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IHC, NGS and liquid biopsy — what each biomarker test actually does

IHC (immunohistochemistry) stains a tissue slide to check one protein, such as PD-L1. NGS (next-generation sequencing) reads a panel of genes from that same tissue in a single run. Liquid biopsy tests a blood draw for tumour DNA when fresh tissue isn't practical. Testing is coordinated at accredited partner labs — this page explains the terms, not your individual report.

Medically reviewed by Dr. C. Raghavendra Reddy, Medical Oncologist · MBBS (Gold Medal) · DNB · DM (Medical Oncology, Gold Medal) · Last reviewed August 2026

  • One test, one protein — IHC checks a single marker such as PD-L1 or a mismatch-repair protein, quickly and at lower cost
  • One test, many genes — NGS profiles a broad gene panel in one run when more than one actionable mutation is possible
  • No new biopsy needed — liquid biopsy uses a blood draw when tissue is scarce or a repeat biopsy carries real risk
  • Coordinated at partner labs — CION arranges IHC, NGS and liquid biopsy testing at accredited partner labs and reviews your report with you
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What does each test actually do?

IHC (immunohistochemistry) stains a slide made from your existing tumour tissue with an antibody that binds to one specific protein — such as PD-L1, HER2, or a mismatch-repair protein — so a pathologist can see how much of it is present. NGS (next-generation sequencing) works on the same kind of tissue sample but reads many genes at once, looking for mutations, gene fusions, and broader signals such as tumour mutational burden or microsatellite instability in a single run instead of one marker at a time. Liquid biopsy is different again: instead of tissue, it tests a blood sample for circulating tumour DNA (ctDNA) — fragments of genetic material a tumour sheds into the bloodstream — and is used mainly when a fresh tissue sample isn't practical to obtain.

These three tests are coordinated for CION patients through accredited partner pathology and molecular-diagnostics laboratories — this page explains what the terms mean in general; it does not interpret what your own report says about your own cancer.

Did you know?

IHC has been part of routine pathology since the 1980s, but tumour panels that sequence dozens of genes from one sample in a single run — what NGS does today — only became practical for everyday cancer care in the last decade or so, once sequencing costs fell sharply.

Side By Side

IHC vs NGS vs liquid biopsy: how they compare

Turnaround and cost brackets are general ranges, indicative as of August 2026 — your lab, panel size and test volume will change the exact figures. This is not a quote for your case.

Test What it measures Sample needed Typical turnaround Relative cost Typically ordered when
IHC Expression of one protein (e.g. PD-L1, HER2, MMR) Existing tissue block Fastest — often a few days Lowest of the three First-line single-marker check
NGS Mutations, fusions, TMB/MSI across a gene panel Existing tissue block with adequate tumour content Slowest — often one to a few weeks Highest of the three Multiple possible actionable markers, or IHC inconclusive
Liquid biopsy Circulating tumour DNA (ctDNA) in blood Blood draw — no fresh tissue required Usually faster than tissue NGS Comparable to or higher than tissue NGS Insufficient tissue, risky repeat biopsy, or resistance monitoring

General ranges only, indicative as of August 2026 — not every tumour sheds enough ctDNA to be reliably detected by liquid biopsy, which is why guideline bodies treat it as complementary to tissue testing rather than an automatic substitute.

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MBBS(Gold Medal), DNB(General Medicine), DM(Medical Oncology)(Gold Medal)

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Dr. Bharati Devi Gorantla

MBBS, MD(General Medicine), DM(Medical Oncology)(Adyar,Chennai), ECMO, MRCP SCE(UK)

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Dr. Owais Mohammed

MBBS, MD (General Medicine), DrNB (Medical Oncology), ECMO, MRCP SCE (Medical Oncology) (UK)

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Medical Oncologist

Dr. T. Raghavender Reddy

MBBS, DM (Medical Oncology), MD (Radiation Oncology)

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MBBS, DM (Medical Oncology), MD (Internal Medicine)

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Dr. Muralidhar Muddusetty

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MBBS, MS (General Surgery), M.Ch (Surgical Oncology)

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M.B.B.S, MS (General Surgery), M.Ch (Surgical Oncology)

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MBBS, MS(General Surgery), M.Ch(Surgical Oncology), FMAS, FARIS(Ongoing)

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Behind The Result

How does a biomarker test move from your biopsy to your report?

Whichever test is ordered, the pathway follows a similar sequence — only the sample type and the lab process in the middle change.

  1. A sample is collected

    IHC and NGS use an existing tissue block from a prior biopsy or surgery where possible; liquid biopsy uses a simple blood draw instead.

  2. The right test is selected

    Your oncologist and tumour board choose IHC, NGS, liquid biopsy, or a combination, based on your cancer type and the clinical question being asked.

  3. Processing at an accredited partner lab

    Staining, sequencing or ctDNA analysis is carried out at an accredited partner pathology or molecular-diagnostics laboratory — not run in-house at CION.

  4. Your oncology team reviews the report with you

    The result is discussed at tumour board and explained to you in the context of your specific treatment options — never read in isolation from your full clinical picture.

