Wnt Signaling and Survival of Women With High-Grade Serous Ovarian Cancer: A Brief Report
Ovarian cancer is the gynecologic malignancy with the highest case-fatality rate due to the development of chemotherapy resistance. Predictors of chemotherapy response are needed to guide chemotherapy selection and improve survival for patients with ovarian cancer. Wnt signaling may impact chemoresi...
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Veröffentlicht in: | International journal of gynecological cancer 2016-07, Vol.26 (6), p.1078 |
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container_title | International journal of gynecological cancer |
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creator | Seagle, Brandon-Luke L Dandapani, Monica Yeh, Judy Y Shahabi, Shohreh |
description | Ovarian cancer is the gynecologic malignancy with the highest case-fatality rate due to the development of chemotherapy resistance. Predictors of chemotherapy response are needed to guide chemotherapy selection and improve survival for patients with ovarian cancer. Wnt signaling may impact chemoresistance in ovarian cancer.
We studied The Cancer Genome Atlas patients with ovarian cancer treated with intraperitoneal or intravenous-only adjuvant chemotherapy. Cox regression tested associations of expression of 26 Wnt pathway genes with progression-free survival and overall survival. Permutation tests compared survival between chemotherapy groups stratified by expression.
values are two-tailed.
Increased
was associated with increased survival (intraperitoneal group, overall survival: hazard ratio [HR], 0.25; 95% confidence interval [CI], 0.11-0.72,
= 0.009; progression-free survival: HR, 0.58; 95% CI, 0.37-0.92,
= 0.020) (intravenous-only group, overall survival: HR, 0.85; 95% CI, 0.72-0.99,
= 0.039; progression-free survival: HR, 0.83; 95% CI, 0.73-0.95,
= 0.006). Low
predicted decreased overall survival after intraperitoneal versus intravenous-only chemotherapy (21.7 vs 33.3 months,
< 0.0001). Increased
was associated with decreased overall survival (HR, 1.22; 95% CI, 1.05-1.42;
= 0.009) and progression-free survival (HR, 1.28; 95% CI, 1.12-1.45;
= 0.0002).
Up-regulated tumor Wnt signaling predicts increased ovarian cancer survival.
may predict benefit from intraperitoneal chemotherapy. |
doi_str_mv | 10.1097/IGC.0000000000000726 |
format | Article |
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We studied The Cancer Genome Atlas patients with ovarian cancer treated with intraperitoneal or intravenous-only adjuvant chemotherapy. Cox regression tested associations of expression of 26 Wnt pathway genes with progression-free survival and overall survival. Permutation tests compared survival between chemotherapy groups stratified by expression.
values are two-tailed.
Increased
was associated with increased survival (intraperitoneal group, overall survival: hazard ratio [HR], 0.25; 95% confidence interval [CI], 0.11-0.72,
= 0.009; progression-free survival: HR, 0.58; 95% CI, 0.37-0.92,
= 0.020) (intravenous-only group, overall survival: HR, 0.85; 95% CI, 0.72-0.99,
= 0.039; progression-free survival: HR, 0.83; 95% CI, 0.73-0.95,
= 0.006). Low
predicted decreased overall survival after intraperitoneal versus intravenous-only chemotherapy (21.7 vs 33.3 months,
< 0.0001). Increased
was associated with decreased overall survival (HR, 1.22; 95% CI, 1.05-1.42;
= 0.009) and progression-free survival (HR, 1.28; 95% CI, 1.12-1.45;
= 0.0002).
Up-regulated tumor Wnt signaling predicts increased ovarian cancer survival.
may predict benefit from intraperitoneal chemotherapy.</description><identifier>EISSN: 1525-1438</identifier><identifier>DOI: 10.1097/IGC.0000000000000726</identifier><identifier>PMID: 30814169</identifier><language>eng</language><publisher>England</publisher><ispartof>International journal of gynecological cancer, 2016-07, Vol.26 (6), p.1078</ispartof><rights>2016 by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30814169$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seagle, Brandon-Luke L</creatorcontrib><creatorcontrib>Dandapani, Monica</creatorcontrib><creatorcontrib>Yeh, Judy Y</creatorcontrib><creatorcontrib>Shahabi, Shohreh</creatorcontrib><title>Wnt Signaling and Survival of Women With High-Grade Serous Ovarian Cancer: A Brief Report</title><title>International journal of gynecological cancer</title><addtitle>Int J Gynecol Cancer</addtitle><description>Ovarian cancer is the gynecologic malignancy with the highest case-fatality rate due to the development of chemotherapy resistance. Predictors of chemotherapy response are needed to guide chemotherapy selection and improve survival for patients with ovarian cancer. Wnt signaling may impact chemoresistance in ovarian cancer.
We studied The Cancer Genome Atlas patients with ovarian cancer treated with intraperitoneal or intravenous-only adjuvant chemotherapy. Cox regression tested associations of expression of 26 Wnt pathway genes with progression-free survival and overall survival. Permutation tests compared survival between chemotherapy groups stratified by expression.
values are two-tailed.
