12月9日（路透社）- BioNTech SE与施贵宝（Bristol Myers Squibb）首次公布PD-L1XVEGF-A双特异性抗体Pumitamig在晚期三阴性乳腺癌中的全球二期研究数据，显示出令人鼓舞的疗效。Pumitamig联合化疗实现了61.5%的确认客观反应率（CORR）、71.8%的未确认客观反应率（UORR）和92.3%的疾病控制率（DCR），与PD-L1表达水平无关。这些数据与先前在中国进行的1L TNBC I期/II期临床试验中报告的数据一致，并确认了关键III期ROSETTA BREAST-01试验的剂量选择。相关数据将于2025年圣安东尼奥乳腺癌研讨会（SABCS）上公布。
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