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Types of Immunotherapy Explained

Tumour-Infiltrating Lymphocyte (TIL) Therapy — What It Is, and Where It Stands in India

TIL therapy takes immune cells that had already found their way inside your tumour, grows them in a laboratory until there are billions, and infuses them back. It was approved in the United States in 2024 for advanced melanoma. It is not approved or routinely available in India, and CION does not provide it. This page explains what it is, who it is being studied for, and what to ask instead.

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

  • Your own cells, not a manufactured drug — the infusion is T cells harvested from your own tumour and multiplied outside the body; nothing is genetically engineered into them
  • Approved in one country, for one cancer — the United States approved a TIL therapy in 2024 for advanced melanoma after checkpoint-inhibitor treatment; every other use is investigational
  • Not available in India today — no TIL product holds CDSCO approval as of August 2026, and CION does not provide, administer or stock TIL therapy or any cell therapy
  • The demands are physical, not only financial — surgery, weeks of manufacturing, lymphodepleting chemotherapy and intensive-care backup are part of the treatment, not optional extras
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What is TIL therapy?

TIL therapy uses immune cells taken from inside your own tumour. A piece of tumour is removed surgically, the T cells living within it are separated out and grown in a laboratory until there are billions, and those cells are infused back into you. Nothing is genetically engineered.

TIL stands for tumour-infiltrating lymphocyte. The name is literal. In many solid tumours, pathologists can see T cells that have already pushed their way into the cancer tissue. Those cells found the tumour on their own and recognised something on it as abnormal. They are simply too few, and too worn down by the environment around them, to do anything decisive.

The idea behind the treatment follows directly from that observation. Rather than designing a new instruction for the immune system, TIL therapy takes the cells that already worked out the answer and multiplies them outside the body, away from the tumour's suppressive influence. It belongs to the family called adoptive cell therapy, where the medicine is living cells belonging to one specific patient and made for that patient alone.

That is also why it cannot be stocked, ordered or kept on a shelf. Every dose is manufactured from one person's tumour, over several weeks, in a specialised facility. It is a manufacturing process as much as a prescription, and that single fact explains most of what follows on this page — including why it is not yet accessible in India.

Did you know?

The cells used in TIL therapy were already inside the tumour before treatment began. Pathologists have described tumour-infiltrating lymphocytes on biopsy slides for decades, long before anyone could do anything with them. TIL therapy does not add a new target or a new instruction — it takes the immune cells that had already recognised the cancer, and grows their numbers outside the body.

The Mechanism

How does TIL therapy actually work, step by step?

Six stages, spread over roughly six to eight weeks. Surgery comes first, laboratory manufacturing takes the longest, and the infusion itself is the shortest part. The demanding portion is what surrounds the infusion, not the infusion.

  1. A tumour lesion is removed surgically

    A surgeon takes out a piece of tumour, usually a centimetre or two across. If no lesion can be safely removed, the treatment cannot begin at all.

  2. The immune cells inside it are separated

    The tissue is broken down in a laboratory and the T cells found within it are isolated from the cancer cells they were sitting among.

  3. Those cells are grown to therapeutic numbers

    Over several weeks the cells are multiplied in culture, often to billions. This is why the wait between surgery and infusion is measured in weeks rather than days.

  4. Lymphodepleting chemotherapy is given first

    A short course clears out existing immune cells so the infused ones have room and signal to expand. Blood counts fall and infection risk rises during this window.

  5. The expanded cells are infused back

    A single infusion returns your own cells to you. There are simply far more of them than your body could ever have produced on its own.

  6. Cytokine support is given, in hospital

    High-dose interleukin-2, a natural immune signalling protein, is usually given to keep the infused cells alive. Intensive-care backup is a requirement for this stage.

Sequence described in general terms, in line with how adoptive cell therapy is presented in NCCN and ASCO patient-education material. Protocols differ between centres and between trials.

Where It Is Used

Which cancers is TIL therapy used for?

Advanced melanoma is the only cancer for which a TIL therapy has been approved by any regulator, and that approval was granted in the United States in 2024. Every other use is investigational, inside clinical trials, with small numbers and short follow-up.

Approved · United States, 2024

Advanced melanoma

The only setting with a regulatory approval anywhere in the world, and it applies to melanoma that has already progressed after checkpoint-inhibitor treatment. It is a later-line option, not a first step.

Investigational

Cervical cancer

Studied on the reasoning that HPV-driven tumours carry viral proteins the immune system can recognise clearly. Trial results have been reported, but no regulator has approved the approach here.

Investigational

Non-small-cell lung cancer

Under study, usually after checkpoint-inhibitor treatment has stopped working. Early-phase work only.

