CD20, CD38 and Other — Antibody Targets in Blood Cancers
Monoclonal antibodies work by finding a specific protein on the surface of blood cancer cells and directing your immune system to destroy them. CD20, CD38 and CD19 are the three most common targets — and the drugs that bind them are now central to treating lymphoma, myeloma and some leukaemias.
Medically reviewed by Dr. T. Raghavender Reddy, Medical Oncologist, MBBS · DM (Medical Oncology) · MD (Radiation Oncology) · Last reviewed August 2026
- CD20 is the target in B-cell lymphomas and CLL — Rituximab and obinutuzumab both lock onto CD20, and one of them is part of nearly every frontline B-cell lymphoma regimen.
- CD38 is the main target in multiple myeloma — Daratumumab and isatuximab target CD38 and are used across multiple lines of myeloma treatment.
- These drugs work with your immune system — Unlike chemotherapy, antibody drugs do not kill cells directly — they flag cancer cells so your own immune system destroys them.
- Most are given as day-care infusions — You receive the drug through a drip and go home the same day. The first infusion is usually the longest.
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Monoclonal antibodies in blood cancer work by locking onto specific proteins on the surface of cancer cells — CD20, CD38, CD19 or CD30 — and signalling the immune system to destroy them. They are standard treatment in B-cell lymphomas, multiple myeloma and some leukaemias, and are usually given alongside chemotherapy or as single agents.
What does CD20, CD38 or CD19 mean on your report?
These are names for proteins that sit on the surface of certain blood cancer cells. CD stands for cluster of differentiation — a numbering system scientists use to identify proteins on white blood cells.
Cancer cells usually carry these proteins in much higher quantities than normal cells. That difference is what makes them useful targets: a drug designed to recognise CD38 will seek out myeloma cells that are densely covered in it.
When your pathology report lists CD20-positive or CD38-positive, it means your cancer cells carry that protein. That result directly shapes which treatment your oncologist recommends.
Which antibody drug targets which blood cancer?
CD20 is the target in B-cell non-Hodgkin lymphomas and chronic lymphocytic leukaemia. Rituximab is the established drug in this class. Obinutuzumab is used in certain CLL and follicular lymphoma regimens where NCCN and ESMO guidance supports it.
CD38 is the principal antibody target in multiple myeloma. Daratumumab and isatuximab both bind CD38 and appear across NCCN-recommended regimens for newly diagnosed and relapsed myeloma, usually combined with other myeloma drugs.
CD19 is present on most B-cell malignancies. Tafasitamab targets CD19 in relapsed diffuse large B-cell lymphoma. CD30 is the target in Hodgkin lymphoma and some T-cell lymphomas, where brentuximab vedotin — an antibody carrying a chemotherapy payload — is listed in standard NCCN regimens.
Your oncologist will match the drug to your specific cancer type, its protein expression and your treatment history. The same protein can appear in more than one cancer type, which is why both the diagnosis and the biomarker result together determine the choice.
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What should you expect during and after an infusion?
Most of these antibodies are given as a slow drip through a vein. The first infusion is given more slowly than later ones because infusion reactions — chills, fever, a brief drop in blood pressure — are most likely the first time.
Nursing staff monitor you throughout. If a reaction occurs, the infusion is paused and managed on the spot; most reactions settle quickly and the drip continues at a slower rate.
Later infusions are usually shorter. You go home the same day. Your team will check your blood counts before each cycle because these drugs can temporarily reduce your normal white cell count, raising infection risk while you are on treatment.
Questions your family is probably asking
Do I need a new biopsy to find out which proteins my cancer has?
In most cases, the testing is done on the biopsy you have already had. The pathology laboratory stains the tumour sample for specific surface proteins and reports which ones are present. If your original sample was too small or the result is borderline, a repeat biopsy may occasionally be needed before the question can be answered. Ask your oncologist which markers were tested and what the results showed — you are entitled to a clear answer, and those results directly determine which treatment options are open to you.
Can these antibody drugs be combined with chemotherapy?
Yes, and for many blood cancers the combination is the standard approach rather than either treatment alone. Rituximab is almost always given alongside a chemotherapy regimen in B-cell lymphoma; daratumumab in myeloma is used with combinations of other myeloma drugs. The reasoning is that the antibody and the chemotherapy attack cancer cells through different mechanisms, which can deepen the response. Your oncologist will explain exactly which combination applies to your situation and what each drug is expected to contribute.
What are the main side effects to watch for?
