Predictors of Spermatogenesis in Orchiectomy Specimens
Objective To evaluate the presence of spermatogenesis in orchiectomy specimens of patients with testicular cancer to determine possible predictors of success with oncologic testicular sperm extraction of the cancerous testis at orchiectomy. Materials and Methods We retrospectively reviewed the patho...
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description | Objective To evaluate the presence of spermatogenesis in orchiectomy specimens of patients with testicular cancer to determine possible predictors of success with oncologic testicular sperm extraction of the cancerous testis at orchiectomy. Materials and Methods We retrospectively reviewed the pathology reports and slides from 83 men who underwent radical orchiectomy for testicular cancer at 2 institutions from 1999 to 2010. The presence or absence of spermatogenesis in each specimen was determined. Data on tumor histopathologic type, serum tumor markers, and tumor size were also obtained and analyzed to detect any associations with the presence of spermatogenesis. Results The 83 specimens included 41 pure seminomas, 36 nonseminomatous and mixed germ cell tumors, and 6 benign lesions. Overall, spermatogenesis was detected in 48 of 77 (62%) cancerous specimens. Spermatogenesis was present in 22 of 41 (54%) pure seminomas and 26 of 36 (72%) nonseminomatous and mixed germ cell tumors, with no significant difference found between the 2 subtypes ( P = .11). No association was found between tumor marker levels and the presence of spermatogenesis. A logistic regression model revealed a statistically significant inverse relationship between tumor size and spermatogenesis presence ( P = .004). Conclusion At orchiectomy, most cancerous testes contained active spermatogenesis and, thus, represent a viable source for sperm cryopreservation with oncologic testicular sperm extraction. A small tumor size proved to be a positive prognostic indicator for the presence of spermatogenesis, although a larger tumor size did not preclude the presence of spermatogenesis. |
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Joseph ; Bell, Stephen W ; Cashy, John ; Brannigan, Robert E ; Köhler, Tobias S</creator><creatorcontrib>Choy, Jeremy T ; Wiser, H. Joseph ; Bell, Stephen W ; Cashy, John ; Brannigan, Robert E ; Köhler, Tobias S</creatorcontrib><description>Objective To evaluate the presence of spermatogenesis in orchiectomy specimens of patients with testicular cancer to determine possible predictors of success with oncologic testicular sperm extraction of the cancerous testis at orchiectomy. Materials and Methods We retrospectively reviewed the pathology reports and slides from 83 men who underwent radical orchiectomy for testicular cancer at 2 institutions from 1999 to 2010. The presence or absence of spermatogenesis in each specimen was determined. Data on tumor histopathologic type, serum tumor markers, and tumor size were also obtained and analyzed to detect any associations with the presence of spermatogenesis. Results The 83 specimens included 41 pure seminomas, 36 nonseminomatous and mixed germ cell tumors, and 6 benign lesions. Overall, spermatogenesis was detected in 48 of 77 (62%) cancerous specimens. Spermatogenesis was present in 22 of 41 (54%) pure seminomas and 26 of 36 (72%) nonseminomatous and mixed germ cell tumors, with no significant difference found between the 2 subtypes ( P = .11). No association was found between tumor marker levels and the presence of spermatogenesis. A logistic regression model revealed a statistically significant inverse relationship between tumor size and spermatogenesis presence ( P = .004). Conclusion At orchiectomy, most cancerous testes contained active spermatogenesis and, thus, represent a viable source for sperm cryopreservation with oncologic testicular sperm extraction. A small tumor size proved to be a positive prognostic indicator for the presence of spermatogenesis, although a larger tumor size did not preclude the presence of spermatogenesis.</description><identifier>ISSN: 0090-4295</identifier><identifier>EISSN: 1527-9995</identifier><identifier>DOI: 10.1016/j.urology.2012.10.038</identifier><identifier>PMID: 23374785</identifier><identifier>CODEN: URGYAZ</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adenomatoid Tumor - pathology ; Adenomatoid Tumor - surgery ; alpha-Fetoproteins - metabolism ; Biological and medical sciences ; Chorionic Gonadotropin, beta Subunit, Human - blood ; Humans ; Leydig Cell Tumor - pathology ; Leydig Cell Tumor - surgery ; Logistic Models ; Male ; Medical sciences ; Neoplasms, Germ Cell and Embryonal - pathology ; Neoplasms, Germ Cell and Embryonal - surgery ; Nephrology. Urinary tract diseases ; Orchiectomy ; Probability ; Retrospective Studies ; Seminoma - pathology ; Seminoma - surgery ; Sperm Retrieval ; Spermatogenesis ; Testicular Neoplasms - pathology ; Testicular Neoplasms - physiopathology ; Testicular Neoplasms - surgery ; Tumor Burden ; Urology</subject><ispartof>Urology (Ridgewood, N.J.), 2013-02, Vol.81 (2), p.288-292</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-d253a2c018f01594846b13d46b4421416d0ed5d2277207d45ba17d874817e5a93</citedby><cites>FETCH-LOGICAL-c450t-d253a2c018f01594846b13d46b4421416d0ed5d2277207d45ba17d874817e5a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0090429512013015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27042263$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23374785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choy, Jeremy T</creatorcontrib><creatorcontrib>Wiser, H. Joseph</creatorcontrib><creatorcontrib>Bell, Stephen W</creatorcontrib><creatorcontrib>Cashy, John</creatorcontrib><creatorcontrib>Brannigan, Robert E</creatorcontrib><creatorcontrib>Köhler, Tobias S</creatorcontrib><title>Predictors of Spermatogenesis in Orchiectomy Specimens</title><title>Urology (Ridgewood, N.J.)</title><addtitle>Urology</addtitle><description>Objective To evaluate the presence of spermatogenesis in orchiectomy specimens of patients with testicular cancer to determine possible predictors of success with oncologic testicular sperm extraction of the cancerous testis at orchiectomy. Materials and Methods We retrospectively reviewed the pathology reports and slides from 83 men who underwent radical orchiectomy for testicular cancer at 2 institutions from 1999 to 2010. The presence or absence of spermatogenesis in each specimen was determined. Data on tumor histopathologic type, serum tumor markers, and tumor size were also obtained and analyzed to detect any associations with the presence of spermatogenesis. Results The 83 specimens included 41 pure seminomas, 36 nonseminomatous and mixed germ cell tumors, and 6 benign lesions. Overall, spermatogenesis was detected in 48 of 77 (62%) cancerous specimens. Spermatogenesis was present in 22 of 41 (54%) pure seminomas and 26 of 36 (72%) nonseminomatous and mixed germ cell tumors, with no significant difference found between the 2 subtypes ( P = .11). No association was found between tumor marker levels and the presence of spermatogenesis. A logistic regression model revealed a statistically significant inverse relationship between tumor size and spermatogenesis presence ( P = .004). Conclusion At orchiectomy, most cancerous testes contained active spermatogenesis and, thus, represent a viable source for sperm cryopreservation with oncologic testicular sperm extraction. A small tumor size proved to be a positive prognostic indicator for the presence of spermatogenesis, although a larger tumor size did not preclude the presence of spermatogenesis.</description><subject>Adenomatoid Tumor - pathology</subject><subject>Adenomatoid Tumor - surgery</subject><subject>alpha-Fetoproteins - metabolism</subject><subject>Biological and medical sciences</subject><subject>Chorionic Gonadotropin, beta Subunit, Human - blood</subject><subject>Humans</subject><subject>Leydig Cell Tumor - pathology</subject><subject>Leydig Cell Tumor - surgery</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neoplasms, Germ Cell and Embryonal - pathology</subject><subject>Neoplasms, Germ Cell and Embryonal - surgery</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Orchiectomy</subject><subject>Probability</subject><subject>Retrospective Studies</subject><subject>Seminoma - pathology</subject><subject>Seminoma - surgery</subject><subject>Sperm Retrieval</subject><subject>Spermatogenesis</subject><subject>Testicular Neoplasms - pathology</subject><subject>Testicular Neoplasms - physiopathology</subject><subject>Testicular Neoplasms - surgery</subject><subject>Tumor Burden</subject><subject>Urology</subject><issn>0090-4295</issn><issn>1527-9995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVFrFDEQx4NY7Fn7EZR7Efqy18kk2ey-KKW0KhQq1D6HXDJbc-5uzuS2cN_eLHcq-OJLApPf_Cf8hrG3HFYceH25WU0p9vFpv0LgWGorEM0LtuAKddW2rXrJFgAtVBJbdcpe57wBgLqu9St2ikJoqRu1YPXXRD64XUx5Gbvlw5bSYHfxiUbKIS_DuLxP7nugQgz7-dmFgcb8hp10ts90frzP2OPtzbfrz9Xd_acv11d3lZMKdpVHJSw64E0HXLWykfWaC19OKZFLXnsgrzyi1gjaS7W2XPtGy4ZrUrYVZ-zikLtN8edEeWeGkB31vR0pTtlwbCQ2LWgsqDqgLsWcE3Vmm8Jg095wMLMyszFHZWZWNpeLstL37jhiWg_k_3T9dlSA90fAZmf7LtnRhfyX0yARa1G4jweOipDnQMlkF2h0xW8q_oyP4b9f-fBPguvDGMrQH7SnvIlTGottw01GA-Zh3u-8Xl5CRBEsfgH9l5-t</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Choy, Jeremy T</creator><creator>Wiser, H. Joseph</creator><creator>Bell, Stephen W</creator><creator>Cashy, John</creator><creator>Brannigan, Robert E</creator><creator>Köhler, Tobias S</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>20130201</creationdate><title>Predictors of Spermatogenesis in Orchiectomy Specimens</title><author>Choy, Jeremy