🔎 Trials Near Me

Home › Esophageal Cancer › NCT06605404

Pan-tumor MRD Study

RecruitingObservational study

Molecular Residual Disease in Solid Tumors: A Prospective Study to Collect Clinical Data and Biospecimens to Support Discovery and Development of Cancer Biomarkers

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Eligibility Criteria:

1. Age 18 years or older.
2. Confirmed histological or cytological diagnosis of a malignant solid tumor that is either specified in one of the pre-defined tumor cohorts or meets the enrollment criteria for the Mix of Solid Tumors (MOST) cohort (Table 1).
3. Eligible for curative intent therapy, with surgical resection of cancer planned.

   a. If surgical resection has occurred, enrollment should occur within 3 months of surgical resection and before initiation of adjuvant therapy.
4. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, 1, or 2.
5. No systemic therapy for current cancer diagnosis administered before enrollment.
6. Willing and able to comply with required study procedures, including blood sample collection and primary tumor tissue submission from diagnostic biopsy or surgical excision.
7. Has completed all therapy (including endocrine therapy) 3 or more years ago for any previous invasive solid organ malignancy (with exception of nonmelanoma skin cancers) or hematologic malignancy. Individuals with a prior history of noninvasive (in situ) carcinomas may participate if they have received definitive treatment (no washout period required).
8. No concurrent diagnosis of another invasive cancer, except for nonmelanoma skin cancers.
9. No prior allogeneic hematopoietic stem cell transplant.
10. Able and willing to provide informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization for the release of personal health information.

    Cohort Specific Criteria
11. Muscle-invasive urothelial carcinoma of the bladder and Melanoma Cohorts: Stage II or operable III cancer:
12. Esophageal, Gastric/GEJ, and NSCLC Cohorts: Stage I, II, or operable III cancer.
13. Pancreatic Cohort: Stage I, II or operable III cancer, exocrine only disease.
14. MOST cohort: Stage II or operable stage III solid tumor diagnosis that meets eligibility criteria and is not included in the other cohorts.

The following tumor types are excluded:

1. Central nervous system (CNS) malignancies
2. Colorectal cancer
3. Breast cancer
4. Squamous cell skin cancer
5. Basal cell carcinoma
6. Gastrointestinal stromal tumors (GIST)
7. Thyroid cancer
8. Uveal melanoma
9. Low or intermediate grade neuroendocrine tumors

   â–  Eligible tumor types: High-grade neuroendocrine tumors, including neuroendocrine carcinomas, Merkel cell carcinomas, and small cell lung cancer are permissible
10. Hematologic cancers including multiple myeloma or other plasma cell dyscrasias, Hodgkin\'s lymphoma, non-Hodgkin\'s lymphoma, acute or chronic leukemias including chronic lymphocytic leukemia / small lymphocytic leukemia

About the study

The purpose of this observational study is to collect clinical information, blood, and tumor tissue samples from participants diagnosed with stage I, stage II, or operable stage III cancer in select solid tumors. The information collected will be used to develop tests to better understand cancer, for example, to improve cancer detection and to assess the risk of cancer coming back.

Participants will receive routine standard of care from their doctor and their involvement is expected to last for approximately five and a half (5.5) years.

What is being tested

Sponsor: Paradigm Health · Participants: 1,350 · Started: Jan 8, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06605404

Locations in the U.S.

AlabamaAlabama Oncology, Birmingham
ArizonaMohtaseb Cancer Center and Blood Disorders, Bullhead City
Cancer & Blood Specialists of Arizona, Casa Grande
ArkansasCARTI, Little Rock
Highlands Oncology Group (HOG), Springdale
CaliforniaLos Angeles Cancer Network (LACN), Glendale
Ventura County Hematology Oncology Specialists, Oxnard
Medical Oncology Associates of San Diego, San Diego
Medical Oncology Associates of San Diego (MOASD), San Diego
Stockton Hematology Oncology Med Group, Stockton
ColoradoThe Melanoma and Skin Cancer Institute, Englewood
FloridaOncology & Hematology Associates of West Broward, Coral Springs
Mid Florida Cancer Centers, Orange City
Comprehensive Hematology Oncology (CHO), St. Petersburg
GeorgiaPiedmont Cancer Institute, Atlanta
IllinoisCancer Care Specialists of Illinois (CCSI), O'Fallon
Carle Health, Urbana
KansasCotton O'Neil Cancer Center [Stormont Vail], Topeka
Cancer Center of Kansas, Wichita
KentuckyBaptist Health Corbin, Corbin
Baptist Health Hardin, Elizabethtown
Baptist Health Lexington, Lexington
Baptist Health Louisville, Louisville
LouisianaPontchartrain Cancer Center, Covington
Christus Health Highlands, Shreveport
MichiganThe Cancer & Hematology Centers (CHC), Grand Rapids
MinnesotaMayo Clinic, Rochester
MissouriCox Health, Springfield
NebraskaCancer Partners of Nebraska, Lincoln
New MexicoSan Juan Oncology Associates, Farmington
New YorkGuthrie Lourdes Memorial Hospital (GLMH), Binghamton
New York Cancer & Blood Specialists, Shirley
North CarolinaCarolina Oncology Specialists, Charlotte
Southeastern Medical Oncology Center (SMOC), Goldsboro
Regional Medical Oncology Center, Wilson
OhioGabrail Cancer Center, Canton
Taylor Cancer Research Center, Maumee
OklahomaOklahoma Cancer Specialists and Research Institute (OCSRI), Tulsa
OregonOregon Health & Science University (OHSU), Portland
PennsylvaniaLancaster General Hospital (UPenn), Lancaster
Guthrie Foundation, Sayre
Cancer Care Associates of York (CCAY), York
TexasOnocology Consultants P.A. (Oncology Consultants [OC Houston]), Houston
Community Clinical Trials, Kingwood
Christus St. Michael's, Texarkana
VirginiaVirginia Cancer Institute, Richmond
WashingtonNorthwest Medical Specialties (NWMS), Tacoma

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.