NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000054048

Registered date:04/04/2024

Progression-free, disease-free, and recurrence-free survivals as surrogate in melanoma perioperative immune checkpoint inhibitor trials.

Basic Information

Recruitment status Pending
Health condition(s) or Problem(s) studiedMalignant melanoma
Date of first enrollment2024/04/04
Target sample size
Countries of recruitmentJapan
Study typeOthers,meta-analysis etc
Intervention(s)

Outcome(s)

Primary OutcomeThe study-level outcomes of our concern will be the hazard ratios (HRs) of event-free survival (EFS, HRefs) and HR of OS (HRos). EFS includes PFS, DFS, and RFS. We will assess the Spearman's rank correlation between HRefs and HRos.
Secondary Outcome

Key inclusion & exclusion criteria

Age minimumNot applicable
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteriaPerioperative ICI combined with radiological treatment will be excluded.

Related Information

Contact

public contact
Name Nobuyuki Horita
Address 3-9, Fukuura, Kanazawa, Yokohama, Japan Japan 236-0004
Telephone 045-787-2800
E-mail horitano@yokohama-cu.ac.jp
Affiliation Yokohama City University Hospital Chemotherapy Center
scientific contact
Name Nobuyuki Horita
Address 3-9, Fukuura, Kanazawa, Yokohama, Japan Japan
Telephone 045-787-2800
E-mail horitano@yokohama-cu.ac.jp
Affiliation Yokohama City University Hospital Chemotherapy Center