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 |
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Health condition(s) or Problem(s) studied | Malignant melanoma |
Date of first enrollment | 2024/04/04 |
Target sample size | |
Countries of recruitment | Japan |
Study type | Others,meta-analysis etc |
Intervention(s) |
Outcome(s)
Primary Outcome | The 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. |
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Secondary Outcome |
Key inclusion & exclusion criteria
Age minimum | Not applicable |
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Age maximum | Not applicable |
Gender | Male and Female |
Include criteria | |
Exclude criteria | Perioperative ICI combined with radiological treatment will be excluded. |
Related Information
Primary Sponsor | Yokohama City University Hospital |
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Secondary Sponsor | |
Source(s) of Monetary Support | Yokohama City University Hospital |
Secondary ID(s) |
Contact
public contact | |
Name | Nobuyuki Horita |
Address | 3-9, Fukuura, Kanazawa, Yokohama, Japan Japan 236-0004 |
Telephone | 045-787-2800 |
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 |
horitano@yokohama-cu.ac.jp | |
Affiliation | Yokohama City University Hospital Chemotherapy Center |