Late effects of medulloblastoma treatment: multidisciplinary approach of survivors

Purpose Medulloblastoma is one of the brain tumors with increased life expectancy due to improvements in treatment approaches. Besides the promising results, various undesirable effects can be encountered. This study’s aim is to review long-term follow-up outcomes of our cases with medulloblastoma....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Child's nervous system 2024-02, Vol.40 (2), p.417-425
Hauptverfasser: Aktekin, Elif Habibe, Kütük, Meryem Özlem, Sangün, Özlem, Yazıcı, Nalan, Çaylaklı, Fatma, Erol, İlknur, Sarıalioğlu, Faik
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 425
container_issue 2
container_start_page 417
container_title Child's nervous system
container_volume 40
creator Aktekin, Elif Habibe
Kütük, Meryem Özlem
Sangün, Özlem
Yazıcı, Nalan
Çaylaklı, Fatma
Erol, İlknur
Sarıalioğlu, Faik
description Purpose Medulloblastoma is one of the brain tumors with increased life expectancy due to improvements in treatment approaches. Besides the promising results, various undesirable effects can be encountered. This study’s aim is to review long-term follow-up outcomes of our cases with medulloblastoma. Methods Age at diagnosis, histological type of medulloblastoma, resection extension, chemotherapy and radiotherapy schemes, follow-up duration, and endocrinological, neuropsychiatric, cardiological, auditory, and visual examination results were evaluated in 20 patients diagnosed between 2007 and 2018 and followed 5 years and more. Results Twenty of 53 patients were included to the study. Eleven (55%) were male. Mean age at diagnosis was 6.95 years; mean age at the time of the study was 14 years. Mean follow-up time was 8.95 years. In terms of surgery, 14 (70%) were gross total, 1 (5%) was near total, and 2 (10%) were subtotal resection. In histopathological examination, 14 (70%) were classical medulloblastoma, 4 (20%) were desmoplastic medulloblastoma, and 1 (5%) was anaplastic medulloblastoma. With regard to endocrinological evaluation, 15 (75%) patients had hypothyroidism, 5 (25%) had growth hormone deficiency, 7 (35%) had clinical growth hormone deficiency, and 5 (25%) had sex hormone disorders. In neuropsychiatric examination, 11 (55%) patients had neurological sequelae, 18 (90%) patients had psychiatric issues, and 14 (70%) patients had two or more neuropsychiatric problems simultaneously. One (5%) patient had mitral valve insufficiency. Twelve patients (60%) had hearing loss. According to visual examination, 6 (30%) patients had refraction problem, 4 (20%) had cataract, and 1 (5%) had dry eye. Conclusion Careful monitoring of long-term side effects is important for improving the quality of life of medulloblastoma patients. Besides endocrinological and other somatic sequelae of the disease and treatment, increased neuropsychiatric problems showed us that only cure is not the issue while treating childhood medulloblastoma.
doi_str_mv 10.1007/s00381-023-06146-1
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2864158338</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2864158338</sourcerecordid><originalsourceid>FETCH-LOGICAL-c298t-a2ccd87ce14df214a70b6b2a4f35314414d5a193196e8e691274f7a619ef00053</originalsourceid><addsrcrecordid>eNp9kEtLxDAUhYMozjj6B1xIl26qN4-mjTsZfMGAILoOaZpoh7Qdk3TAf2_Gji5dXXJzzuGeD6FzDFcYoLwOALTCORCaA8eM5_gAzTGj6UkLOERzIAXPS2AwQychrAFwURFxjGa05KLiTMzRy0pFkxlrjY4hG2zWmWZ0bqidCnHoVBa9UbEzfbzJutHFtmmDbjeu7ZX_ytRm4welP3bGMPptux18OEVHVrlgzvZzgd7u716Xj_nq-eFpebvKNRFVzBXRuqlKbTBrLMFMlVDzmihmaUExY2ldKCwoFtxUhgtMSmZLxbEwFgAKukCXU2664XM0Icou3WacU70ZxiBJapgKU1olKZmk2g8heGPlxrddaiAxyB1LObGUiaX8YSlxMl3s88c6Ufmz_MJLAjoJQvrq342X62H0fer8X-w3O9l_0A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2864158338</pqid></control><display><type>article</type><title>Late effects of medulloblastoma treatment: multidisciplinary approach of survivors</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Aktekin, Elif Habibe ; Kütük, Meryem Özlem ; Sangün, Özlem ; Yazıcı, Nalan ; Çaylaklı, Fatma ; Erol, İlknur ; Sarıalioğlu, Faik</creator><creatorcontrib>Aktekin, Elif Habibe ; Kütük, Meryem