Schettini Francesco, Giuliano Mario, Lambertini Matteo, Bartsch Rupert, Pinato David James, Onesti Concetta Elisa, Harbeck Nadia, Lüftner Diana, Rottey Sylvie, van Dam Peter A, Zaman Khalil, Mustacchi Giorgio, Gligorov Joseph, Awada Ahmad, Campone Mario, Wildiers Hans, Gennari Alessandra, Tjan-Heijnen Vivianne C G, Cortes Javier, Locci Mariavittoria, Paris Ida, Del Mastro Lucia, De Placido Sabino, Martín Miguel, Jerusalem Guy, Venturini Sergio, Curigliano Giuseppe, Generali Daniele
Translational Genomics and Targeted Therapies in Solid Tumors Research Group, 08036 Barcelona, Spain.
Department of Medical Oncology, Hospital Clinic of Barcelona, 08036 Barcelona, Spain.
Cancers (Basel). 2021 Sep 1;13(17):4421. doi: 10.3390/cancers13174421.
Anthracyclines are among the most active chemotherapies (CT) in breast cancer (BC). However, cardiotoxicity is a risk and peculiar side effect that has been limiting their use in clinical practice, especially after the introduction of taxanes. Non-pegylated liposomal doxorubicin (NPLD) has been developed to optimize the toxicity profile induced by anthracyclines, while maintaining its unquestionable therapeutic index, thanks to its delivering characteristics that increase its diffusion in tumor tissues and reduce it in normal tissues. This feature allows NPLD to be safely administered beyond the standard doxorubicin maximum cumulative dose of 450-480 mg/m. Following three pivotal first-line phase III trials in HER2-negative metastatic BC (MBC), this drug was finally approved in combination with cyclophosphamide in this specific setting. Given the increasing complexity of the therapeutic scenario of HER2-negative MBC, we have carefully revised the most updated literature on the topic and dissected the potential role of NPLD in the evolving therapeutic algorithms.
蒽环类药物是乳腺癌(BC)治疗中最有效的化疗药物之一。然而,心脏毒性是一种风险和特殊的副作用,一直限制着它们在临床实践中的应用,尤其是在紫杉烷类药物引入之后。非聚乙二醇化脂质体阿霉素(NPLD)已被开发出来,以优化蒽环类药物诱导的毒性特征,同时保持其无可争议的治疗指数,这得益于其给药特性,即增加其在肿瘤组织中的扩散并减少在正常组织中的扩散。这一特性使得NPLD能够安全地超过阿霉素标准最大累积剂量450-480mg/m²进行给药。在三项针对HER2阴性转移性乳腺癌(MBC)的关键一线III期试验之后,这种药物最终在这种特定情况下被批准与环磷酰胺联合使用。鉴于HER2阴性MBC治疗方案日益复杂,我们仔细查阅了该主题的最新文献,并剖析了NPLD在不断发展的治疗算法中的潜在作用。