“…BEACOPP offers higher cure rates in HL, but is also associated with a higher percentage of short-term and long-term adverse effects (hematologic toxicity, infections, infertility, secondary malignancies) [17]. In the absence of randomisation, the extent of benefit from switching to BEACOPP cannot be assessed from these trials [13,14]. Also, the optimal strategy in these interim-PET-positive patients might evolve in light of the new therapeutic arsenal (targeted therapy, checkpoint inhibitors such as anti-PD-1 therapy, etc.)…”