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Abstract Camrelizumab (a humanized high‐affinity IgG4 mAb against programmed death‐l) showed potent antitumor activity, well tolerance and controllable safety in patients with relapsed or refractory classical Hodgkin lymphoma (r/r cHL), based on the primary analysis of a Phase 2 study. Here, we present the extended follow‐up outcomes. Seventy‐five patients who had failed to achieve a remission or experienced progression after autologous stem cell transplantation or had received at least two lines of systemic chemotherapies were enrolled to receive camrelizumab 200 mg every 2 weeks. With a median follow‐up of 36.2 months (range, 7.2‐38.1), objective response rate per independent central review was 76.0% (95% confidence interval CI, 64.7‐85.1). Among the 57 responders, 31 (54.4%) had ongoing responses. Median duration of response was 31.7 months (95% CI, 16.7‐not reached). Median progression‐free survival was 22.5 months (95% CI, 14.7‐not reached). Thirty‐six‐month overall survival rate was 82.7% (95% CI, 72.0‐89.5). Reactive capillary endothelial proliferation (RCEP) occurred in 97.3% of patients (73/75), but all RCEP were Grade 1 or 2 in severity and 67.1% of these patients (49/73) achieved complete resolution. Occurrence of new RCEP lesions was rare (8/42 19.0% at 12 months; 2/32 6.3% at 24 months). No treatment‐related deaths occurred, and no new toxicities were reported. With extended follow‐up, camrelizumab monotherapy continues to provide a robust and durable response, long survival and manageable safety in r/r cHL patients.
Wu et al. (Thu,) studied this question.