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The Prognostic Value of the Tumor Shrinkage Rate for Progression-Free Survival in Patients with Non-Small Cell Lung Cancer Receiving Gefitinib
The efficacy of epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) therapy can be measured based on the rate of treatment response, based on the Response Evaluation Criteria in Solid Tumors (RECIST) criteria or progression-free survival (PFS). However, there are some patients harb...
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Published in: | Tuberculosis and respiratory diseases 2015, 78(4), 363, pp.315-320 |
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container_start_page | 315 |
container_title | Tuberculosis and respiratory diseases |
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creator | Park, Dong Il Kim, Sun Young Kim, Ju Ock Jung, Sung Soo Park, Hee Sun Moon, Jae Young Chung, Chae Uk Kim, Song Soo Seo, Jae Hee Lee, Jeong Eun |
description | The efficacy of epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) therapy can be measured based on the rate of treatment response, based on the Response Evaluation Criteria in Solid Tumors (RECIST) criteria or progression-free survival (PFS). However, there are some patients harboring sensitive EGFR mutations who responded poorly to EGFR-TKI therapy. In addition, there is variability in the PFS after EGFR-TKI treatment.
We performed a retrospective analysis of the medical records of 85 patients with non-small cell lung cancer, who had achieved a stable disease or better response at the first evaluation of treatment response, after receiving a 2-month course of gefitinib. We calculated the tumor shrinkage rate (TSR) by measuring the longest and perpendicular diameter of the main mass on computed tomography before, and 2 months after, gefitinib therapy.
There was a significant positive correlation between the TSR and PFS (R=0.373, p=0.010). In addition, a simple linear regression analysis showed that the TSR might be an indicator for the PFS (B±standard error, 244.54±66.79; p=0.001). On univariate analysis, the sex, histologic type, smoking history and the number of prior chemotherapy regimens, were significant prognostic factors. On multivariate regression analysis, both the TSR (β=0.257, p=0.029) and adenocarcinoma (β=0.323, p=0.005) were independent prognostic factors for PFS.
Our results showed that the TSR might be an early prognostic indicator for PFS in patients receiving EGFR-TKI therapy. |
doi_str_mv | 10.4046/trd.2015.78.4.315 |
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We performed a retrospective analysis of the medical records of 85 patients with non-small cell lung cancer, who had achieved a stable disease or better response at the first evaluation of treatment response, after receiving a 2-month course of gefitinib. We calculated the tumor shrinkage rate (TSR) by measuring the longest and perpendicular diameter of the main mass on computed tomography before, and 2 months after, gefitinib therapy.
There was a significant positive correlation between the TSR and PFS (R=0.373, p=0.010). In addition, a simple linear regression analysis showed that the TSR might be an indicator for the PFS (B±standard error, 244.54±66.79; p=0.001). On univariate analysis, the sex, histologic type, smoking history and the number of prior chemotherapy regimens, were significant prognostic factors. On multivariate regression analysis, both the TSR (β=0.257, p=0.029) and adenocarcinoma (β=0.323, p=0.005) were independent prognostic factors for PFS.
Our results showed that the TSR might be an early prognostic indicator for PFS in patients receiving EGFR-TKI therapy.</description><identifier>ISSN: 1738-3536</identifier><identifier>EISSN: 2005-6184</identifier><identifier>DOI: 10.4046/trd.2015.78.4.315</identifier><identifier>PMID: 26508917</identifier><language>eng</language><publisher>Korea (South): The Korean Academy of Tuberculosis and Respiratory Diseases</publisher><subject>Original ; 내과학</subject><ispartof>Tuberculosis and Respiratory Diseases, 2015, 78(4), 363, pp.315-320</ispartof><rights>Copyright©2015. The Korean Academy of Tuberculosis and Respiratory Diseases. All rights reserved. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-8786255defd868a99040c031389742d4177ee354a633d17a4b705dbcbde339163</citedby><cites>FETCH-LOGICAL-c432t-8786255defd868a99040c031389742d4177ee354a633d17a4b705dbcbde339163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620323/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620323/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26508917$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002035677$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Dong Il</creatorcontrib><creatorcontrib>Kim, Sun Young</creatorcontrib><creatorcontrib>Kim, Ju Ock</creatorcontrib><creatorcontrib>Jung, Sung Soo</creatorcontrib><creatorcontrib>Park, Hee Sun</creatorcontrib><creatorcontrib>Moon, Jae Young</creatorcontrib><creatorcontrib>Chung, Chae Uk</creatorcontrib><creatorcontrib>Kim, Song Soo</creatorcontrib><creatorcontrib>Seo, Jae Hee</creatorcontrib><creatorcontrib>Lee, Jeong Eun</creatorcontrib><title>The Prognostic Value of the Tumor Shrinkage Rate for Progression-Free Survival in Patients with Non-Small Cell Lung Cancer Receiving Gefitinib</title><title>Tuberculosis and respiratory diseases</title><addtitle>Tuberc Respir Dis (Seoul)</addtitle><description>The efficacy of epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) therapy can be measured based on the rate of treatment response, based on the Response Evaluation Criteria in Solid Tumors (RECIST) criteria or progression-free survival (PFS). However, there are some patients harboring sensitive EGFR mutations who responded poorly to EGFR-TKI therapy. In addition, there is variability in the PFS after EGFR-TKI treatment.
We performed a retrospective analysis of the medical records of 85 patients with non-small cell lung cancer, who had achieved a stable disease or better response at the first evaluation of treatment response, after receiving a 2-month course of gefitinib. We calculated the tumor shrinkage rate (TSR) by measuring the longest and perpendicular diameter of the main mass on computed tomography before, and 2 months after, gefitinib therapy.
There was a significant positive correlation between the TSR and PFS (R=0.373, p=0.010). In addition, a simple linear regression analysis showed that the TSR might be an indicator for the PFS (B±standard error, 244.54±66.79; p=0.001). On univariate analysis, the sex, histologic type, smoking history and the number of prior chemotherapy regimens, were significant prognostic factors. On multivariate regression analysis, both the TSR (β=0.257, p=0.029) and adenocarcinoma (β=0.323, p=0.005) were independent prognostic factors for PFS.
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We performed a retrospective analysis of the medical records of 85 patients with non-small cell lung cancer, who had achieved a stable disease or better response at the first evaluation of treatment response, after receiving a 2-month course of gefitinib. We calculated the tumor shrinkage rate (TSR) by measuring the longest and perpendicular diameter of the main mass on computed tomography before, and 2 months after, gefitinib therapy.
There was a significant positive correlation between the TSR and PFS (R=0.373, p=0.010). In addition, a simple linear regression analysis showed that the TSR might be an indicator for the PFS (B±standard error, 244.54±66.79; p=0.001). On univariate analysis, the sex, histologic type, smoking history and the number of prior chemotherapy regimens, were significant prognostic factors. On multivariate regression analysis, both the TSR (β=0.257, p=0.029) and adenocarcinoma (β=0.323, p=0.005) were independent prognostic factors for PFS.
Our results showed that the TSR might be an early prognostic indicator for PFS in patients receiving EGFR-TKI therapy.</abstract><cop>Korea (South)</cop><pub>The Korean Academy of Tuberculosis and Respiratory Diseases</pub><pmid>26508917</pmid><doi>10.4046/trd.2015.78.4.315</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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title | The Prognostic Value of the Tumor Shrinkage Rate for Progression-Free Survival in Patients with Non-Small Cell Lung Cancer Receiving Gefitinib |
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