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e-Poster Display Session

389P - Updated analysis from the KEYNOTE-042 China study: 1L pembrolizumab (pembro) vs chemotherapy (chemo) in Chinese patients (pts) with advanced NSCLC with PD-L1 TPS ≥1%

Date

22 Nov 2020

Session

e-Poster Display Session

Topics

Cytotoxic Therapy

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Yi-Long Wu

Citation

Annals of Oncology (2020) 31 (suppl_6): S1386-S1406. 10.1016/annonc/annonc367

Authors

Y. Wu1, L. Zhang2, Y. Fan3, J. Zhou4, L. Zhang5, Q. Zhou1, W. Li6, C. Hu7, G. Chen8, X. Zhang9, C. Zhou10, F. Souza11, J. Lin11, J. Wang12, B. Li12, T. Mok13

Author affiliations

  • 1 Department Of Pulmonary Oncology, Guangdong Lung Cancer Institute, 510000 - Guangzhou/CN
  • 2 Department Of Respiratory Medicine, Peking Union Medical College Hospital, Bejing/CN
  • 3 Department Of Medical Oncology, Zhejiang Cancer Hospital, Hangzhou/CN
  • 4 Respiratory Department, The First Affiliated Hospital of Zhejiang University, Hangzhou/CN
  • 5 Department Of Medical Oncology, Sun Yat-Sen University Cancer Center, 510060 - Guangzhou/CN
  • 6 Stem Cell And Cancer Center, The First Hospital of Jilin University, Changchun, Jilin/CN
  • 7 Department Of Respiratory Medicine, Xiangya Hospital Central South University, Hunan/CN
  • 8 Department Of Pulmonary Medicine, The Third Affiliated Hospital of Harbin Medical University, Harbin/CN
  • 9 Respiratory Diseases Department, Zhongshan Hospital Fudan University, Shanghai/CN
  • 10 Department Of Oncology, Shanghai Pulmonary Hospital, 200433 - Shanghai/CN
  • 11 Oncology, Merck & Co., Inc., Kenilworth/US
  • 12 Oncology, MSD China, Shanghai/CN
  • 13 Department Of Clinical Oncology, State Key Laboratory of Translational Oncology, Chinese University of Hong Kong, Shatin, Hong Kong/HK

Resources

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Abstract 389P

Background

Pembro monotherapy significantly improved OS vs chemo in PD-L1–positive (TPS ≥1%) locally advanced/metastatic NSCLC without targetable EGFR/ALK aberrations in the KEYNOTE-042 global study (NCT02220894) and in an analysis of Chinese pts from the KEYNOTE-042 global and China extension (NCT03850444) studies. Here we present an updated analysis of Chinese pts after ∼17 mo additional follow-up.

Methods

The global and extension studies were designed identically. Pts were randomized 1:1 (stratified by ECOG PS 0/1, squamous/nonsquamous histology, TPS ≥50%/1%‒49%) to up to 35 cycles of pembro 200 mg Q3W or up to 6 cycles of paclitaxel/pemetrexed + carboplatin with optional pemetrexed maintenance (nonsquamous only). Primary endpoints were OS in pts with PD-L1 TPS ≥50%, ≥20%, and ≥1%.

Results

262 Chinese pts with PD-L1–positive NSCLC were enrolled (global, n=92; China extension, n=170) and randomized to pembro (n=128) or chemo (n=134). As of Feb 21, 2020, median time from randomization to database cutoff was 33.0 (range, 25.6‒41.9) mo. Pembro improved OS vs chemo in all populations (Table); in pts with PD-L1 TPS ≥1%, the 24-mo rate for OS was 43.8% vs 28.2%, PFS was 15.6% vs 10.6%, and PFS2 was 26.4% vs 8.6%. Grade 3-5 drug-related AEs occurred in 19.5% of pembro-treated pts vs 68.8% of chemo-treated pts. In 22 pts who completed 35 cycles of pembro, ORR was 77.3% and median DOR was 27.6 mo. Additional efficacy and safety outcomes will be presented.

