Health‐related quality of life in patients with metastatic basal cell carcinoma treated with cemiplimab: Analysis of a phase 2 trial

Author:

Peris Ketty1ORCID,Inocencio Timothy J.2,Stratigos Alexander J.3,Lewis Karl D.2,Eroglu Zeynep4,Chang Anne Lynn S.5,Ivanescu Cristina6,Sekulic Aleksandar7,Fury Matthew G.2,Chen Chieh‐I2,Quek Ruben G. W.2

Affiliation:

1. Catholic University Fondazione Policlinico Universitario‐IRCCS Rome Italy

2. Regeneron Pharmaceuticals, Inc. Tarrytown New York USA

3. National and Kapodistrian University of Athens, Andreas Sygros Hospital Athens Greece

4. Department of Cutaneous Oncology Moffitt Cancer Center Tampa Florida USA

5. Dermatology Department Stanford University School of Medicine Redwood City California USA

6. IQVIA Durham North Carolina USA

7. Mayo Clinic Scottsdale Arizona USA

Abstract

AbstractBackgroundA phase 2 cemiplimab study (NCT03132636) demonstrated a 24.1% objective response rate in patients diagnosed with metastatic basal cell carcinoma (mBCC) who were not candidates for continued hedgehog inhibitor (HHI) therapy due to intolerance to previous HHI therapy, disease progression while receiving HHI therapy, or having not better than stable disease on HHI therapy after 9 months. Here, health‐related quality of life (QoL) for this patient population is reported.MethodsAdult patients with mBCC were treated with intravenous cemiplimab at a dose of 350 mg every 3 weeks for 5 treatment cycles of 9 weeks/cycle then 4 treatment cycles of 12 weeks/cycle. Patients completed the European Organisation for Research and Treatment of Cancer Quality of Life‐Core 30 (QLQ‐C30) and Skindex‐16 questionnaires at baseline and Day 1 of each cycle. Across Cycles 2 to 9, the overall change from baseline was analyzed using a mixed model with repeated measures. Responder analyses determined clinically meaningful improvement or deterioration (changes ≥10 points) or maintenance across all scales.ResultsPatients reported low symptom burden and moderate‐to‐high functioning at baseline. Maintenance for QLQ‐C30 global health status (GHS)/QoL and across all functioning and symptom scales was indicated by overall mean changes from baseline. Clinically meaningful improvement or maintenance was reported at Cycle 2 for GHS/QoL (77%), functioning scales (77% to 86%), and symptom scales (70% to 93%), with similar proportions of improvement or maintenance at Cycles 6 and 9, excluding fatigue. On the Skindex‐16, clinically meaningful improvement or maintenance was reported across the emotional, symptom, and functional subscales, in 76%–88% of patients at Cycle 2, which were generally maintained at Cycles 6 and 9. Overall mean changes from baseline showed maintenance across these subscales.ConclusionsThe majority of patients treated with cemiplimab reported improvement or maintenance in GHS/QoL and functioning while maintaining a low symptom burden.

Funder

Regeneron Pharmaceuticals

Sanofi

Publisher

Wiley

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