Health-related quality of life impact of cobimetinib in combination with vemurafenib in patients with advanced or metastatic BRAF mutation-positive melanoma.

Caroline Dutriaux, Antoni Ribas, Grant A McArthur, James Larkin, Daniel O Koralek, Isabelle Rooney, Ilsung Chang, Thomas Karagiannis, Karen Bartley, Claus Garbe, Brigitte Dréno, Luis de la Cruz-Merino, Luc Thomas, Daniil Stroyakovskiy, Lev Demidov, Mario Mandalà, Michele Maio, Gabriella Liszkay, Victoria Atkinson, Paolo A Ascierto

Journal: British journal of cancer 2019;118(6):777-784

PMID: 29438370

Abstract

BACKGROUND

In the coBRIM study, cobimetinib plus vemurafenib (C+V) significantly improved survival outcomes vs placebo and vemurafenib (P+V) in patients with advanced/metastatic BRAF-mutated melanoma. An analysis of health-related quality of life (HRQOL) from coBRIM is reported.

METHODS

Patients completing the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (QLQ-C30) at baseline and ⩾1 time point thereafter constituted the analysis population. Change from baseline ⩾10 points was considered clinically meaningful.

RESULTS

Mean baseline scores for all QLQ-C30 domains were similar between arms. Most on-treatment scores for QLQ-C30 domains were also comparable between arms. A transient deterioration in role function in cycle 1 day 15 (C1D15; -14.7 points) in the P+V arm and improvement in insomnia in the C+V arm at C2D15 (-12.4 points) was observed. Among patients who experienced a ⩾10-point change from baseline (responders), between-group differences were greatest for insomnia (16%), social functioning (10%), fatigue (9%) and pain (7%), all favouring C+V. Diarrhoea, photosensitivity reaction, pyrexia, and rash did not meaningfully affect global health status (GHS). Serous retinopathy was associated with a transient decrease in GHS at C1D15 assessment.

CONCLUSIONS

In patients with advanced/metastatic BRAF-mutated melanoma, treatment with C+V maintained HRQOL compared with P+V, with superior efficacy.

Address: Department of Dermato Cancerology, Nantes University, Nantes 44093, France.; Istituto Nazionale Tumori Fondazione G. Pascale, Naples 80131, Italy.; Princess Alexandra Hospital, Woolloongabba, QLD 4102, Australia.; National Institute of Oncology, Budapest 1122, Hungary.; Azienda Ospedaliera Universitaria Senese, Siena 53100, Italy.; Department of Oncology and Haematology, Papa Giovanni XXIII Hospital, Bergamo 24127, Italy.; N. N. Blokhin Russian Cancer Research Center, Moscow 115478, Russia.; Moscow City Oncology Hospital 62, Krasnogorsk 14301, Russia.; Service de Dermatologie, Centre Hospitalier Lyon Sud, Pierre-Bénite 69495, France.; Hospital Universitario Virgen Macarena, Seville 41009, Spain.; Hôpital Saint André, Bordeaux 33075, France.; Department of Dermatology, University of Tübingen, Tübingen 72074, Germany.; Genentech, Inc., South San Francisco, CA 94080, USA.; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.; Peter MacCallum Cancer Centre, East Melbourne, VIC 3002, Australia.; University of Melbourne, Parkville, VIC 3052, Australia.; Jonsson Comprehensive Cancer Center, University of California Los Angeles, Los Angeles, CA 90095, USA.
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