
Understanding & Preventing Cancer Recurrence: Insights, Strategies, and Advances
Cancer recurrence—the return of cancer following a period of remission—remains a significant challenge, shaped by factors like cancer type, treatment success, and a patient’s overall health. Detecting recurrence early can greatly enhance the effectiveness of subsequent treatments and improve patient outcomes. This guide explores current approaches to monitoring for cancer recurrence and highlights the latest innovations, offering personalized, effective strategies for more reliable detection.
Why Monitor for Cancer Recurrence?
Increased Mortality Risk: Cancer recurrence significantly raises the risk of death—by 2 to 18 times—depending on the cancer type and stage. Early detection enables timely intervention, which can improve survival chances and prognosis.
High Recurrence Rates: Research indicates that 15% to 69% of cancer patients face recurrence, influenced by factors like cancer type, the success of initial treatment, and individual risk profiles. Regular monitoring is critical to identify recurrence at its earliest stages.
Benefits of Early Detection: Spotting recurrence early leads to prompt treatment, offering better outcomes and a stronger chance of recovery.
Current Standard of Care for Monitoring Cancer Recurrence
Monitoring for cancer recurrence is a critical part of follow-up care for patients with breast, colorectal, lung, liver, pancreatic, and biliary tract cancers. The standard approaches include a combination of imaging scans, tumor marker tests, and endoscopic procedures tailored to the specific cancer type. Below are the key methods used today:
1. Regular Imaging Scans
Imaging remains the backbone of recurrence monitoring for many cancers, with the type and frequency of scans varying based on the cancer’s characteristics and stage.
Mammography: The cornerstone of surveillance after curative breast cancer treatment, mammography effectively detects 8% to 50% of ipsilateral (same-side) recurrences and 18% to 80% of contralateral (opposite-side) metachronous cancers, making it essential for ongoing breast cancer monitoring.
Computed Tomography (CT) Scans: Commonly used for lung, colorectal, liver, and pancreatic cancers, CT scans are performed at regular intervals—ranging from every few months to years—to identify tumor regrowth or metastasis.
Positron Emission Tomography (PET) Scans: Often combined with CT scans, PET imaging detects metabolic changes linked to cancer cells, enhancing diagnostic accuracy in select cases.
Magnetic Resonance Imaging (MRI): Employed occasionally for liver and pancreatic cancers when CT results are unclear, offering detailed imaging to guide further evaluation.


2. Tumor Marker Tests
For certain cancers, blood tests measuring specific tumor markers provide additional monitoring support, though they are less precise than imaging.
CEA (Carcinoembryonic Antigen): Regularly checked in colorectal cancer patients to signal potential recurrence.
AFP (Alpha-Fetoprotein): Used in liver cancer follow-up to detect early signs of tumor activity.
3. Endoscopy
Colonoscopy: The gold standard for colorectal cancer surveillance post-surgery, regular colonoscopies help detect recurrence in the colon or rectum, ensuring timely intervention.
Limitations of Current Cancer Recurrence Monitoring
While the methods outlined above—such as regular imaging scans, tumor marker tests, and endoscopy—represent the gold standard for surveillance of cancer recurrence in breast, colorectal, lung, liver, pancreatic, and biliary tract cancers, they come with certain limitations:
- Radiation Exposure: Repeated imaging, particularly with CT and PET scans, exposes patients to ionizing radiation, which may pose cumulative health risks over time.
- Delayed Detection: Imaging often detects recurrence only after tumors have grown large enough to be visible, potentially delaying critical treatment and impacting outcomes.
- Risks of Endoscopy: Procedures like colonoscopy, though highly effective, carry risks such as bleeding, infection, and, in rare cases, intestinal perforation.
These challenges highlight the need for ongoing advancements to complement these established tools, aiming to enhance safety, precision, and timeliness in detecting cancer recurrence.

