Long-term efficacy of
To determine the efficacy of Y [DOTA , D-Phe , Tyr ]-octreotate (DOTATATE) in 67 patients with pancreatic and small bowel neuroendocrine tumors (NETs). The primary efficacy end point was overall survival (OS) and secondary end points were progression-free survival (PFS) and tumor response. Median PF...
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Veröffentlicht in: | Future oncology (London, England) England), 2016-08, Vol.12 (16), p.1877-1885 |
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container_title | Future oncology (London, England) |
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creator | Rogowski, Wojciech Wachu a, Ewa Lewczuk, Anna Buscombe, John R Seklecka, Nina Sankowski, Artur wik a, Jaros aw B |
description | To determine the efficacy of
Y [DOTA
, D-Phe
, Tyr
]-octreotate (DOTATATE) in 67 patients with pancreatic and small bowel neuroendocrine tumors (NETs).
The primary efficacy end point was overall survival (OS) and secondary end points were progression-free survival (PFS) and tumor response.
Median PFS in pancreatic and small bowel NETs was 25 and 28 months, respectively, and median OS was 42 and 38.5 months, respectively. No intergroup differences in median OS (p = 0.945) or PFS (p = 0.174) were found, also after adjustment for tumor origin, secretory status and grade, and patient's gender.
Y-DOTATATE may have similar efficacy in pancreatic and small bowel NETs. Better WHO performance status at baseline seems to be associated with more favorable outcomes. |
doi_str_mv | 10.2217/fon-2016-0031 |
format | Article |
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Y [DOTA
, D-Phe
, Tyr
]-octreotate (DOTATATE) in 67 patients with pancreatic and small bowel neuroendocrine tumors (NETs).
The primary efficacy end point was overall survival (OS) and secondary end points were progression-free survival (PFS) and tumor response.
Median PFS in pancreatic and small bowel NETs was 25 and 28 months, respectively, and median OS was 42 and 38.5 months, respectively. No intergroup differences in median OS (p = 0.945) or PFS (p = 0.174) were found, also after adjustment for tumor origin, secretory status and grade, and patient's gender.
Y-DOTATATE may have similar efficacy in pancreatic and small bowel NETs. Better WHO performance status at baseline seems to be associated with more favorable outcomes.</description><identifier>ISSN: 1479-6694</identifier><identifier>EISSN: 1744-8301</identifier><identifier>DOI: 10.2217/fon-2016-0031</identifier><language>eng</language><publisher>Future Medicine Ltd</publisher><subject>clinical and radiological response ; GEP-NET ; Y-DOTATATE therapy</subject><ispartof>Future oncology (London, England), 2016-08, Vol.12 (16), p.1877-1885</ispartof><rights>Future Medicine Ltd</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>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Rogowski, Wojciech</creatorcontrib><creatorcontrib>Wachu a, Ewa</creatorcontrib><creatorcontrib>Lewczuk, Anna</creatorcontrib><creatorcontrib>Buscombe, John R</creatorcontrib><creatorcontrib>Seklecka, Nina</creatorcontrib><creatorcontrib>Sankowski, Artur</creatorcontrib><creatorcontrib>wik a, Jaros aw B</creatorcontrib><title>Long-term efficacy of</title><title>Future oncology (London, England)</title><description>To determine the efficacy of
Y [DOTA
, D-Phe
, Tyr
]-octreotate (DOTATATE) in 67 patients with pancreatic and small bowel neuroendocrine tumors (NETs).
The primary efficacy end point was overall survival (OS) and secondary end points were progression-free survival (PFS) and tumor response.
Median PFS in pancreatic and small bowel NETs was 25 and 28 months, respectively, and median OS was 42 and 38.5 months, respectively. No intergroup differences in median OS (p = 0.945) or PFS (p = 0.174) were found, also after adjustment for tumor origin, secretory status and grade, and patient's gender.