Conclusions

In this longer-term follow-up (∼3 y), 1L pembro monotherapy continued to improve OS with a manageable safety profile vs platinum-based chemo in Chinese pts with locally advanced/metastatic NSCLC without sensitizing EGFR/ALK aberrations and PD-L1 TPS ≥1%. Most pts who completed 2 y of pembro had durable responses. These findings support 1L use of pembro for PD-L1–positive advanced/metastatic NSCLC in China Table: 389P

n OS
Median (95% CI), mo HR (95% CI)
PD-L1 TPS ≥50% Pembro 72 24.5 (17.4–32.6) 0.63 (0.43–0.94)
Chemo 74 13.8 (10.1–18.3)
PD-L1 TPS ≥20% Pembro 101 21.9 (17.4–30.9) 0.66 (0.47–0.92)
Chemo 103 13.5 (10.1–17.9)
PD-L1 TPS ≥1% Pembro 128 20.2 (17.4–25.3) 0.67 (0.50-0.89)
Chemo 134 13.5 (10.1–17.9)

HR, hazard ratio.

.

Clinical trial identification

Editorial acknowledgement

Writing support was provided by Michael S. McNamara, MS, ICON plc (North Wales, PA, USA) and funded by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA.

Legal entity responsible for the study

Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA.

Funding

Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA.

Disclosure

Y-L. Wu: Honoraria (self), Advisory/Consultancy: AstraZeneca; Honoraria (self): Eli Lilly; Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution): Roche; Honoraria (self): Pierre Fabre; Honoraria (self): Pfizer; Honoraria (self): Sanofi; Advisory/Consultancy: Merck; Advisory/Consultancy, Research grant/Funding (institution): Boehringer Ingelheim. L. Zhang: Research grant/Funding (self): Hengrui; Research grant/Funding (self): BMS; Research grant/Funding (self): Innovent Biologics. Q. Zhou: Honoraria (self): AstraZeneca; Honoraria (self): Roche. C. Zhou: Honoraria (self): Boehringer Ingelheim; Honoraria (self): Eli Lilly; Honoraria (self): Hengrui, MSD; Honoraria (self): Sanofi; Honoraria (self): F. Hoffmann-La Roche Ltd.; Honoraria (self): Qilu. F. Souza: Full/Part-time employment: Merck & Co., Inc., Kenilworth, NJ, USA. J. Lin: Full/Part-time employment: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. J. Wang, B. Li: Full/Part-time employment: MSD China. T. Mok: Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): AstraZeneca; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): Boehringer Ingelheim; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): Bristol-Myers Squibb; Research grant/Funding (self): Clovis Oncology; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): Novartis; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): Pfizer; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): Roche/Genentech; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): SFJ Pharmaceuticals; Honoraria (self), Speaker Bureau/Expert testimony, Research grant/Funding (self): Taiho; Research grant/Funding (self): XCovery; Honoraria (self), Speaker Bureau/Expert testimony: Amoy Diagnostics Co. Ltd.; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony: Eli Lilly; Honoraria (self), Speaker Bureau/Expert testimony: InMed Medical Communication; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony: Merck Serono; Honoraria (self), Speaker Bureau/Expert testimony: PRIME Oncology; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony: Virtus Medical Group; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony: Takeda Oncology; Advisory/Consultancy, Shareholder/Stockholder/Stock options: Biolidics Ltd.; Shareholder/Stockholder/Stock options: Hutchison ChiMed, Loxo-Oncology; Advisory/Consultancy, Shareholder/Stockholder/Stock options: OrigiMed; Shareholder/Stockholder/Stock options: Sanomics Ltd.; Advisory/Consultancy: ACEA Biosciences Inc; Advisory/Consultancy: Alpha Biopharma Co., Ltd.; Advisory/Consultancy: Bayer; Advisory/Consultancy: Daiichi Sankyo; Advisory/Consultancy: Incyte Corporation; Advisory/Consultancy: Celgene; Advisory/Consultancy: Cirina; Advisory/Consultancy: CStone Pharmaceuticals; Advisory/Consultancy: Fishawack Facilitate Ltd.; Advisory/Consultancy: geneDecode Co. Ltd.; Advisory/Consultancy: Hengrui Therapeutics; Advisory/Consultancy: Ignyta Inc.; Advisory/Consultancy: IQVIA; Advisory/Consultancy: Janssen; Advisory/Consultancy: Loxo-Oncology; Advisory/Consultancy: MoreHealth; Advisory/Consultancy: OncoGenex Technologies Inc.; Advisory/Consultancy: Sanofi-Aventis; Advisory/Consultancy: Vertex Pharmaceuticals; Advisory/Consultancy: Yuhan Corp; Leadership role: ASCO; Leadership role: CSCO; Leadership role: IASLC. All other authors have declared no conflicts of interest.

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