Nanoparticle albumin-bound paclitaxel/liposomal-encapsulated doxorubicin in HER2-negative metastatic breast cancer patients

Author:

Fabi Alessandra1ORCID,Ferretti Gianluigi1,Malaguti Paola1,Gasparro Simona1,Nisticò Cecilia1,Arpino Grazia2,Papaldo Paola1,Russillo Michelangelo1,Catania Giovanna1,Schettini Francesco234,Giannarelli Diana5,Cognetti Francesco16

Affiliation:

1. Medical Oncology 1, Regina Elena National Cancer Institute, IRCCS, Rome, Italy

2. Clinical Medicine & Surgery Department, Division of Medical Oncology, University of Naples Federico II, Naples, Italy

3. Translational Genomics and Targeted Therapeuticsin Solid Tumors, IDIBAPS, Barcelona, Spain

4. SOLTI Breast Cancer Research Group, Barcelona, Spain

5. Biostatistic Unit, Regina Elena National Cancer Institute, IRCCS, Rome, Italy

6. Sapienza University of Rome, Rome, Italy

Abstract

Aim: To investigate the toxicity of nab-paclitaxel (wNP)/nonpegylated liposome-encapsulated doxorubicin (wNPLD) combination in HER2-negative metastatic breast cancer (MBC) patients as first-line treatment. Materials & methods: Phase I, single-arm study in metastatic breast cancer patients naive to previous chemotherapy for advanced disease. A 3 + 3 dose-escalation design was used to determine the safety. Primary endpoints were the identification of dose-limiting toxicity and maximum tolerated dose. Results: In total, 12 patients (mean age: 52 years; median metastatic sites: 2) were enrolled and 97 cycles were completed. Maximum tolerated dose was wNP + wNPLD 25 mg/m2. The most common adverse events were neutropenia, nausea, diarrhea and mucositis. The objective response rate was 68% (response mean duration: 12.6 months). Conclusion: wNP/wNPLD combination constitutes an active regimen with mild toxicity.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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