Circulating Tumor Cells and Drug Sensitivity Testing

How Cancer Patients Can Find the Drugs That Truly Work for Them

Free cancer support
The Hong Kong Cancer Support Network provides you with comprehensive, free cancer information and professional assistance, ensuring that every patient and family member does not have to face the challenge alone.

Patients rarely ask first about the name of their cancer. What they really want to know is: “Which drug will actually work for me?” “Is the medicine I’m taking right now doing anything at all?”

 

In real life, most treatment decisions are still based on large-scale statistics and international guidelines. Doctors follow standard protocols when choosing chemotherapy, targeted therapy, or immunotherapy. Yet tumors are extraordinarily heterogeneous — the exact same drug can be dramatically effective in one patient and completely useless (or even harmful) in another. As a result, many patients suffer severe side effects and huge financial burdens from ineffective drugs while missing treatments that would have worked far better.

 

This is precisely why CTC-based drug sensitivity testing is rapidly becoming one of the most sought-after tools in modern oncology. By drawing blood, isolating live circulating tumor cells (CTCs), and testing dozens of drugs directly on those cells in the laboratory, doctors can finally see — before treatment begins — which drugs actually kill that patient’s cancer. This approach sharply reduces trial-and-error and makes truly personalized therapy possible.

The Question on Every Cancer Patient’s Mind

What Are Circulating Tumor Cells (CTCs)?

CTCs are live cancer cells that detach from the primary tumor or metastases and enter the bloodstream. Although extremely rare, they carry the complete molecular signature of the tumor (DNA, RNA, and proteins). Unlike traditional tissue biopsy, CTC testing requires only a routine blood draw — it is minimally invasive and can be repeated anytime.

 

Clinically, CTCs are used for early detection, prognosis, recurrence monitoring, and — most importantly — as living material for functional drug sensitivity testing.

Drug sensitivity testing (DST) exposes a patient’s own tumor cells to different anti-cancer agents or combinations in the lab and directly measures outcomes such as cell death, growth inhibition, or apoptosis. When the source cells are CTCs drawn from the patient’s blood, the test reflects the current, real-time state of the disease — far more relevant than an old biopsy taken months or years earlier.

Drug Sensitivity Testing: The Core Idea

From Blood Draw to Personalized Drug Report: Step-by-Step

1. Blood collection & CTC isolation

10–20 mL blood is drawn; CTCs are separated using marker-based, microfluidic, or marker-independent technologies.

2. Cell culture & expansion

Isolated CTCs are kept alive and often grown into 3D organoids that closely mimic the in-body tumor environment.

3. Drug challenge

50–100+ drugs (chemotherapies, targeted agents, immunotherapies, hormonals, and natural compounds) are tested individually and in combinations.

4. Report generation

A detailed, ranked sensitivity profile is produced: highly effective → moderately effective → resistant.

Patients receive a clear “treatment roadmap” that oncologists can immediately translate into clinical decisions.

Why CTC-Based Drug Sensitivity Testing Is So Meaningful for Patients

  • Eliminates futile treatments before they are ever given
  • Reduces unnecessary toxicity and side effects
  • Enables genuine individualization — the same cancer type and stage can show >10-fold differences in drug response
  • Supports dynamic monitoring — tumors evolve resistance; repeat blood draws provide updated guidance at any time

Limitations Patients Should Understand Realistically

  • CTC numbers can be very low, especially in early-stage or low-tumor-burden disease
  • In-vitro results cannot perfectly replicate the human immune system and metabolic environment (results are strong guidance, not absolute truth)
  • Turnaround time is usually 2–4 weeks — not suitable for rapidly progressing cases
  • Cost remains high and is not yet widely reimbursed

Five Key Questions Patients Should Ask Before Proceeding

  1. Is this test appropriate for my cancer type and current stage?
  2. What is the laboratory’s real-world CTC detection and culture success rate in patients like me?
  3. Do I have the time to wait for results, or should I start standard therapy immediately?
  4. Can I afford the test, and does the potential benefit justify the cost for me?
  5. How will my oncologist integrate the report with genomic testing, imaging, and clinical experience?

Conclusion

For cancer patients, CTC-based drug sensitivity testing is no longer a distant future technology — it is available and helping patients today. It shifts drug selection from “what works on average” to “what actually kills my own cancer cells in the lab.”

Although technical and cost challenges remain, the field is advancing rapidly. In the fight against cancer, every piece of personalized data gives patients a better chance. CTC drug sensitivity testing is delivering exactly that — clearer direction, reduced suffering, and genuine hope.

Want to know how to choose the most suitable adjuvant therapy for cancer?

Contact our specialists now for professional advice and let us work together to find the best solution for you or your family.

Contact our professional team now

References

  • Alix-Panabières, C., & Pantel, K. (2021). Liquid biopsy: From discovery to clinical application. Cancer Discovery, 11(4), 858–873.
  • Gao, D., Vela, I., Sboner, A., Iaquinta, P. J., Karthaus, W. R., Gopalan, A., … & Chen, Y. (2014). Organoid cultures derived from patients with advanced prostate cancer. Cell, 159(1), 176–187.
  • Pauli, C., Hopkins, B. D., Prandi, D., Shaw, R., Fedrizzi, T., Sboner, A., … & Taylor, B. S. (2017). Personalized in vitro and in vivo cancer models to guide precision medicine. Cancer Discovery, 7(5), 462–477.
  • Sachs, N., de Ligt, J., Kopper, O., Gogola, E., Bounova, G., Weeber, F., … & Clevers, H. (2018). A living biobank of breast cancer organoids captures disease heterogeneity. Cell, 172(1–2), 373–386.
  • Tuveson, D., & Clevers, H. (2019). Cancer modeling meets human organoid technology. Science, 364(6444), 952–955.
  • Yang, C., Xia, B. R., Jin, W. L., & Lou, G. (2019). Circulating tumor cells in precision oncology: Clinical applications in liquid biopsy and 3D organoid model. Cancer Cell International, 19(1), 341.
  • Yu, M., Bardia, A., Wittner, B. S., Stott, S. L., Smas, M. E., Ting, D. T., … & Maheswaran, S. (2014). Circulating breast tumor cells exhibit dynamic changes in epithelial and mesenchymal composition. Science, 339(6119), 580–584.
Scroll to Top
0

Subtotal