PD-1 inhibition therapy for advanced cutaneous squamous cell carcinoma: a retrospective analysis from the University of Southern California.
Adult
Aged
Aged, 80 and over
California
/ epidemiology
Carcinoma, Squamous Cell
/ diagnosis
Disease Progression
Female
Humans
Immune Checkpoint Inhibitors
/ therapeutic use
Male
Middle Aged
Neoplasm Metastasis
Progression-Free Survival
Retrospective Studies
Skin Neoplasms
/ diagnosis
Treatment Outcome
Young Adult
Checkpoint blockade
Cutaneous squamous cell carcinoma
Immunotherapy
PD-1
Skin cancer
Journal
Journal of cancer research and clinical oncology
ISSN: 1432-1335
Titre abrégé: J Cancer Res Clin Oncol
Pays: Germany
ID NLM: 7902060
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
received:
26
08
2020
accepted:
06
11
2020
pubmed:
20
11
2020
medline:
26
5
2021
entrez:
19
11
2020
Statut:
ppublish
Résumé
Approximately 5% of patients with cutaneous squamous cell carcinoma (CSCC) may develop recurrent or metastatic disease. The management of such cases is challenging and requires multi-disciplinary care. Immunotherapy using PD-1 inhibition was approved to treat unresectable or metastatic CSCC in 2018. Given limited data regarding clinical outcomes outside of published trials, we describe our experience using this therapy. We retrospectively reviewed all patients treated with PD-1 inhibition as therapy for locally advanced, regionally metastatic or distant metastatic CSCC at the University of Southern California. Clinicopathological characteristics, treatment data using PD-1 inhibitors, and outcomes were assessed. Among 26 patients treated with PD-1 inhibition, the objective response rate was 42.3%, with 19.2% of patients having partial response and 23.1% having complete response to therapy. The median progression-free survival was 5.4 months. Median tumor mutational burden (TMB) was higher among responders compared to non-responders (60 vs. 9 Mut/Mb, p = 0.04). Primary CSCC tumor location on the head/neck was also associated with response to PD-1 inhibition (p = 0.04). Two patients with mutations affecting mismatch repair deficiency were noted to have complete response to treatment. No other variables were associated with treatment outcomes. PD-1 inhibition produces durable responses among patients with advanced or metastatic CSCC. PD-1 inhibition therapy is well tolerated, but patients should be monitored closely for immune-related adverse events, particularly frail or immune-suppressed patients. Further investigation of potential biomarkers to help identify patients who will derive the most benefit from this therapeutic option is needed.
Identifiants
pubmed: 33210210
doi: 10.1007/s00432-020-03458-6
pii: 10.1007/s00432-020-03458-6
doi:
Substances chimiques
Immune Checkpoint Inhibitors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1803-1811Références
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