<p>The goal of this study is to comprehensively and longitudinally evaluate the natural history of patients with rare solid tumors or tumor predisposition syndromes, estimating and defining their clinical spectrum (e.g. disease course and survival). Clinical data, patient reported outcomes (PROs), and biospecimen associated data are collected. Clinical data includes response to treatment, tumor pathology, and imaging. PROs include measures of pain, depression, anxiety, mobility, and cognitive functioning. Biospecimen data includes next-generation sequencing [RNAseq, whole exome sequencing (WES), whole genome sequencing (WGS), EPIC methylation array data, and TruSight Oncology 500 gene panel sequencing], cytokine analysis of plasma, immune phenotyping of circulating peripheral blood mononuclear cells.</p>

My Pediatric and Adult Rare Tumor (MyPART) Natural History Study of Rare    Solid Tumors

Rare Diseases study with SNP/CNV Genotypes (NGS) data on dbGaP (497 participants)

My Pediatric and Adult Rare Tumor (MyPART) Natural History Study of Rare Solid Tumors

Description

Applying For Access

Summary