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Grade migration and important prognostic factors in a pathology specimen for radical radiotherapy in prostate cancer patients
The study aimed to evaluate grade migration and prognosis depending on pathologic features in patients with prostate cancer treated with radical external beam radiotherapy. The study included 139 patients with an initial Gleason score of 7 (3+4 or 4+3) i.e., Grade Group 2-3 (GG2-GG3) treated between...
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Published in: | Polish journal of pathology 2022-01, Vol.73 (1), p.27-33 |
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container_title | Polish journal of pathology |
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creator | Majewski, Wojciech Lange, Dariusz Stanek-Widera, Agata Itrych, Bartosz Krzysztofiak, Tomasz Jarząb, Michał Oczko-Wojciechowska, Małgorzata Kajor, Maciej Tarnawski, Rafał |
description | The study aimed to evaluate grade migration and prognosis depending on pathologic features in patients with prostate cancer treated with radical external beam radiotherapy. The study included 139 patients with an initial Gleason score of 7 (3+4 or 4+3) i.e., Grade Group 2-3 (GG2-GG3) treated between 2008 and 2013. The clinical outcome was assessed with respect to biochemical control (BC) and biochemical disease-free survival (bDFS). After re-evaluation, the majority of patients (96 patients – 69%) were up-graded from GG2-3. Finally, there were 4 patients (3%) with grade GG1, 12 patients (9%) – GG2, 27 patients (19%) – GG3, 51 patients (37%) – GG4 and 45 patients (32%) – GG5. In 42 patients (30%) a cribriform pattern was observed. Among the analyzed factors only the GGs were important for BC (p = 0.011) and the cribriform pattern was of borderline significance (p = 0.06). The 5-year biochemical control was 100% in GG1-3 and 84% in GG4-5. The 5-year biochemical control was 81% and 93%, if cribriform or no cribriform pattern was detected, respectively. In conclusion, re-evaluation and verification of pathology specimens in accordance with contemporary rules upgraded the Gleason score in the majority of patients. The aggressive behavior of prostate cancer starts to occur from GG 4. Cribriform pattern almost tripled the biochemical failure rate. |
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The study included 139 patients with an initial Gleason score of 7 (3+4 or 4+3) i.e., Grade Group 2-3 (GG2-GG3) treated between 2008 and 2013. The clinical outcome was assessed with respect to biochemical control (BC) and biochemical disease-free survival (bDFS). After re-evaluation, the majority of patients (96 patients – 69%) were up-graded from GG2-3. Finally, there were 4 patients (3%) with grade GG1, 12 patients (9%) – GG2, 27 patients (19%) – GG3, 51 patients (37%) – GG4 and 45 patients (32%) – GG5. In 42 patients (30%) a cribriform pattern was observed. Among the analyzed factors only the GGs were important for BC (p = 0.011) and the cribriform pattern was of borderline significance (p = 0.06). The 5-year biochemical control was 100% in GG1-3 and 84% in GG4-5. The 5-year biochemical control was 81% and 93%, if cribriform or no cribriform pattern was detected, respectively. In conclusion, re-evaluation and verification of pathology specimens in accordance with contemporary rules upgraded the Gleason score in the majority of patients. The aggressive behavior of prostate cancer starts to occur from GG 4. Cribriform pattern almost tripled the biochemical failure rate.</description><identifier>ISSN: 1233-9687</identifier><identifier>EISSN: 2084-9869</identifier><identifier>DOI: 10.5114/pjp.2022.117174</identifier><language>eng</language><publisher>Warsaw: Termedia Publishing House</publisher><subject>Biopsy ; Cancer therapies ; Clinical outcomes ; cribriform ; grade migration ; Medical prognosis ; Multivariate analysis ; Pathology ; Patients ; Prostate cancer ; Radiation therapy ; radiotherapy</subject><ispartof>Polish journal of pathology, 2022-01, Vol.73 (1), p.27-33</ispartof><rights>2022. This work is published under http://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). 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The study included 139 patients with an initial Gleason score of 7 (3+4 or 4+3) i.e., Grade Group 2-3 (GG2-GG3) treated between 2008 and 2013. The clinical outcome was assessed with respect to biochemical control (BC) and biochemical disease-free survival (bDFS). After re-evaluation, the majority of patients (96 patients – 69%) were up-graded from GG2-3. Finally, there were 4 patients (3%) with grade GG1, 12 patients (9%) – GG2, 27 patients (19%) – GG3, 51 patients (37%) – GG4 and 45 patients (32%) – GG5. In 42 patients (30%) a cribriform pattern was observed. Among the analyzed factors only the GGs were important for BC (p = 0.011) and the cribriform pattern was of borderline significance (p = 0.06). The 5-year biochemical control was 100% in GG1-3 and 84% in GG4-5. The 5-year biochemical control was 81% and 93%, if cribriform or no cribriform pattern was detected, respectively. 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Cribriform pattern almost tripled the biochemical failure rate.