Investigational

Head, neck and gynaecological cancers

Trial settings, often in tumours linked to HPV. Numbers are small and follow-up is short.

Not the setting

Leukaemias and lymphomas

Blood cancers do not present a solid tumour mass from which lymphocytes can be harvested. That is why engineered cells, not tumour-infiltrating ones, are the cell-therapy approach studied there.

A practical limit is often missed in coverage of this treatment: there must be a lesion a surgeon can safely remove, and it must contain enough lymphocytes to grow. Regulatory filings behind the 2024 United States approval reported an objective response — measurable tumour shrinkage — in roughly one patient in three treated. That means it did not shrink the tumour in the majority. This page names classes and mechanisms only, and makes no comparison of effectiveness between products.

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The Honest Answer

Is TIL therapy available in India?

No. As of August 2026 no tumour-infiltrating lymphocyte product holds CDSCO approval in India, and TIL therapy is not part of routine cancer care here. Any Indian access would be inside a research or clinical-trial setting, and such programmes are very few.

It is worth being precise about why, because “not available” sounds like a licensing delay that might clear next month. It is not only that. The obstacle is the manufacturing. Growing one patient's own tumour lymphocytes to a therapeutic dose needs a dedicated cell-processing facility working to pharmaceutical-grade standards, several weeks of turnaround per patient, and a receiving hospital able to deliver lymphodepleting chemotherapy and intensive cytokine support with critical-care backup. Each of those is a substantial piece of infrastructure. Approval alone would not create them.

CION Cancer Clinics does not provide, administer or stock TIL therapy, CAR-T, or any other cell therapy. We say that plainly because it is the question this page attracts. The immunotherapy CION does provide is checkpoint-inhibitor and related treatment given as day care at our centres, with response-assessment PET-CT coordinated at partner imaging centres. Where a cell therapy is genuinely relevant to a patient's situation, our role is to say so and to refer, not to offer something we do not have.

If you have read about TIL therapy and are wondering whether to pursue it overseas, that is a reasonable question to bring to an oncologist rather than to a search engine. The answer depends on your cancer type, on whether there is a removable lesion, on what treatment you have already had, and on whether you could physically tolerate the lymphodepletion and cytokine phase. Some of those can be settled in one conversation.

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Telling Them Apart

How is TIL therapy different from CAR-T and checkpoint inhibitors?

All three work through T cells, which is why they get mixed up. TIL therapy multiplies T cells taken from the tumour. CAR-T engineers T cells taken from blood. Checkpoint inhibitors are drugs that release a brake on the T cells you already have. The table compares mechanism and logistics only.

Question TIL therapy CAR-T cell therapy Checkpoint inhibitors
What is actually given Living T cells, your own Living T cells, your own, modified An antibody drug, given by drip
Where the cells come from Inside a surgically removed tumour A blood collection procedure Not applicable — no cells are collected
Genetically engineered? No — only multiplied Yes — a new receptor is added No cells are involved
What it aims at Whatever those cells had already recognised on the tumour One chosen target, decided in advance The brake signal, not the tumour itself
Cancers it is used or studied in Solid tumours; approved abroad in advanced melanoma only Mainly blood cancers Many solid tumours, for patients whose biomarkers fit
Preparation before it is given Surgery, weeks of manufacturing, lymphodepleting chemotherapy Cell collection, manufacturing, lymphodepleting chemotherapy Biomarker testing and baseline blood work
Where it is given Inpatient, with intensive-care backup Inpatient, with intensive-care backup Day care, then home the same day
Status in India, August 2026 Not approved, not routinely available Available only at a small number of specialised centres; not at CION Approved for defined indications; given as day care at CION

This table compares how the three approaches work and what they require, not how well they work. For the mechanism in more depth, read Checkpoint Inhibitors: How Releasing the Brakes on Immunity Works and CAR-T Cell Therapy: Reprogramming Your Own Cells. CION does not administer CAR-T or any cell therapy; patients for whom it is relevant are referred to a centre that provides it.

Before You Pursue It

What are the risks, and what should you ask?

The risks come from the preparation and the support, not the cells. Lymphodepleting chemotherapy drops blood counts and opens an infection window. High-dose interleukin-2 causes fluid to leak from blood vessels, dropping blood pressure and straining the kidneys, heart and lungs. Both need hospital-level monitoring.

