Your browser doesn't support javascript.
loading
Three-year follow-up and patient-reported outcomes from CheckMate 078: Nivolumab versus docetaxel in a predominantly Chinese patient population with previously treated advanced non-small cell lung cancer.
Chang, Jianhua; Wu, Yi-Long; Lu, Shun; Wang, Jie; Mok, Tony; Zhang, Li; Feng, Jifeng; Wu, Lin; Tu, Hai-Yan; Zhang, Yiping; Luft, Alexander; Zhou, Jian-Ying; Ma, Zhiyong; Lu, You; Hu, Chengping; Shi, Yuankai; Poddubskaya, Elena; Soo, Ross A; Chia, Yee Hong; Penrod, John R; Taylor, Fiona; Lawrance, Rachael; Blum, Steven I; Sun, Xiaowu; Juarez-Garcia, Ariadna; Moreno-Koehler, Alejandro; Li, Ang; Li, Amy; Cheng, Ying.
Afiliação
  • Chang J; Fudan University Shanghai Cancer Center, 270 Dongan Road, Shanghai 200032, China. Electronic address: changjianhua@163.com.
  • Wu YL; Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, School of Medicine, South China University of Technology, 106 Zhongshan Second Road, Guangzhou 510080, China. Electronic address: syylwu@live.cn.
  • Lu S; Shanghai Chest Hospital, 241 Huaihai West Road, Shanghai 200030, China. Electronic address: shun_lu@hotmail.com.
  • Wang J; National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 17 Panjiayuan Nanli, Chaoyang District, Beijing 100021, China. Electronic address: zlhuxi@163.com.
  • Mok T; State Laboratory of Translational Oncology, The Chinese University of Hong Kong, Prince of Wales Hospital, 30-32 Ngan Shing Street, Hong Kong, China. Electronic address: tony@clo.cuhk.edu.hk.
  • Zhang L; Sun Yat-Sen University Cancer Center, 651 Dong Feng East Road, Guangzhou 510060, China. Electronic address: zhangli@sysucc.org.cn.
  • Feng J; Jiangsu Cancer Hospital, 42 Bai Zi Ting, Nanjing 210000, China. Electronic address: fjif@vip.sina.com.
  • Wu L; Hunan Cancer Hospital, 283 Tongzipo Road, Changsha 410013, China. Electronic address: wulin-calf@vip.163.com.
  • Tu HY; Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, School of Medicine, South China University of Technology, 106 Zhongshan Second Road, Guangzhou 510080, China. Electronic address: thy0934789@163.com.
  • Zhang Y; Zhejiang Cancer Hospital, 1 Banshan East Road, Hangzhou 310022, China. Electronic address: zyp352@163.com.
  • Luft A; Leningrad Regional Clinical Hospital, 45-49 Lunacharskogo Avenue, St. Petersburg 194291, Russian Federation. Electronic address: alexander_luft@mail.ru.
  • Zhou JY; The First Affiliated Hospital of College of Medicine, 79 Qingchun Road, Hangzhou 310003, China. Electronic address: drzjy@163.com.
  • Ma Z; The Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, 127 Dongming Road, Zhengzhou 450008, China. Electronic address: 18638529152@163.com.
  • Lu Y; West China Hospital, Sichuan University, 37 Guoxue Lane, Chengdu 610041, China. Electronic address: radyoulu@hotmail.com.
  • Hu C; Xiangya Hospital of Central South University, 87 Xiangya Road, Changsha 410008, China. Electronic address: huchengp28@csu.edu.cn.
  • Shi Y; National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 17 Panjiayuan Nanli, Chaoyang District, Beijing 100021, China. Electronic address: syuankai@cicams.ac.cn.
  • Poddubskaya E; Clinical Center VitaMed, 10 Seslavinskaya Street, Moscow, Russian Federation. Electronic address: podd-elena@yandex.ru.
  • Soo RA; National University Hospital, 1E Kent Ridge Road, 119228 Singapore, Singapore. Electronic address: ross_soo@nuhs.edu.sg.
  • Chia YH; Johns Hopkins Singapore Pte Ltd, 11 Jalan Tan Tock Seng, 308433 Singapore, Singapore. Electronic address: yee_hong_chia@ttsh.com.sg.
  • Penrod JR; Bristol Myers Squibb, Princeton, NJ 08540, USA. Electronic address: john.penrod@bms.com.
  • Taylor F; Adelphi Values, Boston, MA, USA. Electronic address: fiona.taylor@adelphivalues.com.
  • Lawrance R; Adelphi Values, Boston, MA, USA. Electronic address: rachael.lawrance@adelphivalues.com.
  • Blum SI; Bristol Myers Squibb, Princeton, NJ 08540, USA. Electronic address: steven.blum@bms.com.
  • Sun X; Adelphi Values, Boston, MA, USA. Electronic address: sun.xiaowu2010@gmail.com.
  • Juarez-Garcia A; Bristol Myers Squibb, Princeton, NJ 08540, USA. Electronic address: ariadna.juarezgarcia@bms.com.
  • Moreno-Koehler A; Adelphi Values, Boston, MA, USA. Electronic address: alejandro.moreno-koehler@adelphivalues.com.
  • Li A; Bristol Myers Squibb, Princeton, NJ 08540, USA. Electronic address: angus.lee@bms.com.
  • Li A; Bristol Myers Squibb, Princeton, NJ 08540, USA. Electronic address: 1020936402mail@sina.com.
  • Cheng Y; Jilin Cancer Hospital, 1018 Huguang Road, Changchun 130012, China. Electronic address: chengying@csco.org.cn.
Lung Cancer ; 165: 71-81, 2022 Mar.
Article em En | MEDLINE | ID: mdl-35093625
ABSTRACT

