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Targeted therapy explained

Targeted Therapy vs Immunotherapy: — Which One Is Right for You?

Targeted therapy and immunotherapy are both cancer treatments, but they work in completely different ways — and they are not interchangeable. The question of which one applies to you is answered by testing your tumour tissue, not by your diagnosis alone.

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

  • Different mechanisms — Targeted therapy blocks a specific gene mutation. Immunotherapy removes the checkpoints that let cancer cells hide from your immune system.
  • Testing decides eligibility — Neither is available to every patient. Biomarker results from your tumour tissue determine which, if either, applies to you.
  • Neither is a backup for the other — If targeted therapy is not indicated, immunotherapy is not automatically an alternative — and vice versa. They suit different biological situations.
  • Side effects differ too — Both differ substantially from chemotherapy — and from each other. What you experience depends on which treatment you receive and your individual response.
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Targeted therapy blocks a specific mutation driving your cancer cells to grow. Immunotherapy removes the checkpoints that let cancer cells hide from your immune system. Both are different from chemotherapy and from each other. Your tumour's test results — not the cancer type alone — determine which one, if either, is right for you.

How are targeted therapy and immunotherapy different?

Targeted therapy is a drug that blocks a specific gene mutation or protein driving your cancer cells to grow. Think of it as a key designed for one particular lock: if your tumour carries that specific change, the drug can block it. If it does not, the drug has nothing to act on.

Immunotherapy does not attack the cancer directly. It removes the molecular checkpoints that cancer cells use to hide from your immune system, allowing your own immune system to recognise and attack them. For this to work, the tumour needs to be visible to the immune system in the first place — and most tumours are not.

The two treatments suit different biological situations. Being ineligible for one does not make you eligible for the other, and one is not a fallback if the other is unavailable. Your oncologist's recommendation is based on which molecular markers your tumour actually carries, determined by testing the biopsy tissue you have already provided.

In certain cancers, both treatments are used together as part of a combination regimen. This is a specific clinical decision that your oncologist will discuss with you if it applies to your situation.

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Did you know?

Targeted therapy only works when your tumour carries the exact gene change the drug was designed to block. Giving it to a patient without that mutation offers no benefit — and still carries side effects.

This is why NCCN guidance makes molecular testing a prerequisite before most targeted agents are started, not an optional add-on.

Source: NCCN Biomarkers Compendium and Molecular Testing Guidelines

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Common questions

Frequently asked questions

Is immunotherapy better than targeted therapy?

Neither is better overall — the right one is the one matched to your tumour's biology. Targeted therapy can produce deep responses in patients whose cancers carry the right mutation. Immunotherapy can produce durable responses in patients whose tumours express the right markers. Each is designed for a different biological situation, and neither is useful where its specific conditions are absent. What matters is which one fits your individual tumour, and that is a question your biopsy results answer.

Can I have both targeted therapy and immunotherapy at the same time?

Sometimes, yes — certain treatment protocols combine both, but this is a specific clinical decision, not something you can request as an upgrade. Combination regimens are approved in some cancer types and studied in others. They also carry the side effects of both treatments, which affects who is fit enough to receive them. Your oncologist will tell you whether a combined approach is appropriate for your cancer type and your current health.

What tests do I need before starting targeted therapy or immunotherapy?

Biomarker testing on your tumour tissue determines eligibility for both. For targeted therapy, the laboratory looks for specific gene mutations or alterations — such as EGFR, ALK, BRAF, HER2, or others depending on your cancer type. For immunotherapy, the key markers include PD-L1 expression, microsatellite instability, and tumour mutational burden. Which tests matter depends on where your cancer started. Most can be run on the biopsy tissue you have already provided; a new biopsy is only needed if the original sample is too small or too old.

Why does targeted therapy sometimes stop working?

Cancer cells can develop new mutations over time that allow them to bypass the pathway the drug was blocking. This is called acquired resistance, and it is a recognised limitation of targeted agents. When it happens, your oncologist may order a repeat biopsy or a liquid biopsy to identify the new change, then consider a second-generation drug or a different treatment altogether. Regular monitoring during treatment is partly designed to catch this early, rather than waiting for clear symptoms of progression.

Are the side effects different from chemotherapy?

Yes, substantially. Targeted therapy causes fewer of the classic chemotherapy side effects — severe nausea and widespread hair loss are less common — but it carries its own effects, including rash, diarrhoea, fatigue, and changes to nails or skin, depending on the specific drug. Immunotherapy side effects are different again: they arise from immune activation and can affect the gut, liver, lungs, skin, or hormone glands. Both can cause serious reactions that need prompt medical attention, and your team will tell you which symptoms to report the same day.

How long does targeted therapy treatment last?

Targeted therapy is typically continued for as long as it is working and you can tolerate it — there is no fixed number of cycles the way chemotherapy often has. Treatment is stopped if the cancer stops responding, if side effects become unmanageable, or sometimes when a prolonged complete response has been achieved. Duration varies from months to years depending on the drug, the cancer type, and how the disease behaves. Your oncologist will discuss what monitoring is planned and what the stopping criteria are for your specific regimen.

What happens if I am not eligible for either treatment?

Being ineligible for both targeted therapy and immunotherapy does not mean you are out of options. Chemotherapy, hormone therapy, radiation, surgery, or combinations of these remain effective for many cancers. Eligibility can also change — tumours evolve, and new evidence emerges steadily for different cancer types. If your disease behaves differently later, the question may be worth revisiting. Ask your oncologist to explain clearly which treatment is recommended and what it is expected to achieve, so you have a complete picture of the plan.

Are targeted therapy and immunotherapy available at CION?

Yes. Both targeted therapy and immunotherapy are administered at CION centres across Telangana and Andhra Pradesh, and both are given as day care — most patients do not need an overnight stay. Biomarker testing to determine eligibility is coordinated as part of your treatment workup. Response assessment scans such as PET-CT are done through partner imaging centres. CION does not offer CAR-T or cell therapy; if that becomes relevant to your treatment, your team will refer you to a centre that provides it.

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