Giuseppe Cicero,1 Rossella De Luca,1 Francesco Dieli2 1Department of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Palermo, Italy; 2Central Laboratory of Advanced Diagnosis and Biomedical Research (CLADIBIOR), University of Palermo, Palermo, Italy Background: In many clinical trials designed to assess the efficacy of anticancer treatments, overall survival (OS) is often used as a primary endpoint despite its several points of weakness. Methods: This study evaluated the role of progression-free survival (PFS) in the first three lines of treatment as a potential surrogate endpoint of OS in patients with metastatic colorectal cancer (MCRC). One hundred and twenty patients with MCRC were enrolle...
Background. The impact of the duration of chemotherapy on the overall survival of patients with meta...
International audienceAbstract Background Progression-free survival (PFS) is a surrogate endpoint wi...
Background: The duration and cost of cancer clinical trials could be reduced if a surrogate endpoint...
Background: In many clinical trials designed to assess the efficacy of anticancer treatments, overal...
The traditional end point for assessing efficacy of first-line chemotherapies for advanced cancer is...
Purpose Progression-free survival (PFS) has previously been established as a surrogate for overall s...
To evaluate progression-free survival (PFS) and objective response rate (ORR) as surrogate endpoints...
Background:Progression free survival (PFS) and tumour response (TR) have been investigated as surrog...
The purpose of this study was to evaluate progression-free survival (PFS) and objective response rat...
PURPOSE: Progression-free survival (PFS) has previously been established as a surrogate for over...
Background: Recurrence-free survival has been used as a surrogate endpoint for overall survival in t...
Importance: The Gynecologic Cancer InterGroup (GCIG) recommended that progression-free survival (PFS...
To quantify and compare the treatment effects on three surrogate end points, progression-free surviv...
Background: Progression-free survival (PFS) has been adopted as the primary endpoint in many randomi...
AbstractObjectivesTo quantify and compare the treatment effects on three surrogate end points, progr...
Background. The impact of the duration of chemotherapy on the overall survival of patients with meta...
International audienceAbstract Background Progression-free survival (PFS) is a surrogate endpoint wi...
Background: The duration and cost of cancer clinical trials could be reduced if a surrogate endpoint...
Background: In many clinical trials designed to assess the efficacy of anticancer treatments, overal...
The traditional end point for assessing efficacy of first-line chemotherapies for advanced cancer is...
Purpose Progression-free survival (PFS) has previously been established as a surrogate for overall s...
To evaluate progression-free survival (PFS) and objective response rate (ORR) as surrogate endpoints...
Background:Progression free survival (PFS) and tumour response (TR) have been investigated as surrog...
The purpose of this study was to evaluate progression-free survival (PFS) and objective response rat...
PURPOSE: Progression-free survival (PFS) has previously been established as a surrogate for over...
Background: Recurrence-free survival has been used as a surrogate endpoint for overall survival in t...
Importance: The Gynecologic Cancer InterGroup (GCIG) recommended that progression-free survival (PFS...
To quantify and compare the treatment effects on three surrogate end points, progression-free surviv...
Background: Progression-free survival (PFS) has been adopted as the primary endpoint in many randomi...
AbstractObjectivesTo quantify and compare the treatment effects on three surrogate end points, progr...
Background. The impact of the duration of chemotherapy on the overall survival of patients with meta...
International audienceAbstract Background Progression-free survival (PFS) is a surrogate endpoint wi...
Background: The duration and cost of cancer clinical trials could be reduced if a surrogate endpoint...