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Repeat stereotactic radiosurgery for Cushing’s disease: outcomes of an international, multicenter study
Stereotactic radiosurgery (SRS) is frequently used for Cushing’s disease (CD) after failed pituitary surgery. Management of patients with persistent CD after failed SRS is complex, as the alternative therapeutic options harbor significant risks. The outcomes of repeat pituitary radiosurgery, however...
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Published in: | Journal of neuro-oncology 2018-07, Vol.138 (3), p.519-525 |
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creator | Mehta, Gautam U. Ding, Dale Gupta, Amitabh Kano, Hideyuki Sisterson, Nathaniel D. Martinez-Moreno, Nuria Kršek, Michal Yang, Huai-Che Lee, Cheng-Chia Liščák, Roman Martinez-Alvarez, Roberto Lunsford, L. Dade Vance, Mary Lee Sheehan, Jason P. |
description | Stereotactic radiosurgery (SRS) is frequently used for Cushing’s disease (CD) after failed pituitary surgery. Management of patients with persistent CD after failed SRS is complex, as the alternative therapeutic options harbor significant risks. The outcomes of repeat pituitary radiosurgery, however, have not been described. We sought to determine the outcomes of repeat SRS in patients with CD. We pooled data from five institutions participating in the International Gamma Knife Research Foundation for patients with recurrent or persistent CD ≥ 12 months after initial SRS. Patients were included in the study if they had ≥ 6 months endocrine follow-up after repeat SRS. Twenty patients were included in the study. Repeat single-session SRS was performed 1.3–9.7 years after initial SRS. Median endocrine follow-up was 6.6 years (1.4–19.1 years). Median margin dose was 20 Gy (range 10.8–35 Gy). Endocrine remission after second SRS was noted in 12 patients (60%), with a median time to remission of 6 months (range 2–64 months). Biochemical recurrence occurred in two patients (17%) after initial remission. Overall, the cumulative rates of durable endocrine remission at 5 and 10 years were 47 and 53%, respectively. Two patients (10%) experienced adverse radiation effects, including transient visual loss and permanent diplopia. Repeat SRS achieves lasting biochemical remission in approximately half of patients with CD refractory to both prior microsurgery and SRS. Because of the morbidity of refractory or recurrent CD, repeat SRS should be considered for carefully selected patients with hypercortisolism confirmed one or more years after initial SRS. |
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Dade ; Vance, Mary Lee ; Sheehan, Jason P.</creator><creatorcontrib>Mehta, Gautam U. ; Ding, Dale ; Gupta, Amitabh ; Kano, Hideyuki ; Sisterson, Nathaniel D. ; Martinez-Moreno, Nuria ; Kršek, Michal ; Yang, Huai-Che ; Lee, Cheng-Chia ; Liščák, Roman ; Martinez-Alvarez, Roberto ; Lunsford, L. Dade ; Vance, Mary Lee ; Sheehan, Jason P.</creatorcontrib><description>Stereotactic radiosurgery (SRS) is frequently used for Cushing’s disease (CD) after failed pituitary surgery. Management of patients with persistent CD after failed SRS is complex, as the alternative therapeutic options harbor significant risks. The outcomes of repeat pituitary radiosurgery, however, have not been described. We sought to determine the outcomes of repeat SRS in patients with CD. We pooled data from five institutions participating in the International Gamma Knife Research Foundation for patients with recurrent or persistent CD ≥ 12 months after initial SRS. Patients were included in the study if they had ≥ 6 months endocrine follow-up after repeat SRS. Twenty patients were included in the study. Repeat single-session SRS was performed 1.3–9.7 years after initial SRS. Median endocrine follow-up was 6.6 years (1.4–19.1 years). Median margin dose was 20 Gy (range 10.8–35 Gy). Endocrine remission after second SRS was noted in 12 patients (60%), with a median time to remission of 6 months (range 2–64 months). Biochemical recurrence occurred in two patients (17%) after initial remission. Overall, the cumulative rates of durable endocrine remission at 5 and 10 years were 47 and 53%, respectively. Two patients (10%) experienced adverse radiation effects, including transient visual loss and permanent diplopia. Repeat SRS achieves lasting biochemical remission in approximately half of patients with CD refractory to both prior microsurgery and SRS. Because of the morbidity of refractory or recurrent CD, repeat SRS should be considered for carefully selected patients with hypercortisolism confirmed one or more years after initial SRS.