Skip to content

Target Therapies Resistance Molecular Profiling in Patients With Neoplastic Disease

Non-interventional Study for the Determination of Molecular Resistance Profiling to Targeted Therapies in Patients With Neoplastic Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03347318
Acronym
PROFILING
Enrollment
2500
Registered
2017-11-20
Start date
2011-03-30
Completion date
2026-03-31
Last updated
2026-03-19

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

Conditions

Solid Tumors

Brief summary

The main purpose of this study is to define the molecular profile of selected solid tumors. From each participants will be collected biological materials for molecular analysis, including saliva, blood and vital tumor tissue derived form surgical or biopsy procedures. Whereas possible, vital tumor specimens will be inoculated and propagated in immunocompromised NOD/SCID mice to study the genetic correlations between genetic status and response to target drugs.

Interventions

None listed

Sponsors

Fondazione del Piemonte per l'Oncologia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

Patients with at least one of the following selected solid tumors: * Colorectal Cancer (primary or with synchronous/metachronous liver metastases) * Prostate Cancer * Head \& Neck Tumors * Gastric Cancer * Glioblastoma * Breast Cancer * Hepatocarcinoma * Biliary Tract Carcinoma * Lung Cancer (primary) * Rare Tumors (incidence ≤ 5x10-6) * Metastatic Sarcoma * Metastatic Melanoma

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
number of patient correctly sampledthrough study completion, an average of five yearsnumber of patients with biological samples idoneous for molecular profiling testing (nucleic acid extraction, protein) over all recruited patients.

Secondary

MeasureTime frame
number of patients with detected genetic alterations that respond to treatments assigned by physician.through study completion, an average of five years

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026