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里程碑3期MARIPOSA研究显示RYBREVANT®▼在EGFR突变的非小细胞肺癌癌症患者中,与奥西美替尼相比,(阿米万塔单抗)加拉泽替尼可降低30%的疾病进展或死亡风险

Landmark Phase 3 MARIPOSA Study Shows RYBREVANT®▼(amivantamab) Plus Lazertinib Resulted in 30 Percent Reduction in Risk of Disease Progression or Death Compared to Osimertinib in Patients with EGFR-Mutated Non-Small Cell Lung Cancer

GlobeNewswire 等信源发布 2023-10-23 22:59

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Early data show an overall survival trend favoring the combination of amivantamab and lazertinib compared to osimertinib; consistent results seen in patients with and without brain metastases1 Late-breaking results from the MARIPOSA study featured in a Presidential Symposium at 2023 ESMO Congress1 BEERSE, BELGIUM, Oct.

早期数据显示,与osimertinib相比,有利于amivantamab和lazertinib联合治疗的总体生存趋势;在有和没有脑转移的患者中观察到的一致结果1 MARIPOSA研究的最新结果在2023年ESMO大会的总统研讨会上得到了特色1比利时比尔森,10月。

23, 2023 (GLOBE NEWSWIRE) -- The Janssen Pharmaceutical Companies of Johnson & Johnson today announced results from the Phase 3 MARIPOSA study showing RYBREVANT®▼ (amivantamab) in combination with lazertinib compared to osimertinib resulted in a 30 percent reduction in the risk of disease progression or death (Hazard Ratio [HR]=0.70; 95 percent Confidence Interval [CI], 0.58–0.85; P<0.001) in the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with either epidermal growth factor receptor (EGFR) exon 19 deletions (ex19del) or L858R substitution.1 Results also showed a favourable trend in overall survival (OS) for amivantamab and lazertinib in these patients compared to osimertinib (HR=0.80; 95 percent CI, 0.61–1.05; P=0.11) at a first interim analysis.1 These data were presented in a Presidential Symposium at the European Society for Medical Oncology (ESMO) 2023 Congress taking place 20-24 October in Madrid, Spain (Abstract #LBA14).1 “Despite advances in EGFR-mutated NSCLC treatment, novel targeted therapies and regimens are needed to address resistance and disease progression, which are nearly inevitable with current treatments,” said Byoung Chul Cho*, M.D., Ph.D., medical oncologist and professor in the Division of Medical Oncology at Yonsei Cancer Center, Yonsei University College of Medicine in Seoul, Republic of Korea, and presenting author.

232023(GLOBE NEWSWIRE)-强生的杨森制药公司今天宣布了第3阶段MARIPOSA研究的结果,显示RYBREVANT®▼ (amivantamab)联合lazertinib与osimertinib相比,在局部晚期或转移性非小细胞肺癌(NSCLC)患者的一线治疗中,疾病进展或死亡的风险降低了30%(危险比[HR]0.70;95%置信区间[CI],0.58-0.85;P 0.001)19个缺失(ex19del)或L858R替代[1]。与osimertinib相比,这些患者的amivantamab和lazertinib的总生存期(OS)也有良好的趋势(HR=0.80;95%CI,0.61-1.05;P=0.11)在第一次中期分析中.1这些数据在20-24日举行的欧洲肿瘤内科学会(ESMO)2023大会总统研讨会上发表10月在西班牙马德里(摘要#LBA14).1“尽管EGFR突变NSCLC治疗取得了进展,但仍需要新的靶向治疗和方案来解决耐药性和疾病进展,这在目前的治疗方法中几乎是不可避免的,”Byoung-Chul Cho*博士,医学肿瘤学家和延世癌症中心肿瘤内科教授,延世大学医学院在韩国首尔,并提交作者。

“With the combination of amivantamab and lazertinib.

“与amivantamab和lazertinib的组合。