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Clinical Trials/NCT07356544
NCT07356544
Recruiting
Not Applicable

HER2 in Advanced NSCLC: an Observational, Prospective, Multi-centric Study Exploring HER2 Mutations Incidence and Therapeutic Management in Italy. The HEROS Study - GOIRC-01-2022

Gruppo Oncologico Italiano di Ricerca Clinica22 sites in 1 country50 target enrollmentStarted: August 12, 2025Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Sponsor
Gruppo Oncologico Italiano di Ricerca Clinica
Enrollment
50
Locations
22
Primary Endpoint
Prevalence of HER2 mutation

Overview

Brief Summary

The HEROS study is an Italian observational multicenter prospective study aimed to investigate the current diagnostic and therapeutical approach towards HER2 mutated NSCLC in clinical practice. The enrolment will start in September 2024 until September 2025. A 12-months follow-up window will be performed.

Detailed Description

The HEROS study will be conducted in partnership with ATLAS project: all patients prospectively enrolled in ATLAS project will be used to fulfil primary and secondary objectives. Information will be obtained by querying ATLAS database (59 centers) in aggregated manner. ATLAS project is a multi-centric retrospective/prospective Italian study aimed to describe prevalence of different oncogene alterations in all new diagnosed advanced NSCLC patients (5,000 patients/year). In particular, prevalence of HER2-mutated patients will be calculated on all patients enrolled in ATLAS project. Approximately 100 HER2 mutated patients enrolled in ATLAS study will be studied for secondary and explorative objectives. Moreover, a subset of centers (25 centers) will enrol patients also for Prospective Biomarker Analysis in order to perform exploratory analysis on blood and tissue samples according to the availability of tissue specimens from the primary tumor or metastatic sites. All centers that will participate for Prospective Biomarker Analysis necessarily will be included into ATLAS project.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Cohort 1 (Prevalence study population)
  • Male or female, aged at least 18 years.
  • Pathologically confirmed diagnosis of NSCLC from September 2024 to September
  • Locally advanced (IIIC), not amenable to multimodal approach (chemo-radiotherapy), or metastatic (IV) NSCLC according to TNM VIII edition.
  • Enrolled in ATLAS project. Cohort 2 (HER2 mutations study population)
  • Included in Cohort
  • Presence of HER2 mutation.
  • Enrolled in ATLAS project. Cohort 3 (Prospective Biomarker Analysis population)
  • Included in Cohort
  • Availability of tissue sample from the first 50 patients enrolled in cohort

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Prevalence of HER2 mutation

Time Frame: 1 year

Percentage of advanced NSCLC with HER2 mutations in Italy clinical practice.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Gruppo Oncologico Italiano di Ricerca Clinica
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (22)

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