Özlem ; Sangün, Özlem ; Yazıcı, Nalan ; Çaylaklı, Fatma ; Erol, İlknur ; Sarıalioğlu, Faik</creatorcontrib><description>Purpose Medulloblastoma is one of the brain tumors with increased life expectancy due to improvements in treatment approaches. Besides the promising results, various undesirable effects can be encountered. This study’s aim is to review long-term follow-up outcomes of our cases with medulloblastoma. Methods Age at diagnosis, histological type of medulloblastoma, resection extension, chemotherapy and radiotherapy schemes, follow-up duration, and endocrinological, neuropsychiatric, cardiological, auditory, and visual examination results were evaluated in 20 patients diagnosed between 2007 and 2018 and followed 5 years and more. Results Twenty of 53 patients were included to the study. Eleven (55%) were male. Mean age at diagnosis was 6.95 years; mean age at the time of the study was 14 years. Mean follow-up time was 8.95 years. In terms of surgery, 14 (70%) were gross total, 1 (5%) was near total, and 2 (10%) were subtotal resection. In histopathological examination, 14 (70%) were classical medulloblastoma, 4 (20%) were desmoplastic medulloblastoma, and 1 (5%) was anaplastic medulloblastoma. With regard to endocrinological evaluation, 15 (75%) patients had hypothyroidism, 5 (25%) had growth hormone deficiency, 7 (35%) had clinical growth hormone deficiency, and 5 (25%) had sex hormone disorders. In neuropsychiatric examination, 11 (55%) patients had neurological sequelae, 18 (90%) patients had psychiatric issues, and 14 (70%) patients had two or more neuropsychiatric problems simultaneously. One (5%) patient had mitral valve insufficiency. Twelve patients (60%) had hearing loss. According to visual examination, 6 (30%) patients had refraction problem, 4 (20%) had cataract, and 1 (5%) had dry eye. Conclusion Careful monitoring of long-term side effects is important for improving the quality of life of medulloblastoma patients. Besides endocrinological and other somatic sequelae of the disease and treatment, increased neuropsychiatric problems showed us that only cure is not the issue while treating childhood medulloblastoma.</description><identifier>ISSN: 0256-7040</identifier><identifier>EISSN: 1433-0350</identifier><identifier>DOI: 10.1007/s00381-023-06146-1</identifier><identifier>PMID: 37698649</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescent ; Adult ; Cerebellar Neoplasms - radiotherapy ; Child ; Disease Progression ; Female ; Growth Hormone ; Humans ; Male ; Medicine ; Medicine &amp; Public Health ; Medulloblastoma - pathology ; Neurosciences ; Neurosurgery ; Original Article ; Quality of Life ; Survivors ; Young Adult</subject><ispartof>Child's nervous system, 2024-02, Vol.40 (2), p.417-425</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c298t-a2ccd87ce14df214a70b6b2a4f35314414d5a193196e8e691274f7a619ef00053</cites><orcidid>0000-0002-0394-6219</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00381-023-06146-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00381-023-06146-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37698649$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aktekin, Elif Habibe</creatorcontrib><creatorcontrib>Kütük, Meryem Özlem</creatorcontrib><creatorcontrib>Sangün, Özlem</creatorcontrib><creatorcontrib>Yazıcı, Nalan</creatorcontrib><creatorcontrib>Çaylaklı, Fatma</creatorcontrib><creatorcontrib>Erol, İlknur</creatorcontrib><creatorcontrib>Sarıalioğlu, Faik</creatorcontrib><title>Late effects of medulloblastoma treatment: multidisciplinary approach of survivors</title><title>Child's nervous system</title><addtitle>Childs Nerv Syst</addtitle><addtitle>Childs Nerv Syst</addtitle><description>Purpose Medulloblastoma is one of the brain tumors with increased life expectancy due to improvements in treatment approaches. Besides the promising results, various undesirable effects can be encountered. This study’s aim is to review long-term follow-up outcomes of our cases with medulloblastoma. Methods Age at diagnosis, histological type of medulloblastoma, resection extension, chemotherapy and radiotherapy schemes, follow-up duration, and