In the subgroup analysis, the addition of bevacizumab showed a trend of improved efficacy (Hazard Ratio [HR] = 0.63 [0.47–0.87] versus 0.74 [0.53–1.04] for patients without bevacizumab), suggesting that adjuvant anti-angiogenic therapy combined with immune checkpoint inhibition warrants further investigation.
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Nivolumab plus chemoradiotherapy in locally-advanced cervical cancer: the NICOL phase 1 trial.
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