Health-related quality of life (HRQoL) in the KEYNOTE-045 study of pembrolizumab versus investigator-choice chemotherapy for previously treated advanced urothelial cancer.

Author:

Vaughn David J.1,Bellmunt Joaquim2,De Wit Ronald3,Fradet Yves4,Lee Jae-Lyun5,Fong Lawrence6,Vogelzang Nicholas J.7,Climent Miguel Angel8,Petrylak Daniel Peter9,Choueiri Toni K.10,Necchi Andrea11,Gerritsen Winald R.12,Gurney Howard13,Quinn David I.14,Culine Stephane15,Sternberg Cora N.16,Mai Yabing17,Li Haojie18,Perini Rodolfo F.17,Bajorin Dean F.19

Affiliation:

1. Abramson Cancer Center of the University of Pennsylvania, Philadelphia, PA;

2. Dana-Farber Cancer Institute, Boston, MA;

3. Erasmus MC Cancer Institute, Rotterdam, Netherlands;

4. CHU de Quebec-Universite Laval, Quebec, QC, Canada;

5. Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea;

6. University of California, San Francisco, San Francisco, CA;

7. Comprehensive Cancer Centers of Nevada, Las Vegas, NV;

8. Fundación Instituto Valenciano de Oncología, Valencia, Spain;

9. Yale University School of Medicine, New Haven, CT;

10. Dana-Farber/Harvard Cancer Center, Boston, MA;

11. Fondazione IRCCS-Istituto Nazionale dei Tumori, Milan, Italy;

12. Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands;

13. Westmead Hospital, Westmead, Australia;

14. University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, CA;

15. Department of Medical Oncology, Hopital Saint-Louis, Paris, France;

16. San Camillo and Forlanini Hospitals, Rome, Italy;

17. Merck & Co., Inc., Kenilworth, NJ;

18. Glaxo Smith Kline, Collegeville, PA;

19. Memorial Sloan Kettering Cancer Center, New York, NY;

Abstract

282 Background: In KEYNOTE-045 (NCT02256436) (N = 542), pembro 200 mg Q3W significantly improved OS over investigator’s choice of paclitaxel, docetaxel, or vinflunine as second-line therapy for advanced UC following platinum-based chemo (HR 0.73; P = 0.0022). Fewer treatment-related AEs were reported with pembro. We present results of the prespecified HRQoL analysis of KEYNOTE-045. Methods: The EORTC QLQ-C30 HRQoL instrument was administered electronically at cycles 1–4, then every 2 cycles for up to 1 y and 30 d after discontinuation. The key HRQoL end points were 1) change from baseline to wk 15 and 2) time to deterioration (TTD) (defined as ≥ 10-point decrease from baseline) in the QLQ-C30 global health status/QoL score. HRQoL was assessed in patients (pts) who received ≥ 1 dose of assigned study treatment and completed ≥ 1 HRQoL instrument (N = 520). Score change from baseline was compared using a constrained longitudinal data analysis model. TTD was compared using a stratified log-rank test and Cox proportional hazards model. Results: Baseline global health status/QoL scores were similar between arms. HRQoL compliance at wk 15 was 88% for both arms. From baseline to wk 15, scores were stable for pembro (n = 266) (least squares [LS] mean +0.75 [95% CI –2.34 to +3.83]) but worsened for chemo (n = 254) (LS mean –8.30 [95% CI –11.76 to –4.83]); the difference in LS means between arms was 9.05 (95% CI 4.61-13.48; nominal 2-sided P < 0.001). At wk 15, pts without PD had improved scores with pembro but worsened scores with chemo (LS mean +5.97 vs –4.31), while pts with PD had less worsening with pembro (LS mean –3.54 vs –13.95). TTD was prolonged with pembro (HR 0.70; 95% CI 0.55-0.90; nominal 1-sided P = 0.002; median 3.5 mo vs 2.2 mo). Rates of improvement (defined as ≥ 10-point increase from baseline) at wk 15 were 31.2% with pembro and 22.0% with chemo; rates of deterioration were 28.9% and 40.6%, respectively. Conclusions: Pembro was associated with substantially better HRQoL for a longer duration than investigator-choice chemo in pts with previously treated advanced UC. Along with superior OS, these data support pembro as a new standard-of-care in this population. Clinical trial information: NCT02256436.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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