Adrenocortical carcinoma: Single center experience
Adrenocortical carcinoma is an aggressive endocrine malignancy with an annual incidence of 0.5-2 cases per million. The most important factors that determine prognosis are tumor stage at the time of diagnosis and the success of surgery. However, advanced age, large tumor size, hormone secretion, hig...
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Veröffentlicht in: | Turkish journal of urology 2017-12, Vol.43 (4), p.462-469 |
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creator | Şişman, Pınar Şahin, Ahmet Bilgehan Peynirci, Hande Cander, Soner Gül, Özen Öz Ertürk, Erdinç Ersoy, Canan |
description | Adrenocortical carcinoma is an aggressive endocrine malignancy with an annual incidence of 0.5-2 cases per million. The most important factors that determine prognosis are tumor stage at the time of diagnosis and the success of surgery. However, advanced age, large tumor size, hormone secretion, high Ki-67 index (>10%), tumor necrosis and high mitotic activity are other factors associated with poor prognosis. In the present study, we aimed to evaluate the contribution of the patient and treatment- related factors to the prognosis in adrenocortical carcinoma.
We included 15 adrenocortical carcinoma patients who were followed in our center between 2005 and 2015. The effects of age, gender, tumor size, type of operation, postoperative resection status and adjuvant treatment on disease-free survival and overall survival were analyzed.
Disease-free survival was 23.32±3.69 months and overall survival was 36.60±10.78 months. Gender, tumor size, tumor stage, type of operation, hormonal activity, presence of necrosis, recurrence and development of metastasis were not found to be associated with disease-free survival and overall survival (p>0.05). Postoperatively applied adjuvant treatments including mitotane, chemotherapy and radiotherapy did not significantly affect disease-free survival in our study, but statistically significant increase in overall survival was observed in patients getting adjuvant treatments (p=0.006).
Adrenocortical carcinoma has poor prognosis and short overall survival, and in its clinical course, recurrence and development of metastasis can be commonly observed even after complete resection of the tumor. Therefore, the patients should be evaluated carefully while determining the surgical procedure during the preoperative period, and the operation and post-operative follow-up should be performed in experienced centers. However, due to the positive effects of adjuvant treatments on survival, all patients should be evaluated postoperatively for the necessity of adjuvant treatments, especially mitotane. |
doi_str_mv | 10.5152/tud.2017.81598 |
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We included 15 adrenocortical carcinoma patients who were followed in our center between 2005 and 2015. The effects of age, gender, tumor size, type of operation, postoperative resection status and adjuvant treatment on disease-free survival and overall survival were analyzed.
Disease-free survival was 23.32±3.69 months and overall survival was 36.60±10.78 months. Gender, tumor size, tumor stage, type of operation, hormonal activity, presence of necrosis, recurrence and development of metastasis were not found to be associated with disease-free survival and overall survival (p>0.05). Postoperatively applied adjuvant treatments including mitotane, chemotherapy and radiotherapy did not significantly affect disease-free survival in our study, but statistically significant increase in overall survival was observed in patients getting adjuvant treatments (p=0.006).
Adrenocortical carcinoma has poor prognosis and short overall survival, and in its clinical course, recurrence and development of metastasis can be commonly observed even after complete resection of the tumor. Therefore, the patients should be evaluated carefully while determining the surgical procedure during the preoperative period, and the operation and post-operative follow-up should be performed in experienced centers. However, due to the positive effects of adjuvant treatments on survival, all patients should be evaluated postoperatively for the necessity of adjuvant treatments, especially mitotane.</description><identifier>ISSN: 2149-3235</identifier><identifier>EISSN: 2149-3057</identifier><identifier>EISSN: 2980-1478</identifier><identifier>DOI: 10.5152/tud.2017.81598</identifier><identifier>PMID: 29201509</identifier><language>eng</language><publisher>Turkey: Aves Yayincilik Ltd. STI</publisher><subject>Gangrene ; Medical prognosis ; Metastasis ; Neuroendocrine tumors ; Urology ; Urooncology</subject><ispartof>Turkish journal of urology, 2017-12, Vol.43 (4), p.462-469</ispartof><rights>Copyright Aves Yayincilik Ltd. STI. Dec 2017</rights><rights>Copyright 2017 by Turkish Association of Urology 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-5185bd315567dbeca27e0244a4b6ab442d9a9a7a780d70ba9a1fa51cfdbc4ccf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2021783869/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2021783869?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,21388,21389,27924,27925,33530,33744,43659,43805,53791,53793,64385,64389,72469,74104,74302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29201509$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Şişman, Pınar</creatorcontrib><creatorcontrib>Şahin, Ahmet Bilgehan</creatorcontrib><creatorcontrib>Peynirci, Hande</creatorcontrib><creatorcontrib>Cander, Soner</creatorcontrib><creatorcontrib>Gül, Özen Öz</creatorcontrib><creatorcontrib>Ertürk, Erdinç</creatorcontrib><creatorcontrib>Ersoy, Canan</creatorcontrib><title>Adrenocortical carcinoma: Single center experience</title><title>Turkish journal of urology</title><addtitle>Turk J Urol</addtitle><description>Adrenocortical carcinoma is an aggressive endocrine malignancy with an annual incidence of 0.5-2 cases per million. The most important factors that determine prognosis are tumor stage at the time of diagnosis and the success of surgery. However, advanced age, large tumor size, hormone secretion, high Ki-67 index (>10%), tumor necrosis and high mitotic activity are other factors associated with poor prognosis. In the present study, we aimed to evaluate the contribution of the patient and treatment- related factors to the prognosis in adrenocortical carcinoma.
