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Clinical Trials/CTRI/2023/05/052666
CTRI/2023/05/052666
Not yet recruiting
未知

A Study of Individualized Molecular Profiling Guided Therapy Based on Deciphering Recondite Molecular Alterations and Variations in Advanced Solid Tumors - I-DRAV study

Dr. AV Cancer Institute of Personalized Cancer Treatment and Research0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Dr. AV Cancer Institute of Personalized Cancer Treatment and Research
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational

Investigators

Sponsor
Dr. AV Cancer Institute of Personalized Cancer Treatment and Research

Eligibility Criteria

Inclusion Criteria

  • Male and female patients \>\= 18 years of age, who have agreed to receive either molecularly targeted matched treatment based on molecular profiling analysis or conventional anti\-cancer treatment in routine clinical practice as per their discussion with the treating physician and have provided written informed consent for participation in the study.
  • Patients with incurable malignancies.
  • Patients with cancer of unknown primary, or a rare tumor with no approved therapies.
  • Patients with cancers of hereditary in nature
  • Patients must have the following for a diagnosis/disease status: Relapsed or refractory advanced/metastatic disease, Actionable alterations determined by molecular profiling
  • Molecular profiling (including one or more technologies but not limited to NGS, FISH, IHC, PCR, Microarray, and histopathology) for tumor and/ or blood analysis results should be available with all patients.
  • Known disease status post one or more unmatched systemic therapy regimens.
  • Patients must have a measurable disease for malignancies: defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded for non\-nodal lesions and short axis for nodal lesions) as \>\=20 mm with conventional techniques or as \>\=10 mm with spiral CT scan, PET\-CT, MRI, or calipers by clinical exam or liquid biopsy showing the ctDNA fraction.
  • ECOG Performance Status 0\-2\.
  • New York Heart Association (NYHA) Functional Classification I\-II.

Exclusion Criteria

  • Severe or uncontrolled medical disorder
  • Pregnant or lactating women

Outcomes

Primary Outcomes

Not specified

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