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1007/s11060-018-2817-5</identifier><identifier>PMID: 29500664</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adrenocorticotropic hormone ; Clinical Study ; Cushing syndrome ; Cushing's disease ; Drug dosages ; Hormones ; Hospitals ; Medicine ; Medicine & Public Health ; Microsurgery ; Morbidity ; Nervous system diseases ; Neurology ; Neurosurgery ; Oncology ; Patients ; Pituitary ; Radiation therapy ; Radiosurgery ; Remission ; Remission (Medicine) ; Surgery ; Tumors</subject><ispartof>Journal of neuro-oncology, 2018-07, Vol.138 (3), p.519-525</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>Journal of Neuro-Oncology is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-c3f727c3d2288f71a5257fa5d5e8cfc54e80be878190324d0cb2938de5f2547d3</citedby><cites>FETCH-LOGICAL-c372t-c3f727c3d2288f71a5257fa5d5e8cfc54e80be878190324d0cb2938de5f2547d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29500664$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mehta, Gautam U.</creatorcontrib><creatorcontrib>Ding, Dale</creatorcontrib><creatorcontrib>Gupta, Amitabh</creatorcontrib><creatorcontrib>Kano, Hideyuki</creatorcontrib><creatorcontrib>Sisterson, Nathaniel D.</creatorcontrib><creatorcontrib>Martinez-Moreno, Nuria</creatorcontrib><creatorcontrib>Kršek, Michal</creatorcontrib><creatorcontrib>Yang, Huai-Che</creatorcontrib><creatorcontrib>Lee, Cheng-Chia</creatorcontrib><creatorcontrib>Liščák, Roman</creatorcontrib><creatorcontrib>Martinez-Alvarez, Roberto</creatorcontrib><creatorcontrib>Lunsford, L. Dade</creatorcontrib><creatorcontrib>Vance, Mary Lee</creatorcontrib><creatorcontrib>Sheehan, Jason P.</creatorcontrib><title>Repeat stereotactic radiosurgery for Cushing’s disease: outcomes of an international, multicenter study</title><title>Journal of neuro-oncology</title><addtitle>J Neurooncol</addtitle><addtitle>J Neurooncol</addtitle><description>Stereotactic radiosurgery (SRS) is frequently used for Cushing’s disease (CD) after failed pituitary surgery. Management of patients with persistent CD after failed SRS is complex, as the alternative therapeutic options harbor significant risks. The outcomes of repeat pituitary radiosurgery, however, have not been described. We sought to determine the outcomes of repeat SRS in patients with CD. We pooled data from five institutions participating in the International Gamma Knife Research Foundation for patients with recurrent or persistent CD ≥ 12 months after initial SRS. Patients were included in the study if they had ≥ 6 months endocrine follow-up after repeat SRS. Twenty patients were included in the study. Repeat single-session SRS was performed 1.3–9.7 years after initial SRS. Median endocrine follow-up was 6.6 years (1.4–19.1 years). Median margin dose was 20 Gy (range 10.8–35 Gy). Endocrine remission after second SRS was noted in 12 patients (60%), with a median time to remission of 6 months (range 2–64 months). Biochemical recurrence occurred in two patients (17%) after initial remission. Overall, the cumulative rates of durable endocrine remission at 5 and 10 years were 47 and 53%, respectively. Two patients (10%) experienced adverse radiation effects, including transient visual loss and permanent diplopia. Repeat SRS achieves lasting biochemical remission in approximately half of patients with CD refractory to both prior microsurgery and SRS. Because of the morbidity of refractory or recurrent CD, repeat SRS should be considered for carefully selected patients with hypercortisolism confirmed one or more years after initial SRS.