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The Bigger Picture

Do you need IHC, NGS, liquid biopsy — or more than one?

Most patients start with IHC because it is fast and answers a specific question, such as PD-L1 status. NGS is added when your cancer type has several possible actionable mutations, or when IHC alone doesn't answer the clinical question. Liquid biopsy is used instead of, or alongside, tissue testing when a fresh biopsy isn't practical. Your oncologist decides the sequence for your specific case — this page cannot tell you which one you personally need.

  • Single-marker question — IHC is usually enough on its own, and is often ordered first.
  • Multiple possible actionable mutations — NGS is typically added to screen a broader panel in one run.
  • Insufficient or unsafe-to-repeat tissue — liquid biopsy can stand in for, or supplement, tissue testing.
  • Monitoring over time — liquid biopsy is sometimes repeated later to watch for resistance mutations, without a new invasive procedure.
  • Inconclusive first result — a second test type may be ordered to clarify an unclear IHC or NGS finding.
A Known Limitation

Why can't liquid biopsy simply replace tissue testing?

Liquid biopsy depends on a tumour shedding enough circulating tumour DNA into the bloodstream for the lab to detect reliably — and not every tumour sheds at a level current assays can reliably pick up, particularly in early-stage or low-disease-burden situations. When ctDNA is found, it can be highly informative; when it isn't, that result does not rule out a mutation the way a clear, adequate tissue sample can. This is a recognised, openly discussed limitation in ASCO and CAP guidance on circulating tumour DNA testing, not a flaw specific to any one lab or assay.

This is also why oncologists often treat liquid biopsy as complementary to tissue-based IHC and NGS — used together, or in sequence — rather than as an automatic, one-for-one replacement.

Related Reading

Understanding the wider biomarker-testing journey

This page explains general IHC, NGS and liquid-biopsy terminology for education only and does not interpret any individual patient's report. Testing is coordinated at accredited partner labs. Bring your report to a consultation for a doctor's assessment of what it means for you.

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Common questions

IHC, NGS and liquid biopsy: your questions answered

What is the difference between IHC, NGS and liquid biopsy?
IHC (immunohistochemistry) stains an existing tissue slide to check the expression of one protein at a time, such as PD-L1 or a mismatch-repair protein — it is fast and answers a narrow, specific question. NGS (next-generation sequencing) reads a panel of genes from the same tissue sample in a single run, looking for mutations, fusions and signals such as tumour mutational burden across many genes at once. Liquid biopsy tests a blood draw for circulating tumour DNA rather than a tissue sample, and is most often used when a fresh biopsy is not practical. Each test answers a different clinical question — they are not interchangeable substitutes for one another.
When is IHC enough, and when do I need NGS?
IHC is often the first test ordered because it is quick and inexpensive, and for some cancers a single-protein result — such as PD-L1 or HER2 — is enough to guide the next step. NGS is typically added when your cancer type has several possible actionable mutations that a single-protein stain cannot detect, when IHC results are borderline, or when your oncologist is screening for a broader set of targeted-therapy or immunotherapy options at once. Which sequence applies to you depends on your specific cancer type and case — this page explains the general logic, not a recommendation for your report.
Can liquid biopsy replace a tissue biopsy completely?
Not routinely. Liquid biopsy is useful when tissue is insufficient, a repeat biopsy carries meaningful risk, or ongoing monitoring for resistance mutations is needed without repeated invasive procedures. However, not every tumour sheds enough circulating tumour DNA into the bloodstream to be reliably detected, so a "negative" liquid biopsy does not rule out a mutation the way a clear tissue result can — guideline bodies such as ASCO and CAP describe liquid biopsy as complementary to tissue testing in most current use cases, not a full replacement for it.
Which test is fastest, and which is cheapest?
As a general rule, IHC is both the fastest and the least expensive of the three, because it checks one marker with a shorter, simpler lab process. NGS panels are typically the slowest and the most expensive, since sequencing and analysing a broad gene panel takes more processing time and specialised equipment. Liquid biopsy timelines usually sit between the two, often faster than tissue-based NGS, though its cost can be comparable to or higher than tissue NGS depending on the panel used. Exact turnaround and cost depend on your lab and panel, and figures here are indicative as of August 2026, not a quote.
Can I choose which biomarker test I get, or does my oncologist decide?
Your treating oncologist and tumour board decide which test, or combination of tests, is appropriate — based on your cancer type, the tissue available, prior results, and the specific treatment options being considered. This page explains what each test does in general terms so the conversation makes more sense; it is not a substitute for that clinical decision, and nothing here should be read as telling you which test you personally need.
Where are these tests actually performed for CION patients?
Biomarker testing for CION patients — IHC, NGS and liquid biopsy alike — is coordinated through accredited partner pathology and molecular-diagnostics laboratories; CION does not run these tests in-house. This page explains general testing terminology only and does not interpret any individual patient's report. Bring your report, or your oncologist's testing recommendation, to a free consultation, and a CION oncologist will walk you through what applies to your specific case.
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