Biochemical Control in Acromegaly With Multimodality Therapies: Outcomes From a Pituitary Center and Changes Over Time
Abstract Purpose To determine the prevalence of insulin-like growth factor-1 (IGF-1) normalization with long-term multimodality therapy in a pituitary center and to assess changes over time. Methods Patients with acromegaly (N = 409), with ≥1 year of data after surgery and at least 2 subsequent clin...
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creator | Ghajar, Alireza Jones, Pamela S Guarda, Francisco J Faje, Alex Tritos, Nicholas A Miller, Karen K Swearingen, Brooke Nachtigall, Lisa B |
description | Abstract
Purpose
To determine the prevalence of insulin-like growth factor-1 (IGF-1) normalization with long-term multimodality therapy in a pituitary center and to assess changes over time.
Methods
Patients with acromegaly (N = 409), with ≥1 year of data after surgery and at least 2 subsequent clinic visits were included in long-term analysis (N = 266). Biochemical data, clinical characteristics, and therapeutic interventions were reviewed retrospectively.
Results
At diagnosis, mean [standard deviation] age was 43.4 [14.3] years, body mass index was 28.5 (24.9–32.1) kg/m2 (median, interquartile range), serum IGF-1 index (IGF-1 level/upper limit of normal) was 2.3 [1.7–3.1], and 80.5% had macroadenomas. Patients with transsphenoidal surgery after 2006 were older [46.6 ± 14.3 vs 40.0 ± 13.4 years; P < 0.001]. Age and tumor size correlated inversely. Overall (N = 266), 93.2% achieved a normal IGF-1 level during 9.9 [5.0–15.0] years with multimodality therapy. The interval to first normal IGF-1 level following failed surgical remission was shorter after 2006: 14.0 (95% confidence interval, 10.0–20.0) versus 27.5 (22.0–36.0) months (P = 0.002). Radiation therapy and second surgery were rarer after 2006: 28 (22%) versus 62 (47.0%); P < 0.001 and 12 (9.4%) versus 28 (21.2%); P = 0.010, respectively. Age at diagnosis increased over time periods, possibly reflecting increased detection of acromegaly in older patients with milder disease. Male gender, older age, smaller tumor and lower IGF-1 index at diagnosis predicted long-term sustained IGF-1 control after surgery without adjuvant therapies.
Conclusion
The vast majority of patients with acromegaly can be biochemically controlled with multimodality therapy in the current era. Radiotherapy and repeat pituitary surgery became less frequently utilized over time. Long-term postoperative IGF-1 control without use of adjuvant therapies has improved. |
doi_str_mv | 10.1210/clinem/dgz187 |
format | Article |
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Purpose
To determine the prevalence of insulin-like growth factor-1 (IGF-1) normalization with long-term multimodality therapy in a pituitary center and to assess changes over time.
Methods
Patients with acromegaly (N = 409), with ≥1 year of data after surgery and at least 2 subsequent clinic visits were included in long-term analysis (N = 266). Biochemical data, clinical characteristics, and therapeutic interventions were reviewed retrospectively.
Results
At diagnosis, mean [standard deviation] age was 43.4 [14.3] years, body mass index was 28.5 (24.9–32.1) kg/m2 (median, interquartile range), serum IGF-1 index (IGF-1 level/upper limit of normal) was 2.3 [1.7–3.1], and 80.5% had macroadenomas. Patients with transsphenoidal surgery after 2006 were older [46.6 ± 14.3 vs 40.0 ± 13.4 years; P < 0.001]. Age and tumor size correlated inversely. Overall (N = 266), 93.2% achieved a normal IGF-1 level during 9.9 [5.0–15.0] years with multimodality therapy. The interval to first normal IGF-1 level following failed surgical remission was shorter after 2006: 14.0 (95% confidence interval, 10.0–20.0) versus 27.5 (22.0–36.0) months (P = 0.002). Radiation therapy and second surgery were rarer after 2006: 28 (22%) versus 62 (47.0%); P < 0.001 and 12 (9.4%) versus 28 (21.2%); P = 0.010, respectively. Age at diagnosis increased over time periods, possibly reflecting increased detection of acromegaly in older patients with milder disease. Male gender, older age, smaller tumor and lower IGF-1 index at diagnosis predicted long-term sustained IGF-1 control after surgery without adjuvant therapies.
