Unique ID issued by UMIN | UMIN000049022 |
---|---|
Receipt number | R000053724 |
Scientific Title | Efficacy and safety of Immune check point inhibitors in patients with non-small cell lung cancer harboring rare driver oncogene |
Date of disclosure of the study information | 2022/09/26 |
Last modified on | 2024/12/16 21:49:15 |
A real-world study of efficacy and safety of Immune check point inhibitors in patients with non-small cell lung cancer harboring driver oncogene excepting EGFR
Efficacy and safety of Immune check point inhibitors in patients with non-small cell lung cancer harboring rare driver oncogene
Efficacy and safety of Immune check point inhibitors in patients with non-small cell lung cancer harboring rare driver oncogene
Efficacy and safety of Immune check point inhibitors in patients with non-small cell lung cancer harboring rare driver oncogene
Japan |
Non-small cell lung cancer harboring driver oncogene excepting EGFR
Pneumology |
Malignancy
NO
We will retrospectively evaluate the efficacy and safety of immune checkpoint inhibitor (ICI) therapy in patients with unresectable or postoperatively recurrent non-small cell lung cancer harboring rare driver oncogene mutation/translocation. Secondary, the efficacy and safety of molecular targeted therapy in actual clinical practice will also be retrospectively evaluated.
Safety,Efficacy
Others
Others
Not applicable
Progression-free survival of immune checkpoint inhibitor therapy with or without chemotherapy
Response rate of immune checkpoint inhibitor therapy with or without chemotherapy, Immune-related adverse events, Response rate of molecular targeted therapy, Progression-free survival of molecular targeted therapy, Time to treatment failure of molecular targeted therapy, Overall survival from start date of the first line treatment, Cluster analysis of survival
Observational
Not applicable |
Not applicable |
Male and Female
(1) Patients with histologically or cytologically confirmed non-small cell lung cancer at clinical stage IIIA, IIIB, IIIC, IVA, IVB or postoperative recurrence that is not amenable to local treatment.
(2) ALK, ROS1, MET, BRAF, KRAS, HER2, RET, NTRK are proven.
(3) Patients who have received systemic chemotherapy between January 2015 and December 2021.
(1) Patients who are judged by the principal investigator or sub-investigator to be inappropriate for participation in this study.
(2) Patients who had no driver mutation/translocation or EGFR mutation only.
870
1st name | Takehito |
Middle name | |
Last name | Shukuya |
Juntendo University School of Medicine
Respiratory Medicine
113-8431
Hongo 3-1-3, Bunkyo-ku, Tokyo
0338133111
tshukuya@juntendo.ac.jp
1st name | Atsuto |
Middle name | |
Last name | Mouri |
Saitama Medical University International Medical Center
Respiratory medicine
350-1298
350-1298 Yamane 1397-1, Hidaka-city, Saitama
09016016701
mouria@saitama-med.ac.jp
North East Japan Study Group
Novartis Pharma KK
Profit organization
Saitama Medical University International Medical Center
350-1298 Yamane 1397-1, Hidaka city, Saitama
0429844111
chikens@saitama-med.ac.jp
YES
2022-007
Saitama Medical University International Medical Center
埼玉医科大学国際医療センター
2022 | Year | 09 | Month | 26 | Day |
Unpublished
Open public recruiting
2022 | Year | 05 | Month | 30 | Day |
2022 | Year | 06 | Month | 20 | Day |
2022 | Year | 07 | Month | 01 | Day |
2022 | Year | 12 | Month | 31 | Day |
2023 | Year | 03 | Month | 31 | Day |
Retrospective study
2022 | Year | 09 | Month | 26 | Day |
2024 | Year | 12 | Month | 16 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000053724