Related articles

When we talk about early cancer detection, most people think of imaging tests or tumor markers.
These tools are valuable for identifying structural abnormalities or elevated markers — in other words, when a disease has already begun to manifest.
But what if you could go one step earlier?
Before anything is visible or measurable, is there a way to understand your underlying genetic risk?

Have you ever had a health checkup that came back “normal,” yet you still felt fatigued, foggy, or out of balance?
Or known someone who was diagnosed with cancer shortly after receiving clear test results?
These situations highlight a crucial gap:
Traditional checkups are important—but they focus on detecting existing issues, not predicting future risks.

You may regularly undergo health checkups, including cancer markers and imaging scans.
Yet, it’s not uncommon to hear of individuals being diagnosed with cancer shortly after receiving “normal” test results. Why does this happen?
The truth is, traditional screenings, while essential, have their limitations.
Some risks remain hidden—undetectable by standard scans or blood markers—because they originate at a cellular or molecular level, far before tumors form.
This is where RGCC (Research Genetic Cancer Centre) testing plays a unique and valuable role.

One in three men and one in four women will be diagnosed with cancer in their lifetime. Many types of cancer can develop silently over years, and by the time symptoms appear, the disease may already be in an advanced stage. Recognizing early warning signs and seeking medical advice promptly can be life-changing.

Tumor markers are substances produced either by cancer cells or by the body in response to cancer. These can be found in blood, urine, stool, body fluids, or tissues.