TY - JOUR
T1 - Pembrolizumab in Patients with Refractory Cutaneous Squamous Cell Carcinoma
T2 - A Phase II Trial
AU - Ferrarotto, Renata
AU - Sousa, Luana G.
AU - Qing, Yun
AU - Kaya, Diana
AU - Stephen, Bettzy
AU - Jain, Dipti
AU - Bell, Diana
AU - Pant, Shubham
AU - Tsimberidou, Apostolia M.
AU - Janku, Filip
AU - Blumenschein, George
AU - Glisson, Bonnie S.
AU - Ahnert, Jordi Rodon
AU - Piha-Paul, Sarina A.
AU - Lee, J. Jack
AU - Wong, Michael K.
AU - Lu, Charles
AU - Meric-Bernstam, Funda
AU - Naing, Aung
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Healthcare Ltd., part of Springer Nature.
PY - 2021/8
Y1 - 2021/8
N2 - Introduction: 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. Methods: 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. Results: 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. Conclusion: 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. Trial Registration: ClinicalTrials.gov, NCT02721732, Registered March 29, 2016.
AB - Introduction: 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. Methods: 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. Results: 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. Conclusion: 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. Trial Registration: ClinicalTrials.gov, NCT02721732, Registered March 29, 2016.
KW - Checkpoint inhibitor
KW - Cutaneous squamous cell carcinoma
KW - Pembrolizumab
KW - Rare cancers
KW - Skin cancer
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U2 - 10.1007/s12325-021-01807-6
DO - 10.1007/s12325-021-01807-6
M3 - Article
C2 - 34241781
AN - SCOPUS:85109871476
SN - 0741-238X
VL - 38
SP - 4581
EP - 4591
JO - Advances in Therapy
JF - Advances in Therapy
IS - 8
ER -