  • Is there a lesion that can safely be removed? — No harvestable tumour, no treatment. This is settled by imaging and a surgical opinion, and it rules many patients out at the first step.
  • Under what approval is this being offered? — Ask for the regulator, the indication and the date, in writing. A treatment approved for advanced melanoma in one country is not an approval for your cancer.
  • Is it a registered clinical trial, and can I see the registration? — Trial participation is a legitimate route and is arranged through your treating team. A programme that cannot show you a registration number is not one.
  • What happens to my current treatment during the manufacturing weeks? — Cancer does not pause while cells are grown. Ask specifically what covers that gap and who is monitoring you through it.
  • Does the receiving centre have critical-care backup? — The cytokine phase is the part that puts people in an intensive-care unit. This is a question about the hospital, not about the therapy.
  • What is the full cost, including travel, stay and follow-up? — Ask for it in writing from the treating centre. CION publishes no figure for a treatment it does not provide, and any number quoted to you should be treated as indicative only, as of August 2026.

The side effects here are largely those of chemotherapy and cytokine support rather than the immune-related reactions seen with checkpoint drugs. Those are a different pattern, and How Immunotherapy Actually Causes Side Effects explains why an immune-based treatment can inflame organs that have nothing to do with the cancer.

Related Reading

Where TIL therapy sits among the other classes

This page is general patient education and does not replace a consultation. It describes drug and therapy classes and their mechanisms only, without naming products, and makes no comparison of effectiveness between products. Regulatory status is stated as of August 2026 and can change. CION Cancer Clinics does not provide, administer or stock TIL therapy, CAR-T or any other cell therapy.

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Common questions

TIL therapy: your questions answered

What is TIL therapy?
TIL stands for tumour-infiltrating lymphocyte. These are your own immune cells that have already found their way inside a tumour but are too few, and too suppressed by the tumour environment, to control it. In TIL therapy a piece of tumour is removed surgically, those cells are separated out and grown in a laboratory until there are billions of them, and they are infused back after a short course of lymphodepleting chemotherapy. It belongs to the family called adoptive cell therapy: the medicine is living cells taken from one specific patient and made for that patient alone. Nothing is genetically engineered into the cells - they are only multiplied.
Which cancers is TIL therapy used for?
Advanced melanoma is the only setting in which TIL therapy has reached regulatory approval anywhere in the world, and that approval was granted in the United States in 2024, for melanoma that had already progressed after checkpoint-inhibitor treatment. Everywhere else the approach is investigational. Trials are running in cervical cancer, non-small-cell lung cancer, head and neck cancers and some gynaecological cancers, with small numbers and short follow-up. One practical limitation is often missed: there must be a lesion a surgeon can safely remove, and it must contain enough lymphocytes to grow, so many patients are excluded on technical grounds alone.
Is TIL therapy available in India?
No. As of August 2026 no tumour-infiltrating lymphocyte product holds CDSCO approval in India, and TIL therapy is not part of routine cancer care here. Any Indian access would be inside a research or clinical-trial setting, and such programmes are very few. Manufacturing is as much the obstacle as regulation: growing one patient's own cells to a therapeutic dose needs a dedicated cell-processing facility, several weeks of turnaround, and a hospital able to deliver lymphodepleting chemotherapy and intensive cytokine support with critical-care backup. CION Cancer Clinics does not provide, administer or stock TIL therapy or any other cell therapy.
How is TIL therapy different from CAR-T cell therapy?
Both are adoptive cell therapies that use the patient's own T cells, but the cells are obtained and prepared differently. CAR-T cells are collected from blood and genetically engineered in the laboratory to carry a receptor aimed at one target chosen in advance, which is why CAR-T has been developed mainly for blood cancers where that target is reliably present. TIL cells are not engineered at all. They are the T cells that had already recognised something on the tumour by themselves, harvested from tumour tissue and multiplied. That is why TIL therapy is being studied in solid tumours, where no single target is shared by every cancer cell.
What happens during TIL therapy, and what are the risks?
It is a demanding treatment delivered in hospital, and most of the risk comes from what surrounds the cells rather than the cells themselves. A short course of lymphodepleting chemotherapy is given first, to clear space so the infused cells can expand; that alone causes very low blood counts and a real infection risk for a period. The cells are then infused, and cytokine support, usually high-dose interleukin-2, is given to keep them alive. That cytokine causes fluid to leak from blood vessels, which can drop blood pressure and strain the kidneys, heart and lungs. Intensive-care backup is a requirement, not a precaution.
If TIL therapy is not available here, what should I ask my oncologist instead?
Ask what is genuinely on the table for your diagnosis today. For many solid tumours that means checkpoint-inhibitor immunotherapy, which is given as day care and does have approved indications in India, but only for patients whose biomarker testing and clinical situation fit. Ask whether your tumour has been tested for the markers that decide that. Ask whether a registered clinical trial exists for your cancer, in India or abroad, and what taking part would actually involve. Ask what the plan is if the current treatment stops working. Those questions move your care forward; waiting for a therapy that is not accessible does not.
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