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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04501497
Other study ID # J-TAIL-2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 21, 2020
Est. completion date February 3, 2023

Study information

Verified date April 2024
Source Chugai Pharmaceutical
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a multi-center observational study of atezolizumab combination therapy in patients with unresectable, advanced and recurrent non-small cell lung cancer(NSCLC) or extensive disease small cell lung cancer(ED-SCLC). 800 patients in NSCLC cohort and 400 patients in ED-SCLC cohort will be enrolled in this trial to assess the efficacy and safety of this combination.


Description:

Primary endpoint: 12 months OS, Secondary endpoints: Overall Survival(OS), 6 months survival rate(6mo OS), 12 months survival rate(12mo OS), Progression-Free Survival(PFS), Time to treatment failure (TTF), Objective Response Rate(ORR), Disease Control Rate(DCR), Duration of Response(DOR) ,Safety and Comprehensive geriatric assessment(G8)


Recruitment information / eligibility

Status Completed
Enrollment 1221
Est. completion date February 3, 2023
Est. primary completion date February 3, 2023
Accepts healthy volunteers
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: < non-small cell lung cancer cohort> 1. Patients 20 years of age or older at the time of signed consent. 2. Patients with unresectable, advanced and recurrent non-small cell lung cancer. 3. Patients who are scheduled to start atezolizumab combination therapy in clinical practice, based on the atezolizumab package insert and the Optimal Use Promotion Guideline. 4. Patients who signed informed consent form before enrolling the study. The consent from a legally acceptable representative is required for the patients with uncertain capacity of judgments. <extensive disease small cell lung cancer cohort> 1. Patients 20 years of age or older at the time of signed consent. 2. Patients with extensive disease small cell lung cancer. 3. Patients who are scheduled to start atezolizumab combination therapy in clinical practice, based on the atezolizumab package insert and the Optimal Use Promotion Guideline. 4. Patients who signed informed consent form before enrolling the study. The consent from a legally acceptable representative is required for the patients with uncertain capacity of judgments. Exclusion Criteria: < non-small cell lung cancer cohort> (1) Patients who are unsuitable for enrolment into the study by the investigator's judgment. <extensive disease small cell lung cancer cohort> (1) Patients who are unsuitable for enrolment into the study by the investigator's judgment.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Japan Akashi Medical Center Akashi
Japan Hyogo Cancer Center Akashi
Japan Hyogo Prefectural Amagasaki General Medical Center Amagasaki
Japan Asahikawa Medical University Hospital Asahikawa
Japan National Hospital Organization Asahikawa Medical Center Asahikawa
Japan Juntendo University Hospital Bunkyo-Ku
Japan Nippon Medical School Hospital Bunkyo-Ku
Japan Tokyo Medical And Dental University, Medical Hospital Bunkyo-Ku
Japan Chiba University Hospital Chiba
Japan National Cancer Center Hospital Chuo Ku
Japan Fujisawa City Hospital Fujisawa
Japan Fukui Prefectural Hospital Fukui
Japan Fukuoka University Hospital Fukuoka
Japan Kyushu University Hospital Fukuoka
Japan National Hospital Organization Kyushu Cancer Center Fukuoka
Japan National Hospital Organization Kyushu Medical Center Fukuoka
Japan Fukushima Medical University Hospital Fukushima
Japan Gifu Prefectural General Medical Center Gifu
Japan National Hospital Organization Okinawa National Hospital Ginowan
Japan Hamamatsu University Hospital Hamamatsu
Japan National Hospital Organization Himeji Medical Center Himeji
Japan Kansai Medical University Hospital Hirakata
Japan Hirosaki University Hospital Hirosaki
Japan Hiroshima City Hiroshima Citizens Hospital Hiroshima
Japan Hiroshima Prefectural Hospital Hiroshima
Japan Hiroshima University Hospital Hiroshima
Japan Aso Iizuka Hospital Iizuka
Japan Nippon Medical School Chiba Hokusoh Hospital Inzai
Japan Japanese Red Cross Ise Hospital Ise
Japan Tokai University Hospital Isehara
Japan Teikyo University Hospital Itabashi-Ku
Japan Itami City Hospital Itami
Japan National Hospital Organization Iwakuni Clinical Center Iwakuni
Japan Shimane University Hospital Izumo
Japan Juntendo University Shizuoka Hospital Izunokuni
Japan Kagawa University Hospital Kagawa
Japan Kagoshima University Hospital Kagoshima
Japan Kameda Medical Center Kamogawa
Japan Ishikawa Prefectural Central Hospital Kanazawa
Japan Kanazawa University Hospital Kanazawa
Japan Ibaraki Prefectural Central Hospital Kasama
Japan Kasukabe Medical Center Kasukabe
Japan Kishiwada City Hospital Kishiwada
Japan Hospital of the University of Occupational and Envioronmental Health Kitakyushu
Japan Japan Community Health care Organization Kyushu Hospital Kitakyushu
Japan Kitakyushu Municipal Medical Center Kitakyushu
