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Brief Title: Study of Pemetrexed+Platinum Chemotherapy With or Without Pembrolizumab (MK-3475) in Participants With First Line Metastatic Nonsquamous Non-small Cell Lung Cancer (MK-3475-189/KEYNOTE-189)-Japan Extension Study
Official Title: A Randomized, Double-Blind, Phase III Study of Platinum+Pemetrexed Chemotherapy With or Without Pembrolizumab (MK-3475) in First Line Metastatic Non-squamous Non-small Cell Lung Cancer Subjects (KEYNOTE-189)
Study ID: NCT03950674
Brief Summary: This is a Japan Extension Study of Global Study MK-3475-189 (NCT02578680). This is an efficacy and safety study of pembrolizumab (MK-3475) combined with pemetrexed/platinum chemotherapy versus pemetrexed/platinum chemotherapy alone in adult Japanese participants with advanced or metastatic nonsquamous non-small cell lung cancer (NSCLC) who have not previously received systemic therapy for advanced disease. Participants will be randomly assigned to receive pembrolizumab combined with pemetrexed/platinum (Investigators choice of cisplatin or carboplatin), OR pemetrexed/platinum (Investigators choice of cisplatin or carboplatin). With Amendment 11 (effective date 31-Jan-2022), once the study objectives have been met or the study has ended, participants will be discontinued from this study and will be enrolled in an extension study to continue protocol-defined assessments and treatment. The primary hypothesis is that pembrolizumab in combination with pemetrexed/platinum chemotherapy prolongs Progression-Free Survival (PFS) and Overall Survival (OS) compared to pemetrexed/platinum chemotherapy alone.
Detailed Description: The MK-3475-189-Japan Extension Study will be identical to the global study (e.g. inclusion and exclusion criteria, study primary and secondary outcome measures and study procedures). The MK-3475-189-Japanese Extension Study enrolled a total of 30 participants and the analyses included 10 participants (pembrolizumab =4; control = 6) that had been previously enrolled in the MK-3475-189 global study (NCT02578680), resulting in a total of 40 participants.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
National Hospital Organization Nagoya Medical Center ( Site 0324), Nagoya, Aichi, Japan
Kurume University Hospital ( Site 0326), Kurume, Fukuoka, Japan
Hyogo Cancer Center ( Site 0325), Akashi, Hyogo, Japan
Kanazawa University Hospital ( Site 0328), Kanazawa, Ishikawa, Japan
Kansai Medical University Hospital ( Site 0313), Hirakata, Osaka, Japan
Shizuoka Cancer Center Hospital and Research Institute ( Site 0322), Sunto-gun, Shizuoka, Japan
National Hospital Organization Shikoku Cancer Center ( Site 0303), Matsuyama, , Japan
Okayama University Hospital ( Site 0327), Okayama, , Japan
National Cancer Center Hospital ( Site 0301), Tokyo, , Japan
The Cancer Institute Hospital of JFCR ( Site 0323), Tokyo, , Japan
Name: Medical Director
Affiliation: Merck Sharp & Dohme LLC
Role: STUDY_DIRECTOR