We included 15 adrenocortical carcinoma patients who were followed in our center between 2005 and 2015. The effects of age, gender, tumor size, type of operation, postoperative resection status and adjuvant treatment on disease-free survival and overall survival were analyzed.
Disease-free survival was 23.32±3.69 months and overall survival was 36.60±10.78 months. Gender, tumor size, tumor stage, type of operation, hormonal activity, presence of necrosis, recurrence and development of metastasis were not found to be associated with disease-free survival and overall survival (p>0.05). Postoperatively applied adjuvant treatments including mitotane, chemotherapy and radiotherapy did not significantly affect disease-free survival in our study, but statistically significant increase in overall survival was observed in patients getting adjuvant treatments (p=0.006).
Adrenocortical carcinoma has poor prognosis and short overall survival, and in its clinical course, recurrence and development of metastasis can be commonly observed even after complete resection of the tumor. Therefore, the patients should be evaluated carefully while determining the surgical procedure during the preoperative period, and the operation and post-operative follow-up should be performed in experienced centers. However, due to the positive effects of adjuvant treatments on survival, all patients should be evaluated postoperatively for the necessity of adjuvant treatments, especially mitotane.</description><subject>Gangrene</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Neuroendocrine tumors</subject><subject>Urology</subject><subject>Urooncology</subject><issn>2149-3235</issn><issn>2149-3057</issn><issn>2980-1478</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdUUtLw0AYXESxpfbqUQJevCTuM7vxIJTiCwoe1POyr9SVNFs3iei_N7EP1NM38M03zHwDwCmCGUMMX7adzTBEPBOIFeIAjDGiRUog44c7jAkbgWnTeA0p5TlhAh6DES76MwaLMcAzG10dTIitN6pKjIrG12GlrpInXy8rlxhXty4m7nPtone1cSfgqFRV46bbOQEvtzfP8_t08Xj3MJ8tUkORaFOGBNOWIMZybrUzCnMHMaWK6lxpSrEtVKG44gJaDnWPUakYMqXVhhpTkgm43uiuO71ydvARVSXX0a9U_JJBefl3U_tXuQwfkuWCY1j0AhdbgRjeO9e0cuUb46pK1S50jUQFJxCT_hM99fwf9S10se7jSQwx4oKIfBDMNiwTQ9NEV-7NICiHRmTfiBwakT-N9AdnvyPs6bv_k2-3K4et</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Şişman, Pınar</creator><creator>Şahin, Ahmet Bilgehan</creator><creator>Peynirci, Hande</creator><creator>Cander, Soner</creator><creator>Gül, Özen Öz</creator><creator>Ertürk, Erdinç</creator><creator>Ersoy, Canan</creator><general>Aves Yayincilik Ltd. 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The most important factors that determine prognosis are tumor stage at the time of diagnosis and the success of surgery. However, advanced age, large tumor size, hormone secretion, high Ki-67 index (>10%), tumor necrosis and high mitotic activity are other factors associated with poor prognosis. In the present study, we aimed to evaluate the contribution of the patient and treatment- related factors to the prognosis in adrenocortical carcinoma.
We included 15 adrenocortical carcinoma patients who were followed in our center between 2005 and 2015. The effects of age, gender, tumor size, type of operation, postoperative resection status and adjuvant treatment on disease-free survival and overall survival were analyzed.
Disease-free survival was 23.32±3.69 months and overall survival was 36.60±10.78 months. Gender, tumor size, tumor stage, type of operation, hormonal activity, presence of necrosis, recurrence and development of metastasis were not found to be associated with disease-free survival and overall survival (p>0.05). Postoperatively applied adjuvant treatments including mitotane, chemotherapy and radiotherapy did not significantly affect disease-free survival in our study, but statistically significant increase in overall survival was observed in patients getting adjuvant treatments (p=0.006).
Adrenocortical carcinoma has poor prognosis and short overall survival, and in its clinical course, recurrence and development of metastasis can be commonly observed even after complete resection of the tumor. Therefore, the patients should be evaluated carefully while determining the surgical procedure during the preoperative period, and the operation and post-operative follow-up should be performed in experienced centers. However, due to the positive effects of adjuvant treatments on survival, all patients should be evaluated postoperatively for the necessity of adjuvant treatments, especially mitotane.</abstract><cop>Turkey</cop><pub>Aves Yayincilik Ltd. STI</pub><pmid>29201509</pmid><doi>10.5152/tud.2017.81598</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Gangrene Medical prognosis Metastasis Neuroendocrine tumors Urology Urooncology |
title | Adrenocortical carcinoma: Single center experience |
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