endocrinological, neuropsychiatric, cardiological, auditory, and visual examination results were evaluated in 20 patients diagnosed between 2007 and 2018 and followed 5 years and more. Results Twenty of 53 patients were included to the study. Eleven (55%) were male. Mean age at diagnosis was 6.95 years; mean age at the time of the study was 14 years. Mean follow-up time was 8.95 years. In terms of surgery, 14 (70%) were gross total, 1 (5%) was near total, and 2 (10%) were subtotal resection. In histopathological examination, 14 (70%) were classical medulloblastoma, 4 (20%) were desmoplastic medulloblastoma, and 1 (5%) was anaplastic medulloblastoma. With regard to endocrinological evaluation, 15 (75%) patients had hypothyroidism, 5 (25%) had growth hormone deficiency, 7 (35%) had clinical growth hormone deficiency, and 5 (25%) had sex hormone disorders. In neuropsychiatric examination, 11 (55%) patients had neurological sequelae, 18 (90%) patients had psychiatric issues, and 14 (70%) patients had two or more neuropsychiatric problems simultaneously. One (5%) patient had mitral valve insufficiency. Twelve patients (60%) had hearing loss. According to visual examination, 6 (30%) patients had refraction problem, 4 (20%) had cataract, and 1 (5%) had dry eye. Conclusion Careful monitoring of long-term side effects is important for improving the quality of life of medulloblastoma patients. Besides endocrinological and other somatic sequelae of the disease and treatment, increased neuropsychiatric problems showed us that only cure is not the issue while treating childhood medulloblastoma.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Cerebellar Neoplasms - radiotherapy</subject><subject>Child</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Growth Hormone</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Medulloblastoma - pathology</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><subject>Original Article</subject><subject>Quality of Life</subject><subject>Survivors</subject><subject>Young Adult</subject><issn>0256-7040</issn><issn>1433-0350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxDAUhYMozjj6B1xIl26qN4-mjTsZfMGAILoOaZpoh7Qdk3TAf2_Gji5dXXJzzuGeD6FzDFcYoLwOALTCORCaA8eM5_gAzTGj6UkLOERzIAXPS2AwQychrAFwURFxjGa05KLiTMzRy0pFkxlrjY4hG2zWmWZ0bqidCnHoVBa9UbEzfbzJutHFtmmDbjeu7ZX_ytRm4welP3bGMPptux18OEVHVrlgzvZzgd7u716Xj_nq-eFpebvKNRFVzBXRuqlKbTBrLMFMlVDzmihmaUExY2ldKCwoFtxUhgtMSmZLxbEwFgAKukCXU2664XM0Icou3WacU70ZxiBJapgKU1olKZmk2g8heGPlxrddaiAxyB1LObGUiaX8YSlxMl3s88c6Ufmz_MJLAjoJQvrq342X62H0fer8X-w3O9l_0A</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Aktekin, Elif Habibe</creator><creator>Kütük, Meryem Özlem</creator><creator>Sangün, Özlem</creator><creator>Yazıcı, Nalan</creator><creator>Çaylaklı, Fatma</creator><creator>Erol, İlknur</creator><creator>Sarıalioğlu, Faik</creator><general>Springer Berlin Heidelberg</general><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><orcidid>https://orcid.org/0000-0002-0394-6219</orcidid></search><sort><creationdate>20240201</creationdate><title>Late effects of medulloblastoma treatment: multidisciplinary approach of survivors</title><author>Aktekin, Elif Habibe ; Kütük, Meryem Özlem ; Sangün, Özlem ; Yazıcı, Nalan ; Çaylaklı, Fatma ; Erol, İlknur ; Sarıalioğlu, Faik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c298t-a2ccd87ce14df214a70b6b2a4f35314414d5a193196e8e691274f7a619ef00053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Cerebellar Neoplasms - radiotherapy</topic><topic>Child</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Growth Hormone</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Medulloblastoma - pathology</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><topic>Original Article</topic><topic>Quality of Life</topic><topic>Survivors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aktekin, Elif Habibe</creatorcontrib><creatorcontrib>Kütük, Meryem Özlem</creatorcontrib><creatorcontrib>Sangün, Özlem</creatorcontrib><creatorcontrib>Yazıcı, Nalan</creatorcontrib><creatorcontrib>Çaylaklı, Fatma</creatorcontrib><creatorcontrib>Erol, İlknur</creatorcontrib><creatorcontrib>Sarıalioğlu, Faik</creatorcontrib><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>Child's nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aktekin, Elif Habibe</au><au>Kütük, Meryem Özlem</au><au>Sangün, Özlem</au><au>Yazıcı, Nalan</au><au>Çaylaklı, Fatma</au><au>Erol, İlknur</au><au>Sarıalioğlu, Faik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Late effects of medulloblastoma treatment: multidisciplinary approach of survivors</atitle><jtitle>Child's nervous system</jtitle><stitle>Childs Nerv Syst</stitle><addtitle>Childs Nerv Syst</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>40</volume><issue>2</issue><spage>417</spage><epage>425</epage><pages>417-425</pages><issn>0256-7040</issn><eissn>1433-0350</eissn><abstract>Purpose Medulloblastoma is one of the brain tumors with increased life expectancy due to improvements in treatment approaches. Besides the promising results, various undesirable effects can be encountered. This study’s aim is to review long-term follow-up outcomes of our cases with medulloblastoma. Methods Age at diagnosis, histological type of medulloblastoma, resection extension, chemotherapy and radiotherapy schemes, follow-up duration, and endocrinological, neuropsychiatric, cardiological, auditory, and visual examination results were evaluated in 20 patients diagnosed between 2007 and 2018 and followed 5 years and more. Results Twenty of 53 patients were included to the study. Eleven (55%) were male. Mean age at diagnosis was 6.95 years; mean age at the time of the study was 14 years. Mean follow-up time was 8.95 years. In terms of surgery, 14 (70%) were gross total, 1 (5%) was near total, and 2 (10%) were subtotal resection. In histopathological examination, 14 (70%) were classical medulloblastoma, 4 (20%) were desmoplastic medulloblastoma, and 1 (5%) was anaplastic medulloblastoma. With regard to endocrinological evaluation, 15 (75%) patients had hypothyroidism, 5 (25%) had growth hormone deficiency, 7 (35%) had clinical growth hormone deficiency, and 5 (25%) had sex hormone disorders. In neuropsychiatric examination, 11 (55%) patients had neurological sequelae, 18 (90%) patients had psychiatric issues, and 14 (70%) patients had two or more neuropsychiatric problems simultaneously. One (5%) patient had mitral valve insufficiency. Twelve patients (60%) had hearing loss. According to visual examination, 6 (30%) patients had refraction problem, 4 (20%) had cataract, and 1 (5%) had dry eye. Conclusion Careful monitoring of long-term side effects is important for improving the quality of life of medulloblastoma patients. Besides endocrinological and other somatic sequelae of the disease and treatment, increased neuropsychiatric problems showed us that only cure is not the issue while treating childhood medulloblastoma.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37698649</pmid><doi>10.1007/s00381-023-06146-1</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0394-6219</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0256-7040
ispartof Child's nervous system, 2024-02, Vol.40 (2), p.417-425
issn 0256-7040
1433-0350
language eng
recordid cdi_proquest_miscellaneous_2864158338
source MEDLINE; Springer Nature - Complete Springer Journals
subjects Adolescent
Adult
Cerebellar Neoplasms - radiotherapy
Child
Disease Progression
Female
Growth Hormone
Humans
Male
Medicine
Medicine & Public Health
Medulloblastoma - pathology
Neurosciences
Neurosurgery
Original Article
Quality of Life
Survivors
Young Adult
title Late effects of medulloblastoma treatment: multidisciplinary approach of survivors
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T21%3A10%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Late%20effects%20of%20medulloblastoma%20treatment:%20multidisciplinary%20approach%20of%20survivors&rft.jtitle=Child's%20nervous%20system&rft.au=Aktekin,%20Elif%20Habibe&rft.date=2024-02-01&rft.volume=40&rft.issue=2&rft.spage=417&rft.epage=425&rft.pages=417-425&rft.issn=0256-7040&rft.eissn=1433-0350&rft_id=info:doi/10.1007/s00381-023-06146-1&rft_dat=%3Cproquest_cross%3E2864158338%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2864158338&rft_id=info:pmid/37698649&rfr_iscdi=true