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Pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis
BACKGROUND: To explore the activity of pazopanib (P) + sirolimus (S) in patients who progressed after previous clinical benefit on pazopanib. METHODS: Eight patients with progressing metastatic high grade soft tissue sarcoma (STS) whose disease advanced on P following a response duration of at least...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977830/ https://www.ncbi.nlm.nih.gov/pubmed/27501793 http://dx.doi.org/10.1186/s12885-016-2618-1 |
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author | Katz, D. Azraq, Y. Eleyan, F. Gill, S. Peretz, T. Merimsky, O. |
author_facet | Katz, D. Azraq, Y. Eleyan, F. Gill, S. Peretz, T. Merimsky, O. |
author_sort | Katz, D. |
collection | PubMed |
description | BACKGROUND: To explore the activity of pazopanib (P) + sirolimus (S) in patients who progressed after previous clinical benefit on pazopanib. METHODS: Eight patients with progressing metastatic high grade soft tissue sarcoma (STS) whose disease advanced on P following a response duration of at least 4 months were offered re-challenge of P supplemented by off-label S and a single patient with progressing metastatic chondrosarcoma was offered the combination as compassionate treatment. Patients were treated in two centers: Hadassah Medical Center and Tel Aviv Medical Center. Patients received oral P 200–600 mg once a day supplemented by S 3–4 mg taken separately, 12 h after the P dose. RESULTS: Patients received treatment from December 2012 to February 2016. Four progressed on the combination and their treatment was terminated. Two patients were undergoing treatment when data was summarized. Best Response Evaluation Criteria in Solid Tumour (RECIST) responses were: one partial response (PR), four stable disease (SD), and four progressive disease (PD), corresponding to five PR and four PD on the Choi criteria. Median progression free survival was 5.5 months (range 4–17). CONCLUSIONS: Our series showed that the combination of P + S has activity in STS patients selected by previous response to P and in a patient with chondrosarcoma, suggesting this can serve as a mechanism to reverse resistance to P and extend the chemotherapy-free window. |
format | Online Article Text |
id | pubmed-4977830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49778302016-08-10 Pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis Katz, D. Azraq, Y. Eleyan, F. Gill, S. Peretz, T. Merimsky, O. BMC Cancer Research Article BACKGROUND: To explore the activity of pazopanib (P) + sirolimus (S) in patients who progressed after previous clinical benefit on pazopanib. METHODS: Eight patients with progressing metastatic high grade soft tissue sarcoma (STS) whose disease advanced on P following a response duration of at least 4 months were offered re-challenge of P supplemented by off-label S and a single patient with progressing metastatic chondrosarcoma was offered the combination as compassionate treatment. Patients were treated in two centers: Hadassah Medical Center and Tel Aviv Medical Center. Patients received oral P 200–600 mg once a day supplemented by S 3–4 mg taken separately, 12 h after the P dose. RESULTS: Patients received treatment from December 2012 to February 2016. Four progressed on the combination and their treatment was terminated. Two patients were undergoing treatment when data was summarized. Best Response Evaluation Criteria in Solid Tumour (RECIST) responses were: one partial response (PR), four stable disease (SD), and four progressive disease (PD), corresponding to five PR and four PD on the Choi criteria. Median progression free survival was 5.5 months (range 4–17). CONCLUSIONS: Our series showed that the combination of P + S has activity in STS patients selected by previous response to P and in a patient with chondrosarcoma, suggesting this can serve as a mechanism to reverse resistance to P and extend the chemotherapy-free window. BioMed Central 2016-08-08 /pmc/articles/PMC4977830/ /pubmed/27501793 http://dx.doi.org/10.1186/s12885-016-2618-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Katz, D. Azraq, Y. Eleyan, F. Gill, S. Peretz, T. Merimsky, O. Pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis |
title | Pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis |
title_full | Pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis |
title_fullStr | Pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis |
title_full_unstemmed | Pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis |
title_short | Pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis |
title_sort | pazolimus: pazopanib plus sirolimus following progression on pazopanib, a retrospective case series analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977830/ https://www.ncbi.nlm.nih.gov/pubmed/27501793 http://dx.doi.org/10.1186/s12885-016-2618-1 |
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