Table A1.
Evidence and narrative quality appraisal.
| No. | Study | Design | Principal limitation | Narrative evidence strength |
|---|---|---|---|---|
| 1 | Lee et al. | Consensus guidance | Foundational standardized grading; consensus-based rather than comparative effectiveness evidence | Moderate–high contextual authority |
| 2 | Fatahichegeni et al. | Review | Broad recent synthesis; dependent on included literature and review methods | Contextual review evidence |
| 3 | Ruff et al. | Focused review | Neurologist-oriented practical synthesis; not comparative | Contextual review evidence |
| 4 | Garfall et al. | Implementation review | Operationally useful outpatient roadmap; center/resource dependent | Consensus/implementation evidence |
| 5 | Bayly-McCredie et al. | Systematic review | Aggregates clinical trials; heterogeneity and trial-selection limitations | Systematic-review level |
| 6 | Fonseca et al. | Meta-analysis | Large aggregate safety context; trial heterogeneity and indirect workflow evidence | Meta-analysis level |
| 7 | Cook et al. | Meta-analysis | CNS lymphoma safety context; small heterogeneous cohorts | Meta-analysis with imprecision |
| 8 | He et al. | Clinical cohort/trial | Direct CNS-involved population; product- and setting-specific | Limited–moderate clinical evidence |
| 9 | Shalabi et al. | Prospective pediatric/AYA study | Detailed phenotype; limited generalizability to adults/products | Preliminary prospective evidence |
| 10 | Guo et al. | Pharmacovigilance study | Large real-world signal detection; reporting and denominator bias | Signal-generating observational evidence |
| 11 | Suresh et al. | Prospective pilot | Sensitive serial testing and predictive signal; small pilot requiring validation | Preliminary pilot evidence |
| 12 | Wesley et al. | Observational EEG series | Direct EEG characterization; selected treated population and small sample | Limited observational evidence |
| 13 | Gust et al. | Pediatric EEG study | Prospective physiologic correlations; pediatric/product-specific | Limited prospective evidence |
| 14 | Hernani et al. | Observational EEG study | Baseline association with severity; nonrandomized and modest sample | Limited observational evidence |
| 15 | Storci et al. | Biomarker study | Novel predictive candidate; requires external clinical validation | Exploratory biomarker evidence |
| 16 | Sweiss et al. | Real-world cohort | Exposure–toxicity association; confounding and product specificity | Moderate observational evidence |
| 17 | Abramson et al. | Phase 3 trial | Robust product safety context; workflow not primary endpoint | High product-context evidence |
| 18 | D’Souza et al. | Phase 1 trial | Direct early safety data; small, noncomparative dose-escalation study | Early-phase evidence |
| 19 | Mohan et al. | Real-world cohort | Multicenter practical safety context; retrospective confounding | Moderate observational evidence |
| 20 | Dima et al. | Real-world cohort | Academic-center experience; selection and retrospective limitations | Limited–moderate observational evidence |
| 21 | Lutfi et al. | Case-based report | Highlights rare severe refractory toxicity; cannot estimate incidence | Case-level safety signal |
| 22 | Kowalski et al. | Real-world prophylaxis cohort | Operationally relevant association; no randomized control | Limited–moderate observational evidence |
| 23 | Cohen et al. | CARTITUDE cohort analysis | Program-level delayed toxicity signal; product-specific | Moderate observational safety evidence |
| 24 | Schroeder et al. | Case report | Rare delayed phenotype; no generalizable frequency or causality | Case-report-level evidence |
| 25 | Khoudari et al. | Case report | Severe delayed safety signal; no incidence inference | Case-report-level evidence |
| 26 | Wirk and Lim | Case report | Therapeutically informative single observation; efficacy unproven | Case-report-level evidence only |
| 27 | Alqaisi et al. | Scoping review | Broad neurologic disease context; complementary rather than part of original 26 | Scoping-review context |