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Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer
INTRODUCTION: Rapamycin acts synergistically with platinum agents to induce apoptosis and inhibit proliferation in breast cancer cell lines. Combination of everolimus also known as RAD001 (oral mammalian target of rapamycin (mTOR) inhibitor) and carboplatin may have activity in metastatic triple-neg...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053575/ https://www.ncbi.nlm.nih.gov/pubmed/24684785 http://dx.doi.org/10.1186/bcr3634 |
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author | Singh, Jasmeet Chadha Novik, Yelena Stein, Stacey Volm, Matthew Meyers, Marlene Smith, Julia Omene, Coral Speyer, James Schneider, Robert Jhaveri, Komal Formenti, Silvia Kyriakou, Victoria Joseph, Benson Goldberg, Judith D Li, Xiaochun Adams, Sylvia Tiersten, Amy |
author_facet | Singh, Jasmeet Chadha Novik, Yelena Stein, Stacey Volm, Matthew Meyers, Marlene Smith, Julia Omene, Coral Speyer, James Schneider, Robert Jhaveri, Komal Formenti, Silvia Kyriakou, Victoria Joseph, Benson Goldberg, Judith D Li, Xiaochun Adams, Sylvia Tiersten, Amy |
author_sort | Singh, Jasmeet Chadha |
collection | PubMed |
description | INTRODUCTION: Rapamycin acts synergistically with platinum agents to induce apoptosis and inhibit proliferation in breast cancer cell lines. Combination of everolimus also known as RAD001 (oral mammalian target of rapamycin (mTOR) inhibitor) and carboplatin may have activity in metastatic triple-negative breast cancer (TNBC). METHODS: The primary objective of this study was to determine clinical benefit rate (CBR), that is (complete remission (CR) + partial remission (PR) + stable disease (SD) lasting ≥6 months) and the toxicity of everolimus/carboplatin in women with metastatic TNBC. Prior carboplatin was allowed. Treatment consisted of intravenous carboplatin area under the curve (AUC) 6 (later decreased to AUC 5 and subsequently to AUC 4) every 3 weeks with daily 5 mg everolimus. RESULTS: We enrolled 25 patients in this study. Median age was 58 years. There were one CR, six PRs, seven SDs and eight PDs (progression of disease). CBR was 36% (95% confidence interval (CI) 21.1 to 57.4%). One SD was achieved in a patient progressing on single agent carboplatin. The median progression free survival (PFS) was 3 months (95% CI 1.6 to 4.6 months) and overall survival (OS) was 16.6 months (95% CI 7.3 months to not reached). There were seven patients (28%) with ≥ grade 3 thrombocytopenia; three (12%) with grade 3 neutropenia (no bleeding/febrile neutropenia) and one (4%) with grade 3 anemia. Greater hematological toxicity was seen in the first seven patients treated with carboplatin AUC5/6. After the amendment for starting dose of carboplatin to AUC 4, the regimen was well tolerated with only one out of 18 patients with grade 3 neutropenia and two patients with grade 3 thrombocytopenia. There was only one case of mucositis. CONCLUSION: Everolimus-carboplatin was efficacious in metastatic TNBC. Dose limiting hematological toxicity was observed when AUC5/6 of carboplatin was combined with everolimus. However, carboplatin AUC 4 was well tolerated in combination with everolimus with continuing responses. TRIAL REGISTRATIONS: ClinicalTrials.gov NCT01127763. |
format | Online Article Text |
id | pubmed-4053575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40535752014-06-12 Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer Singh, Jasmeet Chadha Novik, Yelena Stein, Stacey Volm, Matthew Meyers, Marlene Smith, Julia Omene, Coral Speyer, James Schneider, Robert Jhaveri, Komal Formenti, Silvia Kyriakou, Victoria Joseph, Benson Goldberg, Judith D Li, Xiaochun Adams, Sylvia Tiersten, Amy Breast Cancer Res Research Article INTRODUCTION: Rapamycin acts synergistically with platinum agents to induce apoptosis and inhibit proliferation in breast cancer cell lines. Combination of everolimus also known as RAD001 (oral mammalian target of rapamycin (mTOR) inhibitor) and carboplatin may have activity in metastatic triple-negative breast cancer (TNBC). METHODS: The primary objective of this study was to determine clinical benefit rate (CBR), that is (complete remission (CR) + partial remission (PR) + stable disease (SD) lasting ≥6 months) and the toxicity of everolimus/carboplatin in women with metastatic TNBC. Prior carboplatin was allowed. Treatment consisted of intravenous carboplatin area under the curve (AUC) 6 (later decreased to AUC 5 and subsequently to AUC 4) every 3 weeks with daily 5 mg everolimus. RESULTS: We enrolled 25 patients in this study. Median age was 58 years. There were one CR, six PRs, seven SDs and eight PDs (progression of disease). CBR was 36% (95% confidence interval (CI) 21.1 to 57.4%). One SD was achieved in a patient progressing on single agent carboplatin. The median progression free survival (PFS) was 3 months (95% CI 1.6 to 4.6 months) and overall survival (OS) was 16.6 months (95% CI 7.3 months to not reached). There were seven patients (28%) with ≥ grade 3 thrombocytopenia; three (12%) with grade 3 neutropenia (no bleeding/febrile neutropenia) and one (4%) with grade 3 anemia. Greater hematological toxicity was seen in the first seven patients treated with carboplatin AUC5/6. After the amendment for starting dose of carboplatin to AUC 4, the regimen was well tolerated with only one out of 18 patients with grade 3 neutropenia and two patients with grade 3 thrombocytopenia. There was only one case of mucositis. CONCLUSION: Everolimus-carboplatin was efficacious in metastatic TNBC. Dose limiting hematological toxicity was observed when AUC5/6 of carboplatin was combined with everolimus. However, carboplatin AUC 4 was well tolerated in combination with everolimus with continuing responses. TRIAL REGISTRATIONS: ClinicalTrials.gov NCT01127763. BioMed Central 2014 2014-03-31 /pmc/articles/PMC4053575/ /pubmed/24684785 http://dx.doi.org/10.1186/bcr3634 Text en Copyright © 2014 Singh et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Singh, Jasmeet Chadha Novik, Yelena Stein, Stacey Volm, Matthew Meyers, Marlene Smith, Julia Omene, Coral Speyer, James Schneider, Robert Jhaveri, Komal Formenti, Silvia Kyriakou, Victoria Joseph, Benson Goldberg, Judith D Li, Xiaochun Adams, Sylvia Tiersten, Amy Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer |
title | Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer |
title_full | Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer |
title_fullStr | Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer |
title_full_unstemmed | Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer |
title_short | Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer |
title_sort | phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053575/ https://www.ncbi.nlm.nih.gov/pubmed/24684785 http://dx.doi.org/10.1186/bcr3634 |
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