Your browser doesn't support javascript.
loading
Ixazomib in combination with carboplatin in pretreated women with advanced triple-negative breast cancer, a phase I/II trial of the AGMT (AGMT MBC-10 trial).
Rinnerthaler, Gabriel; Gampenrieder, Simon Peter; Petzer, Andreas; Burgstaller, Sonja; Fuchs, David; Rossmann, Dieter; Balic, Marija; Egle, Daniel; Rumpold, Holger; Singer, Christian F; Bartsch, Rupert; Petru, Edgar; Melchardt, Thomas; Ulmer, Hanno; Mlineritsch, Brigitte; Greil, Richard.
Afiliação
  • Rinnerthaler G; IIIrd Medical Department with Hematology and Medical Oncology, Hemostaseology, Rheumatology and Infectious Diseases, Oncologic Center, Paracelsus Medical University Salzburg, Müllner Hauptstrasse 48, 5020, Salzburg, Austria.
  • Gampenrieder SP; Salzburg Cancer Research Institute with Laboratory of Immunological and Molecular Cancer Research and Center for Clinical Cancer and Immunology Trials, Salzburg, Austria.
  • Petzer A; Cancer Cluster Salzburg, Salzburg, Austria.
  • Burgstaller S; IIIrd Medical Department with Hematology and Medical Oncology, Hemostaseology, Rheumatology and Infectious Diseases, Oncologic Center, Paracelsus Medical University Salzburg, Müllner Hauptstrasse 48, 5020, Salzburg, Austria.
  • Fuchs D; Salzburg Cancer Research Institute with Laboratory of Immunological and Molecular Cancer Research and Center for Clinical Cancer and Immunology Trials, Salzburg, Austria.
  • Rossmann D; Cancer Cluster Salzburg, Salzburg, Austria.
  • Balic M; Internal Department I for Medical Oncology and Hematology, Ordensklinikum Linz Barmherzige Schwestern, Linz, Austria.
  • Egle D; IVth Department of Internal Medicine with Hematology and Medical Oncolocy, Klinikum Wels-Grieskirchen, Wels, Austria.
  • Rumpold H; Department of Internal Medicine 3 - Hematology and Oncology, Kepler University Hospital, Linz, Austria.
  • Singer CF; 2nd Medical Department, County Hospital Steyr, Steyr, Austria.
  • Bartsch R; Division of Oncology, Department of Internal Medicine, Medical University Graz, Graz, Austria.
  • Petru E; Department of Obstetrics and Gynaecology, Innsbruck Medical University, Innsbruck, Austria.
  • Melchardt T; Department of Oncology, Hematology and Gastroenterology, Academic Teaching Hospital Feldkirch, Feldkirch, Austria.
  • Ulmer H; Department of Obstetrics and Gynecology, Cancer Comprehensive Center, Medical University of Vienna, Vienna, Austria.
  • Mlineritsch B; Department of Internal Medicine 1, Division of Oncology, Cancer Comprehensive Center, Medical University of Vienna, Vienna, Austria.
  • Greil R; Department of Obstetrics and Gynaecology, Clinical Department of Gynecology, Medical University Graz, Graz, Austria.
BMC Cancer ; 18(1): 1074, 2018 Nov 06.
Article em En | MEDLINE | ID: mdl-30400780
ABSTRACT

BACKGROUND:

Triple-negative breast cancer (TNBC) comprises a heterogeneous group of diseases which are generally associated with poor prognosis. Up to now, no targeted treatment beyond anti-VEGF therapy has been approved for TNBC and cytotoxic agents remain the mainstay of treatment. Ixazomib is a selective and reversible inhibitor of the proteasome, which has been mainly investigated in the treatment of multiple myeloma. In a preclinical study TNBC cells were treated with the first-generation proteasome inhibitor bortezomib in combination with cisplatin and synergistic efficacy was demonstrated. Clinical data are available for carboplatin plus bortezomib in metastatic ovarian and lung cancers showing remarkable antitumor activity and good tolerability (Mol Cancer 1126 2012, J Thorac Oncol 487-92 2009, J Thorac Oncol 71032-1040, 2012). Based on this evidence, the phase I/II MBC-10 trial will evaluate the toxicity profile and efficacy of the second-generation proteasome inhibitor ixazomib in combination with carboplatin in patients with advanced TNBC.

METHODS:

Patients with metastatic TNBC pretreated with at least one prior line of chemotherapy for advanced disease with a confirmed disease progression and measurable disease according to RECIST criteria 1.1 are eligible for this study. Patients will receive ixazomib in combination with carboplatin on days 1, 8, and 15 in a 28-day cycle. The phase I part of this study utilizes an alternate dose escalation accelerated titration design. After establishing the maximum tolerated dose (MTD), the efficacy and safety of the combination will be further evaluated (phase II, including 41 evaluable patients). All patients will continue on study drugs until disease progression, unacceptable toxicity or discontinuation for any other reason. Primary endpoint of the phase II is overall response rate, secondary endpoints include progression-free survival, safety, and quality of life. This trial is open for patient enrollment since November 2016 in six Austrian cancer centers. Accrual is planned to be completed within 2 years.

DISCUSSION:

Based on preclinical and clinical findings an ixazomib and carboplatin combination is thought to be effective in metastatic TNBC patients. The MBC-10 trial is accompanied by a broad biomarker program investigating predictive biomarkers for treatment response and potential resistance mechanisms to the investigational drug combination. TRIAL REGISTRATION EudraCT Number 2016-001421-13 received on March 31, 2016, ClinicalTrials.gov Identifier NCT02993094 first posted on December 15, 2016. This trial was registered prospectively.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Boro / Protocolos de Quimioterapia Combinada Antineoplásica / Carboplatina / Neoplasias de Mama Triplo Negativas / Glicina Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Boro / Protocolos de Quimioterapia Combinada Antineoplásica / Carboplatina / Neoplasias de Mama Triplo Negativas / Glicina Idioma: En Ano de publicação: 2018 Tipo de documento: Article