What Is a Molecular Tumour Board — and Why Should You Want One?
A molecular tumour board is a specialist panel that reviews your tumour's DNA alongside your clinical history to find treatment options a standard team may not have reached. Not every patient needs one — but knowing when to ask is the question this page answers.
Medically reviewed by Dr. C. Raghavendra Reddy, Medical Oncologist, MBBS (Gold Medal) · DNB · DM (Medical Oncology, Gold Medal) · Last reviewed August 2026
- A panel built around genomics — The board includes specialists whose primary expertise is interpreting DNA sequencing reports, not just treating cancer.
- Finds what standard meetings miss — It looks systematically for matched targeted drugs and open trials based on your specific molecular profile.
- Not a replacement for your team — The MTB makes a recommendation. Your oncologist discusses it with you and decides the plan.
- Not standard everywhere yet — In India, access to an MTB often depends on asking. Most patients who would benefit are not referred automatically.
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A molecular tumour board is a specialist panel — oncologists, pathologists, and molecular scientists — that reviews your tumour's DNA profile together to find treatment options a standard team may not have considered. It is most useful when standard treatments have not worked or when your cancer carries an unusual molecular pattern.
How does a molecular tumour board differ from a standard MDT?
| Standard MDT | Molecular Tumour Board (MTB) | |
|---|---|---|
| Who reviews your case | Oncologist, radiologist, surgeon, pathologist | All MDT members plus molecular pathologist and genomics specialist |
| What they review | Imaging, histology, and clinical staging | All of the above plus your tumour's full DNA sequencing report |
| Treatment options considered | Approved drugs for your cancer type | Approved drugs, off-label therapies, and matched clinical trials |
| Best suited for | Newly diagnosed patients with standard treatment options available | Treatment-resistant disease, rare mutations, complex genomic profiles |
| When to consider | After every new diagnosis | When standard options have not worked or NGS results need expert interpretation |
When should you ask for an MTB review?
- Your cancer has not responded to, or has stopped responding to, standard treatment.
- You have a rare cancer type, or a common cancer with an unusual or rare mutation.
- Your oncologist has ordered next-generation sequencing (NGS) and the results are complex or uncertain.
- You want to know whether any open clinical trial matches your molecular profile.
- You have already had the standard drugs approved for your cancer type.
- Your NGS report names mutations that your current team is not sure how to act on.
What actually happens at an MTB review?
The board meets — usually weekly or fortnightly — and your case is presented alongside your sequencing report. Specialists in oncology, molecular pathology, and genomics review the actionable alterations together and cross-reference them against approved drugs, clinical trial databases, and published evidence.
The output is a written recommendation that names each actionable mutation, the matched drug or trial, and the evidence level behind it. Your oncologist receives that recommendation and discusses it with you.
You do not attend the board itself. The clinical conversation — what the findings mean for your actual situation — happens between you and your treating oncologist after the review.
17+ senior cancer specialists. One panel for your case.
Trained at AIIMS, Tata Memorial, and leading international centres. Combined 150+ years of experience. Every complex case is reviewed by 3+ of them — together.
Dr. C. Raghavendra Reddy
MBBS(Gold Medal), DNB(General Medicine), DM(Medical Oncology)(Gold Medal)
Dr. Bharati Devi Gorantla
MBBS, MD(General Medicine), DM(Medical Oncology)(Adyar,Chennai), ECMO, MRCP SCE(UK)
Dr. Owais Mohammed
MBBS, MD (General Medicine), DrNB (Medical Oncology), ECMO, MRCP SCE (Medical Oncology) (UK)
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MBBS (AIIMS), MS (Surgery) (AIIMS), DNB (Surgical Oncology), MRCS (Edinburgh)
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MBBS, MS(General Surgery), M.Ch(Surgical Oncology), FMAS, FARIS(Ongoing)
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MBBS, MS (General Surgery), DrNB (Surgical Oncology), FALS Oncology
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What will you get from it, and how long does the process take?
The most useful outcome is clarity: a clear answer on whether your tumour has an actionable target, what drug or trial is matched to it, and whether that option is accessible in India. Sometimes the answer is that no actionable target was found — and that too is a decision-useful result, not a failure.
Turnaround depends on two steps: how long your NGS report takes to come back after the tissue sample is sent, and how quickly the board can schedule your case once results are available. Ask your oncologist when to expect each step so you are not waiting without a timeline.
Cost varies by centre and by which tests are still needed. Ask for a written estimate before you commit, and tell your team upfront if cost is a constraint — there may be trial access or assistance schemes that change what is realistic for you.
The questions families ask most about MTB reviews
We have already seen several oncologists. Will an MTB actually add anything?
An MTB adds something structurally different from more oncologists: it adds specialists whose whole focus is genomic data. Where a standard team reads your NGS report as part of a broader meeting, an MTB is built around it. The board can identify matches to drugs approved for a different cancer type, or to open clinical trials not widely known outside genomic medicine. If your tumour has no actionable alterations, the board will say so clearly — and that is a useful answer, not a wasted step.