Y-DOTATATE may have similar efficacy in pancreatic and small bowel NETs. Better WHO performance status at baseline seems to be associated with more favorable outcomes.</description><subject>clinical and radiological response</subject><subject>GEP-NET</subject><subject>Y-DOTATATE therapy</subject><issn>1479-6694</issn><issn>1744-8301</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqlzr0KwjAUBeCLKFh_xu59gei9TWzsLIqDo3so6Y1EbApNO_j2tugbOJ1zhgMfQEq4y3PSe9cGkSMVAlHSDBLSSomjRJqPXelSFEWplrCK8YmotDxgAumtDQ_Rc9dk7Jy3lX1nrdvAwlWvyNtfrqG8nO-nq3BDP3Qcredg2XxXw7W3PrAhNJPDjA4zOczkkP98P246Pow</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Rogowski, Wojciech</creator><creator>Wachu a, Ewa</creator><creator>Lewczuk, Anna</creator><creator>Buscombe, John R</creator><creator>Seklecka, Nina</creator><creator>Sankowski, Artur</creator><creator>wik a, Jaros aw B</creator><general>Future Medicine Ltd</general><scope/></search><sort><creationdate>20160801</creationdate><title>Long-term efficacy of</title><author>Rogowski, Wojciech ; Wachu a, Ewa ; Lewczuk, Anna ; Buscombe, John R ; Seklecka, Nina ; Sankowski, Artur ; wik a, Jaros aw B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-futurescience_futuremedicine_10_2217_fon_2016_00313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>clinical and radiological response</topic><topic>GEP-NET</topic><topic>Y-DOTATATE therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rogowski, Wojciech</creatorcontrib><creatorcontrib>Wachu a, Ewa</creatorcontrib><creatorcontrib>Lewczuk, Anna</creatorcontrib><creatorcontrib>Buscombe, John R</creatorcontrib><creatorcontrib>Seklecka, Nina</creatorcontrib><creatorcontrib>Sankowski, Artur</creatorcontrib><creatorcontrib>wik a, Jaros aw B</creatorcontrib><jtitle>Future oncology (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rogowski, Wojciech</au><au>Wachu a, Ewa</au><au>Lewczuk, Anna</au><au>Buscombe, John R</au><au>Seklecka, Nina</au><au>Sankowski, Artur</au><au>wik a, Jaros aw B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term efficacy of</atitle><jtitle>Future oncology (London, England)</jtitle><date>2016-08-01</date><risdate>2016</risdate><volume>12</volume><issue>16</issue><spage>1877</spage><epage>1885</epage><pages>1877-1885</pages><issn>1479-6694</issn><eissn>1744-8301</eissn><abstract>To determine the efficacy of
Y [DOTA
, D-Phe
, Tyr
]-octreotate (DOTATATE) in 67 patients with pancreatic and small bowel neuroendocrine tumors (NETs).
The primary efficacy end point was overall survival (OS) and secondary end points were progression-free survival (PFS) and tumor response.
Median PFS in pancreatic and small bowel NETs was 25 and 28 months, respectively, and median OS was 42 and 38.5 months, respectively. No intergroup differences in median OS (p = 0.945) or PFS (p = 0.174) were found, also after adjustment for tumor origin, secretory status and grade, and patient's gender.
Y-DOTATATE may have similar efficacy in pancreatic and small bowel NETs. Better WHO performance status at baseline seems to be associated with more favorable outcomes.</abstract><pub>Future Medicine Ltd</pub><doi>10.2217/fon-2016-0031</doi></addata></record> |
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identifier | ISSN: 1479-6694 |
ispartof | Future oncology (London, England), 2016-08, Vol.12 (16), p.1877-1885 |
issn | 1479-6694 1744-8301 |
language | eng |
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source | PubMed Central |
subjects | clinical and radiological response GEP-NET Y-DOTATATE therapy |
title | Long-term efficacy of |
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