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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03928964
Other study ID # P/2017/342
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date January 15, 2018
Est. completion date April 2019

Study information

Verified date April 2019
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The hypothesis of this study are as follows:

- Prognostic evaluation of patients based on an integrative model provides better assessment of overall survival, and thus improves setting of care goals.

- In a routine care population, antitumour drugs may have a significant impact on overall survival through their targeted antitumor effect, but also through their toxicity profile and their impact on comorbidities.

- The optimization of patient support (supportive care, drug tolerance monitoring) can have an impact on the prognosis.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 440
Est. completion date April 2019
Est. primary completion date October 3, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria:

1. Patients with locally advanced or metastatic renal cell carcinoma

2. Whose first-line treatment included at least one anti-angiogenic agent (tyrosine kinase inhibitor or monoclonal antibodies) and / or an mTOR inhibitor;

3. Whatever was the overall ECOG-PS score (Eastern Cooperative Oncology Group Performance Status) at treatment initiation time

4. With first-line treatment carried out between 2007 and June 2016.

Exclusion criteria:

1. Patient previously treated with only one cytokine (Interferon a2a, high-dose interleukin-2)

2. Refusal of processing of personal data

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU de Besançon Besançon
France Hôpital Henri Mondor Créteil
France Hôpital Nord Franche-Comté Montbéliard Montbéliard
France Hôpital Cochin Paris
France Hôpital Européen Georges Pompidou Paris
France Hôpital Saint-Louis Paris
France Institut Mutualiste Montsouris Paris
France Hôpital d'Instruction des Armées de Bégin Saint-Mandé

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival after the first line of treatment Time elapsed between initiation date for 2nd line treatment et the date of death, whatever the cause. year 11
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