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Performance of Tumor Surveillance for Children With Cancer Predisposition.
Blake, Alise; Perrino, Melissa R; Morin, Cara E; Taylor, Leslie; McGee, Rose B; Lewis, Sara; Hines-Dowell, Stacy; Pandey, Arti; Turner, Paige; Kubal, Manish; Su, Yin; Tang, Li; Howell, Laura; Harrison, Lynn W; Abramson, Zachary; Schechter, Ann; Sabin, Noah D; Nichols, Kim E.
Afiliação
  • Blake A; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Perrino MR; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Morin CE; Department of Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Taylor L; Now with Department of Radiology, Cincinnati Children's Hospital Medical Center, Ohio.
  • McGee RB; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Lewis S; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Hines-Dowell S; Department of Hematology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Pandey A; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Turner P; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Kubal M; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Su Y; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Tang L; Department of Biostatistics, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Howell L; Department of Biostatistics, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Harrison LW; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Abramson Z; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Schechter A; Department of Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Sabin ND; Department of Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, Tennessee.
  • Nichols KE; Department of Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, Tennessee.
JAMA Oncol ; 10(8): 1060-1067, 2024 Aug 01.
Article em En | MEDLINE | ID: mdl-38900420
ABSTRACT
Importance 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.

Objective:

To evaluate the performance of surveillance across a wide spectrum of CPSs. Design, Setting, and

Participants:

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. Exposure Cancer predisposition syndrome. Main Outcomes and

Measures:

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.

Results:

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%]; P < .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. Conclusions and Relevance 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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: JAMA Oncol Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: JAMA Oncol Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos