{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,6]],"date-time":"2026-11-06T19:45:27Z","timestamp":1793994327422,"version":"4.8.0"},"reference-count":45,"publisher":"American Medical Association (AMA)","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Oncol"],"published-print":{"date-parts":[[2024,8,1]]},"abstract":"<jats:sec id=\"ab-coi240023-4\"><jats:title>Importance<\/jats:title><jats:p>Pediatric oncology patients are increasingly recognized as having an underlying cancer predisposition syndrome (CPS). Surveillance is often recommended to detect new tumors at their earliest and most curable stages. Data on the effectiveness and outcomes of surveillance for children with CPS are limited.<\/jats:p><\/jats:sec><jats:sec id=\"ab-coi240023-5\"><jats:title>Objective<\/jats:title><jats:p>To evaluate the performance of surveillance across a wide spectrum of CPSs.<\/jats:p><\/jats:sec><jats:sec id=\"ab-coi240023-6\"><jats:title>Design, Setting, and Participants<\/jats:title><jats:p>This cohort study reviewed surveillance outcomes for children and young adults from birth to age 23 years with a clinical and\/or molecular CPS diagnosis from January 1, 2009, through September 31, 2021. Patients were monitored using standard surveillance regimens for their corresponding CPS at a specialty pediatric oncology center. Patients with hereditary retinoblastoma and bone marrow failure syndromes were excluded. Data were analyzed between August 1, 2021, and December 6, 2023.<\/jats:p><\/jats:sec><jats:sec id=\"ab-coi240023-7\"><jats:title>Exposure<\/jats:title><jats:p>Cancer predisposition syndrome.<\/jats:p><\/jats:sec><jats:sec id=\"ab-coi240023-8\"><jats:title>Main Outcomes and Measures<\/jats:title><jats:p>Outcomes of surveillance were reviewed to evaluate the incidence, spectrum, and clinical course of newly detected tumors. Surveillance modalities were classified for accuracy and assessed for common strengths and weaknesses.<\/jats:p><\/jats:sec><jats:sec id=\"ab-coi240023-9\"><jats:title>Results<\/jats:title><jats:p>A total of 274 children and young adults (mean age, 8 years [range, birth to 23 years]; 144 female [52.6%]) with 35 different CPSs were included, with a median follow-up of 3 years (range, 1 month to 12 years). During the study period, 35 asymptomatic tumors were detected in 27 patients through surveillance (9.9% of the cohort), while 5 symptomatic tumors were detected in 5 patients (1.8% of the cohort) outside of surveillance, 2 of whom also had tumors detected through surveillance. Ten of the 35 tumors (28.6%) were identified on first surveillance imaging. Malignant solid and brain tumors identified through surveillance were more often localized (20 of 24 [83.3%]) than similar tumors detected before CPS diagnosis (71 of 125 [56.8%]; <jats:italic>P<\/jats:italic>\u2009&amp;amp;lt;\u2009.001). Of the 24 tumors identified through surveillance and surgically resected, 17 (70.8%) had completely negative margins. When analyzed across all imaging modalities, the sensitivity (96.4%), specificity (99.6%), positive predictive value (94.3%), and negative predictive value (99.6%) of surveillance were high, with few false-positive (6 [0.4%]) or false-negative (5 [0.3%]) findings.<\/jats:p><\/jats:sec><jats:sec id=\"ab-coi240023-10\"><jats:title>Conclusions and Relevance<\/jats:title><jats:p>These findings suggest that standardized surveillance enables early detection of new tumors across a wide spectrum of CPSs, allowing for complete surgical resection and successful treatment in the majority of patients.<\/jats:p><\/jats:sec>","DOI":"10.1001\/jamaoncol.2024.1878","type":"journal-article","created":{"date-parts":[[2024,6,20]],"date-time":"2024-06-20T15:02:22Z","timestamp":1718895742000},"page":"1060","source":"Crossref","is-referenced-by-count":19,"title":["Performance of Tumor Surveillance for Children With Cancer 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