Skip to main content
Premium Trial:

Request an Annual Quote

FDA Approves Expanded Use of Agilent CDx for Keytruda in Head and Neck Cancer

NEW YORK (360Dx) – Agilent Technologies announced on Tuesday that the US Food and Drug Administration has expanded its approval of the firm's Dako PD-L1 IHC 22C3 pharmDx assay as a companion diagnostic test for Merck's anti-PDL-1 immunotherapy pembrolizumab (Keytruda) for head and neck squamous cell carcinoma (HNSCC).

Keytruda is approved for the first-line treatment of patients with metastatic or unresectable, recurrent HNSCC whose tumors express PD-L1. Agilent's test is the only CDx approved by the FDA to aid in the identification of HNSCC patients for treatment with Keytruda, the company said.

"Targeted immunotherapies are redefining standards of care in cancer treatment, and PD-L1 testing plays a crucial role in identifying patients who may benefit from this treatment," Sam Raha, president of Agilent's diagnostics and genomics group, said in a statement. "By expanding the use of PD-L1 IHC 22C3 pharmDx, Agilent enables more patients to be identified for treatment with Keytruda."

Merck and Agilent's Dako subsidiary developed the assay in partnership, and the FDA initially approved it in October 2015 to determine whether patients with advanced non-small cell lung cancer (NSCLC) were likely to respond to Keytruda. In October 2016, the FDA expanded the assay's approval as a CDx for Keytruda to determine expression status and inform treatment in a broader range of metastatic NSCLC patients.

In September 2017, the FDA approved the assay as a CDx for Keytruda for gastric or gastroesophageal junction adenocarcinoma, and followed that with an approval for use in cervical cancer patients in June 2018 and in urothelial carcinoma patients in August 2018.

This past April, Agilent said the assay had also been approved to identify patients with stage III NSCLC who are not candidates for surgical resection or definitive chemoradiation, or patients with metastatic NSCLC whose tumors express a PD-L1 Tumor Proportion Score greater than or equal to 1 percent, and who are eligible for first-line treatment with Keytruda.

The diagnostic was also granted CE marking in August 2016 as a CDx for Keytruda for patients with previously treated, advanced NSCLC with PD-L1 expressing tumors. In January 2017, the CE marking was expanded to include patients with metastatic NSCLC with no EGFR or ALK mutations who had not yet been treated. And in August 2018, the CE marking was expanded again to include urothelial carcinoma.