Biomarker Conversation Guide
Understanding Your Biomarker Results
What are biomarkers?
Biomarkers are clues in your cancer cells or blood. They can help your care team choose treatments, avoid medicines that may or may not work well, or watch for signs that cancer may come back.
Bring to your visit:
- Your biomarker report
- This guide
- A person you trust or a place to take notes
My Test Results at a Glance
At diagnosis
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- DNA repair (MMR/MSI): ☐ Tested / ☐ Not yet
☐ MSI-H (dMMR) ☐ MSS (pMMR) ☐ Unsure
- DNA repair (MMR/MSI): ☐ Tested / ☐ Not yet
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- Tumor side: ☐ Left ☐ Right ☐ Unsure
- Rectal tumors are often grouped with left-sided tumors for some treatment discussions. Ask your care team how tumor location applies to you.
Before certain chemotherapy medicines
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- DPYD (before 5-FU/capecitabine): ☐ Tested / ☐ Not yet
☐ Normal function ☐ Reduced function ☐ No Function ☐ Unsure
- DPYD (before 5-FU/capecitabine): ☐ Tested / ☐ Not yet
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- This test can help your care team choose a safer starting dose and monitoring plan
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- UGT1A1 (before irinotecan in some cases): ☐ Tested / ☐ Not yet
☐ Typical-risk ☐ Higher-risk ☐ Unsure
- UGT1A1 (before irinotecan in some cases): ☐ Tested / ☐ Not yet
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- This test may help your care team understand side-effect risk and decide whether dose changes or extra monitoring are needed
If you have stage IV (metastatic), before your first treatment
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- KRAS: ☐ Tested / ☐ Not yet ☐ Wild-type ☐ Positive ☐ Unsure
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- KRAS G12C: ☐ Detected ☐ Not detected ☐ Unsure
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- NRAS: ☐ Wild-type ☐ Positive ☐ Unsure
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- BRAF: ☐ Wild-type ☐ V600E ☐ Other: ☐ Unsure
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- HER2 (ERBB2): ☐ Positive ☐ Negative ☐ Unsure
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- NTRK fusion: ☐ Detected ☐ Not detected ☐ Unsure
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- KRAS G12C is one specific KRAS change that may open certain treatment options later.
Other results my report may include
POLE/POLD1, PIK3CA, RET, ALK, HER2 mutation, and others. Ask which results matter for your care.
Other: ____________
Plain words first, medical words second: NGS = broad tumor profiling. ctDNA or MRD = tumor DNA in blood. CEA = blood tumor marker.
Timing at a Glance
| When | Why this matters | How long it may take | Sample |
| At diagnosis | MMR or MSI can help guide treatment and genetic counseling conversations. | Often within days to about 2 weeks | Tumor tissue |
| Before certain chemotherapy medicines | DPYD and sometimes UGT1A1 can help personalize dosing and monitoring | About 3 to 10 business days, sometimes longer | Blood draw or saliva or cheek swab |
| If metastatic, before first treatment | NGS helps identify targets before choosing first-line therapy. | Tissue NGS about 2 to 3 weeks. Liquid biopsy often about 5 to 10 business days | Tumor tissue and or blood |
| After surgery or if cancer changes | CtDNA can help guide follow-up and trial conversations, but it does not replace scans, exams, CEA testing, or your care team’s judgement | Varies by test | Usually blood, sometimes tissue for setup |
***Times vary by lab, insurance steps, and sample quality. Ask your clinic when to expect results and whether they will appear in your patient portal.
Questions That Put You in Control
Only have time for 3 questions? Start here:
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If you were just diagnosed
- What is my MMR/MSI result?
- Could this affect my treatment?
- Do I need genetic counseling for possible Lynch syndrome?
- Can I get a printed copy of my results?
Before certain chemotherapy medicines
- Did we check DPYD and, if needed, UGT1A1 before treatment starts?
- How will these results affect my starting dose or monitoring plan?
- What side effects should I watch for in the first 1 to 2 weeks?
- Who should I call if I have symptoms?
If you have stage IV (metastatic) disease
- Do we have my NGS results before choosing first treatment?
- Does my report include KRAS, NRAS, BRAF, HER2, KRAS G12C, and NTRK?
- What are my top treatment options and why?
- If I am RAS wild-type and left sided, should we discuss whether an anti-EGFR approach fits my care?
After surgery
- Should we do a ctDNA, also called MRD testing, now?
