cfDNA Assay Prospective Observational Validation for Early Cancer Detection and Minimal Residual Disease

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age40+
SponsorAdela, Inc

About this trial

This is an observational case-control study to train and validate a genome-wide methylome enrichment platform to detect multiple cancer types and to differentiate amongst cancer types. The cancers included in this study are brain, breast, bladder, cervical, colorectal, endometrial, esophageal, gastric, head and neck, hepatobiliary, leukemia, lung, lymphoma, multiple myeloma, ovarian, pancreatic, prostate, renal, sarcoma, and thyroid. These cancers were selected based on their prevalence and mortality to maximize impact on clinical care.

Additionally, the ability of the whole-genome methylome enrichment platform to detect minimal residual disease after completion of cancer treatment and to detect relapse prior to clinical presentation will be evaluated in lung cancer. This cancer was selected based on the existing clinical landscape and treatment availability.

Eligibility criteria

Qualifiers

Newly diagnosed (within 120 days) with cancer or a recurrence of a cancer diagnosed >5 years ago of one of the following subtypes: Invasive Brain, Breast, Bladder, Cervical, Colorectal, Endometrial, Esophageal, Gastric, Head and Neck, Hepatobiliary, Lung, Ovarian, Pancreatic, Prostate, Renal, Sarcoma, Thyroid; Leukemia, Lymphoma, Multiple Myeloma

Able and willing to provide informed consent

≥40 years of age

Disqualifiers

Currently receiving any treatment for cancer

Currently taking any demethylating agents/DNA hypomethylating agents

Simultaneously diagnosed with two or more invasive cancers

Diagnosed with any invasive or non-invasive cancer in addition to the index cancer in the last 5 years

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

7,000 Participants
are grouped into 2 trial groups

Sponsors and collaborators