LucenceMONITOR: Personalised Detection of Cancer Recurrence
LucenceMONITOR is an effective blood test designed to monitor six key cancers—breast, colorectal, lung, liver, pancreatic, and biliary tract—and detect minimal residual disease (MRD) as early as 18 months after surgical treatment.
Minimal Residual Disease (MRD) refers to the small number of cancer cells that may linger in the body after treatment, often undetectable by traditional imaging or tests. These residual cells, though few, carry a significant risk of multiplying over time, potentially leading to cancer recurrence or progression. MRD is especially critical in blood cancers (like leukemia and lymphoma) and solid tumors, where even tiny traces of cancer cells can trigger a relapse.
By leveraging advances in circulating tumor DNA (ctDNA) testing, LucenceMONITOR analyses minute fragments of tumor DNA in the bloodstream, offering a highly sensitive and precise way to spot recurrence earlier than conventional methods. This MRD testing revolutionizes cancer surveillance by assessing treatment effectiveness, predicting relapse risk, and guiding personalized treatment plans—empowering patients and clinicians with actionable insights for better outcomes.

Key Benefits of MRD Testing:
✅ Earlier Detection: MRD testing can identify recurrence months before tumors become visible on CT scans.
✅ Non-Invasive: A simple blood draw replaces the need for frequent high-radiation imaging.
✅ More Accurate Monitoring: Unlike traditional tumor markers, ctDNA analysis provides specific genetic insights into tumor activity and progression.
✅ Personalized Treatment Decisions: Helps oncologists determine when to start or adjust treatment, improving patient outcomes.
How LucenceMONITOR Outperforms Traditional Cancer Surveillance?
LucenceMONITOR leverages circulating tumor DNA (ctDNA) testing to revolutionize recurrence monitoring, offering clear advantages over conventional methods:
Assesses Recurrence Risk: Studies show 93% of cancer patients with detectable ctDNA after surgery experience recurrence, while 96% of those with consistently undetectable ctDNA remain cancer-free long-term.
Detects Recurrence Earlier: ctDNA identifies recurrence an average of 5.8 months sooner than standard radiologic imaging, enabling faster intervention.
Monitors Therapy Response: Unlike traditional protein markers, ctDNA provides a more precise way to track recurrence, while also detecting actionable mutations and resistance to targeted therapies.
These benefits make LucenceMONITOR a powerful tool for proactive, personalized cancer management.
The Role of MRD Testing in Cancer Recurrence Monitoring

While CT scans remain a cornerstone of cancer follow-up care, LucenceMONITOR’s minimal residual disease (MRD) testing with circulating tumor DNA (ctDNA) analysis offers a powerful complement. This approach enables earlier and more accurate detection of recurrence compared to imaging alone.
Increasingly, oncologists are incorporating liquid biopsy tests like LucenceMONITOR into post-treatment surveillance for cancers such as lung, colorectal, liver, and pancreatic. By reducing dependence on imaging, this DNA-based monitoring minimizes radiation exposure, enhances timely interventions, and marks a significant leap forward in precision oncology—ultimately improving long-term survival outcomes.
MRD testing at scheduled intervals serves several critical functions in post-treatment cancer surveillance:
Evaluating Recurrence Risk: Studies show that 93% of cancer patients with detectable circulating tumor DNA (ctDNA) after surgery experience recurrence, whereas 96% of those with undetectable ctDNA remain disease-free in the long term.
- Early Recurrence Detection: MRD testing with ctDNA can detect cancer recurrence up to 5.8 months earlier than standard radiologic imaging, allowing for timely intervention.
- Tracking Treatment Response: ctDNA provides a more accurate measure of recurrence risk compared to traditional protein-based tumor markers. It also helps identify treatment-resistant mutations and actionable genetic changes, guiding more precise, targeted therapies.

Understanding Cancer Recurrence
Cancer recurrence—the return of cancer after a period of remission—can be a challenging and emotional experience for patients and their families.
- Types of Recurrence:
- Local recurrence – Cancer returns at the original site.
- Regional recurrence – Cancer spreads to nearby lymph nodes.
- Distant/metastatic recurrence – Cancer appears in distant organs.
- Risk Factors:
- Type and stage of the original cancer.
- Response to initial treatment.
- Genetic and lifestyle factors.
- Early Detection:
- Regular follow-ups and screenings improve chances of early intervention.
- Being aware of new or unusual symptoms is crucial.
How is LucenceMONITOR™ Used in Clinical Practice?
LucenceMONITOR™ is a liquid biopsy test, plays a vital role in detecting MRD with high sensitivity.
It tracks tumor specific mutations in a patient’s ctDNA and ctRNA using Lucence’s mirror barcoding technology.
LucenceMONITOR™ is complementary to standard-of-care radiologic imaging, meaning it works alongside CT scans, MRIs, and other imaging techniques to enhance recurrence detection and guide treatment decisions.
When is MRD testing recommended?
🔹 4-6 weeks post-surgery to assess if any residual cancer cells remain.
🔹 At 3-month intervals to continuously monitor for recurrence.Why is this important?
✅ Early intervention: Detecting recurrence before imaging scans show visible tumors allows for faster treatment adjustments.
✅ Reduced reliance on radiation-based scans: Fewer CT scans may be needed, minimizing radiation exposure.
✅ More personalized treatment planning: Physicians can adjust therapies based on real-time tumor DNA/RNA analysis.


