Feasibility of functional precision medicine for guiding treatment of relapsed or refractory pediatric cancers.
Arlet M Acanda De La RochaNoah E BerlowMaggie FaderEbony R CoatsCima SaghiraPaula S EspinalJeanette GalanoZiad KhatibHaneen AbdellaOssama M MaherYana VorontsovaCristina M Andrade-FeraudAimee DaccacheAlexa JacomeVictoria ReisBaylee HolcombYasmin GhuraniLilliam RimblasTomás R GuilarteNan HuDaria SalyakinaDiana J AzzamPublished in: Nature medicine (2024)
Children with rare, relapsed or refractory cancers often face limited treatment options, and few predictive biomarkers are available that can enable personalized treatment recommendations. The implementation of functional precision medicine (FPM), which combines genomic profiling with drug sensitivity testing (DST) of patient-derived tumor cells, has potential to identify treatment options when standard-of-care is exhausted. The goal of this prospective observational study was to generate FPM data for pediatric patients with relapsed or refractory cancer. The primary objective was to determine the feasibility of returning FPM-based treatment recommendations in real time to the FPM tumor board (FPMTB) within a clinically actionable timeframe (<4 weeks). The secondary objective was to assess clinical outcomes from patients enrolled in the study. Twenty-five patients with relapsed or refractory solid and hematological cancers were enrolled; 21 patients underwent DST and 20 also completed genomic profiling. Median turnaround times for DST and genomics were within 10 days and 27 days, respectively. Treatment recommendations were made for 19 patients (76%), of whom 14 received therapeutic interventions. Six patients received subsequent FPM-guided treatments. Among these patients, five (83%) experienced a greater than 1.3-fold improvement in progression-free survival associated with their FPM-guided therapy relative to their previous therapy, and demonstrated a significant increase in progression-free survival and objective response rate compared to those of eight non-guided patients. The findings from our proof-of-principle study illustrate the potential for FPM to positively impact clinical care for pediatric and adolescent patients with relapsed or refractory cancers and warrant further validation in large prospective studies. ClinicalTrials.gov registration: NCT03860376 .
Keyphrases
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- healthcare
- acute lymphoblastic leukemia
- peritoneal dialysis
- acute myeloid leukemia
- prognostic factors
- squamous cell carcinoma
- primary care
- mental health
- gene expression
- multiple myeloma
- copy number
- dna methylation
- electronic health record
- single cell
- combination therapy
- bone marrow
- chronic pain
- lymph node metastasis
- human health
- cell therapy
- genome wide