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 ------------------------------------------- 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