OncologyDr. Mohit AgarwalCancer Treatment

Principal Director & Unit Head - Medical Oncology, Fortis Hospital, Shalimar Bagh, New Delhi, India

Part 3 of 18 in Cancer: Myths Facts and Advances

Does a Biopsy Spread Cancer? Diagnosis Myths Explained

August 7, 2026

A biopsy does not cause cancer to spread, despite this being one of the most persistent myths patients raise before starting cancer treatment in India, and a normal blood test does not rule out cancer either. Understanding what diagnostic tests can and cannot tell you is essential before assuming the worst, or the best, based on limited information.

Does Taking a Biopsy Cause Cancer to Spread?

Dr. Mohit Agarwal is clear that numerous studies have shown a biopsy does not cause cancer to spread, despite the widespread fear that inserting a needle into a tumour will make it worse. In fact, what is suspected to be cancer, particularly in Africa and India, sometimes turns out on biopsy to be tuberculosis or another infection instead, which changes the treatment plan entirely.

How Precise Are Modern Biopsy Techniques?

Modern image-guided biopsies, such as a CT-guided biopsy of a lung mass, allow doctors to target a suspicious area directly and extract a small sample with a high degree of precision and safety. This level of precision is part of why biopsy remains a safe, essential step in accurately diagnosing cancer before any treatment decision is made.

Does a Normal Blood Test Rule Out Cancer?

A normal hemogram, kidney function test or liver function test does not rule out cancer, particularly in its early stages, since blood is not always affected by cancer elsewhere in the body. Patients should not dismiss a persistent symptom or lump simply because routine blood tests have come back normal, as this is a common but potentially dangerous misconception.

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This article is based on a Jivo Masterclass session conducted by Dr. Mohit Agarwal, Principal Director and Unit Head, Medical Oncology, Fortis Hospital, Shalimar Bagh, New Delhi, India. The article has been summarised with the assistance of an AI tool from the original masterclass recording. Watch the full Masterclass recording

This guide is based on a live Jivo Masterclass — Dr. Mohit Agarwal taught doctors across Africa on September 7, 2025.

FROM THE LIVE Q&A

DR

Dr. Ashetu (Ethiopia)

What investigations help us identify targets on cancer cells?

MA

Dr. Mohit Agarwal

We take a biopsy from the specimen, cut it into sections, make blocks, and apply immunohistochemistry staining, which lets us identify targets on the cells. We then do mutation testing to see what mutations are present in the genes, to identify further targets we can address. We also do PD-L1 testing, which tells us whether the patient can receive immunotherapy. It is a combination of these staining protocols along with NGS that tells us the best way forward for the patient.

See all 6 questions from this masterclass →

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Frequently Asked Questions

Could you elaborate more on the next generation sequencing (NGS) you mentioned?

We take the biopsy specimen and extract the DNA from the cancer cell, then sequence it to identify where something has gone wrong in the DNA or RNA, which tells us why that individual developed the cancer. Through this we identify specific mutations that may be the probable reason. Research is ongoing to counteract every change found on NGS, but currently we have a few drugs available for certain specific mutations — if we find one of those, we give that specific drug and the patient benefits.

Doctors practising in Africa face the challenge of exact diagnosis in the absence of PET-CT scan machines, which are not available in most countries, forcing guesswork. If the protocol decided in the home country is chemotherapy, what is the difference between chemotherapy administered in a country like Nigeria or Ethiopia compared to an advanced centre like Fortis Shalimar Bagh, and how can that gap be filled?

If you don't have a PET-CT, the second-best modality is a CT scan of the probable areas — chest, abdomen, and maybe head and neck depending on the cancer — which will give some answers on staging. As for treatment: chemotherapy is calculated as per the height, weight and profile of the patient, not given as a simple fixed dose. There are specific mixing criteria — it cannot be mixed like an antibiotic — and India has specific mixing units where care is taken over contamination and dosing. Drugs also have to be given over an appropriate infusion time, since infusing over the wrong duration causes more side effects. We also have monitoring systems running during chemotherapy to catch problems early, and targeted therapies and immunotherapies have specific temperature and light-sensitivity handling requirements that are important to follow correctly.

Isn't the next generation sequencing procedure going to take a long time before giving the patient medication? How many days does it take to get the precise DNA gene mutation result and start the exact medication?

Previously it used to take 30 days, and it still does in most institutes, but with the advanced machines we now have, our turnaround time is only about five to six working days — even including a Sunday, a comprehensive NGS report is usually ready by about the seventh day.

Can you give an approximate idea of the cost range for cancer treatment, since doctors often get asked this even before a formal case file is created?

The cost is very different for every cancer and every stage — it can vary from a few thousand rupees to a million rupees. The good news is that targeted therapy and immunotherapy drugs, which used to be very costly, now have more reasonable generic alternatives. For example, a drug that used to cost about $5,000 for a single dose as immunotherapy now costs just around $1,000 for a single dose. We also try to provide assistance programmes through indications approved by the companies that manufacture these drugs, to help patients financially.

Do we have targeted therapy and immunotherapy for all forms of cancer, or only for a few?

It is not available for everyone blanketly — you first need to identify the target on the cell, which is where NGS and special staining come in. Not every individual harbours those targets, but many do, and we then use specific targeted drugs. Immunotherapy is not available for all cancers either, but with present indications it is available for the majority of advanced cancers — about 70% of advanced cancers would be candidates for some form of immunotherapy. There are specific criteria that must be met; giving it without meeting those criteria would not help the patient and would just be a financial waste.

Does having a biopsy cause cancer to spread?

No. Numerous studies have shown that a biopsy does not cause cancer to spread, despite the widespread fear that inserting a needle into a tumour will make it worse.

Can a biopsy reveal something other than cancer even when cancer is suspected?

Yes. What is suspected to be cancer, particularly in Africa and India, sometimes turns out on biopsy to be tuberculosis or another infection instead, which changes the treatment plan entirely.

How precise are modern biopsy techniques such as a CT-guided biopsy?

A CT-guided biopsy allows doctors to target a suspicious area, such as a lung mass, directly and extract a small sample with a high degree of precision and safety.

Does a normal blood test rule out cancer?

No. A normal hemogram, kidney function test or liver function test does not rule out cancer, particularly in its early stages, since blood is not always affected by cancer elsewhere in the body.

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