Prognostic factors affecting the risk of thoracic progression in extensive-stage small cell lung cancer
The efficacy of combined modality therapy is evaluated for patients with extensive-stage (ES) small cell lung cancer (SCLC). This study evaluated prognostic factors affecting the risk of thoracic progression in ES-SCLC patients likely to undergo thoracic radiotherapy combined chemotherapy. A retrosp...
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description | The efficacy of combined modality therapy is evaluated for patients with extensive-stage (ES) small cell lung cancer (SCLC). This study evaluated prognostic factors affecting the risk of thoracic progression in ES-SCLC patients likely to undergo thoracic radiotherapy combined chemotherapy.
A retrospective review of ES-SCLC patients who had received systemic chemotherapy at our hospital was performed. Tumor size, metastatic sites, and laboratory data at diagnosis were evaluated as potential prognostic factors. In ES-SCLC patients without pleural dissemination, the rate of thoracic progression after initial chemotherapy was assessed.
Eighty-three of 96 consecutive ES-SCLC patients were analyzed. The overall response rate was 55 %, median progression free survival was 5.0 months (mo), and overall survival (OS) was 9.2 mo. Tumor size (19.4 mo for ≤3 cm vs. 8.5 mo for >3 cm, p = 0.017) and the number of metastatic sites (12.9 mo for single sites vs. 7.1 mo for multiple sites, p = 0.015) were prognostic factors, in addition to known prognostic factors such as performance status and the levels of LDH and sodium. Cox proportional hazard model showed that the OS was significantly worse in patients with large (>3 cm) primary tumor size {HR 2.44 [95 % confidential interval (CI) 1.05-5.68], p = 0.038} and multiple metastatic sites [HR 1.81 (95 % CI 1.08-3.04), p = 0.026]. In 51 cases without pleural dissemination, the number of metastatic sites was associated with thoracic progression after initial chemotherapy (65 % for single sites vs. 36 % for multiple sites, p = 0.036).
Large tumor size and multiple metastatic sites at diagnosis significantly predicted poor survival in ES-SCLC patients. Based on the high rate of thoracic progression in ES-SCLC patients with single site of distant metastasis, we should consider thoracic radiotherapy combined with chemotherapy for this population. |
doi_str_mv | 10.1186/s12885-016-2222-4 |
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A retrospective review of ES-SCLC patients who had received systemic chemotherapy at our hospital was performed. Tumor size, metastatic sites, and laboratory data at diagnosis were evaluated as potential prognostic factors. In ES-SCLC patients without pleural dissemination, the rate of thoracic progression after initial chemotherapy was assessed.
Eighty-three of 96 consecutive ES-SCLC patients were analyzed. The overall response rate was 55 %, median progression free survival was 5.0 months (mo), and overall survival (OS) was 9.2 mo. Tumor size (19.4 mo for ≤3 cm vs. 8.5 mo for >3 cm, p = 0.017) and the number of metastatic sites (12.9 mo for single sites vs. 7.1 mo for multiple sites, p = 0.015) were prognostic factors, in addition to known prognostic factors such as performance status and the levels of LDH and sodium. Cox proportional hazard model showed that the OS was significantly worse in patients with large (>3 cm) primary tumor size {HR 2.44 [95 % confidential interval (CI) 1.05-5.68], p = 0.038} and multiple metastatic sites [HR 1.81 (95 % CI 1.08-3.04), p = 0.026]. In 51 cases without pleural dissemination, the number of metastatic sites was associated with thoracic progression after initial chemotherapy (65 % for single sites vs. 36 % for multiple sites, p = 0.036).