How is this different from getting a second opinion from another oncologist?
A second opinion from another oncologist gives you a second clinical judgement on the same information your current team has. An MTB gives you a different kind of expertise: molecular pathologists and genomics specialists who spend their time interpreting sequencing data rather than treating patients directly. The two serve different purposes and are not alternatives. If you are uncertain about your diagnosis or overall plan, a second clinical opinion is the right first step. If you have NGS data that needs deep interpretation, an MTB adds the most value.
What if the MTB recommends a drug that is not available or affordable in India?
It is possible, and worth asking about upfront. An MTB may identify a drug approved abroad but not yet cleared through CDSCO in India, or one accessible only through a clinical trial. Some matched drugs are available off-label in India, and your oncologist can discuss whether that is feasible in your case. A responsible MTB recommendation includes an honest appraisal of what is actually accessible — not just what the biology suggests. If cost is a concern, say so clearly: there may be trial access, compassionate use, or a locally available alternative.
What if my original biopsy tissue is no longer available?
The MTB works from your NGS report, and that report requires tumour tissue. If your original biopsy sample has been used up or cannot be located, a repeat biopsy may be needed before the review can begin. In some cases a liquid biopsy — a blood test that detects tumour DNA circulating in the bloodstream — can be used instead, though it does not always give the same depth of information as a tissue sample. Ask your oncologist whether your stored tissue is sufficient before waiting for an MTB slot.
My oncologist has not mentioned this. Is it appropriate to bring it up?
Yes, entirely. An MTB is not yet standard practice across all centres in India, which means access depends partly on whether it is raised in the consultation. Your oncologist may not have offered it because it was not indicated at your current stage, because NGS results were still pending, or simply because the conversation moved in a different direction. You can ask directly: 'My NGS results are back — would a molecular tumour board review add anything for my case?' That is a clinical question, and a reasonable one.
Does the MTB recommendation replace what my oncologist decides?
No. The MTB makes a recommendation — it does not prescribe treatment. Your oncologist weighs that recommendation against your full clinical picture: your general fitness, other treatments you have had, your goals, and what is available and affordable for you. There will be cases where the MTB identifies something actionable but your oncologist decides it is not appropriate for your specific situation, and that is a legitimate clinical judgement. The MTB is one important input into the decision, not the final word.
Did you know?
Across published molecular tumour board programmes, a substantial proportion of reviewed cases result in a change or addition to the treatment plan — most often by identifying a matched drug approved for a different cancer type, or an open clinical trial the treating team had not previously considered.
The MTB can only review your case once your NGS results are in hand. If sequencing has not yet been ordered, that is the step to ask about now.
Source: ESMO Precision Medicine Working Group; ASCO Molecular Oncology Working Group
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Frequently asked questions
Do I need to specifically ask for an MTB, or will my oncologist refer me automatically?
In most centres in India, an MTB referral is not automatic — it depends on whether your oncologist considers it appropriate and whether the facility runs one. If you have received a complex NGS report, if standard treatments have not worked, or if you have a rare cancer type, it is reasonable to ask directly whether an MTB review would help your case. The question will not seem unusual to a team familiar with genomic medicine.
What information does the MTB need to review my case?
The board primarily needs your NGS or molecular sequencing report, your diagnosis and stage, your treatment history, and your current clinical status. In most cases this information comes from your existing records — you do not need to gather anything separately. Your oncologist's team typically prepares the case summary for submission. If your NGS has not been done yet, that is the step to complete first.
How long does the full process take from referral to recommendation?
Total time depends on two steps: how long your NGS report takes after tissue is sent to the lab, and when the board can schedule your case once results are available. Boards typically meet weekly or fortnightly. Ask your team for an estimate at each stage — when the report is expected, and when the board's recommendation will follow — so you are not waiting without a timeline.
What if the MTB finds an actionable mutation but the matched drug is very expensive?
Cost is a legitimate part of the treatment discussion, and a good recommendation should acknowledge it. Some matched drugs are available through clinical trials at no cost to the patient. Others may be accessible through compassionate use programmes or manufacturer assistance schemes. Tell your oncologist if affordability is a constraint before the recommendation is finalised — knowing that upfront shapes which options the team focuses on.
Is an MTB review available at CION?
CION coordinates molecular tumour board reviews for eligible patients across its network of 35-plus centres in Telangana and Andhra Pradesh. Immunotherapy and targeted treatments identified through the MTB process are administered as day care where indicated. PET-CT and other response-assessment scans are coordinated with partner imaging centres. CION does not provide CAR-T or cell therapy; patients recommended for those would be referred to a centre that offers them.
What does a useful MTB written recommendation look like?
It should name each actionable alteration found, the drug or trial matched to it, the evidence level behind the match — citing NCCN, ESMO, published trial data, or a similar body — and whether the option is accessible in India. If the report uses technical language without explanation, ask for a plain-language summary. You are entitled to understand what was found, what it means, and what your options are — not just a list of gene names and drug codes.