Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
1500

Summary

Conditions
  • Cancer of Cervix
  • Bladder Cancer
  • Glioblastoma
  • BRCA Gene Rearrangement
  • Breast Cancer
  • Cancer
  • Cancer, Advanced
  • Myelodysplastic Syndromes
  • Cancer Liver
  • Cancer of Neck
  • Non -Small Cell Lung Cancer
  • Cancer of Rectum
  • Endometrial Cancer
  • Melanoma
  • Neuroendocrine Tumors
  • Mantle Cell Lymphoma
  • Cancer of Colon
  • Urothelial Carcinoma
  • Myeloproliferative Disorders
  • Testicular Cancer
  • Cancer of Esophagus
  • Myelofibrosis
  • Non Hodgkin Lymphoma
  • Cholangiocarcinoma
  • Ovarian Cancer
  • Leukemia
  • Cancer of Kidney
  • Cancer of Skin
  • Cancer Breast
  • Cancer, Lung
  • COVID
  • Cancer Prostate
  • Marginal Zone Lymphoma
  • Mismatch Repair Deficiency
  • Cancer of Larynx
  • Follicular Lymphoma
  • Cancer of Liver
  • Central Nervous System Tumor
  • Carcinoma
  • Cancer of Pancreas
  • Cancer of Stomach
  • Cancer Metastatic
  • Myeloproliferative Neoplasm
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Younger than 125 years
Gender
Both males and females

Description

The SYNERGY Registry is an international prospective, observational cohort study of eligible adult and pediatric pts with advanced solid and hematological malignancies, for whom the decision to consider CTE has already been made by their primary providers (PP). Using a proprietary application progra...

The SYNERGY Registry is an international prospective, observational cohort study of eligible adult and pediatric pts with advanced solid and hematological malignancies, for whom the decision to consider CTE has already been made by their primary providers (PP). Using a proprietary application programming interface (API) linked to existing electronic health records (EHR) platforms, individual clinical data is extracted, analyzed and matched to a parametric database of existing institutional and non-institutional CT. Machine learning algorithms allow for dynamic matching based on CT allocation and availability for optimized matching. Patients voluntarily enroll into the registry, which is non-interventional with no protocol-mandated tests/procedures - all treatment decisions are made at the discretion of PP in consultation with their pts, based on the AI CT matching report, and VTB support. CTE will be assessed on variables including biomarkers, barriers to enrollment. Study duration anticipated as ~36 mo (~24-mo enrollment followed by 12 mo of data collection, to occur every 3 mo). The primary analysis will be performed 12 mo after last pt enrolled. The impact time to initiation of CTE on PFS and OS will be estimated by Kaplan-Meier and Cox multivariable survival analysis. Enrollment is ongoing, with a target of ?1500 patients.

Tracking Information

NCT #
NCT03452774
Collaborators
Not Provided
Investigators
Principal Investigator: Selin Kurnaz, PhD Massive Bio, Inc.