Childhood Cancer Data Initiative Annual Symposium (Abstract Registration): Submission #41
Submission information
Submission Number: 41
Submission ID: 148393
Submission UUID: 0152f5c9-da71-4180-9908-037cc01084ed
Submission URI: /nci/ccdisymposium/abstract
Created: Thu, 08/07/2025 - 13:55
Completed: Thu, 08/07/2025 - 14:24
Changed: Thu, 08/07/2025 - 14:24
Remote IP address: 10.208.28.64
Submitted by: Anonymous
Language: English
Is draft: No
Abstract Submission for Poster Presentation
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Abstract Title:: Pediatric PRISSMM model for real world medical record data to capture stage, treatment and cancer outcomes
Abstract::
Background: Approaches to obtaining structured clinical oncology data from the medical record are not standardized. PRISSMM was developed to reliably and reproducibly capture real-world oncology clinical data for adult solid malignancies from the medical record. We adapted the PRISSMM method to pediatric solid tumors(pediPRISSM) and assessed the feasibility of using pediPRISSMM to determine stage at presentation and progression-free survival(PFS) in patients with Ewing sarcoma(EWS). Methods: Patients diagnosed with EWS who had tumor molecular profiling had medical records abstracted using pediPRISSMM at two institutions. Staging was derived from disease site information from imaging performed during staging (4 weeks from diagnosis). PFS from the diagnosis was based on disease status from radiology reports(PFSimaging) and chemotherapy drug regimen start and stop dates(PFSdrugs). Results: 158 patients with a confirmed EWS-associated fusion were included. Median age at diagnosis was 17 years (range of 1-75), 63% were male and 80% had primary bone disease. Currently, complete pediPRISSM data are available for 43 patients. It was possible to derive stage from pediPRISSMM radiology data for 63% of patients. PFSimaging and PFSdrugs were concordant in 74% of patients. Medical record review for patients with a difference of >6 weeks in PFS revealed multi-institutional care as the most common reason for discordance. Conclusions: Although further analysis is ongoing, these data support the universal implementation of accurate staging forms as part of routine clinical documentation. Concordant findings using PFSimaging and PFSdrugs were achieved in the majority of patients, with highest success seen in patients treated at single institutions.
Abstract:: {Empty}
Authors::
1. First Name: Sidney
Middle Initial: N
Last Name: Benich
Degree(s): M.S.
Organization: Dana-Farber Cancer Institute
2. First Name: Stephanie
Last Name: Suser
Degree(s): B.A.
Organization: Memorial Sloan Kettering Cancer Center
3. First Name: Evelina
Last Name: Ceca
Degree(s): MBA
Organization: Dana-Farber Cancer Institute
4. First Name: Liliana
Last Name: Rodriguez
Organization: Memorial Sloan Kettering Cancer Center
5. First Name: Madhumitha
Last Name: Sridharan
Degree(s): B.E.
Organization: Dana-Farber Cancer Institute
6. First Name: Julian
Last Name: Schwartz
Degree(s): B.S.
Organization: Memorial Sloan Kettering Cancer Center
7. First Name: Zachary
Last Name: Kahn
Degree(s): B.S.
Organization: Dana-Farber Cancer Institute
8. First Name: Anita
Last Name: Bowman
Degree(s): M.S.
Organization: Memorial Sloan Kettering Cancer Center
9. First Name: Joseph
Last Name: White
Degree(s): Ph.D.
Organization: Dana-Farber Cancer Institute
10. First Name: Rose
Last Name: Brannon
Degree(s): Ph.D.
Organization: Memorial Sloan Kettering Cancer Center
11. First Name: Wendy
Middle Initial: B
Last Name: London
Degree(s): Ph.D.
Organization: Dana-Farber Cancer Institute
12. First Name: Neerav
Middle Initial: N
Last Name: Shukla
Degree(s): M.D.
Organization: Memorial Sloan Kettering Cancer Center
13. First Name: Katherine
Middle Initial: A
Last Name: Janeway
Degree(s): M.D., MMSc
Organization: Dana-Farber Cancer Institute
Presenting Author:: Sidney Benich
Institution:: Dana-Farber Cancer Institute
Email Address:: sidneyn_benich@dfci.harvard.edu