The most common early effect is an infusion reaction — chills, flushing or fever during the drip — which is managed by slowing the infusion and giving medication beforehand. Over the course of treatment, these drugs can reduce the number of normal white blood cells, which raises the risk of infection. Report any fever, shaking or sudden feeling of being unwell between cycles to your team the same day — do not wait for your next appointment. Fatigue is common. Your team will brief you on side effects specific to your drug before you start.
If the antibody drug stops working, are there other options?
Yes. Blood cancers are an area where several lines of treatment may be available. If one CD20-directed regimen stops controlling the disease, a drug targeting a different protein or working by a different mechanism may still respond. In myeloma, if a CD38-based regimen stops working, BCMA-directed therapies are among the options that NCCN and ESMO list for later lines of treatment. What is available depends on your cancer type, its biology and what you have already received. Ask your oncologist what the plan would be if the current regimen stops responding — it is a reasonable question to ask upfront.
How long does each infusion take?
The first infusion of most antibody drugs takes several hours because it is given slowly to reduce the chance of a reaction. Subsequent infusions are usually faster — often two to three hours or less, depending on the drug and whether there were any reactions earlier. You will be in the day-care unit for the full duration plus a short observation period afterwards. Most people read, watch something on their phone or sleep through it. Your team will give you the expected timing before your first visit so you can plan.
Are these treatments available at CION?
Targeted antibody treatments and immunotherapy are administered as day care at CION centres. Your oncologist will confirm which agents are appropriate for your diagnosis and discuss the full regimen with you before treatment begins. CION does not provide CAR-T or cell therapy; if that is being considered for your situation, you would be referred to a centre that offers it. PET-CT scans to assess your response to treatment are coordinated with partner imaging centres.
Did you know?
Rituximab, which targets CD20, was among the first targeted antibody therapies approved for any cancer.
ASCO has identified its introduction as one of the advances that most changed outcomes in B-cell lymphomas — it is now incorporated into nearly every frontline regimen for these cancers worldwide.
Source: ASCO Clinical Progress Reports; ESMO Clinical Practice Guidelines on aggressive and indolent B-cell lymphoma
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Frequently asked questions
How is a monoclonal antibody different from chemotherapy?
Chemotherapy drugs are broadly toxic to dividing cells — cancer and healthy ones alike. Monoclonal antibodies are designed to recognise a specific protein on cancer cells and direct the immune system to destroy them, leaving most other cells alone. The side effect profile is different from chemotherapy, though it is not side-effect free. The two are often combined because they attack the cancer through different mechanisms, which can improve the overall response.
Will biomarker testing tell me which antibody drug is right for me?
Pathology testing of your tumour tissue is the starting point. It establishes which surface proteins your cancer cells carry — CD20, CD38, CD19, CD30 and others — and that result narrows down which drug classes apply. The final decision also takes into account your cancer type, stage, general fitness and prior treatment. Biomarker testing answers whether a drug can work; clinical judgement determines which combination makes most sense for your situation.
Are these drugs used alone or always with other treatments?
Both, depending on the cancer and the situation. In B-cell lymphomas, rituximab is almost always given alongside a chemotherapy regimen because the evidence for the combination is stronger than for the antibody alone. In myeloma, daratumumab is typically part of a multi-drug regimen. In certain relapsed settings, some antibody drugs are used as single agents or two-drug combinations without chemotherapy. Your oncologist will explain the specific regimen and the evidence behind the approach they are recommending.
What is an infusion reaction and how serious is it?
An infusion reaction is your body's response to the antibody drug going in — typically chills, flushing, a mild fever or a brief drop in blood pressure. It is most common during the first infusion and is why the first dose is given slowly, with medication given beforehand. Nursing staff monitor you throughout and are trained to manage it. Most reactions are mild and settle quickly when the drip is paused or slowed. Tell your nurse immediately if you feel unwell during the infusion.
How do you know if the treatment is working?
Your team will assess response at planned intervals — through blood tests, imaging or bone marrow examination depending on your cancer type. In lymphomas, a PET-CT scan is the standard tool. In myeloma, blood and urine protein markers are checked regularly. A response does not always mean the cancer disappears completely; a significant reduction in measurable disease is considered a meaningful response under NCCN and ESMO criteria. Your oncologist will explain what they are measuring and what the results mean for your situation.
Will these drugs raise my risk of infection?
Yes, and this is one of the most important things to monitor during treatment. Drugs targeting CD20 and CD38 reduce normal immune cells alongside cancer cells, temporarily lowering your resistance to infection. Your team will check your blood counts before each cycle. Report any fever, shaking, unusual tiredness or signs of infection to your oncology team the same day — do not wait for your next appointment. In some cases your oncologist may recommend preventive antiviral or antifungal medication alongside treatment.