Large tumor size and multiple metastatic sites at diagnosis significantly predicted poor survival in ES-SCLC patients. Based on the high rate of thoracic progression in ES-SCLC patients with single site of distant metastasis, we should consider thoracic radiotherapy combined with chemotherapy for this population.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-016-2222-4</identifier><identifier>PMID: 26955807</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Aged ; Aged, 80 and over ; Analysis ; Cancer therapies ; Chemotherapy ; Combined Modality Therapy ; Confidence intervals ; Data collection ; Development and progression ; Disease Progression ; Female ; Hospitals ; Humans ; Kaplan-Meier Estimate ; Lung cancer ; Lung cancer, Small cell ; Lung Neoplasms - mortality ; Lung Neoplasms - pathology ; Lung Neoplasms - therapy ; Male ; Medical imaging ; Medical prognosis ; Metastasis ; Middle Aged ; Multivariate analysis ; Neoplasm Metastasis ; Neoplasm Staging ; Patient outcomes ; Prognosis ; Proportional Hazards Models ; Radiation therapy ; Radiotherapy ; Risk Factors ; Small Cell Lung Carcinoma - mortality ; Small Cell Lung Carcinoma - pathology ; Small Cell Lung Carcinoma - therapy ; Thorax - pathology ; Treatment Outcome ; Tumor Burden</subject><ispartof>BMC cancer, 2016-03, Vol.16 (199), p.197-197, Article 197</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>Fukui et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c559t-e4c30f2e66a4c168eb3f6701c6a4c877e00d113879eb4a2aaff592052a314b033</citedby><cites>FETCH-LOGICAL-c559t-e4c30f2e66a4c168eb3f6701c6a4c877e00d113879eb4a2aaff592052a314b033</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/PMC4782389/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782389/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26955807$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fukui, Tomoya</creatorcontrib><creatorcontrib>Itabashi, Michiko</creatorcontrib><creatorcontrib>Ishihara, Mikiko</creatorcontrib><creatorcontrib>Hiyoshi, Yasuhiro</creatorcontrib><creatorcontrib>Kasajima, Masashi</creatorcontrib><creatorcontrib>Igawa, Satoshi</creatorcontrib><creatorcontrib>Sasaki, Jiichiro</creatorcontrib><creatorcontrib>Masuda, Noriyuki</creatorcontrib><title>Prognostic factors affecting the risk of thoracic progression in extensive-stage small cell lung cancer</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>The efficacy of combined modality therapy is evaluated for patients with extensive-stage (ES) small cell lung cancer (SCLC). This study evaluated prognostic factors affecting the risk of thoracic progression in ES-SCLC patients likely to undergo thoracic radiotherapy combined chemotherapy.
A retrospective review of ES-SCLC patients who had received systemic chemotherapy at our hospital was performed. Tumor size, metastatic sites, and laboratory data at diagnosis were evaluated as potential prognostic factors. In ES-SCLC patients without pleural dissemination, the rate of thoracic progression after initial chemotherapy was assessed.
Eighty-three of 96 consecutive ES-SCLC patients were analyzed. The overall response rate was 55 %, median progression free survival was 5.0 months (mo), and overall survival (OS) was 9.2 mo. Tumor size (19.4 mo for ≤3 cm vs. 8.5 mo for >3 cm, p = 0.017) and the number of metastatic sites (12.9 mo for single sites vs. 7.1 mo for multiple sites, p = 0.015) were prognostic factors, in addition to known prognostic factors such as performance status and the levels of LDH and sodium. Cox proportional hazard model showed that the OS was significantly worse in patients with large (>3 cm) primary tumor size {HR 2.44 [95 % confidential interval (CI) 1.05-5.68], p = 0.038} and multiple metastatic sites [HR 1.81 (95 % CI 1.08-3.04), p = 0.026]. In 51 cases without pleural dissemination, the number of metastatic sites was associated with thoracic progression after initial chemotherapy (65 % for single sites vs. 36 % for multiple sites, p = 0.036).
