The relative value of conventional staging procedures for developing prognostic models in extensive-stage small-cell lung cancer
Published prognostic models for small-cell lung cancer (SCLC) have either combined limited- and extensive-stage patients or have not included standard anatomic staging information to assess the relative value of the knowledge of specific sites and number of sites of metastases in predicting survival...
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Veröffentlicht in: | Journal of clinical oncology 1990-12, Vol.8 (12), p.2047-2053 |
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creator | Sheehan, R G Balaban, E P Cox, J V Frenkel, E P |
description | Published prognostic models for small-cell lung cancer (SCLC) have either combined limited- and extensive-stage patients or have not included standard anatomic staging information to assess the relative value of the knowledge of specific sites and number of sites of metastases in predicting survival in extensive-stage disease. We studied 136 extensive-stage patients in whom traditional staging procedures were performed and in whom other previously demonstrated significant pretreatment variables were determined. Using the Cox proportional hazards model, when all data were included, three variables were significant: performance status (PS) (P = .0001), number of sites of metastases (P = .0010), and age (P = .0029). A prognostic algorithm was developed using these variables, which divided the patients into three distinct groups. When the anatomic staging data were omitted, the serum albumin (P = .0313) was the only variable in addition to PS (P = .0001) and age (P = .0064) that was significant. An alternative algorithm using these three variables was nearly as predictive as the original. Therefore, in extensive-stage patients, reasonable pretreatment prognostic information can be obtained without using the number or specific sites of metastases as variables once the presence of distant metastases has been demonstrated. |
doi_str_mv | 10.1200/jco.1990.8.12.2047 |
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We studied 136 extensive-stage patients in whom traditional staging procedures were performed and in whom other previously demonstrated significant pretreatment variables were determined. Using the Cox proportional hazards model, when all data were included, three variables were significant: performance status (PS) (P = .0001), number of sites of metastases (P = .0010), and age (P = .0029). A prognostic algorithm was developed using these variables, which divided the patients into three distinct groups. When the anatomic staging data were omitted, the serum albumin (P = .0313) was the only variable in addition to PS (P = .0001) and age (P = .0064) that was significant. An alternative algorithm using these three variables was nearly as predictive as the original. 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We studied 136 extensive-stage patients in whom traditional staging procedures were performed and in whom other previously demonstrated significant pretreatment variables were determined. Using the Cox proportional hazards model, when all data were included, three variables were significant: performance status (PS) (P = .0001), number of sites of metastases (P = .0010), and age (P = .0029). A prognostic algorithm was developed using these variables, which divided the patients into three distinct groups. When the anatomic staging data were omitted, the serum albumin (P = .0313) was the only variable in addition to PS (P = .0001) and age (P = .0064) that was significant. An alternative algorithm using these three variables was nearly as predictive as the original. Therefore, in extensive-stage patients, reasonable pretreatment prognostic information can be obtained without using the number or specific sites of metastases as variables once the presence of distant metastases has been demonstrated.</description><subject>Carcinoma, Small Cell - mortality</subject><subject>Carcinoma, Small Cell - pathology</subject><subject>Humans</subject><subject>Lung Neoplasms - mortality</subject><subject>Lung Neoplasms - pathology</subject><subject>Neoplasm Staging - methods</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Survival Analysis</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc2KFDEUhYMoYzv6AoKQlbtqb_4qVUtp_GVgNiO4C-nUre4MqaRNqlrd-eimnMZZhUvO-XL5QshrBlvGAd7du7RlfQ_brs5bDlI_IRumuG60Vuop2YAWvGGd-P6cvCjlHoDJTqgrcsWZ5lLLDflzd0SaMdjZn5GebViQppG6FM8YZ5-iDbTM9uDjgZ5ycjgsGQsdU6YDnjGk0-XmEFOZvaNTGjAU6iPFXzPGUrHNCkBaJhtC4zAEGpZacjY6zC_Js9GGgq8u5zX59vHD3e5zc3P76cvu_U3jRK_mxgoH7QC2HfYSBwGsFaKXTDrlBOularkc9KiUZbzbI1fW9apHKTW0AFZqcU3ePnDrrj8WLLOZfFmXsRHTUkwH0MkeoAb5Q9DlVErG0Zyyn2z-bRiYVbv5urs1q3bT1dms2mvpzYW-7Ccc_lcunh9fP_rD8afPaP7ZqGlu6i8-gv4CnQqNcg</recordid><startdate>19901201</startdate><enddate>19901201</enddate><creator>Sheehan, R G</creator><creator>Balaban, E P</creator><creator>Cox, J V</creator><creator>Frenkel, E P</creator><general>American Society of Clinical Oncology</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>7X8</scope></search><sort><creationdate>19901201</creationdate><title>The relative value of conventional staging procedures for developing prognostic models in extensive-stage small-cell lung cancer</title><author>Sheehan, R G ; Balaban, E P ; Cox, J V ; Frenkel, E P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-a3c06d0a6db4ed3016339414c5c31945624d7f55a128be25ac959e4470600a473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Carcinoma, Small Cell - mortality</topic><topic>Carcinoma, Small Cell - pathology</topic><topic>Humans</topic><topic>Lung Neoplasms - mortality</topic><topic>Lung Neoplasms - pathology</topic><topic>Neoplasm Staging - methods</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheehan, R G</creatorcontrib><creatorcontrib>Balaban, E P</creatorcontrib><creatorcontrib>Cox, J V</creatorcontrib><creatorcontrib>Frenkel, E P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sheehan, R G</au><au>Balaban, E P</au><au>Cox, J V</au><au>Frenkel, E P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The relative value of conventional staging procedures for developing prognostic models in extensive-stage small-cell lung cancer</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>1990-12-01</date><risdate>1990</risdate><volume>8</volume><issue>12</issue><spage>2047</spage><epage>2053</epage><pages>2047-2053</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>Published prognostic models for small-cell lung cancer (SCLC) have either combined limited- and extensive-stage patients or have not included standard anatomic staging information to assess the relative value of the knowledge of specific sites and number of sites of metastases in predicting survival in extensive-stage disease. We studied 136 extensive-stage patients in whom traditional staging procedures were performed and in whom other previously demonstrated significant pretreatment variables were determined. Using the Cox proportional hazards model, when all data were included, three variables were significant: performance status (PS) (P = .0001), number of sites of metastases (P = .0010), and age (P = .0029). A prognostic algorithm was developed using these variables, which divided the patients into three distinct groups. When the anatomic staging data were omitted, the serum albumin (P = .0313) was the only variable in addition to PS (P = .0001) and age (P = .0064) that was significant. An alternative algorithm using these three variables was nearly as predictive as the original. Therefore, in extensive-stage patients, reasonable pretreatment prognostic information can be obtained without using the number or specific sites of metastases as variables once the presence of distant metastases has been demonstrated.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>2172474</pmid><doi>10.1200/jco.1990.8.12.2047</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; Journals@Ovid Complete |
subjects | Carcinoma, Small Cell - mortality Carcinoma, Small Cell - pathology Humans Lung Neoplasms - mortality Lung Neoplasms - pathology Neoplasm Staging - methods Prognosis Prospective Studies Survival Analysis |
title | The relative value of conventional staging procedures for developing prognostic models in extensive-stage small-cell lung cancer |
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