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Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials
Background: There is often a finite progression-free interval of time between one systemic therapy and the next when treating patients with advanced cancer. While it appears that progression-free survival (PFS) between systemic therapies tends to get shorter for a number of factors, there has not be...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245603/ https://www.ncbi.nlm.nih.gov/pubmed/22211140 |
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author | Bailey, Christopher H. Jameson, Gayle Sima, Chao Fleck, Sharon White, Erica Von Hoff, Daniel D. Weiss, Glen J. |
author_facet | Bailey, Christopher H. Jameson, Gayle Sima, Chao Fleck, Sharon White, Erica Von Hoff, Daniel D. Weiss, Glen J. |
author_sort | Bailey, Christopher H. |
collection | PubMed |
description | Background: There is often a finite progression-free interval of time between one systemic therapy and the next when treating patients with advanced cancer. While it appears that progression-free survival (PFS) between systemic therapies tends to get shorter for a number of factors, there has not been a formal evaluation of diverse tumor types in an advanced cancer population treated with commercially-available systemic therapies. Methods: In an attempt to clarify the relationship between PFS between subsequent systemic therapies, we analyzed the records of 165 advanced cancer patients coming to our clinic for consideration for participation in six different phase I clinical trials requiring detailed and extensive past medical treatment history documentation. Results: There were 77 men and 65 women meeting inclusion criteria with a median age at diagnosis of 55.3 years (range 9.4-81.6). The most common cancer types were colorectal (13.9%), other gastrointestinal (11.8%), prostate (11.8%). A median of 3 (range 1-11) systemic therapies were received prior to phase I evaluation. There was a significant decrease in PFS in systemic therapy for advanced disease from treatment 1 to treatment 2 to treatment 3 (p = 0.002), as well as, from treatment 1 through treatment 5 (p < 0.001). Conclusions: In an advanced cancer population of diverse tumor types, we observe a statistically significant decrease in PFS with each successive standard therapy. Identification of new therapies that reverse this trend of decreasing PFS may lead to improved clinical outcomes. |
format | Online Article Text |
id | pubmed-3245603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-32456032012-01-01 Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials Bailey, Christopher H. Jameson, Gayle Sima, Chao Fleck, Sharon White, Erica Von Hoff, Daniel D. Weiss, Glen J. J Cancer Research Paper Background: There is often a finite progression-free interval of time between one systemic therapy and the next when treating patients with advanced cancer. While it appears that progression-free survival (PFS) between systemic therapies tends to get shorter for a number of factors, there has not been a formal evaluation of diverse tumor types in an advanced cancer population treated with commercially-available systemic therapies. Methods: In an attempt to clarify the relationship between PFS between subsequent systemic therapies, we analyzed the records of 165 advanced cancer patients coming to our clinic for consideration for participation in six different phase I clinical trials requiring detailed and extensive past medical treatment history documentation. Results: There were 77 men and 65 women meeting inclusion criteria with a median age at diagnosis of 55.3 years (range 9.4-81.6). The most common cancer types were colorectal (13.9%), other gastrointestinal (11.8%), prostate (11.8%). A median of 3 (range 1-11) systemic therapies were received prior to phase I evaluation. There was a significant decrease in PFS in systemic therapy for advanced disease from treatment 1 to treatment 2 to treatment 3 (p = 0.002), as well as, from treatment 1 through treatment 5 (p < 0.001). Conclusions: In an advanced cancer population of diverse tumor types, we observe a statistically significant decrease in PFS with each successive standard therapy. Identification of new therapies that reverse this trend of decreasing PFS may lead to improved clinical outcomes. Ivyspring International Publisher 2011-11-28 /pmc/articles/PMC3245603/ /pubmed/22211140 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. |
spellingShingle | Research Paper Bailey, Christopher H. Jameson, Gayle Sima, Chao Fleck, Sharon White, Erica Von Hoff, Daniel D. Weiss, Glen J. Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials |
title | Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials |
title_full | Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials |
title_fullStr | Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials |
title_full_unstemmed | Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials |
title_short | Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials |
title_sort | progression-free survival decreases with each subsequent therapy in patients presenting for phase i clinical trials |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245603/ https://www.ncbi.nlm.nih.gov/pubmed/22211140 |
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