Disease Control after Radiotherapy for Adult Craniopharyngioma: Clinical Outcomes from a Large Single-Institution Series

Purpose To report disease control and treatment-related side effects among adult patients with craniopharyngioma treated with radiotherapy. Methods We performed a single-institution review of adult patients (> 21 years old) with craniopharyngioma treated with radiotherapy either definitively or p...

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Veröffentlicht in:Journal of neuro-oncology 2022-05, Vol.157 (3), p.425-433
Hauptverfasser: Rutenberg, Michael S., Holtzman, Adam L., Indelicato, Daniel J., Huh, Soon, Rao, Dinesh, Fiester, Peter J., Morris, Christopher G., Tavanaiepour, Daryoush, Amdur, Robert J.
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container_end_page 433
container_issue 3
container_start_page 425
container_title Journal of neuro-oncology
container_volume 157
creator Rutenberg, Michael S.
Holtzman, Adam L.
Indelicato, Daniel J.
Huh, Soon
Rao, Dinesh
Fiester, Peter J.
Morris, Christopher G.
Tavanaiepour, Daryoush
Amdur, Robert J.
description Purpose To report disease control and treatment-related side effects among adult patients with craniopharyngioma treated with radiotherapy. Methods We performed a single-institution review of adult patients (> 21 years old) with craniopharyngioma treated with radiotherapy either definitively or postoperatively for gross residual disease. We report disease control, survival, and radiotherapy-related side effects. Results A total of 49 adult patients with craniopharyngioma were included, 27 of whom were treated at initial presentation and 22 for recurrent disease following initial surgery and observation. Overall, 77% received radiotherapy postoperatively (either after primary surgery or surgery for recurrence). With a median clinical and radiographic follow-up of 4.2 (range, 0.4–21.6) years and 3.0 (range, 0–21.5) years, the 5- and 10-year local control rates were 100 and 94%, respectively. The 5- and 10-year overall survival rates were 80 and 66%, respectively. Eleven percent of patients experienced grade 2 vision deterioration and 18% suffered grade 2 endocrinopathies following radiotherapy. Conclusions Radiotherapy provides excellent disease control with acceptable toxicity among adult patients with craniopharyngioma. These data support the use of fractionated radiotherapy in adult patients with recurrent or gross residual disease after surgery. For inoperable patients or those with moderate or high surgical risk to neurologic and/or vascular structures, we advocate for limited surgical resection and postoperative radiotherapy to balance optimal tumor control with tumor- and treatment-related morbidity.
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Methods We performed a single-institution review of adult patients (&gt; 21 years old) with craniopharyngioma treated with radiotherapy either definitively or postoperatively for gross residual disease. We report disease control, survival, and radiotherapy-related side effects. Results A total of 49 adult patients with craniopharyngioma were included, 27 of whom were treated at initial presentation and 22 for recurrent disease following initial surgery and observation. Overall, 77% received radiotherapy postoperatively (either after primary surgery or surgery for recurrence). With a median clinical and radiographic follow-up of 4.2 (range, 0.4–21.6) years and 3.0 (range, 0–21.5) years, the 5- and 10-year local control rates were 100 and 94%, respectively. The 5- and 10-year overall survival rates were 80 and 66%, respectively. Eleven percent of patients experienced grade 2 vision deterioration and 18% suffered grade 2 endocrinopathies following radiotherapy. Conclusions Radiotherapy provides excellent disease control with acceptable toxicity among adult patients with craniopharyngioma. These data support the use of fractionated radiotherapy in adult patients with recurrent or gross residual disease after surgery. For inoperable patients or those with moderate or high surgical risk to neurologic and/or vascular structures, we advocate for limited surgical resection and postoperative radiotherapy to balance optimal tumor control with tumor- and treatment-related morbidity.