Japan Japan Anti-Tuberculosis Association Fukujuji Hospital Kiyose
Japan National Hospital Organization Tokyo National Hospital Kiyose
Japan Kobe City Medical Center General Hospital Kobe
Japan Kobe Minimally Invasive Cancer Center Kobe
Japan Kobe University Hospital Kobe
Japan Dokkyo Medical University Saitama Medical Center Koshigaya
Japan The Cancer Institute Hospital of Japanese Foundation For Cancer Research Koto-Ku
Japan Kurashiki Central Hospital Kurashiki
Japan National Hospital Organization Kure Medical Center and Chugoku Cancer Kure
Japan Kurume University Hospital Kurume
Japan Kyoto City Hospital Kyoto
Japan Kyoto University Hospital Kyoto
Japan Kyoto-Katsura Hospital Kyoto
Japan National Hospital Organization Kyoto Medical Center Kyoto
Japan University Hospital, Kyoto Prefectural University of Medicine Kyoto
Japan Shinshu University Hospital Matsumoto
Japan Matsusaka Municipal Hospital Matsusaka
Japan National Hospital Organization Shikoku Cancer Center Matsuyama
Japan National Hospital Organization Tokyo Medical Center Meguro-Ku
Japan The Jikei University Hospital Minato-Ku
Japan Tokyo Saiseikai Central Hospital Minato-Ku
Japan Kyorin University Hospital Mitaka
Japan Miyazaki Prefectural Miyazaki Hospital Miyazaki
Japan Nagahama City Hospital Nagahama
Japan Aichi Medical University Hospital Nagakute
Japan Nagasaki University Hospital Nagasaki
Japan Aichi Cancer Center Nagoya
Japan Japanese Red Cross Nagoya Daini Hospital Nagoya
Japan Nagoya City University Hospital Nagoya
Japan Nagoya Ekisaikai Hospital Nagoya
Japan Nagoya University Hospital Nagoya
Japan National Hospital Organization Nagoya Medical Center Nagoya
Japan Miyagi Cancer Center Natori
Japan Niigata Cancer Center Hospital Niigata
Japan Niigata University Medical and Dental Hospital Niigata
Japan The Hospital of Hyogo College of Medicine Nishinomiya
Japan Obihiro Kosei Hospital Obihiro
Japan Ogaki Municipal Hospital Ogaki
Japan Oita Prefectural Hospital Oita
Japan Japanese Red Cross Okayama Hospital Okayama
Japan Kawasaki Medical School General Medical Center Okayama
Japan Okayama Rosai Hospital Okayama
Japan Okayama University Hospital Okayama
Japan Osaka City General Hospital Osaka
Japan Osaka General Medical Center Osaka
Japan Osaka International Cancer Institute Osaka
Japan Osaka Saiseikai Nakatsu Hospital Osaka
Japan Kindai University Hospital Osaka-sayama
Japan Osaki Citizen Hospital Osaki
Japan Gunma Prefectural Cancer Center Ota
Japan Shiga University of Medical Science Hospital Otsu
Japan Saga University Hospital Saga
Japan Kitasato University Hospital Sagamihara
Japan Jichi Medical University Saitama Medical Center Saitama
Japan Saitama medical university International medical Center Saitama
Japan Saitama Prefectural Cancer Center Saitama
Japan Saitama Red Cross Hospital Saitama
Japan National Hospital Organization Kinki-Chuo Chest Medical Center Sakai
Japan Hokkaido University Hospital Sapporo
Japan National Hospital Organization Hokkaido Cancer Center Sapporo
Japan Sapporo Medical University Hospital Sapporo
Japan Teine Keijinkai Hospital Sapporo
Japan Sendai Kousei Hospital Sendai
Japan Tohoku Medical And Pharmaceutical University Hospital Sendai
Japan Tohoku University Hospital Sendai
Japan Japanese Red Cross Medical Center Shibuya-Ku
Japan Jichi Medical University Hospital Shimotsuke
Japan Showa University Hospital Shinagawa-Ku
Japan Center Hospital of the National Center for Global Health and Medicine Shinjuku-Ku
Japan Keio University Hospital Shinjuku-Ku
Japan Tokyo Medical University Hospital Shinjuku-Ku
Japan Iwate Medical University Hospital Shiwa-gun
Japan Shizuoka Cancer Center Shizuoka
Japan Shizuoka General Hospital Shizuoka
Japan Osaka University Hospital Suita
Japan Saiseikai Suita Hospital Suita
Japan Kagawa Prefectural Central Hospital Takamatsu
Japan JA Toyama Kouseiren Takaoka Hospital Takaoka
Japan Takarazuka City Hospital Takarazuka
Japan Osaka Medical and Pharmaceutical University Hospital Takatsuki
Japan Tenri Hospital Tenri
Japan Dokkyo Medical University Hospital Tochigi
Japan Tokushima Prefectural Central Hospital Tokushima
Japan Tokushima University Hospital Tokushima
Japan Ehime University Hospital Toon
Japan Toyama Prefectural Central Hospital Toyama
Japan Fujita Health University Hospital Toyoake
Japan National Hospital Organization Osaka Toneyama Medical Center Toyonaka
Japan TOYOTA Memorial Hospital Toyota
Japan Tsukuba Medical Center Hospital Tsukuba
Japan University of Tsukuba Hospital Tsukuba
Japan National Hospital Organization Yamaguchi-Ube Medical Center Ube
Japan Juntendo University Urayasu Hospital Urayasu
Japan Japanese Red Cross Wakayama Medical Center Wakayama
Japan Wakayama Medical University Hospital Wakayama
Japan Kanagawa Cancer Center Yokohama
Japan Kanagawa Cardiovascular and Respiratory Center Yokohama
Japan Yokohama City University Hospital Yokohama
Japan Yokohama Municipal Citizen's Hospital Yokohama
Japan Yokosuka Kyosai Hospital Yokosuka
Japan Tottori University Hospital Yonago
Japan Oita University Hospital Yufu