Large tumor size and multiple metastatic sites at diagnosis significantly predicted poor survival in ES-SCLC patients. Based on the high rate of thoracic progression in ES-SCLC patients with single site of distant metastasis, we should consider thoracic radiotherapy combined with chemotherapy for this population.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Analysis</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Combined Modality Therapy</subject><subject>Confidence intervals</subject><subject>Data collection</subject><subject>Development and progression</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Lung cancer</subject><subject>Lung cancer, Small cell</subject><subject>Lung Neoplasms - mortality</subject><subject>Lung Neoplasms - pathology</subject><subject>Lung Neoplasms - therapy</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Neoplasm Metastasis</subject><subject>Neoplasm Staging</subject><subject>Patient outcomes</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Radiation therapy</subject><subject>Radiotherapy</subject><subject>Risk Factors</subject><subject>Small Cell Lung Carcinoma - mortality</subject><subject>Small Cell Lung Carcinoma - pathology</subject><subject>Small Cell Lung Carcinoma - therapy</subject><subject>Thorax - pathology</subject><subject>Treatment Outcome</subject><subject>Tumor Burden</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkt1r1TAYxosobk7_AG-kIIi76MxXm_RGGEPnYKD4cR1yct70ZLbJMW869L835cx5jphCkja_50mT96mq55ScUaq6N0iZUm1DaNew0hrxoDqmQtKGCSIf7s2PqieIN4RQqYh6XB2xrm9bReRxNXxKcQgRs7e1MzbHhLVxDmz2YajzBurk8XsdXZnHZGzBtkWRANHHUPtQw88MAf0tNJjNADVOZhxrC6Ub5-JhTbCQnlaPnBkRnt2NJ9W39---Xnxorj9eXl2cXze2bfvcgLCcOAZdZ4SlnYIVd50k1C7vSkogZE0pV7KHlTDMlF9te0ZaZjgVK8L5SfV257udVxOsLYSczKi3yU8m_dLReH24EvxGD_FWC6kYV30xeH1nkOKPGTDryeNyGhMgzqiplIyKrqfLXi__QW_inEI5XqF6qXgvOflLDWYE7YOLZV-7mOpz0XKlWKlLoc7-Q5VnDZO3MYDz5fuB4PRAUJhcSjGYGVFfffl8yL7aYzdgxrzBOM65lBAPQboDbYqICdz9xVGil8jpXeR0iZxeIqdF0bzYv_F7xZ-M8d_iQ8_j</recordid><startdate>20160308</startdate><enddate>20160308</enddate><creator>Fukui, Tomoya</creator><creator>Itabashi, Michiko</creator><creator>Ishihara, Mikiko</creator><creator>Hiyoshi, Yasuhiro</creator><creator>Kasajima, Masashi</creator><creator>Igawa, Satoshi</creator><creator>Sasaki, Jiichiro</creator><creator>Masuda, Noriyuki</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160308</creationdate><title>Prognostic factors affecting the risk of thoracic progression in extensive-stage small cell lung cancer</title><author>Fukui, Tomoya ; Itabashi, Michiko ; Ishihara, Mikiko ; Hiyoshi, Yasuhiro ; Kasajima, Masashi ; Igawa, Satoshi ; Sasaki, Jiichiro ; Masuda, Noriyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c559t-e4c30f2e66a4c168eb3f6701c6a4c877e00d113879eb4a2aaff592052a314b033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Analysis</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Combined Modality Therapy</topic><topic>Confidence intervals</topic><topic>Data collection</topic><topic>Development and progression</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Lung cancer</topic><topic>Lung cancer, Small cell</topic><topic>Lung Neoplasms - mortality</topic><topic>Lung Neoplasms - pathology</topic><topic>Lung Neoplasms - therapy</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Multivariate analysis</topic><topic>Neoplasm Metastasis</topic><topic>Neoplasm Staging</topic><topic>Patient outcomes</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Radiation therapy</topic><topic>Radiotherapy</topic><topic>Risk Factors</topic><topic>Small Cell Lung Carcinoma - mortality</topic><topic>Small Cell Lung Carcinoma - pathology</topic><topic>Small Cell Lung Carcinoma - therapy</topic><topic>Thorax - pathology</topic><topic>Treatment Outcome</topic><topic>Tumor