AIO-BNHO Comprehensive Clinico-genomics Database Network - AIO-BNHO CONNECT

Sponsor
AIO-Studien-gGmbH (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05701150
Collaborator
(none)
3,000
2
34.6
1500
43.4

Study Details

Study Description

Brief Summary

National, retro- and prospective, observational, multicenter clinical research platform to connect clinical and genomic data of patients with advanced (locally advanced, inoperable, or metastatic) solid tumors (excluding NSCLC, SCLC, and mesothelioma) with results from multi-gene next-generation sequencing (NGS) panels (>30 genes)

Condition or Disease Intervention/Treatment Phase
  • Other: Minimal documentation
  • Other: Extended documentation

Detailed Description

The AIO-BNHO CONNECT research platform is a clinic-genomic database collecting data on NGS results and corresponding clinical outcomes in patients with advanced solid tumors (excluding NSCLC, SCLC, and mesothelioma). Data of deceased patients will be included. The platform will provide insight into the current state of precision oncology in Germany by compiling real-world data encompassing a broad spectrum of care providers including but not limited to practice-based oncologists, community hospitals, and university hospitals. The platform also comprises a decentral tissue repository with clinically annotated tumor specimens retrieved within routine clinical care that can be used in future collaborative research projects.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
3000 participants
Observational Model:
Cohort
Time Perspective:
Other
Official Title:
AIO-BNHO Comprehensive Clinico-genomics Database Network - AIO-BNHO CONNECT
Anticipated Study Start Date :
Jan 20, 2023
Anticipated Primary Completion Date :
Dec 8, 2025
Anticipated Study Completion Date :
Dec 8, 2025

Arms and Interventions

Arm Intervention/Treatment
MIN Data Set

Patients who did not receive a targeted therapy based on NGS results (outside of a clinical trial)

Other: Minimal documentation
Minimal data documentation only of patients without targeted therapy based on NGS results

Other: Extended documentation
Extended data documentation of patients with targeted therapy based on NGS results

EXT Data Set

Patients who received a targeted therapy based on NGS results (outside of a clinical trial)

Other: Extended documentation
Extended data documentation of patients with targeted therapy based on NGS results

Outcome Measures

Primary Outcome Measures

  1. Molecular tumorboard utilization [3 years]

    Proportion of patients who's case was discussed in a Molecular tumorboard

  2. Treatment reality after NGS analysis [3 years]

    Proportion of patients who received at least one targeted therapy based on NGS results, who exclusively received therapies other than targeted therapies based on NGS results or who did not receive any therapy

  3. NGS [3 years]

    Genomic alterations identified by multi-gene NGS panels

  4. Molecular tumorboard [3 years]

    Descriptive analysis of MTB-based therapy recommendations, their implementation rate and reasons for non-implementation

  5. Overall response rate [3 years]

    Overall response rate of targeted therapy based on NGS results

  6. Progression-free survival (PFS) [3 years]

    Progression-free survival from start of targeted therapy based on NGS results

  7. Overall survival [3 years]

    Overall survival from start of targeted therapy based on NGS results

  8. PFS ratio [3 years]

    PFS interval associated with targeted therapy(ies) administered after NGS analysis divided by the time to progression (TTP) interval associated with the last prior treatment(s)

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 (i.e., locally advanced, inoperable, or metastatic) solid tumor, ineligible for curative surgery and/or curative systemic therapy

  • Available results of commercial or non-commercial RNA- and/or DNA-based multi-gene NGS panels with >30 genes analyzed; for non-commercial panels a list of all tested genes and multiple gene biomarkers (e.g., tumor mutational burden (TMB), microsatellite status) must be provided

  • Age ≥ 18 years

  • Signed and dated informed consent form (not applicable for inclusion of deceased patients)

Exclusion Criteria:
  • Diagnosis of NSCLC/SCLC (C34) or mesothelioma (C45)

  • NGS results older than two years at the date of patient inclusion

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medizinische Fakultät Mannheim der Universität Heidelberg Mannheim Baden-Württemberg Germany 68167
2 Klinikum der Universität München München Bayern Germany 81377

Sponsors and Collaborators

  • AIO-Studien-gGmbH

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
AIO-Studien-gGmbH
ClinicalTrials.gov Identifier:
NCT05701150
Other Study ID Numbers:
  • AIO-TF-0122
First Posted:
Jan 27, 2023
Last Update Posted:
Jan 27, 2023
Last Verified:
Jan 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 27, 2023