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1007/s11060-022-03983-z</identifier><identifier>PMID: 35278157</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adult ; Brain cancer ; Clinical outcomes ; Clinical Study ; Craniopharyngioma - radiotherapy ; Craniopharyngioma - surgery ; Disease control ; Endocrine disorders ; Humans ; Medicine ; Medicine &amp; Public Health ; Morbidity ; Neoplasia ; Neoplasm Recurrence, Local - radiotherapy ; Neoplasm Recurrence, Local - surgery ; Neoplasm, Residual - surgery ; Neurology ; Oncology ; Patients ; Pituitary ; Pituitary Neoplasms - radiotherapy ; Pituitary Neoplasms - surgery ; Radiation therapy ; Retrospective Studies ; Side effects ; Surgery ; Survival ; Survival Rate ; Toxicity ; Treatment Outcome ; Tumors ; Young Adult</subject><ispartof>Journal of neuro-oncology, 2022-05, Vol.157 (3), p.425-433</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022</rights><rights>2022. 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Methods We performed a single-institution review of adult patients (&gt; 21 years old) with craniopharyngioma treated with radiotherapy either definitively or postoperatively for gross residual disease. We report disease control, survival, and radiotherapy-related side effects. Results A total of 49 adult patients with craniopharyngioma were included, 27 of whom were treated at initial presentation and 22 for recurrent disease following initial surgery and observation. Overall, 77% received radiotherapy postoperatively (either after primary surgery or surgery for recurrence). With a median clinical and radiographic follow-up of 4.2 (range, 0.4–21.6) years and 3.0 (range, 0–21.5) years, the 5- and 10-year local control rates were 100 and 94%, respectively. The 5- and 10-year overall survival rates were 80 and 66%, respectively. Eleven percent of patients experienced grade 2 vision deterioration and 18% suffered grade 2 endocrinopathies following radiotherapy. 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Methods We performed a single-institution review of adult patients (&gt; 21 years old) with craniopharyngioma treated with radiotherapy either definitively or postoperatively for gross residual disease. We report disease control, survival, and radiotherapy-related side effects. Results A total of 49 adult patients with craniopharyngioma were included, 27 of whom were treated at initial presentation and 22 for recurrent disease following initial surgery and observation. Overall, 77% received radiotherapy postoperatively (either after primary surgery or surgery for recurrence). With a median clinical and radiographic follow-up of 4.2 (range, 0.4–21.6) years and 3.0 (range, 0–21.5) years, the 5- and 10-year local control rates were 100 and 94%, respectively. The 5- and 10-year overall survival rates were 80 and 66%, respectively. Eleven percent of patients experienced grade 2 vision deterioration and 18% suffered grade 2 endocrinopathies following radiotherapy. Conclusions Radiotherapy provides excellent disease control with acceptable toxicity among adult patients with craniopharyngioma. These data support the use of fractionated radiotherapy in adult patients with recurrent or gross residual disease after surgery. For inoperable patients or those with moderate or high surgical risk to neurologic and/or vascular structures, we advocate for limited surgical resection and postoperative radiotherapy to balance optimal tumor control with tumor- and treatment-related morbidity.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>35278157</pmid><doi>10.1007/s11060-022-03983-z</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6945-7883</orcidid></addata></record>
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subjects Adult
Brain cancer
Clinical outcomes
Clinical Study
Craniopharyngioma - radiotherapy
Craniopharyngioma - surgery
Disease control
Endocrine disorders
Humans
Medicine
Medicine & Public Health
Morbidity
Neoplasia
Neoplasm Recurrence, Local - radiotherapy
Neoplasm Recurrence, Local - surgery
Neoplasm, Residual - surgery
Neurology
Oncology
Patients
Pituitary
Pituitary Neoplasms - radiotherapy
Pituitary Neoplasms - surgery
Radiation therapy
Retrospective Studies
Side effects
Surgery
Survival
Survival Rate
Toxicity
Treatment Outcome
Tumors
Young Adult
title Disease Control after Radiotherapy for Adult Craniopharyngioma: Clinical Outcomes from a Large Single-Institution Series
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