Burden</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fukui, Tomoya</creatorcontrib><creatorcontrib>Itabashi, Michiko</creatorcontrib><creatorcontrib>Ishihara, Mikiko</creatorcontrib><creatorcontrib>Hiyoshi, Yasuhiro</creatorcontrib><creatorcontrib>Kasajima, Masashi</creatorcontrib><creatorcontrib>Igawa, Satoshi</creatorcontrib><creatorcontrib>Sasaki, Jiichiro</creatorcontrib><creatorcontrib>Masuda, Noriyuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fukui, Tomoya</au><au>Itabashi, Michiko</au><au>Ishihara, Mikiko</au><au>Hiyoshi, Yasuhiro</au><au>Kasajima, Masashi</au><au>Igawa, Satoshi</au><au>Sasaki, Jiichiro</au><au>Masuda, Noriyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic factors affecting the risk of thoracic progression in extensive-stage small cell lung cancer</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2016-03-08</date><risdate>2016</risdate><volume>16</volume><issue>199</issue><spage>197</spage><epage>197</epage><pages>197-197</pages><artnum>197</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>The efficacy of combined modality therapy is evaluated for patients with extensive-stage (ES) small cell lung cancer (SCLC). This study evaluated prognostic factors affecting the risk of thoracic progression in ES-SCLC patients likely to undergo thoracic radiotherapy combined chemotherapy.
A retrospective review of ES-SCLC patients who had received systemic chemotherapy at our hospital was performed. Tumor size, metastatic sites, and laboratory data at diagnosis were evaluated as potential prognostic factors. In ES-SCLC patients without pleural dissemination, the rate of thoracic progression after initial chemotherapy was assessed.
Eighty-three of 96 consecutive ES-SCLC patients were analyzed. The overall response rate was 55 %, median progression free survival was 5.0 months (mo), and overall survival (OS) was 9.2 mo. Tumor size (19.4 mo for ≤3 cm vs. 8.5 mo for >3 cm, p = 0.017) and the number of metastatic sites (12.9 mo for single sites vs. 7.1 mo for multiple sites, p = 0.015) were prognostic factors, in addition to known prognostic factors such as performance status and the levels of LDH and sodium. Cox proportional hazard model showed that the OS was significantly worse in patients with large (>3 cm) primary tumor size {HR 2.44 [95 % confidential interval (CI) 1.05-5.68], p = 0.038} and multiple metastatic sites [HR 1.81 (95 % CI 1.08-3.04), p = 0.026]. In 51 cases without pleural dissemination, the number of metastatic sites was associated with thoracic progression after initial chemotherapy (65 % for single sites vs. 36 % for multiple sites, p = 0.036).
Large tumor size and multiple metastatic sites at diagnosis significantly predicted poor survival in ES-SCLC patients. Based on the high rate of thoracic progression in ES-SCLC patients with single site of distant metastasis, we should consider thoracic radiotherapy combined with chemotherapy for this population.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26955807</pmid><doi>10.1186/s12885-016-2222-4</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Analysis Cancer therapies Chemotherapy Combined Modality Therapy Confidence intervals Data collection Development and progression Disease Progression Female Hospitals Humans Kaplan-Meier Estimate Lung cancer Lung cancer, Small cell Lung Neoplasms - mortality Lung Neoplasms - pathology Lung Neoplasms - therapy Male Medical imaging Medical prognosis Metastasis Middle Aged Multivariate analysis Neoplasm Metastasis Neoplasm Staging Patient outcomes Prognosis Proportional Hazards Models Radiation therapy Radiotherapy Risk Factors Small Cell Lung Carcinoma - mortality Small Cell Lung Carcinoma - pathology Small Cell Lung Carcinoma - therapy Thorax - pathology Treatment Outcome Tumor Burden |
title | Prognostic factors affecting the risk of thoracic progression in extensive-stage small cell lung cancer |
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