Skip to content

Observational Study for Lung Cancer Patients Treated With Nivolumab

EVIDENS: Lung Cancer Patients Treated With Nivolumab: A Longitudinal, Prospective, Observational, Multicentric Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03382496
Acronym
EVIDENS
Enrollment
1462
Registered
2017-12-26
Start date
2016-10-01
Completion date
2020-12-23
Last updated
2022-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Brief summary

This study will describe the characteristics of patients initiating nivolumab treatment for lung cancer and their outcomes over 3 years in France

Interventions

OTHERNon-Interventional

Non-Interventional

Sponsors

Bristol-Myers Squibb
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female: 18 age at the time of nivolumab initiation * Pathologically confirmed diagnosis of lung cancer * Patient initiating nivolumab :therapeutic decision to initiate nivolumab must be taken by the physician prior to enrolling a patient in the study

Exclusion criteria

-Patient taking part in an interventional study for lung cancer treatment for which nivolumab is 1 of the investigational drugs Other protocol defined inclusion or

Design outcomes

Primary

MeasureTime frameDescription
(OS) Overall SurvivalUp to 3 yearsTime from index date (treatment with nivolumab) until date of death due to any cause
Number of patients exposed to other lung cancer treatmentsAt baseline
Distribution of current smokers, former smokers, and non-smokers at initial diagnosisAt baseline
Distribution of cancer stage at initial diagnosis and at nivolumab initiationAt baseline
Distribution of Lung cancer histology at initial diagnosisAt baseline
Number of patients with untreated brain metastasis at nivolumab initiationAt baseline
Number of patients with treated brain metastasis at nivolumab initiationAt baseline
Number of patients with PD-L1 expression at nivolumab initiationAt baselinePD-LI (Programmed death-ligand 1)
Number of patients with mutations at nivolumab initiationAt baseline
Distribution of concomitant diseases at nivolumab initiationAt baseline
Number of patients with corticosteroids treatment at nivolumab initiationAt baseline
Distribution of genderAt baseline
Distribution of ageAt baseline
Distribution of line of therapy at nivolumab initiationAt baseline
Distribution of ECOG PSAt baselineEastern Cooperative Oncology Group Performance Status (ECOG PS) A scale used to assess how a patient's disease is progressing, assess how the disease affects the daily living abilities of the patient, and determine appropriate treatment and prognosis
Distribution of patients working status at nivolumab initiationAt baseline
QoL (EQ-5D) at nivolumab initiationAt baselineQuality of Life (QoL) as assessed by European Quality of Life-5 Dimensions (EQ-5D) EQ-5D: the descriptive system consists of 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, each with 3 levels (eg, no problems, moderate problems, extreme problems)
Median time from initial diagnosis to nivolumab initiationAt baselineMedian time from initial diagnosis to nivolumab initiation (derived from date of initial diagnosis and date of first dose of nivolumab, assumed to be the date of D0 visit). Any lung cancer declaring more than 5 years after another cancer is defined as an initial diagnosis of lung cancer

Secondary

MeasureTime frameDescription
Distribution of patients with progression of pre-existing sitesUp to 3 years
Overall Survival after initiation of nivolumabUp to 2 years
Distribution of nivolumab adverse drug reactionAt 3 years after nivolumab initiation
Progression Free Survival (PFS)Up to 3 years after nivolumab initiationPFS measured by time since index date (initial treatment with nivolumab) to either the first disease progression date or last known tumor assessment date, or death due to any cause, whichever occurs first as assessed by RECIST 1.1
Objective Response Rate (ORR)Up to 3 years after nivolumab initiationORR is measured by the sum of partial responses plus complete responses as assessed by (RECIST 1.1) Response Evaluation Criteria In Solid Tumors
Quality of Life (QoL)Baseline to 3 years after nivolumab initiation
Distribution of patient management treatment patternsBaseline to 3 years
Mean weight change in kilogram from baselineBaseline up to 3 years
Mean ECOG PS change from baselineBaseline up to 3 years
Distribution of patients with new metastasisUp to 3 years

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026