THE MODERN BIO← Testing Lab

MODERN BIO / TESTING LAB / PRECISION ONCOLOGY

Emerging + use-dependent

Advanced
cancer testing.

Start with the clinical question—not the most comprehensive panel.

RGCC International offers liquid-biopsy and molecular tests that examine circulating tumor cells and related cancer signals. Some are positioned for early detection; others for monitoring known cancer or exploring treatment sensitivity. Those are different decisions with different evidence, risks and follow-up needs.

Find the right testing lane ↓View RGCC's test portfolio ↗
Advanced blood testing and cellular biomarker visualization
LIQUID BIOPSY / CTC / MOLECULAR SIGNALSInformation for a clinician-led decision.

01 / START HERE

What brings you here?

Choose a situation to focus the guide. This organizes the information; your clinician determines whether a test is appropriate.
Not sure which situation fits?

You can browse all six tests below or use the questions to prepare for a clinician conversation.

Help me prepare →
Keep standard care in place.

These tests do not replace mammography, colonoscopy or FIT, cervical screening, low-dose CT, pathology or imaging. A detected signal needs conventional clinical evaluation and confirmation. No therapy, supplement or oncology plan should change from this report alone.

02 / UNDERSTAND THE OPTIONS

What does each test look for?

Open a test for its purpose and limits. These are RGCC’s reported uses, not a recommendation to order. Confirm current panels, specimens, methods and availability with RGCC and your ordering clinician.

All 6 tests

Screening signalOnco-D-Clare

What RGCC reports

Designed by RGCC for early-detection risk signals before symptoms.

What to keep in view

Does not diagnose cancer, cover every cancer or replace organ-specific screening.

Baseline + broad monitoringOncotrace

What RGCC reports

Evaluates circulating tumor cell count, phenotype and stemness markers.

What to keep in view

Interpret changes with tumor type, stage, treatment, imaging and the same laboratory method.

Treatment-response monitoringOncocount

What RGCC reports

Measures the presence and concentration of circulating tumor cells.

What to keep in view

A count alone does not establish treatment success, recurrence or progression.

Cancer-specific monitoringOncotrail RGCC

What RGCC reports

Tracks markers associated with selected cancers, including breast, colon, GI, lung, melanoma, prostate and sarcoma.

What to keep in view

Availability and clinical fit depend on the confirmed cancer type and the treating clinician's plan.

Conventional therapy profilingOnconomics

What RGCC reports

RGCC reports cellular and molecular sensitivity to selected chemotherapy and targeted agents.

What to keep in view

An ex-vivo result is one input; it is not a prescription or proof of patient benefit.

Expanded therapy profilingOnconomics Plus

What RGCC reports

Adds RGCC-reported sensitivity to selected natural substances and other modalities.

What to keep in view

Natural does not mean safe or compatible. Oncology and pharmacy review are essential.

Next: prepare for the clinician conversation

03 / PREPARE YOUR NEXT STEP

Start with a conversation.

A qualified clinician decides whether to order, how to interpret and what happens next. Modern Bio can help you organize records; coordinated oncology testing is not an available ordering service here.

Bring the full picture

Gather prior results, imaging, pathology and your current medicine and supplement list.

Organize my records →
See the complete seven-step testing workflow

Future coordination should organize the record and route requests. Clinical decisions remain with the qualified oncology team.

  1. 01
    Clarify the situation

    Symptoms, no known cancer, confirmed diagnosis, active treatment or post-treatment surveillance.

  2. 02
    Assemble the source record

    Pathology, stage, imaging, prior biomarkers, inherited risk, treatments, medicines and supplements.

  3. 03
    Practitioner eligibility review

    Confirm that the test can answer a defined question and that the correct oncology team is involved.

  4. 04
    Test-specific consent

    Review evidence, limits, privacy, full cost, possible results and downstream diagnostic burden.

  5. 05
    Qualified collection + laboratory processing

    Use the exact specimen, handling and shipping requirements for the selected assay.

  6. 06
    Reconcile the report

    Compare it with pathology, imaging, authorized biomarkers, symptoms and clinical guidelines.

  7. 07
    Document the next decision

    Confirm, monitor, repeat, refer or take no action—with an owner and timeline for follow-up.

READING A REPORT

What could the result mean?

A report needs context and a clinician-owned next step.
Explore detected, negative and sensitivity results
POSITIVE OR DETECTED SIGNAL

Confirm—do not label.

A screening signal is not proof of cancer. It should trigger a coordinated diagnostic pathway, which may include imaging, endoscopy or tissue biopsy depending on the predicted site and clinical context.

NEGATIVE OR NO SIGNAL

Continue standard care.

A negative blood result does not exclude cancer, clear concerning symptoms or cancel recommended screening. Early cancers may release too little circulating material for detection.

SENSITIVITY RESULT

Reconcile—do not prescribe.

Laboratory response categories must be weighed against the cancer type, stage, patient health, drug approval, dosing evidence, interactions and the treating oncologist's plan.

04 / TAKE THIS TO YOUR CLINICIAN

Make the conversation count.

Use this checklist before payment or sample collection. A credible testing pathway welcomes specific questions about evidence, cost and follow-up.
Open the 10-question appointment checklist
  1. 01

    What exact decision will this result change?

  2. 02

    Is this intended for screening, monitoring, recurrence surveillance or treatment selection?

  3. 03

    What evidence supports this exact test in my cancer type and stage?

  4. 04

    What is the test's regulatory and laboratory status where I live?

  5. 05

    What are its sensitivity, specificity and false-positive or false-negative risks?

  6. 06

    How will a result be confirmed with pathology, imaging or an authorized diagnostic?

  7. 07

    Who will interpret the report and own follow-up?

  8. 08

    Will my oncologist review it before any treatment or supplement changes?

  9. 09

    What is the complete cost, including repeat testing and downstream workup?

  10. 10

    How are my sample, genetic data and results stored, shared and deleted?

START WITH WHAT IS ALREADY PROVEN

Build the complete cancer-prevention record first.

Keep standard screening current, capture family history and prior results, then decide whether an advanced test adds information that could genuinely change care.
Open the screening navigator →Review hereditary testing →Organize records for review →

CHECK THE EVIDENCE

Sources behind the guide.

RGCC pages explain what the company says each assay is designed to do. NCI and FDA sources provide the broader evidence and regulatory context needed to interpret those claims responsibly.
View all seven primary and official sources