Post-ATU Study of Nivolumab

Melanoma Clinical Trial

— Post-ATU  

Official title:

Two-years Follow-up of Melanoma Patients Treated by Nivolumab During the French ATU Program

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03325257
• Other study ID #: RC17_0027
• Status: Completed
• Start date: March 9, 2017
• Est. completion date: March 1, 2019

Study information

• Verified date: September 2021
• Source: Nantes University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Nivolumab obtained European Marketing authorization in June 2015. Before this date, a Temporary Authorization for Use (ATU) Program in France for nivolumab was set up between September 2014 and August 2015. This program enrolled approximately 600 melanoma patients (unresectable or metastatic).

It appears relevant to conduct a study on patients treated during the ATU to assess thoroughly patient characteristics, efficacy, safety, and patterns of use of nivolumab in real-life conditions.

Description:

In order to reach goals of this study, collaboration had been established between BMS and the RIC-Mel network (network for Research and Clinical Investigational Research on Melanoma) (NCT03315468).

The RIC-Mel network has set up a national database in order to reference the active file of melanoma patients in France. The RIC-Mel database, supported by Nantes University Hospital, had been approved by French authorities (CCTIRS and CNIL). The RIC-Mel network is coordinated by Pr B. DRENO (Nantes University Hospital) and Pr C. LEBBE (Saint-Louis Hospital, AP-HP, Paris). Nowadays, 49 centres located all over the country are participating, with more than 19,000 melanoma patients included in the database. The RIC-Mel database is referred as one of the privileged access to any research program on melanoma by the Cancerology Group (GCC) of the French Society of Dermatology .

Based on this, BMS and the RIC-Mel network had established a partnership to set up a study in order to estimate the overall survival of melanoma patients treated by Nivolumab during the French ATU program.

Data are collected in the RIC-Mel database by participating centres. Information of centres, follow-up of activity, data reviewing and extractions are realized by the RIC-Mel network. Data analysis is performed by BMS following a developed statistical protocol.

Patients included in the study were patients with unresectable or advanced metastatic melanoma, which received at least one of Nivolumab, dispensed during the French ATU program.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 350
• Est. completion date: March 1, 2019
• Est. primary completion date: September 6, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with unresectable or metastatic melanoma cared in participating sites,

• Patients included in French nivolumab ATU program,

• Patients treated by at least one perfusion of nivolumab,

• Patients agreed to participate to the study.

Exclusion Criteria:

• Patients with unresectable or metastatic melanoma not included in French nivolumab ATU program,

• Patients having initiated Nivolumab after the 31th December 2015,

• Patients disagreed to participate.

Related Conditions & MeSH terms

• Melanoma

Intervention

Other:
• Routine care
This study is an observational one - there is no change to the routine care. Patients received the Nivolumab independently of the study. Only data will be collected during this project.

Locations

Country	Name	City	State
France	Chu Amiens	Amiens
France	Hopital St andré-CHU DE Bordeaux	Bordeaux
France	Chu Clermont-Ferrand	Clermont-Ferrand
France	Chu Dijon	Dijon
France	CHU de Grenoble	Grenoble	La Tronche
France	CH du Mans	Le Mans
France	Chru Lille	Lille
France	Centre Léon Bérard de Lyon	Lyon
France	Hospices Civils de Lyon: Lyon Sud	Lyon
France	Hôpitaux de Marseille	Marseille
France	CHU NICE	Nice
France	AP-HP Hôpital Ambroise Paré	Paris	Boulogne Billancourt
France	CH de PAU	Pau
France	CHU de Rouen	Rouen
France	Chu Toulouse	Toulouse
France	Ch Valence	Valence
France	Institut Gustave Roussy	Villejuif

Sponsors (2)

Lead Sponsor	Collaborator
Nantes University Hospital	Bristol-Myers Squibb

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Survival of patients included in the study thanks to subgroups of interest	Overall survival is defined as the time from index date (initiation of Nivolumab) until date of death due to any cause. Overall survival will be censored on the last date a subject was known to be alive. Estimates of survival rates will be realized for 1-year and 2-year survival. Median time will also be calculated.; Subgroups of interest are described in the description of the first Secondary Outcome Measure.; Safety Issue: No	2 years
Secondary	Distribution of melanoma patients included in the study in all subgroups of interest thanks to their clinical features at the time of treatment initiation	Subgroups of interest, based on information collected in medical records, were : ECOG performance status (PF). ECOG PF is attempted to quantify cancer patients' general well-being and activities of daily life. The classifications were 0, 1 or =2.; LDH level. This level is considered as a prognostic factor: higher the LDH level, the worst the prognosis. The classifications were =Upper Limit of Normal (ULN), >ULN, >2 ULN or N/R (Unknown).; History of brain metastasis. These metastases are considered as one of the most difficult-to-treat complications of melanoma. The classifications were No or Yes.; Line of therapy. The classifications were 0, 1, 2 or >2.; BRAF status. BRAF is a proto-oncogene. Melanoma patients with BRAF mutation are eligible to targeted therapy.The classifications were Yes (mutated), No (wild-type) and Unknown (no research).; Number of metastatic sites. Safety Issue: No	Day 1
Secondary	Proportion of melanoma patients included in the study categorized by genders overall and by subgroups of interest	Distribution of females and males. This analyse will be performed for all the study population and by subgroups of interest (as defined in the primary Outcome Measure).Safety Issue: No	Day 1
Secondary	Distribution of age of melanoma patients included in the study overall and by subgroups of interest	Age of patients is the age at the start of Nivolumab treatment Safety Issue: No	Day 1
Secondary	Description of Nivolumab treatment of melanoma patients included in the study	Average and median of Nivolumab treatment duration and infusion number will be assessed. Median time to discontinuation, whatever the reason and median time to discontinuation of dose related to adverse events. Distribution of reasons for discontinuation.; Safety Issue: No	2 years
Secondary	Incidence of select grade 3, 4 and 5 adverse events (AE) in melanoma patients included in the study and related to Nivolumab treatment	An AE is defined as any undesirable experience or manifestation associated with the use of a medical product in a patient. AEs are categorized by grades, which refer to severity : Grade 3 - Severe or medically significant but not immediately life-threatening, hospitalization or prolongation of hospitalization indicated, disabling, limiting self-care activities of daily living, Grade 4 - Life-threatening consequences, urgent intervention indicated, Grade 5 - Death related to AE. Proportion of patients with at least one or more select AE, distribution, average and median time of AE occurrence, duration and evolution of AEs as well as description of action on Nivolumab treatment will also be assessed.; Safety Issue: Yes	2 years
Secondary	Progression-free survival of melanoma patients included in the study	Progression-free survival is defined as the time since Nivolumab initiation to either the first disease progression date or at last known tumour assessment date, or death due to any cause, whichever occurs first.; Safety Issue: No	2 years
Secondary	Objective response rate of melanoma patients included in the study	Objective response rate as the number of subjects with a best objective response of either a partial response of a complete response. Objective response rate is the proportion of patients with an objective response. Safety Issue: No	2 years