Temozolomide post pazopanib treatment failure in patients with advanced sarcoma: A case series.

Sarcomas are rare, heterogeneous tumors for which prognosis remains dismal in patients with advanced disease. Pazopanib, a vascular endothelial growth factor receptor inhibitor, has shown modest efficacy in patients with soft tissue sarcoma who fail cytotoxic chemotherapy. The cytotoxic agent temozo...

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Main Authors: Manojkumar Bupathi, John L Hays, James L Chen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5687737?pdf=render
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author Manojkumar Bupathi
John L Hays
James L Chen
author_facet Manojkumar Bupathi
John L Hays
James L Chen
author_sort Manojkumar Bupathi
collection DOAJ
description Sarcomas are rare, heterogeneous tumors for which prognosis remains dismal in patients with advanced disease. Pazopanib, a vascular endothelial growth factor receptor inhibitor, has shown modest efficacy in patients with soft tissue sarcoma who fail cytotoxic chemotherapy. The cytotoxic agent temozolomide has also demonstrated activity in patients with advanced sarcoma.We performed a retrospective case series to evaluate the feasibility of adding temozolomide to pazopanib in advanced sarcoma patients following single-agent pazopanib failure.Patients with recurrent, metastatic sarcomas who had progressed on single-agent pazopanib and continued on pazopanib with the addition of temozolomide were included in this retrospective analysis to examine the tolerability and responses associated with the treatment combination.Nine patients with a range of sarcoma subtypes were identified (55% female; median age, 48 years; median number of therapies prior to pazopanib, 3). All patients received combination therapy. One patient was recently started on therapy and was excluded from the analysis (n = 8 evaluable patients). Median PFS for single-agent pazopanib was 7.5 months (range 2-19). For the eight evaluable patients (63% female), best response at 4 months with pazopanib plus temozolomide was partial response (n = 1), stable disease (n = 3) and progressive disease (n = 4), with a median PFS of 3.5 months (range 0-15). Median PFS with combination treatment in patients with stable disease or response was 8 months (range 5-15). All four patients who achieved clinical benefit remain on therapy and are tolerating the combination therapy with expected but manageable side effects.In heavily pretreated patients with advanced sarcoma, the addition of temozolomide to pazopanib was found to be tolerable. Future prospective trials are required to deduce whether temozolomide extends the clinical benefit of pazopanib.
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spelling doaj.art-aad60a1e46a04ccc85aa8bd1743738d02022-12-22T03:36:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011211e018811610.1371/journal.pone.0188116Temozolomide post pazopanib treatment failure in patients with advanced sarcoma: A case series.Manojkumar BupathiJohn L HaysJames L ChenSarcomas are rare, heterogeneous tumors for which prognosis remains dismal in patients with advanced disease. Pazopanib, a vascular endothelial growth factor receptor inhibitor, has shown modest efficacy in patients with soft tissue sarcoma who fail cytotoxic chemotherapy. The cytotoxic agent temozolomide has also demonstrated activity in patients with advanced sarcoma.We performed a retrospective case series to evaluate the feasibility of adding temozolomide to pazopanib in advanced sarcoma patients following single-agent pazopanib failure.Patients with recurrent, metastatic sarcomas who had progressed on single-agent pazopanib and continued on pazopanib with the addition of temozolomide were included in this retrospective analysis to examine the tolerability and responses associated with the treatment combination.Nine patients with a range of sarcoma subtypes were identified (55% female; median age, 48 years; median number of therapies prior to pazopanib, 3). All patients received combination therapy. One patient was recently started on therapy and was excluded from the analysis (n = 8 evaluable patients). Median PFS for single-agent pazopanib was 7.5 months (range 2-19). For the eight evaluable patients (63% female), best response at 4 months with pazopanib plus temozolomide was partial response (n = 1), stable disease (n = 3) and progressive disease (n = 4), with a median PFS of 3.5 months (range 0-15). Median PFS with combination treatment in patients with stable disease or response was 8 months (range 5-15). All four patients who achieved clinical benefit remain on therapy and are tolerating the combination therapy with expected but manageable side effects.In heavily pretreated patients with advanced sarcoma, the addition of temozolomide to pazopanib was found to be tolerable. Future prospective trials are required to deduce whether temozolomide extends the clinical benefit of pazopanib.http://europepmc.org/articles/PMC5687737?pdf=render
spellingShingle Manojkumar Bupathi
John L Hays
James L Chen
Temozolomide post pazopanib treatment failure in patients with advanced sarcoma: A case series.
PLoS ONE
title Temozolomide post pazopanib treatment failure in patients with advanced sarcoma: A case series.
title_full Temozolomide post pazopanib treatment failure in patients with advanced sarcoma: A case series.
title_fullStr Temozolomide post pazopanib treatment failure in patients with advanced sarcoma: A case series.
title_full_unstemmed Temozolomide post pazopanib treatment failure in patients with advanced sarcoma: A case series.
title_short Temozolomide post pazopanib treatment failure in patients with advanced sarcoma: A case series.
title_sort temozolomide post pazopanib treatment failure in patients with advanced sarcoma a case series
url http://europepmc.org/articles/PMC5687737?pdf=render
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