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Updated: Dec 1, 2025

Quantification of Protein Interaction Network Dynamics using Multiplexed Co-Immunoprecipitation
Published on: August 21, 2019
Abstract:
The NCI Molecular Analysis for Therapy Choice trial has demonstrated the feasibility of sequencing tumor DNA and matching patients to targeted therapies according to their cancer's mutation profile. However, response rates of those assigned to a therapy were generally low.
Insights
The Molecular Analysis for Therapy Choice trial showed it is possible to match cancer patients to targeted therapies using tumor DNA sequencing. However, the effectiveness of these targeted treatments was limited, with generally low response rates observed.
Area of Science:
- Oncology
- Genomics
- Precision Medicine
Background:
- The NCI Molecular Analysis for Therapy Choice (MATCH) trial investigated the feasibility of matching patients to targeted therapies based on tumor molecular alterations.
- This trial aimed to determine if comprehensive genomic profiling could guide treatment selection in cancer patients.
Discussion:
- While the trial successfully demonstrated the feasibility of molecular profiling and treatment assignment, the overall response rates to the assigned targeted therapies were low.
- This suggests a gap between identifying targetable mutations and achieving significant clinical benefit.
Key Insights:
- Tumor DNA sequencing is a feasible approach for identifying actionable mutations in cancer patients.
- Matching patients to therapies based on genomic profiles is achievable in a clinical trial setting.
- Low response rates indicate challenges in the efficacy of current targeted therapies or the selection criteria.
Outlook:
- Further research is needed to improve the efficacy of targeted therapies and optimize patient selection strategies.
- Exploring novel therapeutic combinations and biomarkers may enhance treatment outcomes in precision oncology.
- The findings highlight the need for continued innovation in molecularly guided cancer treatment.
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