NCI-MATCH, also known as National Cancer Institute-Molecular Analysis for Therapy Choice, or study EAY131, is a phase II precision medicine trial that seeks to determine whether matching certain drugs or drug combinations in adults whose tumors have specific gene abnormalities will effectively treat their cancer, regardless of their cancer type. Such discoveries could be eligible to move on to larger, more definitive trials.
Precision medicine refers to the tailoring of treatment based on the characteristics of each individual. Treatment focuses on molecular abnormalities instead of the organ site of the cancer.
There are several broad categories of resources for this trial to help website visitors locate the most relevant information. Please see the buttons to the right to access additional information for the trial.
NCI-MATCH was co-developed by the ECOG-ACRIN Cancer Research Group and the National Cancer Institute. It is being led by ECOG-ACRIN through its Biomarker Sciences Program.
NEW! We are now accepting proposals for ctDNA analysis of blood specimens collected from patients in the NCI-MATCH / EAY131 trial
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A Unique Trial
- NCI-MATCH is a unique cancer treatment trial because it is the largest, most scientifically rigorous precision medicine cancer trial to date
- NCI-MATCH is considered the largest precision medicine cancer trial to date based on the number of patients, treatment options, and types of cancer being studied in a single clinical trial
- The 30 or more treatment options explore a large number of genetic abnormalities and drugs—far more than any other cancer trial
- It includes a large number of cancer types (most other trials address a single cancer) and has many more drugs available than most other cancer trials
Other Ways that NCI-MATCH is Unique
- Unlike many clinical trials, this trial is not comparing the drugs or drug combinations with each other, but is studying each treatment’s effectiveness on its own
- The depth and breadth of expertise among the investigators and staff involved in the trial is unprecedented, and includes hundreds of translational scientists, clinical oncologists, community practitioners, and research personnel all with deep experience in clinical trials
- The inclusion of uncommon types of cancer in NCI-MATCH offers patients an unusual opportunity to have their disease assessed to see if it has the same genetic abnormalities found in more common cancer types
- It also offers researchers a unique opportunity to study the effectiveness of new treatments on rare diseases
- Use of the NCI Central Institutional Review Board is mandatory
For an overview, visit the Patient Eligibility section.
Trial Availability and Patient Identification
- NCI-MATCH is a nationwide trial that is open and enrolling patients at nearly 1100 cancer centers and community hospitals in every state, the District of Columbia, and Puerto Rico. For locations, visit the NCI website.
- A new study entry process is currently being implemented to identify potentially eligible patients at participating sites through genomic tumor sequencing that is performed independently (outside of the trial) by designated commercial and academic laboratories. This process was announced on June 7, 2017. To read the press release, go here.
- Trial researchers expect that only a small number of those screened will have one or more molecular abnormalities that match one of the 30 or more treatment options being studied
- Once enrolled, patients will be treated with a drug or drug combination that targets the molecular changes in their tumor for as long as their tumor shrinks or remains stable
- The drugs included in the trial have all either been approved by the U.S. Food and Drug Administration (FDA) for specific cancer types or are still being tested in other clinical trials but have shown some effectiveness against tumors with a particular genetic alteration(s)
- NCI-MATCH was co-developed by the National Cancer Institute (NCI), part of the National Institutes of Health (NIH), and the ECOG-ACRIN Cancer Research Group, one of five NCI National Clinical Trials Network groups
- The trial is publicly funded by the NCI
- ECOG-ACRIN is leading the trial, a role that involves coordinating the genetic testing and supporting trial sites with training, laboratory services, trial assignments, biostatistical support, data management, auditing, quality control, and public awareness
- Patient advocates were engaged in the development of the trial and are giving input on its implementation and other aspects of the study
- To learn more about this trial, patients should start by speaking with their doctor or healthcare team
- Visit the NCI website to obtain study contact information for the participating clinical sites nationwide where this trial is open and enrolling patients
- Trained information specialists at the NCI Contact Center are available to answer cancer-related questions in English and Spanish
- Read NCI-MATCH Keeps Enrolling, a series of three in-depth articles by The Cancer Letter
Study Overview PowerPoint
Accrual as of October 30, 2016
Towards the overall goal to complete tumor gene testing for 6000 patients, 2734 had registered and submitted tumor samples for gene testing. Of these:
Study Summary for Patients [In Revision]