On August 11, 2022, Roche announced the U.S. Food and Drug Administration (FDA) approval of a label expansion for the Ventana MMR RxDx Panel. The Ventana MMR RxDx Panel is the first immunohistochemistry companion diagnostic test to aid in identifying patients whose solid tumors are deficient in DNA mismatch repair (dMMR) and who may be eligible for therapy with the PD-1 inhibitor pembrolizumab.
The panel is also the first companion diagnostic test to aid in identifying patients with endometrial cancer whose tumors are proficient in DNA mismatch repair (pMMR) and who may be eligible for a combination of pembrolizumab and the tyrosine kinase inhibitor lenvatinib. The test evaluates a panel of MMR proteins in tumors in order to provide relevant treatment information to clinicians.
What Is MMR?
MMR is a naturally occurring mechanism that scans DNA, correcting errors that cause disease. When MMR is deficient (dMMR), mutations are not corrected, and this can lead to cancer. Although MMR deficiency is most common in endometrial cancer, other high-prevalence dMMR tumor types include gastric, colorectal, small intestine, cervical, and neuroendocrine cancers. In the United States, prevalence of dMMR across patients with solid tumors has been estimated at 14%. PD-1 inhibitors may be an effective treatment in cancers with MMR deficiency. For patients with endometrial cancer without this MMR deficiency (pMMR), PD-1 inhibitors may retain activity when combined with a tyrosine kinase inhibitor.
Approval of Label Expansion
FDA approval of the label expansion for the Ventana MMR RxDx Panel provides clinicians with access to a fully automated panel of MMR biomarkers tested by immunohistochemistry. This label expansion follows the April 2021 FDA approval of the Ventana MMR RxDx Panel as the first immunohistochemistry predictive test to identify patients with endometrial carcinoma who may be eligible for treatment with the anti–PD-1 immunotherapy dostarlimab-gxly. That approval was expanded for the following indications on the dates below:
Pembrolizumab for MSI-H or dMMR Cancers
In May 2017, pembrolizumab became the first cancer treatment approved by the FDA for a tissue-agnostic indication—the FDA granted accelerated approval to the therapy for adult and pediatric patients with unresectable or metastatic, microsatellite instability–high (MSI-H) or dMMR solid tumors, as determined by an FDA-approved test, whose disease has progressed following prior treatment and who have no satisfactory alternative treatment options.
Pembrolizumab for Endometrial Carcinoma
Subsequently, pembrolizumab was approved by the FDA in combination with lenvatinib for the treatment of patients with advanced endometrial carcinoma that is not MSI-H or dMMR who experience disease progression after prior systemic therapy in any setting and are not candidates for curative surgery or radiation therapy. At the same time, prembrolizumab was approved as a single agent for the treatment of patients with advanced endometrial carcinoma that is MSI-H or dMMR, as determined by an FDA-approved test, who have disease progression after prior systemic therapy in any setting and are not candidates for curative surgery or radiation therapy.