Pembrolizumab in Patients with Refractory Cutaneous Squamous Cell Carcinoma: A Phase II Trial.


Journal

Advances in therapy
ISSN: 1865-8652
Titre abrégé: Adv Ther
Pays: United States
ID NLM: 8611864

Informations de publication

Date de publication:
08 2021
Historique:
received: 19 04 2021
accepted: 25 05 2021
pubmed: 10 7 2021
medline: 7 9 2021
entrez: 9 7 2021
Statut: ppublish

Résumé

Patients with advanced cutaneous squamous cell carcinoma (CSCC) have a poor prognosis. Blocking the PD-1-PD-L1 axis has shown promising activity in this patient population. We assessed the safety and antitumor activity of PD-1 inhibitor pembrolizumab in patients with refractory advanced CSCC. This was a prespecified subgroup analysis of patients with advanced CSCC who enrolled in an open-label, phase II clinical trial for pembrolizumab in patients with refractory rare cancers during 2016-2018. Patients received pembrolizumab 200 mg intravenously every 21 days until progressive disease, unacceptable adverse event, or completion of 24 months of treatment. The primary endpoint was nonprogression rate (NPR) at 27 weeks; secondary endpoints included safety, objective response rate (ORR) per irRECIST, clinical benefit rate (CBR), progression-free survival, and overall survival. Twenty patients with refractory CSCC enrolled; 19 were evaluable for efficacy. Median follow-up time was 44.1 months. The NPR at 27 weeks was 37% (95% CI 0.16-0.62). Three patients had a complete response (CR), three had a partial response, and one had stable disease, for an ORR of 32% and a CBR of 37%; median duration of response was 27.3 months. All three patients with a CR remained free of recurrence at the time of writing. Severe treatment-related adverse events (grade ≥ 3) occurred in 10% of patients (2/20). PD-L1 expression was not correlated with response to pembrolizumab. A long-term follow-up confirms pembrolizumab's antitumor activity and safety profile in patients with refractory CSCC. Patients with a CR may experience cure. ClinicalTrials.gov, NCT02721732, Registered March 29, 2016.

Identifiants

pubmed: 34241781
doi: 10.1007/s12325-021-01807-6
pii: 10.1007/s12325-021-01807-6
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
pembrolizumab DPT0O3T46P

Banques de données

ClinicalTrials.gov
['NCT02721732']

Types de publication

Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Pagination

4581-4591

Subventions

Organisme : NCI NIH HHS
ID : P30CA016672
Pays : United States

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Healthcare Ltd., part of Springer Nature.

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Auteurs

Renata Ferrarotto (R)

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. rferrarotto@mdanderson.org.

Luana G Sousa (LG)

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Yun Qing (Y)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Diana Kaya (D)

Department of Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Bettzy Stephen (B)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Dipti Jain (D)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Diana Bell (D)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Shubham Pant (S)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Apostolia M Tsimberidou (AM)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Filip Janku (F)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

George Blumenschein (G)

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Bonnie S Glisson (BS)

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Jordi Rodon Ahnert (JR)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Sarina A Piha-Paul (SA)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

J Jack Lee (JJ)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Michael K Wong (MK)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Charles Lu (C)

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Funda Meric-Bernstam (F)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Aung Naing (A)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

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