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Weekly gemcitabine and docetaxel in refractory soft tissue sarcoma: a retrospective analysis
The combination of gemcitabine and docetaxel (GD) is used to effectively treat patients with soft tissue sarcoma (STS). It is widely considered that the conventional doses used are too high for long term use and many patients must discontinue GD treatment due to its toxicity. Therefore, to determine...
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Published in: | Cancer research and treatment 2012, 44(1), , pp.43-49 |
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container_title | Cancer research and treatment |
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creator | Lee, Ha-Young Shin, Sang Joon Kim, Hyo Song Hong, Soo Jung Han, Jung Woo Lim, Seung Taek Roh, Jae Kyung Rha, Sun Young |
description | The combination of gemcitabine and docetaxel (GD) is used to effectively treat patients with soft tissue sarcoma (STS). It is widely considered that the conventional doses used are too high for long term use and many patients must discontinue GD treatment due to its toxicity. Therefore, to determine the appropriate dose meeting acceptable efficacy results, while minimizing toxic side effects, we treated patients with a weekly infusion of GD (weekly GD).
A total of 22 patients presenting a variety of STSs were treated at Yonsei Cancer Center. All patients had metastatic or recurrent cancer and had previously received doxorubicin and ifosfamide combination chemotherapy. In all cases, gemcitabine (1,000 mg/m(2)) and docetaxel (35 mg/m(2)) were administered intravenously on days 1 and 8 of a 21-day cycle. We retrospectively reviewed the medical records of these patients.
The response rate was 4.5%, with one patient diagnosed with leiomyosarcoma having a partial response, and the disease control rate was 40.9%. The median progression-free survival (PFS) duration was 2.7 months and the PFS was correlated with the treatment response to a weekly GD. The median overall survival (OS) duration was 7.8 months and the OS was correlated with histology. There was no significant difference in OS between patients who received weekly GD as a 2nd line chemotherapy and those who received 3rd line or more. Treatment was generally well tolerated.
Weekly GD was well tolerated and showed moderate efficacy, indicating that this could be a reasonable option as a salvage treatment for metastatic STS. |
doi_str_mv | 10.4143/crt.2012.44.1.43 |
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A total of 22 patients presenting a variety of STSs were treated at Yonsei Cancer Center. All patients had metastatic or recurrent cancer and had previously received doxorubicin and ifosfamide combination chemotherapy. In all cases, gemcitabine (1,000 mg/m(2)) and docetaxel (35 mg/m(2)) were administered intravenously on days 1 and 8 of a 21-day cycle. We retrospectively reviewed the medical records of these patients.
The response rate was 4.5%, with one patient diagnosed with leiomyosarcoma having a partial response, and the disease control rate was 40.9%. The median progression-free survival (PFS) duration was 2.7 months and the PFS was correlated with the treatment response to a weekly GD. The median overall survival (OS) duration was 7.8 months and the OS was correlated with histology. There was no significant difference in OS between patients who received weekly GD as a 2nd line chemotherapy and those who received 3rd line or more. Treatment was generally well tolerated.
Weekly GD was well tolerated and showed moderate efficacy, indicating that this could be a reasonable option as a salvage treatment for metastatic STS.</description><identifier>ISSN: 1598-2998</identifier><identifier>EISSN: 2005-9256</identifier><identifier>DOI: 10.4143/crt.2012.44.1.43</identifier><identifier>PMID: 22500160</identifier><language>eng</language><publisher>Korea (South): Korean Cancer Association</publisher><subject>Original ; 의약학</subject><ispartof>Cancer Research and Treatment, 2012, 44(1), , pp.43-49</ispartof><rights>Copyright © 2012 by the Korean Cancer Association 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c495t-d3712aa9bb5b8a213a64c8c59ef88258fea669f9ea14f71093bf1c654cd8d86c3</citedby><cites>FETCH-LOGICAL-c495t-d3712aa9bb5b8a213a64c8c59ef88258fea669f9ea14f71093bf1c654cd8d86c3</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/PMC3322200/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322200/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22500160$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001647763$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Ha-Young</creatorcontrib><creatorcontrib>Shin, Sang Joon</creatorcontrib><creatorcontrib>Kim, Hyo Song</creatorcontrib><creatorcontrib>Hong, Soo Jung</creatorcontrib><creatorcontrib>Han, Jung Woo</creatorcontrib><creatorcontrib>Lim, Seung Taek</creatorcontrib><creatorcontrib>Roh, Jae Kyung</creatorcontrib><creatorcontrib>Rha, Sun Young</creatorcontrib><title>Weekly gemcitabine and docetaxel in refractory soft tissue sarcoma: a retrospective analysis</title><title>Cancer research and treatment</title><addtitle>Cancer Res Treat</addtitle><description>The combination of gemcitabine and docetaxel (GD) is used to effectively treat patients with soft tissue sarcoma (STS). It is widely considered that the conventional doses used are too high for long term use and many patients must discontinue GD treatment due to its toxicity. Therefore, to determine the appropriate dose meeting acceptable efficacy results, while minimizing toxic side effects, we treated patients with a weekly infusion of GD (weekly GD).
A total of 22 patients presenting a variety of STSs were treated at Yonsei Cancer Center. All patients had metastatic or recurrent cancer and had previously received doxorubicin and ifosfamide combination chemotherapy. In all cases, gemcitabine (1,000 mg/m(2)) and docetaxel (35 mg/m(2)) were administered intravenously on days 1 and 8 of a 21-day cycle. We retrospectively reviewed the medical records of these patients.
