Frontline Pembrolizumab Combo Obtains EU Approval for HER2+ Gastric Cancer

News
Article

Data from the phase 3 KEYNOTE-811 trial highlight a trend towards improved overall survival among patients with HER2-positive, PD-L1–positive advanced gastric or gastroesophageal junction adenocarcinoma receiving pembrolizumab, trastuzumab, and chemotherapy.

The FDA granted accelerated approval to pembrolizumab, trastuzumab, and chemotherapy as a treatment for locally advanced or metastatic gastric or GEJ carcinoma that is HER2 positive in May 2021.

The FDA granted accelerated approval to pembrolizumab, trastuzumab, and chemotherapy as a treatment for locally advanced or metastatic gastric or GEJ carcinoma that is HER2 positive in May 2021.

The European Commission has approved a combination of pembrolizumab (Keytruda) plus trastuzumab (Herceptin) and fluoropyrimidine- and platinum-based chemotherapy for the frontline treatment of patients with locally advanced unresectable or metastatic HER2-positive, PD-L1–positive gastric or gastroesophageal junction (GEJ) adenocarcinoma, according to a press release from Merck.1

The approval was supported by findings from the phase 3 KEYNOTE-811 study (NCT03615326) in which investigators reported a statistically significant improvement in progression-free survival and objective response rate with the pembrolizumab combo vs trastuzumab and chemotherapy.2 A trend towards improved overall survival was also observed in the experimental arm, although it was not considered to be statistically significant.

“Patients in the [European Union] EU diagnosed with HER2-positive advanced gastric cancer [have] an aggressive disease associated with a poor prognosis, underscoring the need for additional first-line treatment options for these patients,” Scot Ebbinghaus, MD, vice president of global clinical development at Merck Research Laboratories, said in the press release. “With today’s approval of [pembrolizumab], we’re proud that patients whose tumors express PD-L1 with a combined positive score [of 1 or higher] and health care providers in the EU will have an option that includes immunotherapy for this difficult-to-treat disease.”

The FDA granted accelerated approval to pembrolizumab, trastuzumab, and chemotherapy as a treatment for locally advanced or metastatic gastric or GEJ carcinoma that is HER2 positive in May 2021.3 The regulatory decision was also based on data from the phase 3 KEYNOTE-811 study.

References

  1. European Commission approves KEYTRUDA® (pembrolizumab) plus trastuzumab and chemotherapy as first-line treatment for HER2-positive advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma expressing PD-L1 (CPS ≥1). News release. Merck. August 29, 2023. Accessed August 29, 2023. https://bit.ly/3PhgAeA
  2. KEYTRUDA® (pembrolizumab) plus trastuzumab and chemotherapy met primary endpoint of progression-free survival as first-line treatment in patients With HER2-positive advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma. News release. Merck. News release. June 16, 2023. Accessed August 29, 2023. bit.ly/3p903iB
  3. FDA approves Merck’s KEYTRUDA (pembrolizumab) combined with trastuzumab and chemotherapy as first-line treatment in locally advanced unresectable or metastatic HER2-positive gastric or gastroesophageal junction adenocarcinoma. News release. Merck. May 5, 2021. Accessed August 29, 2023. https://bit.ly/2SjmdOj
Related Videos
Data from a ctDNA analysis of the phase 3 INTRIGUE study indicate that KIT mutational status may be associated with response to certain Tyrosine kinase inhibitors in GIST, according to an expert from the Yale Cancer Center in New Haven, Massachusetts.
Future research into the management of unresectable hepatocellular carcinoma may involve combining local therapies with checkpoint inhibitors like durvalumab and tremelimumab, according to Ghassan K. Abou-Alda, MD.
Patients with unresectable hepatocellular carcinoma who have recurrent disease following surgery or locally advanced diseases who will likely progress on local therapy may have an opportunity to benefit from tremelimumab and durvalumab following its FDA approval, according to Ghassan K. Abou-Alfa, MD.
Ghassan K. Abou-Alfa, MD, discusses the importance of improving access to novel therapies and combinations for patients with hepatocellular carcinoma across the world.
Ghassan K. Abou-Alfa, MD, spoke about the recent approval of tremelimumab plus durvalumab for patients with unresectable hepatocellular carcinoma, based on results from the phase 3 HIMALAYA trial.
Howard A. Burris, MD, highlighted previous findings of the phase 3 TOPAZ-1 trial assessing durvalumab plus gemcitabine and cisplatin vs placebo plus gemcitabine and cisplatin in advanced biliary tract cancer and patient-reported outcomes (PRO)data that were presented at 2022 ASCO.
Shubham Pant, MD discusses key findings from a basket trial examining the use of erdafitinib in patients with gastrointestinal cancers.
Related Content