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Comparing the Efficacy and Safety of a New Additional Treatment With Tislelizumab in Non-Small Cell Lung Cancer (NSCLC)

Phase 3
Active, not recruiting
Conditions
Non Small Cell Lung Cancer
Interventions
Registration Number
NCT04379635
Lead Sponsor
BeiGene
Brief Summary

The primary objective of this study is to evaluate and compare major pathological response(MPR) rate and event-free survival (EFS) in participants receiving tislelizumab plus platinum-based doublet chemotherapy as the new additional treatment followed by tislelizumab as adjuvant treatment versus participants receiving placebo plus platinum-based doublet chemotherapy as neoadjuvant treatment followed by placebo as adjuvant treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
453
Inclusion Criteria
  1. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1
  2. Histologically confirmed Stage II or IIIA NSCLC
  3. Measurable disease as assessed per RECIST v1.1
  4. Confirm eligibility for an R0 resection with curative intent

Key

Exclusion Criteria
  1. Any prior therapy for current lung cancer, including chemotherapy, or radiotherapy
  2. Known Epidermal growth factor receptor (EGFR) mutation or Anaplastic Lymphoma Kinase (ALK) gene translocation
  3. Any condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days before randomization
  4. Active autoimmune diseases or history of autoimmune diseases that may relapse
  5. History of interstitial lung disease, non-infectious pneumonitis or uncontrolled diseases including pulmonary fibrosis, acute lung diseases, etc.

NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant TislelizumabTislelizumabTislelizumab + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant TislelizumabCarboplatinTislelizumab + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant TislelizumabCisplatin injectionTislelizumab + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant TislelizumabPaclitaxel injectionTislelizumab + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant TislelizumabPemetrexed DisodiumTislelizumab + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant PlaceboCisplatin injectionPlacebo + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant PlaceboPaclitaxel injectionPlacebo + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant PlaceboPemetrexed DisodiumPlacebo + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant PlaceboPlacebosPlacebo + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Neoadjuvant chemotherapy + Neoadjuvant/Adjuvant PlaceboCarboplatinPlacebo + cisplatin/carboplatin + paclitaxel or Pemetrexed Disodium
Primary Outcome Measures
NameTimeMethod
Major pathological response (MPR) in Intent-to-Treat (ITT) analysis setUp to 3 months following completion of neoadjuvant treatment
Event-free survival (EFS) in ITT analysis set as Assessed by the Blinded Independent Central Review (BICR)Up to 5 years
Secondary Outcome Measures
NameTimeMethod
Overall survival (OS) in the ITT setUp to 5 years
Pathological complete response (pCR) rateUp to 5 years
Objective Response Rate (ORR)Up to 5 years
Disease-Free Survival (DFS) in ITT analysis setUp to 5 years
Event-free survival (EFS) Assessed by the InvestigatorUp to 5 years
Number of participants experiencing treatment-emergent adverse events (TEAEs)Up to 5 years
Efficacy and Safety as Assessed by Health-related quality of life (HRQoL) QuestionnaireUp to 5 years

Trial Locations

Locations (44)

Affiliated Zhongshan Hospital of Fudan University

🇨🇳

Shanghai, Shanghai, China

Fujian Cancer Hospital

🇨🇳

Fuzhou, Fujian, China

Quanzhou First Affliated Hospital of Fujian Medical University

🇨🇳

Quanzhou, Fujian, China

The First Affiliated Hospital of Xiamen University

🇨🇳

Xiamen, Fujian, China

Sun Yat Sen University Cancer Center

🇨🇳

Guangzhou, Guangdong, China

Cancer Hospital of Shantou University Medical College

🇨🇳

Shantou, Guangdong, China

The Tumor Hospital Affiliated to Guangxi Medical University

🇨🇳

Nanning, Guangxi, China

Nanjing Drum Tower Hospital,the Affiliated Hospital of Nanjing University Medical School

🇨🇳

Nanjing, Jiangsu, China

The First Affiliated Hospital of Nanchang University Branch Donghu

🇨🇳

Nanchang, Jiangxi, China

The First Affiliated Hospital of Nanchang University Branch Xianghu

🇨🇳

Nanchang, Jiangxi, China

The First Hospital of Jilin University

🇨🇳

Changchun, Jilin, China

Liaoning Cancer Hospital and Institute

🇨🇳

Shenyang, Liaoning, China

The First Affiliated Hospital of Xian Jiaotong University

🇨🇳

Xian, Shaanxi, China

First Hospital of Shanxi Medical University

🇨🇳

Taiyuan, Shanxi, China

Sichuan Cancer Hospital and Institute

🇨🇳

Chengdu, Sichuan, China

West China Hospital, Sichuan University

🇨🇳

Chengdu, Sichuan, China

Tianjin Medical University General Hospital

🇨🇳

Tianjin, Tianjin, China

The First Affiliated Hospital, Zhejiang University School of Medicine

🇨🇳

Hangzhou, Zhejiang, China

Hwa Mei Hospital, University of Chinese Academy of Sciences (Ningbo No Hospital)

🇨🇳

Ningbo, Zhejiang, China

Anhui Provincial Hospital

🇨🇳

Hefei, Anhui, China

Peking University Peoples Hospital

🇨🇳

Beijing, Beijing, China

Beijing Friendship Hospital, Capital Medical University

🇨🇳

Beijing, Beijing, China

Xuanwu Hospital Capital Medical University

🇨🇳

Beijing, Beijing, China

Beijing Cancer Hospital

🇨🇳

Beijing, Beijing, China

Beijing Hospital

🇨🇳

Beijing, Beijing, China

Peking Union Medical College Hospital

🇨🇳

Beijing, Beijing, China

Fujian Medical University Union Hospital

🇨🇳

Fuzhou, Fujian, China

Cancer Center of Guangzhou Medical University

🇨🇳

Guangzhou, Guangdong, China

Jiangmen Central Hospital

🇨🇳

Jiangmen, Guangdong, China

Hainan Cancer Hospital

🇨🇳

Haikou, Hainan, China

Harbin Medical University Cancer Hospital

🇨🇳

Harbin, Heilongjiang, China

Luoyang Central Hospital

🇨🇳

Luoyang, Henan, China

Union Hospital of Tongji Medical College, Huazhong University of Science and Technology

🇨🇳

Wuhan, Hubei, China

Hubei Cancer Hospital

🇨🇳

Wuhan, Hubei, China

Hunan Cancer Hospital

🇨🇳

Changsha, Hunan, China

Jilin Cancer Hospital

🇨🇳

Changchun, Jilin, China

General Hospital of Ningxia Medical University

🇨🇳

Yinchuan, Ningxia, China

Fudan University Shanghai Cancer Center

🇨🇳

Shanghai, Shanghai, China

Shanghai Chest Hospital

🇨🇳

Shanghai, Shanghai, China

Shanghai Pulmonary Hospital

🇨🇳

Shanghai, Shanghai, China

Tianjin Medical University Cancer Institute and Hospital

🇨🇳

Tianjin, Tianjin, China

Yunnan Cancer Hospital

🇨🇳

Kunming, Yunnan, China

The Second Affiliated Hospital of Zhejiang University School of Medicine

🇨🇳

Hangzhou, Zhejiang, China

Zhejiang Cancer Hospital

🇨🇳

Hangzhou, Zhejiang, China

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