
Dr Duska on the Efficacy of Pembrolizumab Plus Concurrent CRT in Advanced Cervical Cancer
Linda R. Duska, MD, MPH, discusses OS and PFS2 outcomes with concurrent pembrolizumab and chemoradiotherapy in high-risk advanced cervical cancer.
Linda R. Duska, MD, MPH, a gynecologic oncologist at the University of Virginia Health, discussed efficacy outcomes with the combination of pembrolizumab (Keytruda) and chemoradiotherapy followed by pembrolizumab monotherapy, in patients with newly diagnosed, high-risk, stage IB2 to IIB, node-positive or stage III to IVA locally advanced cervical cancer.
Data from
At the second interim analysis, the median OS was not reached (NR) in both arms, with 14.2% of patients in the pembrolizumab arm experiencing an OS event compared with 20.5% of those in the placebo arm (HR, 0.67; 95% CI, 0.50-0.90; P = .0040). The 36-month OS rates were 82.6% (95% CI, 78.4%-86.1%) in the pembrolizumab arm compared with 74.8% (95% CI, 70.1%-78.8%) in the placebo arm.
Regarding PFS2, the median time to event was NR in both arms, with events occurring in 15.3% of patients in the pembrolizumab arm and 24.3% of those in the placebo arm (HR, 0.60; 95% CI, 0.46-0.80). The PFS data showed that 29.3% of patients in the pembrolizumab arm experienced a PFS event compared with 39.5% of those in the placebo arm. The median PFS was NR in both arms (HR, 0.68; 95% CI, 0.56-0.84). The 36-month PFS rates were 62.7% (95% CI, 56.4%-68.4%) in the pembrolizumab arm and 54.5% (95% CI, 49.3%-59.3%) in the placebo arm. These data are exciting as they represent a significant treatment advancement for patients with high-risk locally advanced cervical cancer, Duska concluded.



