Personalised Cancer Recurrence Detection
Monitoring Recurrence in 6 Cancers
Breast Cancer: A malignant tumor that originates in the breast tissue, often in the milk ducts or lobules. It is one of the most common cancers in women but can also occur in men. Early detection through mammograms improves outcomes.
Colorectal Cancer: Cancer that begins in the colon or rectum, often developing from precancerous polyps. Risk factors include age, diet, genetics, and inflammatory bowel diseases. Screening through colonoscopies is key for early detection.
Lung Cancer: A leading cause of cancer-related deaths, often linked to smoking but also seen in non-smokers. It originates in the lung tissues and includes types like small-cell and non-small-cell lung cancer. Treatment depends on the stage and type.
Liver Cancer: Typically develops in people with chronic liver disease, cirrhosis, or hepatitis infections. Hepatocellular carcinoma (HCC) is the most common type. Early-stage treatment includes surgery or liver transplantation.
Pancreatic Cancer: An aggressive cancer with a low survival rate, as symptoms often appear late. It arises in the pancreas, affecting digestion and hormone regulation. Risk factors include smoking, diabetes, and chronic pancreatitis.
Biliary Tract Cancer: Includes cancers of the bile ducts and gallbladder, which are rare but often diagnosed late. Risk factors include gallstones, chronic inflammation, and liver fluke infections. Treatment is challenging due to late detection.
LucenceMONITOR™ MRD Program Overview
The LucenceMONITOR™ MRD Program is a structured two-step process designed for Minimal Residual Disease (MRD) detection and cancer recurrence monitoring. It leverages tumor-specific mutations identified from patient samples to provide precise and personalized surveillance.
Step 1: Eligibility Assessment
- Patients undergo an initial LucenceMONITOR™ TissueBASELINE test.
- This test detects tumor-specific mutations from the patient’s tissue sample.
- To proceed with ongoing monitoring, the identified mutation must be included in the LucenceMONITOR™ LiquidMRD gene list.
Step 2: Ongoing Monitoring
- Patients receive four LucenceMONITOR™ LiquidMRD tests at regular intervals.
- These liquid biopsy tests analyze circulating tumor DNA (ctDNA) and circulating tumor RNA (ctRNA) in the bloodstream.
- The program helps detect cancer recurrence earlier than traditional imaging methods, enabling timely intervention.
- Physicians should refer to the test order form for the full list of eligible mutations.

FAQ
Cancer recurrence happens when some cancer cells survive treatment and remain in the body undetected. These residual cells can later multiply, leading to a relapse. Factors influencing recurrence include the cancer type, stage at diagnosis, treatment effectiveness, and individual health conditions. In some cases, cancer cells may become resistant to treatment, making recurrence more likely.
LucenceINSIGHT is particularly beneficial for:
- Cancer survivors who want to monitor for recurrence proactively.
- Individuals with a family history of cancer who may be at a higher risk.
- Patients undergoing post-treatment surveillance who want a convenient, non-invasive option for monitoring.
By integrating LucenceINSIGHT into routine follow-ups, patients and doctors can detect potential recurrences earlier and take appropriate action.
The signs of recurrence vary based on the type of cancer but may include persistent pain, unexplained weight loss, fatigue, lumps or swelling, changes in bowel or bladder habits, and unusual bleeding. Some recurrences are detected through routine scans or blood tests before symptoms appear. If you notice any unusual or persistent symptoms, it’s important to consult your doctor for further evaluation. Regular follow-ups and screenings are crucial in detecting recurrence early.