Patient-reported outcomes (PROs) with first-line durvalumab (D) ± tremelimumab (T) versus chemotherapy (CT) in metastatic NSCLC: Results from MYSTIC.

Authors

null

Edward B. Garon

David Geffen School of Medicine, University of California/TRIO-US Network, Los Angeles, CA

Edward B. Garon , Byoung Chul Cho , Niels Reinmuth , Ki Hyeong Lee , Alexander Luft , Myung-Ju Ahn , Gilles Robinet , Sylvestre Le Moulec , Ronald Natale , Jeffrey Gary Schneider , Frances A. Shepherd , Marina Chiara Garassino , Sarayut Lucien Geater , Zsolt Papai-Szekely , Tran Van Ngoc , Feng Liu , Urban J. Scheuring , Anna Rydén , Solange Peters , Naiyer A. Rizvi

Organizations

David Geffen School of Medicine, University of California/TRIO-US Network, Los Angeles, CA, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea, Asklepios Lung Clinic, Munich-Gauting, Germany, Chungbuk National University Hospital, Cheongju, South Korea, Leningrad Regional Clinical Hospital, Oncology Department, Lunacharskogo Prospect, Russian Federation, Samsung Medical Center, Seoul, South Korea, CHRU de Brest-Hôpital Morvan, Brest, France, Institut Bergonnié, Bordeaux Cedex, France, Cedars-Sinai Comprehensive Cancer Center, Los Angeles, CA, NYU Winthrop Hospital, Mineola, NY, Cancer Clinical Research Unit, Princess Margaret Cancer Centre, Toronto, ON, Canada, Fondazione IRCCS-Istituto Nazionale dei Tumori, Milan, Italy, Prince of Songkla University, Hat Yai, Thailand, St George Hospital of Fejer County, Szekesfehervar, Hungary, Cho Ray Hospital, Ho Chi Minh, Viet Nam, AstraZeneca, Gaithersburg, MD, AstraZeneca, Cambridge, United Kingdom, AstraZeneca, Gothenburg, Sweden, Centre Hospitalier Universitaire Vaudois, Lausanne University, Lausanne, Switzerland, Columbia University Medical Center, New York, NY

Research Funding

Pharmaceutical/Biotech Company

Background: MYSTIC, an open-label, Phase 3 trial of first-line D (anti-PD-L1) ± T (anti-CTLA-4) vs platinum CT in mNSCLC, showed an improvement in overall survival (OS) with D vs CT in pts with tumor cell PD-L1 expression ≥25% (TC ≥25% [primary analysis population]; D vs CT, HR 0.76 [97.54% CI 0.56–1.02], p = 0.036; D+T vs CT, HR 0.85 [98.77% CI 0.61–1.17], p = 0.202). Here we summarize PROs from MYSTIC. Methods: Immunotherapy/CT-naïve mNSCLC pts were randomized (1:1:1) to D, D+T, or CT. Symptoms, function, and global health status/quality of life (QoL) were assessed using the EORTC QLQ-C30 v3 questionnaire and its lung cancer module, QLQ-LC13. A change in score from baseline ≥10 points was predefined as clinically meaningful (CM). Mean changes from baseline (over 12 mos) for prespecified symptoms were analyzed using a mixed model for repeated measures (MMRM). Time from randomization to the first CM deterioration (TTD) was analyzed. Results: Among pts with PD-L1 TC ≥25% (n = 488), there were no differences between arms in symptoms, function, or global health status/QoL at baseline. Compliance with completing the questionnaires was ≥60% to wk 120 in the D±T arms, and to wk 40 (C30) and wk 44 (LC13) in the CT arm. MMRM analysis showed significant between-arm differences in changes from baseline in favor of D for fatigue (difference vs CT −9.5) and appetite loss (−11.9; CM), and D+T for fatigue (−11.7; CM). Significantly longer TTD (median, mos) was seen with D and D+T vs CT for appetite loss (12.8 and 5.6 vs 4.5), constipation (14.6 and 9.0 vs 5.5), nausea/vomiting (16.7 and 9.7 vs 4.5), and dyspnea (10.6 and 7.4 vs 5.6); D vs CT for diarrhea (16.3 vs 9.0), insomnia (9.3 vs 6.2), and hemoptysis (not reached vs 10.3); and D+T vs CT for fatigue (5.6 vs 2.0). Significantly longer TTD (median, mos) was also seen with D and D+T vs CT for function (cognitive [9.1 and 6.6 vs 5.2], physical [9.0 and 7.4 vs 4.2], role [D vs CT only; 7.3 vs 3.7], social [12.9 and 5.4 vs 5.2]), and global health status/QoL (5.9 and 6.8 vs 5.5). Conclusions: Pts with PD-L1 TC ≥25% treated with D±T had a reduced symptom burden over time and longer TTD for symptoms, function, and global health status/QoL compared to pts receiving CT. Clinical trial information: NCT02453282

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Abstract Details

Meeting

2019 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Lung Cancer—Non-Small Cell Metastatic

Track

Lung Cancer

Sub Track

Metastatic Non–Small Cell Lung Cancer

Clinical Trial Registration Number

NCT02453282

Citation

J Clin Oncol 37, 2019 (suppl; abstr 9048)

DOI

10.1200/JCO.2019.37.15_suppl.9048

Abstract #

9048

Poster Bd #

371

Abstract Disclosures