Increased
was associated with increased survival (intraperitoneal group, overall survival: hazard ratio [HR], 0.25; 95% confidence interval [CI], 0.11-0.72,
= 0.009; progression-free survival: HR, 0.58; 95% CI, 0.37-0.92,
= 0.020) (intravenous-only group, overall survival: HR, 0.85; 95% CI, 0.72-0.99,
= 0.039; progression-free survival: HR, 0.83; 95% CI, 0.73-0.95,
= 0.006). Low
predicted decreased overall survival after intraperitoneal versus intravenous-only chemotherapy (21.7 vs 33.3 months,
< 0.0001). Increased
was associated with decreased overall survival (HR, 1.22; 95% CI, 1.05-1.42;
= 0.009) and progression-free survival (HR, 1.28; 95% CI, 1.12-1.45;
= 0.0002).
Up-regulated tumor Wnt signaling predicts increased ovarian cancer survival.
may predict benefit from intraperitoneal chemotherapy.</description><issn>1525-1438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFjssKgkAUhocgur9BxHkBa0a72a6ktFWQgbSKU442oaMcL9Db16KgXf_mg49v8TM2FHwsuL2Y7F1nzH-3MOcN1hEzc2aIqbVss25RPN7eNrndYm2LL8VUzO0OOwe6BF_FGhOlY0Adgl9RrWpMIIsgyFKpIVDlHTwV3w2XMJTgS8qqAg41kkINDuqbpBWsYUNKRnCUeUZlnzUjTAo5-LDHRrvtyfGMvLqmMrzkpFKk5-X7xfobvAB0SkPM</recordid><startdate>201607</startdate><enddate>201607</enddate><creator>Seagle, Brandon-Luke L</creator><creator>Dandapani, Monica</creator><creator>Yeh, Judy Y</creator><creator>Shahabi, Shohreh</creator><scope>NPM</scope></search><sort><creationdate>201607</creationdate><title>Wnt Signaling and Survival of Women With High-Grade Serous Ovarian Cancer: A Brief Report</title><author>Seagle, Brandon-Luke L ; Dandapani, Monica ; Yeh, Judy Y ; Shahabi, Shohreh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_308141693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seagle, Brandon-Luke L</creatorcontrib><creatorcontrib>Dandapani, Monica</creatorcontrib><creatorcontrib>Yeh, Judy Y</creatorcontrib><creatorcontrib>Shahabi, Shohreh</creatorcontrib><collection>PubMed</collection><jtitle>International journal of gynecological cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seagle, Brandon-Luke L</au><au>Dandapani, Monica</au><au>Yeh, Judy Y</au><au>Shahabi, Shohreh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Wnt Signaling and Survival of Women With High-Grade Serous Ovarian Cancer: A Brief Report</atitle><jtitle>International journal of gynecological cancer</jtitle><addtitle>Int J Gynecol Cancer</addtitle><date>2016-07</date><risdate>2016</risdate><volume>26</volume><issue>6</issue><spage>1078</spage><pages>1078-</pages><eissn>1525-1438</eissn><abstract>Ovarian cancer is the gynecologic malignancy with the highest case-fatality rate due to the development of chemotherapy resistance. Predictors of chemotherapy response are needed to guide chemotherapy selection and improve survival for patients with ovarian cancer. Wnt signaling may impact chemoresistance in ovarian cancer.
We studied The Cancer Genome Atlas patients with ovarian cancer treated with intraperitoneal or intravenous-only adjuvant chemotherapy. Cox regression tested associations of expression of 26 Wnt pathway genes with progression-free survival and overall survival. Permutation tests compared survival between chemotherapy groups stratified by expression.
values are two-tailed.
Increased
was associated with increased survival (intraperitoneal group, overall survival: hazard ratio [HR], 0.25; 95% confidence interval [CI], 0.11-0.72,
= 0.009; progression-free survival: HR, 0.58; 95% CI, 0.37-0.92,
= 0.020) (intravenous-only group, overall survival: HR, 0.85; 95% CI, 0.72-0.99,
= 0.039; progression-free survival: HR, 0.83; 95% CI, 0.73-0.95,
= 0.006). Low
predicted decreased overall survival after intraperitoneal versus intravenous-only chemotherapy (21.7 vs 33.3 months,
< 0.0001). Increased
was associated with decreased overall survival (HR, 1.22; 95% CI, 1.05-1.42;
= 0.009) and progression-free survival (HR, 1.28; 95% CI, 1.12-1.45;
= 0.0002).
Up-regulated tumor Wnt signaling predicts increased ovarian cancer survival.
may predict benefit from intraperitoneal chemotherapy.</abstract><cop>England</cop><pmid>30814169</pmid><doi>10.1097/IGC.0000000000000726</doi></addata></record> |
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issn | 1525-1438 |
language | eng |
recordid | cdi_pubmed_primary_30814169 |
source | Journals@Ovid Complete |
title | Wnt Signaling and Survival of Women With High-Grade Serous Ovarian Cancer: A Brief Report |
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