Unique ID issued by UMIN | UMIN000025908 |
---|---|
Receipt number | R000029772 |
Scientific Title | Retrospective cohort study of correlation between immune check point molecular inhibitor and response factor, side effect, and post treatment |
Date of disclosure of the study information | 2017/01/31 |
Last modified on | 2017/03/26 20:34:28 |
Retrospective cohort study of correlation between immune check point molecular inhibitor and response factor, side effect, and post treatment
The rerashonship between immune check point molecular inhibitor and response factor, side effect, or post treatment
Retrospective cohort study of correlation between immune check point molecular inhibitor and response factor, side effect, and post treatment
The rerashonship between immune check point molecular inhibitor and response factor, side effect, or post treatment
Japan |
Patients with non-resectable advanced or recurrent NSCLC receiving treatment with nivolumab
Medicine in general | Pneumology | Hematology and clinical oncology |
Malignancy
NO
To investigate of factors influencing the response rate and adverse reactions to an immune checkpoint inhibitor, as well as subsequent therapy
Others
A: Relation between pretreatment patient characteristics and the efficacy of nivolumab and its ARs.
B: Response patterns, sites of response (anatomical regions), and ARs
C: Influence of nivolumab on subsequent treatment
D: Correlation with effect of nivolumab and IHC of PD-L1
Confirmatory
Pragmatic
Not applicable
To investigate whether retrospective analysis of nivolumab therapy in the real clinical setting reproduces the RR shown by primary analysis of the CheckMate trial.
A: Relation between pretreatment patient characteristics and the efficacy of nivolumab and its ARs.
B: Response patterns, sites of response (anatomical regions), and ARs
C: Influence of nivolumab on subsequent treatment
D: Correlation with effect of nivolumab and IHC of PD-L1
Others,meta-analysis etc
Not applicable |
Not applicable |
Male and Female
1) Patients with a definite diagnosis of NSCLC based on histology or cytology.
2) Patients unsuitable for curative radiation therapy who have a clinical diagnosis of either recurrent disease or stage IV NSCLC.
3) Patients who receive at least one dose of nivolumab.
Patients who have previously received nivolumab in a clinical trial will be excluded
200
1st name | |
Middle name | |
Last name | Imamura Fumio |
Osaka Medical Center for Cancer and Cardiovascular Diseases
Thoracic Oncology
1-3-3 Nakamichi, Higashinari-ku, Osaka
06-6972-1181
imamura-fu@mc.pref.osaka.jp
1st name | |
Middle name | |
Last name | Tamiya Motohiro |
Osaka Medical Center for Cancer and Cardiovascular Diseases
Thoracic Oncology
1-3-3 Nakamichi, Higashinari-ku, Osaka
06-6972-1181
moto19781205@yahoo.co.jp
Osaka Medical Center for Cancer and Cardiovascular
ONO PHARMACEUTICAL CO., LTD.
Bristol-Myers Squibb K.K.
Profit organization
National Hospital Organization Kinki Chuo Chest Medical Center
Osaka Prefectural Medical Center for Respiratory and Allergic Diseases
NO
2017 | Year | 01 | Month | 31 | Day |
Unpublished
No longer recruiting
2016 | Year | 12 | Month | 14 | Day |
2017 | Year | 02 | Month | 01 | Day |
Primary endpoint:
To investigate whether retrospective analysis of nivolumab therapy in the real clinical setting reproduces the RR shown by primary analysis of the CheckMate trial.
Secondary endpoints:
A: Relation between pretreatment patient characteristics and the efficacy of nivolumab and its ARs.
B: Response patterns, sites of response (anatomical regions), and ARs
C: Influence of nivolumab on subsequent treatment
D: Correlation with effect of Nivolumab and IHC of PD-L1
2017 | Year | 01 | Month | 30 | Day |
2017 | Year | 03 | Month | 26 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029772