Sponsors (2)

Lead Sponsor Collaborator
Chugai Pharmaceutical Japan Lung Cancer Society

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary 12 months survival rate Percentage of participants alive 12 months after initiation of treatment Baseline up to 12 Months
Secondary Overall Survival OS was defined as the time from the first day of study treatment to death due to any cause Up to death (up to 3 years)
Secondary 6 moths survival rate Percentage of participants alive 6 months after initiation of treatment Up to 6 months
Secondary 18 moths survival rate Percentage of participants alive 18 months after initiation of treatment Up to 18 months
Secondary Progression-Free Survival(PFS) PFS based on disease status as evaluated by the investigator in accordance with Response Evaluation Criteria in Solid Tumors (RECIST), Version 1.1 (v1.1) Up to disease progression or death whichever occurs first (up to 3 years)
Secondary Time to treatment failure (TTF) TTF was defined as the time from the first day of study treatment to treatment discontinuation for any reason, including disease progression, treatment toxicity, patient preference, or death Up to 3 years
Secondary Post-treatment transfer rate Rate of patients who received drug therapy for primary disease after study treatment Up to post-treatment is started (up to 3 years)
Secondary Objective Response Rate(ORR) Percentage of participants with objective response as assessed by the investigator according to RECIST v1.1 Up to disease progression or death whichever occurs first (up to 3 years)
Secondary Duration of Response(DOR) Duration of Response as Assessed by the Investigator According to RECIST v1.1 From date of first objective response up to disease progression or death whichever occurs first (up to 3 years)
Secondary Disease Control Rate(DCR) Percentage of patients with controled disease as Assessed by the investigator according to RECIST v1.1 Up to 3 years
Secondary Percentage of Participants with adverse events(Adverse Reactions) The incidence of worst-grade adverse events on study as graded by NCI-CTCAE v5.0 Up to 3 years
Secondary Comprehensive geriatric assessment (G8) The G-8 screening tool was developed to identify elderly cancer patients who would benefit from comprehensive geriatric assessment At baseline
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