The response rate was 4.5%, with one patient diagnosed with leiomyosarcoma having a partial response, and the disease control rate was 40.9%. The median progression-free survival (PFS) duration was 2.7 months and the PFS was correlated with the treatment response to a weekly GD. The median overall survival (OS) duration was 7.8 months and the OS was correlated with histology. There was no significant difference in OS between patients who received weekly GD as a 2nd line chemotherapy and those who received 3rd line or more. Treatment was generally well tolerated.
Weekly GD was well tolerated and showed moderate efficacy, indicating that this could be a reasonable option as a salvage treatment for metastatic STS.</description><subject>Original</subject><subject>의약학</subject><issn>1598-2998</issn><issn>2005-9256</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpVkUtPGzEUha2qiITHvivkZTcz9XNis0CKUIFIkSohEBsk647HpiaTmcg2qPn3dUiLYHUX95zvPg5C3yipBRX8h425ZoSyWoia1oJ_QVNGiKw0k81XNKVSq4pprSboKKVnQhrBZ_QQTRiThNCGTNHjg3Orfouf3NqGDG0YHIahw91oXYY_rsdhwNH5CDaPcYvT6DPOIaUXhxNEO67hHENR5DimjbM5vO4A0G9TSCfowEOf3Om_eozur37eXd5Uy1_Xi8v5srJCy1x1ZSkGoNtWtgoY5dAIq6zUzivFpPIOmkZ77YAKP6NE89ZT20hhO9WpxvJj9H3PHaI3KxvMCOGtPo1mFc389m5hmBRyNivSi71089KuXWfdkCP0ZhPDGuL2zfi5M4TfBfNqOGes_LYAyB5gy8GpfObdS4nZhWJKKGYXihHCUCN4sZx9nPlu-J8C_wsInouC</recordid><startdate>20120301</startdate><enddate>20120301</enddate><creator>Lee, Ha-Young</creator><creator>Shin, Sang Joon</creator><creator>Kim, Hyo Song</creator><creator>Hong, Soo Jung</creator><creator>Han, Jung Woo</creator><creator>Lim, Seung Taek</creator><creator>Roh, Jae Kyung</creator><creator>Rha, Sun Young</creator><general>Korean Cancer Association</general><general>대한암학회</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>ACYCR</scope></search><sort><creationdate>20120301</creationdate><title>Weekly gemcitabine and docetaxel in refractory soft tissue sarcoma: a retrospective analysis</title><author>Lee, Ha-Young ; Shin, Sang Joon ; Kim, Hyo Song ; Hong, Soo Jung ; Han, Jung Woo ; Lim, Seung Taek ; Roh, Jae Kyung ; Rha, Sun Young</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c495t-d3712aa9bb5b8a213a64c8c59ef88258fea669f9ea14f71093bf1c654cd8d86c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Original</topic><topic>의약학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Ha-Young</creatorcontrib><creatorcontrib>Shin, Sang Joon</creatorcontrib><creatorcontrib>Kim, Hyo Song</creatorcontrib><creatorcontrib>Hong, Soo Jung</creatorcontrib><creatorcontrib>Han, Jung Woo</creatorcontrib><creatorcontrib>Lim, Seung Taek</creatorcontrib><creatorcontrib>Roh, Jae Kyung</creatorcontrib><creatorcontrib>Rha, Sun Young</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Ha-Young</au><au>Shin, Sang Joon</au><au>Kim, Hyo Song</au><au>Hong, Soo Jung</au><au>Han, Jung Woo</au><au>Lim, Seung Taek</au><au>Roh, Jae Kyung</au><au>Rha, Sun Young</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Weekly gemcitabine and docetaxel in refractory soft tissue sarcoma: a retrospective analysis</atitle><jtitle>Cancer research and treatment</jtitle><addtitle>Cancer Res Treat</addtitle><date>2012-03-01</date><risdate>2012</risdate><volume>44</volume><issue>1</issue><spage>43</spage><epage>49</epage><pages>43-49</pages><issn>1598-2998</issn><eissn>2005-9256</eissn><abstract>The combination of gemcitabine and docetaxel (GD) is used to effectively treat patients with soft tissue sarcoma (STS). It is widely considered that the conventional doses used are too high for long term use and many patients must discontinue GD treatment due to its toxicity. Therefore, to determine the appropriate dose meeting acceptable efficacy results, while minimizing toxic side effects, we treated patients with a weekly infusion of GD (weekly GD).
A total of 22 patients presenting a variety of STSs were treated at Yonsei Cancer Center. All patients had metastatic or recurrent cancer and had previously received doxorubicin and ifosfamide combination chemotherapy. In all cases, gemcitabine (1,000 mg/m(2)) and docetaxel (35 mg/m(2)) were administered intravenously on days 1 and 8 of a 21-day cycle. We retrospectively reviewed the medical records of these patients.
The response rate was 4.5%, with one patient diagnosed with leiomyosarcoma having a partial response, and the disease control rate was 40.9%. The median progression-free survival (PFS) duration was 2.7 months and the PFS was correlated with the treatment response to a weekly GD. The median overall survival (OS) duration was 7.8 months and the OS was correlated with histology. There was no significant difference in OS between patients who received weekly GD as a 2nd line chemotherapy and those who received 3rd line or more. Treatment was generally well tolerated.
Weekly GD was well tolerated and showed moderate efficacy, indicating that this could be a reasonable option as a salvage treatment for metastatic STS.</abstract><cop>Korea (South)</cop><pub>Korean Cancer Association</pub><pmid>22500160</pmid><doi>10.4143/crt.2012.44.1.43</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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title | Weekly gemcitabine and docetaxel in refractory soft tissue sarcoma: a retrospective analysis |
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