Five leading cancer research organizations in the United States are jointly announcing the start of patient enrollment in Molecular Analysis for Combination Therapy Choice (ComboMATCH), a unique, precision medicine initiative to test new combinations of cancer drugs guided by tumor biology. The Alliance for Clinical Trials in Oncology, Children's Oncology Group, ECOG-ACRIN Cancer Research Group, NRG Oncology, and SWOG Cancer Research Network plan to conduct many early-phase treatment trials through this platform in collaboration with the National Cancer Institute (NCI) National Clinical Trials Network (NCTN). NCI is part of the National Institutes of Health.
"Through ComboMATCH, the NCTN groups and NCI are taking advantage of translational ideas, pre-clinical investigations, and early clinical experience from a large number of investigators working closely together," said James M. Ford, MD , of the Stanford University School of Medicine. Dr. Ford is a co-leader of ComboMATCH and is leading the coordination effort by the ECOG-ACRIN Cancer Research Group.
Each treatment trial will explore the evidence-based addition of a genomically-targeted agent to another anti-cancer therapy—whether that therapy is a single targeted agent or a standard chemotherapy agent or regimen. The hypothesis is that the combination will produce greater clinical activity than the standard treatment without the added targeted agent.
Some studies will measure the contribution of the additional targeted agent in a randomized cohort. Other studies will be single-arm designs, in cases where there are adequate data on the activity of the component agents individually to assess with confidence the activity of the combination.
Targeted therapy is a type of cancer treatment that targets proteins that control how cancer cells grow, divide, and spread. It is the foundation of precision medicine. As researchers learn more about the DNA changes and proteins that drive cancer, they are better able to design treatments that target these proteins.
Can pre-clinical data from in vivo models of drug combinations in the setting of known tumor genomic variants predict clinical activity in defined patient groups? ComboMATCH aims to find out.
"The central hypothesis of ComboMATCH is that a precision medicine initiative organized around pre-clinical in vivo evidence will efficiently generate clinical studies that are likely to reach their clinical activity endpoints," said Funda Meric-Bernstam, MD , of The University of Texas MD Anderson Cancer Center. Dr. Meric-Bernstam is a co-leader of ComboMATCH.
This hypothesis sets ComboMATCH apart from other early-phase trials evaluating drug combinations, Drs. Meric-Bernstam and Ford explained in a recent publication. As a result, investigators expect ComboMATCH to become a primary vehicle for advancing the field of precision medicine in oncology.
"If successful, we expect the ComboMATCH model to become routinely implemented for early development of molecularly targeted oncology drug combinations in the future," said Dr. Ford . "This structure is also designed to identify beneficial therapies for patients with rare malignancies and/or rare molecular abnormalities in their tumors."
Three ComboMATCH treatment trials are already open for enrollment , with the network groups planning to open several more in the next few months. Overall, investigators expect to enroll about 2,000 patients, but that number could grow.
The combinations to be evaluated in ComboMATCH will include approved drugs and investigational agents that pharmaceutical companies contribute by collaborating under individual Cooperative Research and Development Agreements (CRADAs) with NCI.
Multiple researchers are leading each treatment trial, offering opportunities for both junior and senior investigators to collaborate with translational researchers.
"This is the era of team science and biomarker-directed therapy. The ComboMATCH collaboration is extensive and includes health care providers, clinical and translational researchers, statisticians, patient advocates, and industry partners. It is the great promise to improve patient outcomes that brings these stakeholders together," said Dr. Meric-Bernstam.
Precision medicine refers to the tailoring of treatment based on each person’s individual characteristics. In ComboMATCH, treatment focuses on specific molecular abnormalities known to drive cancer growth in cancerous tumors. The drug combinations show evidence that they may be more effective than single therapy in treating some cancers.
ComboMATCH is for patients with solid tumors that have spread to nearby tissue or lymph nodes (locally advanced) or have spread to other places in the body (advanced or metastatic) and have progressed on at least one line of standard systemic therapy. ComboMATCH is also for patients with a type of advanced cancer for which no standard treatment exists that has been shown to prolong overall survival.
Participants will be assigned to treatment based on laboratory tests that look at the unique genetic material (genes) of tumor cells. Patients with gene abnormalities included in ComboMATCH may benefit from the therapies being studied.
Each treatment trial has its own research goals, patient eligibility criteria, and enrollment timeline.
Statements by the NCTN Trial Group Leaders
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1 Meric-Bernstam F, Ford JM, O’Dwyer PJ, et al on behalf of the ComboMATCH study team. National Cancer Institute Combination Therapy Platform Trial with Molecular Analysis for Therapy Choice (ComboMATCH). Clin Cancer Res. 14 April 2023; 29 (8): 1412–1422.
2 Parsons DW, Janeway KA, Patton DR, et al. Actionable tumor alterations and treatment protocol enrollment of 1000 pediatric and young adult patients with refractory cancers in the NCI-COG Pediatric MATCH Trial. J Clin Oncol. 2022; 40:2224-2234.