- If positive or negative, how would that affect follow-up or trial options?
- How often would we repeat ctDNA?
- Was my tumor tested for PIK3CA or another PI3K pathway change, and should we talk about whether aspirin is safe and appropriate for me?
ctDNA can help guide follow-up and trial conversations, but it should not be used by itself to make treatment decisions.
During follow-up
- What is my CEA trend?
- When is my next scan?
- If CEA rises, when would we move the scan sooner?
- What symptoms should prompt me to call early?
If cancer changes or returns
- Should we re-test now to look for new options?
- Would a liquid biopsy be faster while planning a tissue biopsy?
- What new targets or clinical trials are we hoping to find?
Insurance Help
- Ask your care team for prior authorization and a letter of medical necessity.
- If coverage is denied, ask for the denial in writing and appeal quickly.
- Ask the lab or testing company about financial assistance or capped cash-pay programs.
- Ask your financial counselor or navigator for help with codes, deadlines, and appeals.
Take Control of Your Health
- Keep asking until you understand.
- Bring someone with you or take notes.
- Leave with a next step: what’s happening, when, and how we’ll follow up.
This resource is for education and conversation support. It does not replace medical advice. Use it with your care team to make decisions that are right for you.
Biomarker Conversation Guide Supporters

Citations
- National Comprehensive Cancer Network. (2026). NCCN Clinical Practice Guidelines in Oncology: Colon Cancer (Version 2.2026). https://www.nccn.org/guidelines/guidelines-detail?category=1&id=1428
- National Comprehensive Cancer Network. (2026). NCCN Clinical Practice Guidelines in Oncology: Rectal Cancer (Version 2.2026). https://www.nccn.org/guidelines/guidelines-detail?category=1&id=1461
- Sepulveda, A. R., Hamilton, S. R., Allegra, C. J., et al. (2017). Molecular biomarkers for the evaluation of colorectal cancer: Guideline from ASCP, CAP, AMP, and ASCO. Archives of Pathology & Laboratory Medicine, 141(5), 625–657. https://doi.org/10.5858/arpa.2016-0554-CP
- College of American Pathologists; Association for Molecular Pathology; American Society of Clinical Oncology. (2022). Mismatch repair and microsatellite instability testing for immune checkpoint inhibitor therapy. Archives of Pathology & Laboratory Medicine, 146(10), 1194–1210. https://doi.org/10.5858/arpa.2021-0632-CP
- Clinical Pharmacogenetics Implementation Consortium (CPIC). (2017, updated 2024). CPIC guideline for fluoropyrimidines and DPYD. https://cpicpgx.org/guidelines/guideline-for-fluoropyrimidines-and-dpyd/
- Dutch Pharmacogenetics Working Group (DPWG). (2022). Guideline for the gene–drug interaction between UGT1A1 and irinotecan. European Journal of Human Genetics. https://doi.org/10.1038/s41431-022-01243-2
- Watanabe, J., Muro, K., Shitara, K., et al. (2023). Panitumumab vs bevacizumab added to first-line chemotherapy for RAS wild-type, left-sided mCRC (PARADIGM). JAMA, 329(15), 1271–1282. https://doi.org/10.1001/jama.2023.4428
- U.S. Food & Drug Administration. (2023). Tucatinib with trastuzumab for RAS WT, HER2-positive mCRC (accelerated approval). https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-tucatinib-trastuzumab-colorectal-cancer
- U.S. Food & Drug Administration. (2024). FDA approvals and labels for targeted therapies, including HER2-positive, BRAF V600E, and KRAS G12C metastatic colorectal cancer. https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-encorafenib-cetuximab-and-mfolfox6-metastatic-colorectal-cancer-braf
- U.S. Food & Drug Administration. (2024). Adagrasib + cetuximab for KRAS G12C–mutated mCRC (accelerated approval). https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-adagrasib-cetuximab-kras-g12c-mutated-colorectal-cancer
- U.S. Food & Drug Administration. (2025). Sotorasib + panitumumab for KRAS G12C–mutated mCRC (approval). https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-sotorasib-panitumumab-kras-g12c-mutated-colorectal-cancer
- Caughey, B. A., & Parikh, A. R. (2024). ctDNA/MRD testing for colon cancer: A work in progress or ready for prime time? Journal of the National Comprehensive Cancer Network, 22(10), e247049. https://jnccn.org/view/journals/jnccn/22/10/article-e247049.xml