T ; Wiser, H. Joseph ; Bell, Stephen W ; Cashy, John ; Brannigan, Robert E ; Köhler, Tobias S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-d253a2c018f01594846b13d46b4421416d0ed5d2277207d45ba17d874817e5a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenomatoid Tumor - pathology</topic><topic>Adenomatoid Tumor - surgery</topic><topic>alpha-Fetoproteins - metabolism</topic><topic>Biological and medical sciences</topic><topic>Chorionic Gonadotropin, beta Subunit, Human - blood</topic><topic>Humans</topic><topic>Leydig Cell Tumor - pathology</topic><topic>Leydig Cell Tumor - surgery</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neoplasms, Germ Cell and Embryonal - pathology</topic><topic>Neoplasms, Germ Cell and Embryonal - surgery</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Orchiectomy</topic><topic>Probability</topic><topic>Retrospective Studies</topic><topic>Seminoma - pathology</topic><topic>Seminoma - surgery</topic><topic>Sperm Retrieval</topic><topic>Spermatogenesis</topic><topic>Testicular Neoplasms - pathology</topic><topic>Testicular Neoplasms - physiopathology</topic><topic>Testicular Neoplasms - surgery</topic><topic>Tumor Burden</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choy, Jeremy T</creatorcontrib><creatorcontrib>Wiser, H. Joseph</creatorcontrib><creatorcontrib>Bell, Stephen W</creatorcontrib><creatorcontrib>Cashy, John</creatorcontrib><creatorcontrib>Brannigan, Robert E</creatorcontrib><creatorcontrib>Köhler, Tobias S</creatorcontrib><collection>Pascal-Francis</collection><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>Urology (Ridgewood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choy, Jeremy T</au><au>Wiser, H. Joseph</au><au>Bell, Stephen W</au><au>Cashy, John</au><au>Brannigan, Robert E</au><au>Köhler, Tobias S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictors of Spermatogenesis in Orchiectomy Specimens</atitle><jtitle>Urology (Ridgewood, N.J.)</jtitle><addtitle>Urology</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>81</volume><issue>2</issue><spage>288</spage><epage>292</epage><pages>288-292</pages><issn>0090-4295</issn><eissn>1527-9995</eissn><coden>URGYAZ</coden><abstract>Objective To evaluate the presence of spermatogenesis in orchiectomy specimens of patients with testicular cancer to determine possible predictors of success with oncologic testicular sperm extraction of the cancerous testis at orchiectomy. Materials and Methods We retrospectively reviewed the pathology reports and slides from 83 men who underwent radical orchiectomy for testicular cancer at 2 institutions from 1999 to 2010. The presence or absence of spermatogenesis in each specimen was determined. Data on tumor histopathologic type, serum tumor markers, and tumor size were also obtained and analyzed to detect any associations with the presence of spermatogenesis. Results The 83 specimens included 41 pure seminomas, 36 nonseminomatous and mixed germ cell tumors, and 6 benign lesions. Overall, spermatogenesis was detected in 48 of 77 (62%) cancerous specimens. Spermatogenesis was present in 22 of 41 (54%) pure seminomas and 26 of 36 (72%) nonseminomatous and mixed germ cell tumors, with no significant difference found between the 2 subtypes ( P = .11). No association was found between tumor marker levels and the presence of spermatogenesis. A logistic regression model revealed a statistically significant inverse relationship between tumor size and spermatogenesis presence ( P = .004). Conclusion At orchiectomy, most cancerous testes contained active spermatogenesis and, thus, represent a viable source for sperm cryopreservation with oncologic testicular sperm extraction. A small tumor size proved to be a positive prognostic indicator for the presence of spermatogenesis, although a larger tumor size did not preclude the presence of spermatogenesis.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>23374785</pmid><doi>10.1016/j.urology.2012.10.038</doi><tpages>5</tpages></addata></record> |
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subjects | Adenomatoid Tumor - pathology Adenomatoid Tumor - surgery alpha-Fetoproteins - metabolism Biological and medical sciences Chorionic Gonadotropin, beta Subunit, Human - blood Humans Leydig Cell Tumor - pathology Leydig Cell Tumor - surgery Logistic Models Male Medical sciences Neoplasms, Germ Cell and Embryonal - pathology Neoplasms, Germ Cell and Embryonal - surgery Nephrology. Urinary tract diseases Orchiectomy Probability Retrospective Studies Seminoma - pathology Seminoma - surgery Sperm Retrieval Spermatogenesis Testicular Neoplasms - pathology Testicular Neoplasms - physiopathology Testicular Neoplasms - surgery Tumor Burden Urology |
title | Predictors of Spermatogenesis in Orchiectomy Specimens |
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