Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma
<p>Abstract</p> <p>Background</p> <p>We wished to evaluate the clinical response following ATP-Tumor Chemosensitivity Assay (ATP-TCA) directed salvage chemotherapy in a series of UK patients with advanced ovarian cancer. The results are compared with that of a similar a...
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doaj-2014def2588e477187de57dae782a3852020-11-25T01:08:06ZengBMCBMC Cancer1471-24072003-07-01311910.1186/1471-2407-3-19Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinomaLamont AlanHiggins Bernard RMercer Stuart JWhitehouse Pauline AKnight Louise ADi Nicolantonio FedericaNeale Michael HSharma SanjayOsborne RichardHindley Andrew CKurbacher Christian MCree Ian A<p>Abstract</p> <p>Background</p> <p>We wished to evaluate the clinical response following ATP-Tumor Chemosensitivity Assay (ATP-TCA) directed salvage chemotherapy in a series of UK patients with advanced ovarian cancer. The results are compared with that of a similar assay used in a different country in terms of evaluability and clinical endpoints.</p> <p>Methods</p> <p>From November 1998 to November 2001, 46 patients with pre-treated, advanced ovarian cancer were given a total of 56 courses of chemotherapy based on in-vitro ATP-TCA responses obtained from fresh tumor samples or ascites. Forty-four patients were evaluable for results. Of these, 18 patients had clinically platinum resistant disease (relapse < 6 months after first course of chemotherapy). There was evidence of cisplatin resistance in 31 patients from their first ATP-TCA. Response to treatment was assessed by radiology, clinical assessment and tumor marker level (CA 125).</p> <p>Results</p> <p>The overall response rate was 59% (33/56) per course of chemotherapy, including 12 complete responses, 21 partial responses, 6 with stable disease, and 15 with progressive disease. Two patients were not evaluable for response having received just one cycle of chemotherapy: if these were excluded the response rate is 61%. Fifteen patients are still alive. Median progression free survival (PFS) was 6.6 months per course of chemotherapy; median overall survival (OAS) for each patient following the start of TCA-directed therapy was 10.4 months (95% confidence interval 7.9–12.8 months).</p> <p>Conclusion</p> <p>The results show similar response rates to previous studies using ATP-TCA directed therapy in recurrent ovarian cancer. The assay shows high evaluability and this study adds weight to the reproducibility of results from different centres.</p> http://www.biomedcentral.com/1471-2407/3/19 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lamont Alan Higgins Bernard R Mercer Stuart J Whitehouse Pauline A Knight Louise A Di Nicolantonio Federica Neale Michael H Sharma Sanjay Osborne Richard Hindley Andrew C Kurbacher Christian M Cree Ian A |
spellingShingle |
Lamont Alan Higgins Bernard R Mercer Stuart J Whitehouse Pauline A Knight Louise A Di Nicolantonio Federica Neale Michael H Sharma Sanjay Osborne Richard Hindley Andrew C Kurbacher Christian M Cree Ian A Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma BMC Cancer |
author_facet |
Lamont Alan Higgins Bernard R Mercer Stuart J Whitehouse Pauline A Knight Louise A Di Nicolantonio Federica Neale Michael H Sharma Sanjay Osborne Richard Hindley Andrew C Kurbacher Christian M Cree Ian A |
author_sort |
Lamont Alan |
title |
Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma |
title_short |
Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma |
title_full |
Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma |
title_fullStr |
Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma |
title_full_unstemmed |
Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma |
title_sort |
outcome of atp-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma |
publisher |
BMC |
series |
BMC Cancer |
issn |
1471-2407 |
publishDate |
2003-07-01 |
description |
<p>Abstract</p> <p>Background</p> <p>We wished to evaluate the clinical response following ATP-Tumor Chemosensitivity Assay (ATP-TCA) directed salvage chemotherapy in a series of UK patients with advanced ovarian cancer. The results are compared with that of a similar assay used in a different country in terms of evaluability and clinical endpoints.</p> <p>Methods</p> <p>From November 1998 to November 2001, 46 patients with pre-treated, advanced ovarian cancer were given a total of 56 courses of chemotherapy based on in-vitro ATP-TCA responses obtained from fresh tumor samples or ascites. Forty-four patients were evaluable for results. Of these, 18 patients had clinically platinum resistant disease (relapse < 6 months after first course of chemotherapy). There was evidence of cisplatin resistance in 31 patients from their first ATP-TCA. Response to treatment was assessed by radiology, clinical assessment and tumor marker level (CA 125).</p> <p>Results</p> <p>The overall response rate was 59% (33/56) per course of chemotherapy, including 12 complete responses, 21 partial responses, 6 with stable disease, and 15 with progressive disease. Two patients were not evaluable for response having received just one cycle of chemotherapy: if these were excluded the response rate is 61%. Fifteen patients are still alive. Median progression free survival (PFS) was 6.6 months per course of chemotherapy; median overall survival (OAS) for each patient following the start of TCA-directed therapy was 10.4 months (95% confidence interval 7.9–12.8 months).</p> <p>Conclusion</p> <p>The results show similar response rates to previous studies using ATP-TCA directed therapy in recurrent ovarian cancer. The assay shows high evaluability and this study adds weight to the reproducibility of results from different centres.</p> |
url |
http://www.biomedcentral.com/1471-2407/3/19 |
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