{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,5]],"date-time":"2026-03-05T19:56:10Z","timestamp":1772740570659,"version":"3.50.1"},"reference-count":40,"publisher":"American Medical Association (AMA)","issue":"12","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi251309-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Associations with chemotherapy, occurrence of multiple meningiomas, and mortality after subsequent meningioma diagnosis among survivors of childhood cancer remain unclear.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251309-5\">\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>To report the incidence of meningioma among childhood cancer survivors, identify novel risk factors for meningiomas, characterize survivors with multiple meningiomas, and describe cause-specific mortality following meningioma occurrence.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251309-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>The Childhood Cancer Survivor Study is a retrospective cohort study with longitudinal prospective follow-up of childhood cancer survivors diagnosed between 1970 to 1999 in the US and Canada. Eligibility included diagnosis of cancer before age 21 years and surviving more than 5 years after diagnosis. Meningiomas were self-reported and confirmed by review of pathology reports. Childhood cancer diagnosis, chemotherapy details, and radiation therapy exposures from up to 5 years from diagnosis were abstracted from medical records.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251309-7\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Cumulative incidence of meningioma was calculated starting from 5 years from the diagnosis. Overall survival (OS) from diagnosis of the first subsequent meningioma was estimated using Kaplan-Meier methods.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251309-8\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>The CCSS cohort included 24\u202f886 survivors initially diagnosed from 1970 to 1999, including 471 survivors (263 female [56%]; median [range] age at last follow-up, 42.5 [19.7-66.3] years; median [range] age at primary cancer diagnosis, 5.6 [0-20.9] years) who were diagnosed with 710 meningiomas. Thirty-five years after primary cancer diagnosis, the cumulative incidence of a subsequent meningioma was 2.3% (95% CI, 2.1%-2.6%). Of the 471 survivors who developed meningioma, 137 (29.0%) had at least 2 meningiomas, and 80 (16%) met criteria for meningiomatosis. An increased risk of meningioma was associated with higher doses of cranial radiation therapy (eg, HR, 125.3 [95% CI, 58.1-270.5]), younger age at primary cancer diagnosis (eg, 0 to 4 years: HR, 4.0 [95% CI, 2.4-6.1]), female sex (HR, 1.6 [95% CI, 1.3-1.9]), and exposure to platinum, antimetabolite chemotherapy, and intrathecal chemotherapy, and a lower risk was associated with non-Hispanic Black race (HR, 0.5 [95% CI, 0.3-1.0]) and exposure to alkylating agents (HR,\u20090.6 [95% CI, 0.5-0.8]). The all-cause cumulative mortality was 4.9%, 10.5% and 18.4% at 5, 10, and 15 years from the first subsequent meningioma diagnosis.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251309-9\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>Meningiomas have a relatively high incidence and mortality for childhood cancer survivors. Results from this study could justify screening for meningiomas in high-risk populations.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2025.48715","type":"journal-article","created":{"date-parts":[[2025,12,11]],"date-time":"2025-12-11T16:00:38Z","timestamp":1765468838000},"page":"e2548715","source":"Crossref","is-referenced-by-count":1,"title":["Subsequent Meningiomas Among Survivors of Childhood Cancer"],"prefix":"10.1001","volume":"8","author":[{"given":"Daniel C.","family":"Bowers","sequence":"first","affiliation":[{"name":"Division of Pediatric Hematology\/Oncology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical School, Dallas"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Table","family":"Cooney","sequence":"additional","affiliation":[{"name":"Dana Farber\/Boston Children\u2019s Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts"},{"name":"Tango Therapeutics, Boston, 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