Dostarlimab/Chemo Earns Positive CHMP Opinion in Advanced Endometrial Cancer

News
Article
Currently, dostarlimab has conditional approval as a monotherapy for treating adult patients with dMMR/MSI-H, recurrent or advanced endometrial cancer that has progressed. If the European Commission approves dostarlimab plus chemotherapy, it is expected that the conditional approval will convert to a full approval.

Data from the phase 3 RUBY/ENGOT-EN6/GOG3031/NSGO trial support the use of frontline dostarlimab plus chemotherapy for dMMR/MSI-H primary advanced or recurrent endometrial cancer.

The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion in favor of the approval of dostarlimab (Jemperli) and chemotherapy for adults diagnosed with mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H), primary advanced or recurrent endometrial cancer who are eligible for systemic therapy, according to a press release from GSK.1

The CHMP’s opinion is one of the final steps before the European Commission can authorize use of the combination regimen.

Supporting data for the positive opinion came from the first part of the phase 3 RUBY/ENGOT-EN6/GOG3031/NSGO trial(NCT03981796), which were presented at the European Society for Medical Oncology (ESMO) Virtual Plenary and the Society of Gynecologic Oncology (SGO) Annual Meeting.

Part 1 of the RUBY trial met its primary endpoint of progression-free survival (PFS) in patients treated with dostarlimab plus carboplatin and paclitaxel in the dMMR/MSI-H population. Investigators observed a 72% reduction in the risk of disease progression or death compared with placebo plus chemotherapy (HR, 0.28; 95% CI, 0.16-0.50).2 Additionally, there was a 70% reduction in the risk of death with the combination regimen compared with chemotherapy alone in the dMMR/MSI-H population, according to a prespecified exploratory analysis (HR, 0.30; 95% CI, 0.13-0.70).

“We are pleased with this positive CHMP opinion and the potential for dostarlimab with chemotherapy to treat patients with this very challenging form of endometrial cancer,” Hesham Abdullah, senior vice president and Global Head Oncology, R&D at GSK, said in the press release. “If approved, dostarlimab plus chemotherapy will be the first new treatment option in decades for these patients in the European Union, offering long-awaited new hope for improved long-term outcomes. This opinion further reinforces our confidence in dostarlimab’s important role in the immuno-oncology treatment landscape.”

In the two-part global, randomized, double-blind, multicenter trial, 494 patients with primary advanced or recurrent endometrial cancer were randomly assigned either dostarlimab or a placebo. The study’s dual-primary endpoints were PFS and OS.

Frequent adverse effects (AEs) associated with dostarlimab plus carboplatin and paclitaxel include rash, hypothyroidism, increased alanine aminotransferase and aspartate aminotransferase, pyrexia, and dry skin. Frequent AEs specific to dostarlimab include anemia, nausea, diarrhea, vomiting, joint pain, itching, rash, fever, and hypothyroidism.Investigators have reported several immune system AEs, as well, such as inflammation, rash, and infusion reactions.3

Currently, dostarlimab has conditional approval as a monotherapy for treating adult patients with dMMR/MSI-H, recurrent or advanced endometrial cancer that has progressed. If the European Commission approves dostarlimab plus chemotherapy, it is expected that the conditional approval will convert to a full approval.

Dostarlimab/chemotherapy was approved by the FDA for dMMR/MSI-H, primary advanced or recurrent endometrial cancer in July 2023 based on findings from the RUBY trial.4

References

  1. GSK receives positive CHMP opinion recommending approval of JEMPERLI (dostarlimab) plus chemotherapy as a new frontline treatment for dMMR/MSI-H Primary advanced or recurrent endometrial cancer. News Release. GSK. October 16, 2023. Accessed October 26, 2023. https://bit.ly/3QxXUb6
  2. Phase III RUBY clinical trial demonstrates potential of JEMPERLI (dostarlimab) plus chemotherapy to redefine the treatment of primary advanced or recurrent endometrial cancer versus chemotherapy alone. News release. GSK. March 27, 2023. Accessed October 26, 2023. https://bit.ly/3tX12Es
  3. Jemperli. European Medicines Agency. August 21, 2023. Accessed October 26, 2023. https://bit.ly/3tLkrbv
  4. Jemperli (dostarlimab) plus chemotherapy approved in the US as the first new frontline treatment option in decades for dMMR/MSI-H primary advanced or recurrent endometrial cancer. News release. GSK. July 31, 2023. Accessed October 26, 2023. https://shorturl.at/izGL9

Related Videos
Although immature, overall survival data from the KEYNOTE-868 trial may support the use of pembrolizumab plus chemotherapy in patients with endometrial cancer.
Dostarlimab plus chemotherapy appears to yield favorable overall survival in patients with mismatch repair proficient endometrial cancer.
Pembrolizumab combined with carboplatin and paclitaxel resulted in response rates in patients with recurrent endometrial cancer.
Future analyses will look at durvalumab/olaparib for endometrial cancer populations with TP53 and POLE alterations, as well as those with estrogen receptor and progesterone receptor positivity.
Patients with mismatch repair proficient, newly diagnosed, advanced or recurrent endometrial cancer may have enhanced benefit with the addition of olaparib to durvalumab.
Dostarlimab plus chemotherapy produces notable benefits among patients with advanced, mismatch repair deficient endometrial cancer in the phase 3 RUBY trial.
Ritu Salani, MD, details the health-related quality of life benefits associated with dostarlimab in the treatment of advanced endometrial cancer, which includes improvements in back and pelvic pain.
Ritu Salani, MD, describes the concordance between blinded independent central review and provider-assessed outcomes with dostarlimab among patients with advanced recurrent endometrial cancer in the phase 3 RUBY trial.