A Study Called VICTORIA to Learn More About How Well Larotrectinib Works in Adults With TRK Fusion-positive Cancer by Comparing Larotrectinib Data From Clinical Studies With Data of Other Treatments From Actual Practice

Sponsor
Bayer (Industry)
Overall Status
Active, not recruiting
CT.gov ID
NCT05192642
Collaborator
(none)
368
1
11.9
30.9

Study Details

Study Description

Brief Summary

This is an observational study in which patient data from the past of adult people with solid tumors harboring NTRK gene fusion are studied. This study will focus on 5 tumor types which have been at the late stage or have spread to other parts of the body. These 5 tumor types are:

  • Non-small-cell-lung cancer

  • Colorectal cancer (located in the intestine)

  • Thyroid cancer

  • Sarcomas (located in the connective tissue like bones or body fat)

  • Salivary gland carcinoma

In some people with cancer, the cancer cells have specific changes in their building plans (genes) called NTRK gene fusion. NTRK stands for neurotrophic tyrosine receptor kinase, the specific gene that is changed. Due to this change in the gene, an altered protein known as a TRK fusion protein is made, which can cause cancer cells to grow and survive. While NTRK is the gene, TRK (tropomyosin receptor kinase) is the name of the protein. The specific cancer is therefore also called TRK fusion-positive cancer.

The study drug, larotrectinib works by blocking the altered TRK fusion protein. Larotrectinib is already available in the US, Europe, and in other countries and is approved for doctors to prescribe to patients with TRK fusion cancer.

The main purpose of this study is to learn more about how well larotrectinib works in adults with TRK fusion-positive cancer compared to other treatments. Researchers will compare how long participants who received larotrectninib lived to how long participants who received other treatments lived. To do this, larotrectinib data from past clinical studies will be compared with data on other treatments gathered from different health data sources. The data will cover the time between January 2013 and end of August 2022.

Besides this data collection, no further tests or examinations are planned and no visits are required in this study.

Condition or Disease Intervention/Treatment Phase
  • Drug: Larotrectinib(Vitrakvi, BAY2757556)
  • Drug: Data on other treatments

Study Design

Study Type:
Observational
Anticipated Enrollment :
368 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Comparative Effectiveness Study of Real-world Control of TRK Fusion Positive Cancer With Patients From Larotrectinib (Vitrakvi) Clinical Trials
Actual Study Start Date :
Dec 3, 2021
Anticipated Primary Completion Date :
Nov 30, 2022
Anticipated Study Completion Date :
Nov 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Larotrectinib clinical trial cohort

Drug: Larotrectinib(Vitrakvi, BAY2757556)
Clinical trials

RW external comparator cohort

Drug: Data on other treatments
Real word data

Outcome Measures

Primary Outcome Measures

  1. Overall survival (OS) [Retrospective analysis from January 2013 to August 2022]

Secondary Outcome Measures

  1. Overall Treatment patterns [Retrospective analysis from January 2013 to August 2022]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of advanced stage of disease or metastatic disease.
Exclusion Criteria:
  • Patients involved in TRK inhibitor clinical trials will be excluded from RW control cohort.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bayer Whippany New Jersey United States 07981

Sponsors and Collaborators

  • Bayer

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Bayer
ClinicalTrials.gov Identifier:
NCT05192642
Other Study ID Numbers:
  • 21993
First Posted:
Jan 14, 2022
Last Update Posted:
Aug 23, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 23, 2022