Summary

Location
at UCSF
Dates
study started
study ends around

Description

Summary

International registry for cancer patients evaluating the feasibility and clinical utility of an Artificial Intelligence-based precision oncology clinical trial matching tool, powered by a virtual tumor boards (VTB) program, and its clinical impact on pts with advanced cancer to facilitate clinical trial enrollment (CTE), as well as the financial impact, and potential outcomes of the intervention.

Details

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 ≥50,000 patients.

Keywords

Cancer, Metastatic, Cancer, Cancer of Pancreas, Cancer of Liver, Cancer of Stomach, Cancer Liver, Cancer of Rectum, Cancer of Kidney, Cancer of Esophagus, Cancer of Cervix, Cancer of Colon, Cancer of Larynx, Cancer, Lung, Cancer, Breast, Cancer, Advanced, Cancer Prostate, Cancer of Neck, Cancer of Skin, Neuroendocrine Tumors, Carcinoma, Mismatch Repair Deficiency, BRCA Gene Rearrangement, Non Hodgkin Lymphoma, Leukemia, Non Small Cell Lung Cancer, Cholangiocarcinoma, Glioblastoma, Central Nervous System Tumor, Melanoma, Urothelial Carcinoma, Bladder Cancer, Ovarian Cancer, Endometrial Cancer, Testicular Cancer, Breast Cancer, COVID, Myelofibrosis, Myeloproliferative Neoplasm, Myeloproliferative Disorders, Follicular Lymphoma, Mantle Cell Lymphoma, Marginal Zone Lymphoma, Myelodysplastic Syndromes, artificial intelligence, virtual tumor board, clinical trial, clinical trial matching, electronic medical record, machine learning, cost of care, targeted therapy, immunotherapy, precision medicine, precision oncology, value based care, real world data, data analytics, Neoplasm Metastasis, Neoplasms, Pancreatic Neoplasms, Liver Neoplasms, Stomach Neoplasms, Hepatocellular Carcinoma, Rectal Neoplasms, Kidney Neoplasms, Esophageal Neoplasms, Uterine Cervical Neoplasms, Colonic Neoplasms, Laryngeal Neoplasms, Lung Neoplasms, Breast Neoplasms, Prostatic Neoplasms, Head and Neck Neoplasms, Skin Neoplasms, Turcot syndrome, Non-Hodgkin Lymphoma, Non-Small-Cell Lung Carcinoma, Central Nervous System Neoplasms, Transitional Cell Carcinoma, Urinary Bladder Neoplasms, Ovarian Neoplasms, Endometrial Neoplasms, Testicular Neoplasms, Primary Myelofibrosis, Mantle-Cell Lymphoma, Lymphoma, B-Cell, Marginal Zone

Eligibility

You can join if…

  • Pts with solid and hematological malignancies;
  • Pts cancer-related biomarkers, gene variants, fusion and rearrangements (by immunohistochemistry, PCR, FISH or NGS): PD-L1, MSI (MMR), Claudin18.2, HER2/Neu, Tumor mutational burden/load (TMB), ABL1, ACVR1B, AKT1, AKT2, AKT3, ALK, APC, AR, ATM, ATRX, AURKA, AURKB, BAP1, BCL2, BCL6, BRAF, BRCA1, BRCA2, BTK, CCND1, CCND2, CCND3, CDK4, CDK6, CDKN1A/B, CEBPA, CHEK1, CHEK2, CSF1R, CTNNB1, DAXX, DDR1/2, DNMT3A, EGFR, ERBB2, ERBB3, ERBB4, ERCC4, ER, ESR1, FANCA, FAS, FBXW7, FGFR1, FGFR2, FGFR3, FGFR4, FLT3, GATA3, GATA6, GNAS, HDAC1, HGF, HRAS, IDH1, IDH2, IGF1R, JAK1, JAK2, JAK3, KDR (VEGFR2), KIT, KRAS, MAP2K2 (MEK2), MAP3K1, MCL1, MDM2, MDM4, MEN1, MET, MSH2, MSH3, MSH6, MTOR, MUTYH, MYC, MYCL (MYCL1), NF1, NF2, NOTCH1, NPM1, NRAS, NTRK1, NTRK2, NTRK3, PALB2, PARP1, PARP2, PARP3, PBRM1, PDCD1 (PD1), PDCD1LG2 (PD-L2), PDGFRA, PDGFRB, PIK3C, PMS2, POLD1, POLE, PRDM1, PTCH1, PTEN, RAF1, RB1, RET, RICTOR, ROS1, RPTOR, SDHA/B/C, SMAD, SMARC, SMO, STK11, TGFBR2, TP53, TSC1, TSC2, VEGFA, VHL, WT1, ZNF217, ZNF703, CEACAM, NRG1, among others.

These biomarkers should be determined by local laboratory, external vendor, or next generation sequencing platform

  • Decision to consider clinical trial pre-screening enrollment (CTE) by primary provider and/or patient

You CAN'T join if...

  • ECOG PS > 2;
  • Abnormal organ function;
  • Hospice enrollment

Locations

  • Massive Bio SYNERGY-AI site accepting new patients
    San Francisco 5391959 California 5332921 94143 United States
  • Massive Bio SYNERGY-AI site accepting new patients
    Houston 4699066 Texas 4736286 77030 United States
  • Massive Bio SYNERGY-AI site accepting new patients
    Boca Raton 4148411 Florida 4155751 33487 United States
  • Massive Bio, Inc accepting new patients
    New York 5128581 New York 5128638 10006 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Massive Bio, Inc.
ID
NCT03452774
Study Type
Observational [Patient Registry]
Participants
Expecting 50000 study participants
Last Updated