医学
拉帕蒂尼
曲妥珠单抗
肿瘤科
帕妥珠单抗
内科学
乳腺癌
紫杉烷
封锁
转移性乳腺癌
新辅助治疗
蒽环类
表阿霉素
化疗
环磷酰胺
多西紫杉醇
紫杉醇
癌症
受体
作者
Juan C Vazquez,Silvia Antolín,Manuel Ruíz‐Borrego,Sònia Servitja,Emilio Alba,Agustí Barnadas,Aña Lluch,Miguel Martín,Álvaro Rodríguez-Lescure,Iván Solà,Xavier Bonfill,Gerard Urrútia,Pedro Sánchez‐Rovira
标识
DOI:10.1007/s12094-022-02998-2
摘要
We aimed to determine the effect of dual anti-HER2 blockade compared to monotherapy on clinically important outcomes. We carried out a systematic review updated until July 2022. The outcomes included pathological complete response (pCR), clinical response, event-free survival, and overall survival. We identified eleven randomized clinical trials (2836 patients). When comparing paclitaxel plus dual treatment versus paclitaxel plus trastuzumab or lapatinib, dual treatment was associated with a higher probability of achieving a pathological complete response (OR 2.88, 95% CI 2.02–4.10). Addition of a taxane to an anthracycline plus cyclophosphamide and fluorouracil, plus lapatinib or trastuzumab, showed that the dual treatment was better than lapatinib alone (OR 2.47, 95% CI 1.41–4.34), or trastuzumab alone (OR 1.89, 95% CI 1.13–3.16). Dual treatment may result in an increase in survival outcomes and tumour clinical response, although such benefits are not consistent for all the combinations studied. The use of dual blockade with combinations of trastuzumab and pertuzumab can be recommended for the neoadjuvant treatment of women with HER2-positive breast cancer. PROSPERO Registration number: CRD42018110273.
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