</description><subject>Adrenocorticotropic hormone</subject><subject>Clinical Study</subject><subject>Cushing syndrome</subject><subject>Cushing's disease</subject><subject>Drug dosages</subject><subject>Hormones</subject><subject>Hospitals</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Microsurgery</subject><subject>Morbidity</subject><subject>Nervous system diseases</subject><subject>Neurology</subject><subject>Neurosurgery</subject><subject>Oncology</subject><subject>Patients</subject><subject>Pituitary</subject><subject>Radiation therapy</subject><subject>Radiosurgery</subject><subject>Remission</subject><subject>Remission (Medicine)</subject><subject>Surgery</subject><subject>Tumors</subject><issn>0167-594X</issn><issn>1573-7373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kc-KFDEQh4Mo7uzqA3iRgBcP21pJOpO0t2XwHywsiIK3kEkqa5buzph0DnPzNXw9n2QzzKqwsJcEKl99RepHyAsGbxiAelsYgzV0wHTHNVOdfERWTCrRKaHEY7ICtm7Fof9-Qk5LuQGAXgn2lJzwQQKs1_2KxC-4Q7vQsmDGtFi3REez9TGVmq8x72lImW5q-RHn6z-_fhfqY0Fb8B1NdXFpwkJToHamcW6K2S4xzXY8p1MdmwoPxSavfv-MPAl2LPj87j4j3z68_7r51F1effy8ubjsnFB8aWdQXDnhOdc6KGYllypY6SVqF5zsUcMWtdJsAMF7D27LB6E9ysBlr7w4I6-P3l1OPyuWxUyxOBxHO2OqxXBg0CYp0A19dQ-9SbX9YTxQMOh-EII1ih0pl1MpGYPZ5TjZvDcMzCEHc8zBtBzMIQcjW8_LO3PdTuj_dfxdfAP4ESjtaW6L_j_6YestFoCUxg</recordid><startdate>20180701</startdate><enddate>20180701</enddate><creator>Mehta, Gautam U.</creator><creator>Ding, Dale</creator><creator>Gupta, Amitabh</creator><creator>Kano, Hideyuki</creator><creator>Sisterson, Nathaniel D.</creator><creator>Martinez-Moreno, Nuria</creator><creator>Kršek, Michal</creator><creator>Yang, Huai-Che</creator><creator>Lee, Cheng-Chia</creator><creator>Liščák, Roman</creator><creator>Martinez-Alvarez, Roberto</creator><creator>Lunsford, L. 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Dade</au><au>Vance, Mary Lee</au><au>Sheehan, Jason P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Repeat stereotactic radiosurgery for Cushing’s disease: outcomes of an international, multicenter study</atitle><jtitle>Journal of neuro-oncology</jtitle><stitle>J Neurooncol</stitle><addtitle>J Neurooncol</addtitle><date>2018-07-01</date><risdate>2018</risdate><volume>138</volume><issue>3</issue><spage>519</spage><epage>525</epage><pages>519-525</pages><issn>0167-594X</issn><eissn>1573-7373</eissn><abstract>Stereotactic radiosurgery (SRS) is frequently used for Cushing’s disease (CD) after failed pituitary surgery. Management of patients with persistent CD after failed SRS is complex, as the alternative therapeutic options harbor significant risks. The outcomes of repeat pituitary radiosurgery, however, have not been described. We sought to determine the outcomes of repeat SRS in patients with CD. We pooled data from five institutions participating in the International Gamma Knife Research Foundation for patients with recurrent or persistent CD ≥ 12 months after initial SRS. Patients were included in the study if they had ≥ 6 months endocrine follow-up after repeat SRS. Twenty patients were included in the study. Repeat single-session SRS was performed 1.3–9.7 years after initial SRS. Median endocrine follow-up was 6.6 years (1.4–19.1 years). Median margin dose was 20 Gy (range 10.8–35 Gy). Endocrine remission after second SRS was noted in 12 patients (60%), with a median time to remission of 6 months (range 2–64 months). Biochemical recurrence occurred in two patients (17%) after initial remission. Overall, the cumulative rates of durable endocrine remission at 5 and 10 years were 47 and 53%, respectively. Two patients (10%) experienced adverse radiation effects, including transient visual loss and permanent diplopia. Repeat SRS achieves lasting biochemical remission in approximately half of patients with CD refractory to both prior microsurgery and SRS. Because of the morbidity of refractory or recurrent CD, repeat SRS should be considered for carefully selected patients with hypercortisolism confirmed one or more years after initial SRS.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>29500664</pmid><doi>10.1007/s11060-018-2817-5</doi><tpages>7</tpages></addata></record> |
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subjects | Adrenocorticotropic hormone Clinical Study Cushing syndrome Cushing's disease Drug dosages Hormones Hospitals Medicine Medicine & Public Health Microsurgery Morbidity Nervous system diseases Neurology Neurosurgery Oncology Patients Pituitary Radiation therapy Radiosurgery Remission Remission (Medicine) Surgery Tumors |
title | Repeat stereotactic radiosurgery for Cushing’s disease: outcomes of an international, multicenter study |
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