</description><subject>Biopsy</subject><subject>Cancer therapies</subject><subject>Clinical outcomes</subject><subject>cribriform</subject><subject>grade migration</subject><subject>Medical prognosis</subject><subject>Multivariate analysis</subject><subject>Pathology</subject><subject>Patients</subject><subject>Prostate cancer</subject><subject>Radiation therapy</subject><subject>radiotherapy</subject><issn>1233-9687</issn><issn>2084-9869</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkc1r3DAQxUVooUuac6-CXHrxRl-WpWMJbRII9NKexVgeb7TYlitpD3vo_145G3LoMDAgfvOYp0fIF872Lefqbj2ue8GE2HPe8U5dkZ1gRjXWaPuB7LiQsrHadJ_ITc5HVksz0Wm5I38fEgxI53BIUEJcKCwDDfMaU4Gl0DXFwxJzCZ6O4EtMmYbK0BXKS5zi4Uzzij7MuNAxJlq1gofpdcbyggnW87ZQZXKBgtTD4jFt6wGXkj-TjyNMGW_e5jX5_eP7r_vH5vnnw9P9t-fGK2ZLwyVabXXvLW9tZ3qu5IAjMlMblB0sF8h4Z6WUgxTjIFlvlLTSc2vZqIW8Jk8X3SHC0a0pzJDOLkJwrw8xHRykanJCpz3DFlQrBjYqDr1BP2LfehTY9txsWl8vWtXUnxPm4uaQPU4TLBhP2QltudKs07ait_-hx3hKS3VaKWOY2UKq1N2F8vWXcsLx_UDO3Jauq-m6LV13SVf-A-JMmTE</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Majewski, Wojciech</creator><creator>Lange, Dariusz</creator><creator>Stanek-Widera, Agata</creator><creator>Itrych, Bartosz</creator><creator>Krzysztofiak, Tomasz</creator><creator>Jarząb, Michał</creator><creator>Oczko-Wojciechowska, Małgorzata</creator><creator>Kajor, Maciej</creator><creator>Tarnawski, Rafał</creator><general>Termedia Publishing House</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20220101</creationdate><title>Grade migration and important prognostic factors in a pathology specimen for radical radiotherapy in prostate cancer patients</title><author>Majewski, Wojciech ; Lange, Dariusz ; Stanek-Widera, Agata ; Itrych, Bartosz ; Krzysztofiak, Tomasz ; Jarząb, Michał ; Oczko-Wojciechowska, Małgorzata ; Kajor, Maciej ; Tarnawski, Rafał</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-13e9696bc915978b143defe08e08a49d912e0179333d32fd30b84393c1990f623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biopsy</topic><topic>Cancer therapies</topic><topic>Clinical outcomes</topic><topic>cribriform</topic><topic>grade migration</topic><topic>Medical prognosis</topic><topic>Multivariate analysis</topic><topic>Pathology</topic><topic>Patients</topic><topic>Prostate cancer</topic><topic>Radiation therapy</topic><topic>radiotherapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Majewski, Wojciech</creatorcontrib><creatorcontrib>Lange, Dariusz</creatorcontrib><creatorcontrib>Stanek-Widera, Agata</creatorcontrib><creatorcontrib>Itrych, Bartosz</creatorcontrib><creatorcontrib>Krzysztofiak, Tomasz</creatorcontrib><creatorcontrib>Jarząb, Michał</creatorcontrib><creatorcontrib>Oczko-Wojciechowska, Małgorzata</creatorcontrib><creatorcontrib>Kajor, Maciej</creatorcontrib><creatorcontrib>Tarnawski, Rafał</creatorcontrib><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest - 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>DOAJ Directory of Open Access Journals</collection><jtitle>Polish journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Majewski, Wojciech</au><au>Lange, Dariusz</au><au>Stanek-Widera, Agata</au><au>Itrych, Bartosz</au><au>Krzysztofiak, Tomasz</au><au>Jarząb, Michał</au><au>Oczko-Wojciechowska, Małgorzata</au><au>Kajor, Maciej</au><au>Tarnawski, Rafał</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Grade migration and important prognostic factors in a pathology specimen for radical radiotherapy in prostate cancer patients</atitle><jtitle>Polish journal of pathology</jtitle><date>2022-01-01</date><risdate>2022</risdate><volume>73</volume><issue>1</issue><spage>27</spage><epage>33</epage><pages>27-33</pages><issn>1233-9687</issn><eissn>2084-9869</eissn><abstract>The study aimed to evaluate grade migration and prognosis depending on pathologic features in patients with prostate cancer treated with radical external beam radiotherapy. The study included 139 patients with an initial Gleason score of 7 (3+4 or 4+3) i.e., Grade Group 2-3 (GG2-GG3) treated between 2008 and 2013. The clinical outcome was assessed with respect to biochemical control (BC) and biochemical disease-free survival (bDFS). After re-evaluation, the majority of patients (96 patients – 69%) were up-graded from GG2-3. Finally, there were 4 patients (3%) with grade GG1, 12 patients (9%) – GG2, 27 patients (19%) – GG3, 51 patients (37%) – GG4 and 45 patients (32%) – GG5. In 42 patients (30%) a cribriform pattern was observed. Among the analyzed factors only the GGs were important for BC (p = 0.011) and the cribriform pattern was of borderline significance (p = 0.06). The 5-year biochemical control was 100% in GG1-3 and 84% in GG4-5. The 5-year biochemical control was 81% and 93%, if cribriform or no cribriform pattern was detected, respectively. In conclusion, re-evaluation and verification of pathology specimens in accordance with contemporary rules upgraded the Gleason score in the majority of patients. The aggressive behavior of prostate cancer starts to occur from GG 4. Cribriform pattern almost tripled the biochemical failure rate.</abstract><cop>Warsaw</cop><pub>Termedia Publishing House</pub><doi>10.5114/pjp.2022.117174</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biopsy Cancer therapies Clinical outcomes cribriform grade migration Medical prognosis Multivariate analysis Pathology Patients Prostate cancer Radiation therapy radiotherapy |
title | Grade migration and important prognostic factors in a pathology specimen for radical radiotherapy in prostate cancer patients |
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