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N/A N=260

LUME BioNIS: a Biomarker Study in Patients With NSCLC

Carcinoma, Non-Small-Cell Lung

Enrolled (actual)
260
Serious AEs
49.4%
Results posted
Sep 2020
Primary outcome: Primary: Number of Participants With Overall Survival (OS) Event — 206 Participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Boehringer Ingelheim
Primary completion
Sep 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Overall Survival (OS) Event
206

Summary

At present there are no approved predictive tumour- or serum-derived biomarkers guiding usage of anti-angiogenic therapies in patients with adenocarcinoma of NSCLC.The objective of this NIS is to examine whether genetic/genomic markers (alone or combined with clinical covariates) could be used to predict OS in NSCLC patients eligible for treatment with Vargatef®. The investigations in this study are exploratory in nature and considered to be hypothesis generating. The results from these investigations may help to expand our understanding of the disease and the response to Vargatef®.

Eligibility Criteria

Inclusion criteria

  • Age = 18 years.
  • Women and men with locally advanced, metastatic or locally recurrent NSCLC with histology of adenocarcinoma.
  • Signed and dated written informed consent.
  • Vargatef ® is initiated and administered in accordance with the SPC.
  • Available fixed and paraffin embedded (FPE) tumour tissue routinely obtained at diagnosis and/or at re-biopsy before the initiation of the first line treatment (either block or slides, minimum of 10 slides and up to 20 slides if possible at 5µm thickness).

Exclusion criteria

  • Any contraindication to Vargatef® or docetaxel as specified in their respective labels.
  • Vargatef® initiated more than 7 days prior to inclusion in this NIS.
  • Patients participating simultaneously in a clinical trial.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02671422). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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