OBJECTIVES:

In the phase 3 CheckMate 078 study, nivolumab prolonged overall survival (OS) and showed a favorable safety profile versus docetaxel in a predominantly Chinese patient population with previously treated advanced non-small cell lung cancer (aNSCLC). However, long-term efficacy, safety, and health-related quality of life findings with second-line nivolumab are very limited in Asian patients with previously treated aNSCLC. Here, we report updated clinical data and patient-reported outcomes (PROs) from the phase 3 CheckMate 078 trial with a 3-year minimum follow-up. MATERIALS AND

METHODS:

Patients with aNSCLC and disease progression after platinum-doublet chemotherapy were randomized 21 to nivolumab (3 mg/kg every 2 weeks) or docetaxel (75 mg/m2 every 3 weeks) until progression or unacceptable toxicity. The primary endpoint was OS; secondary endpoints included objective response rate, progression-free survival, safety, and disease-related symptom deterioration assessed using the Lung Cancer Symptom Scale (LCSS) by Week 12. Additional PRO assessments were exploratory endpoints.

RESULTS:

At ≥ 37.3 months follow-up, 3-year OS rates were 19% with nivolumab and 12% with docetaxel; 30% and 0% of responders remained in response for ≥ 3 years, respectively. Incidence of treatment-related adverse events occurring after 2 years was lower than during the first 2 years. No new treatment-related deaths were reported. By Week 12 of treatment, rates of disease-related symptom deterioration were 32% with nivolumab and 47% with docetaxel. Completion rates for PRO questionnaires were ≥ 80% in both arms. Clinically meaningful and sustained improvements in LCSS Average Symptom Burden Index scores and delayed time to first symptom deterioration were observed with nivolumab against docetaxel.

CONCLUSIONS:

At 3 years, nivolumab continued to demonstrate survival benefit versus docetaxel, exhibiting improvements in disease-related symptoms and overall health status in a predominantly Chinese patient population with previously treated aNSCLC. No new safety signals were observed. These findings are similar to the global population.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article