PF-B
Posterior Fossa B — better-prognosis posterior-fossa subgroup. Chromosomal instability without H3K27me3 loss.
Standard of care, prognosis, and what's under investigation
Standard of care. Maximal safe surgery followed by focal radiation. PF-B generally responds well to this combination. Chemotherapy is not standard.
Prognosis. 5-year overall survival is approximately 95% in published series — the most favorable of the major posterior-fossa ependymoma subgroups. PF-B typically presents in older children and young adults rather than infants.
What's being investigated here. No PF-B-specific computational hypothesis is currently under active test in this module. PF-B's favorable prognosis means it is not the highest research priority — the program prioritizes high-mortality subgroups such as PFA. Atlas exploration through the cohort browser is still useful for context and reference.
Research Use Only — no entry below is clinical-grade evidence.
Active hypotheses, data status, and blockers
- Leading hypotheses. None of the five active hypotheses in this module target PF-B specifically. This is by prioritization, not oversight.
- Data status — strengths. PF-B is a clean molecular reference class with a clear outcome signal in the literature (favorable). Useful as a contrast for PFA hypotheses.
- Data status — weaknesses. Sample count in the atlas is small — too few to anchor a PF-B-only computational test. Sample expansion would be required before any subgroup-specific finding could be trusted.
- Key blockers. Cohort expansion. Other ependymoma resources (St. Jude, CBTN, Children's Brain Tumor Network) have additional PF-B cases that would need ingest into the ETL pipeline.
Tools for this subgroup
Small cohort — tools may surface fewer results for this subgroup.