Conclusion
The vast majority of patients with acromegaly can be biochemically controlled with multimodality therapy in the current era. Radiotherapy and repeat pituitary surgery became less frequently utilized over time. Long-term postoperative IGF-1 control without use of adjuvant therapies has improved.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/clinem/dgz187</identifier><identifier>PMID: 31701145</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Acromegaly ; Age ; Body mass index ; Diagnosis ; Insulin ; Insulin-like growth factor I ; Insulin-like growth factors ; Online Only ; Patients ; Pituitary ; Radiation therapy ; Remission ; Surgery ; Therapeutic applications</subject><ispartof>The journal of clinical endocrinology and metabolism, 2020-03, Vol.105 (3), p.e532-e543</ispartof><rights>Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2019</rights><rights>Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c492t-3e8ea55c0cb9eb40cad97ffbf3cf49a01e5bae2c3a7551a7154c2311516ba9173</citedby><cites>FETCH-LOGICAL-c492t-3e8ea55c0cb9eb40cad97ffbf3cf49a01e5bae2c3a7551a7154c2311516ba9173</cites><orcidid>0000-0001-9534-7186</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2431027280?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,776,780,881,21368,21369,27903,27904,33509,33510,33723,33724,43638,43784,64362,64364,64366,72216,72870,72875,72876,72878</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31701145$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ghajar, Alireza</creatorcontrib><creatorcontrib>Jones, Pamela S</creatorcontrib><creatorcontrib>Guarda, Francisco J</creatorcontrib><creatorcontrib>Faje, Alex</creatorcontrib><creatorcontrib>Tritos, Nicholas A</creatorcontrib><creatorcontrib>Miller, Karen K</creatorcontrib><creatorcontrib>Swearingen, Brooke</creatorcontrib><creatorcontrib>Nachtigall, Lisa B</creatorcontrib><title>Biochemical Control in Acromegaly With Multimodality Therapies: Outcomes From a Pituitary Center and Changes Over Time</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>Abstract
Purpose
To determine the prevalence of insulin-like growth factor-1 (IGF-1) normalization with long-term multimodality therapy in a pituitary center and to assess changes over time.
Methods
Patients with acromegaly (N = 409), with ≥1 year of data after surgery and at least 2 subsequent clinic visits were included in long-term analysis (N = 266). Biochemical data, clinical characteristics, and therapeutic interventions were reviewed retrospectively.
Results
At diagnosis, mean [standard deviation] age was 43.4 [14.3] years, body mass index was 28.5 (24.9–32.1) kg/m2 (median, interquartile range), serum IGF-1 index (IGF-1 level/upper limit of normal) was 2.3 [1.7–3.1], and 80.5% had macroadenomas. Patients with transsphenoidal surgery after 2006 were older [46.6 ± 14.3 vs 40.0 ± 13.4 years; P < 0.001]. Age and tumor size correlated inversely. Overall (N = 266), 93.2% achieved a normal IGF-1 level during 9.9 [5.0–15.0] years with multimodality therapy. The interval to first normal IGF-1 level following failed surgical remission was shorter after 2006: 14.0 (95% confidence interval, 10.0–20.0) versus 27.5 (22.0–36.0) months (P = 0.002). Radiation therapy and second surgery were rarer after 2006: 28 (22%) versus 62 (47.0%); P < 0.001 and 12 (9.4%) versus 28 (21.2%); P = 0.010, respectively. Age at diagnosis increased over time periods, possibly reflecting increased detection of acromegaly in older patients with milder disease. Male gender, older age, smaller tumor and lower IGF-1 index at diagnosis predicted long-term sustained IGF-1 control after surgery without adjuvant therapies.
Conclusion
The vast majority of patients with acromegaly can be biochemically controlled with multimodality therapy in the current era. Radiotherapy and repeat pituitary surgery became less frequently utilized over time. Long-term postoperative IGF-1 control without use of adjuvant therapies has improved.</description><subject>Acromegaly</subject><subject>Age</subject><subject>Body mass index</subject><subject>Diagnosis</subject><subject>Insulin</subject><subject>Insulin-like growth factor I</subject><subject>Insulin-like growth factors</subject><subject>Online Only</subject><subject>Patients</subject><subject>Pituitary</subject><subject>Radiation therapy</subject><subject>Remission</subject><subject>Surgery</subject><subject>Therapeutic applications</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkc-P1CAcxYnRuOPq0ash8eKlLt8CZerBZG1cNVkzHsbojVBKp2wojEAnGf96MbOuPy6evgnfD4_3eAg9BfISaiAX2llv5oth9x3W4h5aQct4JaAV99GKkBqqVtRfz9CjlG4IAcY4fYjOKAgCwPgKHd7YoCczW60c7oLPMThsPb7UMcxmp9wRf7F5wh8Xl-0cBuVsPuLtZKLaW5Ne4c2SdSETvioXsMKfbF5sVvGIO-OziVj5AXeT8rvCbA7lYGtn8xg9GJVL5sntPEefr95uu_fV9ebdh-7yutKsrXNFzdoozjXRfWt6RrQaWjGO_Uj1yFpFwPBemVpTJTgHJYAzXVMADk2vWhD0HL0-6e6XfjaDLpaicnIf7VwsyqCs_Hvj7SR34SDXTUOggSLw4lYghm-LSVnONmnjnPImLEmW1ygVnLGmoM__QW_CEn2JJ2tGgdSiXpNCVSeqfHBK0Yx3ZoDIn43KU6Py1Gjhn_2Z4I7-VeFvh2HZ_0frB9KArog</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Ghajar, Alireza</creator><creator>Jones, Pamela S</creator><creator>Guarda, Francisco J</creator><creator>Faje, Alex</creator><creator>Tritos, Nicholas A</creator><creator>Miller, Karen K</creator><creator>Swearingen, Brooke</creator><creator>Nachtigall, Lisa B</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9534-7186</orcidid></search><sort><creationdate>20200301</creationdate><title>Biochemical Control in Acromegaly With Multimodality Therapies: Outcomes From a Pituitary Center and Changes Over Time</title><author>Ghajar, Alireza ; Jones, Pamela S ; Guarda, Francisco J ; Faje, Alex ; Tritos, Nicholas A ; Miller, Karen K ; Swearingen, Brooke ; Nachtigall, Lisa B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c492t-3e8ea55c0cb9eb40cad97ffbf3cf49a01e5bae2c3a7551a7154c2311516ba9173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acromegaly</topic><topic>Age</topic><topic>Body mass index</topic><topic>Diagnosis</topic><topic>Insulin</topic><topic>Insulin-like growth factor I</topic><topic>Insulin-like growth factors</topic><topic>Online Only</topic><topic>Patients</topic><topic>Pituitary</topic><topic>Radiation therapy</topic><topic>Remission</topic><topic>Surgery</topic><topic>Therapeutic applications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ghajar, Alireza</creatorcontrib><creatorcontrib>Jones, Pamela S</creatorcontrib><creatorcontrib>Guarda, Francisco J</creatorcontrib><creatorcontrib>Faje, Alex</creatorcontrib><creatorcontrib>Tritos, Nicholas A</creatorcontrib><creatorcontrib>Miller, Karen K</creatorcontrib><creatorcontrib>Swearingen, Brooke</creatorcontrib><creatorcontrib>Nachtigall, Lisa B</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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>PubMed Central (Full Participant titles)</collection><jtitle>The journal of clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ghajar, Alireza</au><au>Jones, Pamela S</au><au>Guarda, Francisco J</au><au>Faje, Alex</au><au>Tritos, Nicholas A</au><au>Miller, Karen K</au><au>Swearingen, Brooke</au><au>Nachtigall, Lisa B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biochemical Control in Acromegaly With Multimodality Therapies: Outcomes From a Pituitary Center and Changes Over Time</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>105</volume><issue>3</issue><spage>e532</spage><epage>e543</epage><pages>e532-e543</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><abstract>Abstract
Purpose
To determine the prevalence of insulin-like growth factor-1 (IGF-1) normalization with long-term multimodality therapy in a pituitary center and to assess changes over time.
Methods
Patients with acromegaly (N = 409), with ≥1 year of data after surgery and at least 2 subsequent clinic visits were included in long-term analysis (N = 266). Biochemical data, clinical characteristics, and therapeutic interventions were reviewed retrospectively.
Results
At diagnosis, mean [standard deviation] age was 43.4 [14.3] years, body mass index was 28.5 (24.9–32.1) kg/m2 (median, interquartile range), serum IGF-1 index (IGF-1 level/upper limit of normal) was 2.3 [1.7–3.1], and 80.5% had macroadenomas. Patients with transsphenoidal surgery after 2006 were older [46.6 ± 14.3 vs 40.0 ± 13.4 years; P < 0.001]. Age and tumor size correlated inversely. Overall (N = 266), 93.2% achieved a normal IGF-1 level during 9.9 [5.0–15.0] years with multimodality therapy. The interval to first normal IGF-1 level following failed surgical remission was shorter after 2006: 14.0 (95% confidence interval, 10.0–20.0) versus 27.5 (22.0–36.0) months (P = 0.002). Radiation therapy and second surgery were rarer after 2006: 28 (22%) versus 62 (47.0%); P < 0.001 and 12 (9.4%) versus 28 (21.2%); P = 0.010, respectively. Age at diagnosis increased over time periods, possibly reflecting increased detection of acromegaly in older patients with milder disease. Male gender, older age, smaller tumor and lower IGF-1 index at diagnosis predicted long-term sustained IGF-1 control after surgery without adjuvant therapies.
Conclusion
The vast majority of patients with acromegaly can be biochemically controlled with multimodality therapy in the current era. Radiotherapy and repeat pituitary surgery became less frequently utilized over time. Long-term postoperative IGF-1 control without use of adjuvant therapies has improved.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>31701145</pmid><doi>10.1210/clinem/dgz187</doi><orcidid>https://orcid.org/0000-0001-9534-7186</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acromegaly Age Body mass index Diagnosis Insulin Insulin-like growth factor I Insulin-like growth factors Online Only Patients Pituitary Radiation therapy Remission Surgery Therapeutic applications |
title | Biochemical Control in Acromegaly With Multimodality Therapies: Outcomes From a Pituitary Center and Changes Over Time |
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