of recurrent/metastatic HNSCC patients, the ORR and OS to systemic therapy after progression on ICI were higher than historical controls for second-line or beyond. Further investigations are warranted to better characterize optimal sequencing and combination strategies.
Identifiants
pubmed: 31864957
pii: S1368-8375(19)30433-6
doi: 10.1016/j.oraloncology.2019.104523
pii:
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
104523Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.