Medicines
T-DM1 infusion day: what fourteen cycles look like
T-DM1 is given as a drip in a day-care unit every three weeks, usually for fourteen cycles after surgery. Each visit includes weighing, blood tests and a symptom check before the pharmacy prepares your dose. The first drip runs slowly with a longer wait afterwards, and later ones are usually quicker. This page walks you through the day.
On this page
- What happens on a T-DM1 infusion day?
- How a treatment visit usually runs
- What the fourteen cycles look like
- The vocabulary, in plain language
- Honest realities of treatment days
- How to prepare for your visit
- What to tell the nurse straight away
- What people assume about infusion days
- Common questions about T-DM1 infusion days
The short answer
What happens on a T-DM1 infusion day?
T-DM1, also called trastuzumab emtansine or Kadcyla, is given as a drip into a vein in a hospital day-care unit, once every three weeks. After surgery, for people whose cancer was not fully cleared by chemotherapy before the operation, the usual plan is fourteen of these visits, which takes a little under a year. In advanced cancer, visits continue for as long as the treatment is working and side effects are manageable. Each visit follows a similar pattern. You are weighed, because the dose depends on your body weight. A blood sample is checked, mainly your platelet count and liver tests, to make sure it is safe to go ahead. A nurse asks how you have been since the last dose, including any bleeding, tingling, breathlessness or tiredness. The pharmacy then prepares your dose, which can take some time. The first infusion is given slowly, over about an hour and a half, and you are watched for around the same time afterwards in case of a reaction. If that goes well, later infusions usually run over about half an hour, with a shorter wait afterwards. A heart scan is also repeated every few months. Most people can go home the same day and many travel back independently, though having a companion for the first visit is helpful. Knowing the routine makes the day less stressful.
A day-care visit every three weeks
There is no overnight stay, and most of the time is spent on checks and waiting for the pharmacy.
The first visit takes longest
The slower first drip and longer observation mean you should plan for most of the day.
Later visits are shorter
If you cope well, the drip runs faster and the wait afterwards is shorter.
This page gives general information only. Timings and routines differ between hospitals, so ask your own unit what to expect.Four stages
How a treatment visit usually runs
The order may vary slightly, but most visits include these steps.
Checks on arrival
Your weight, blood pressure, pulse and temperature are measured, and a blood sample is taken if it was not done the day before.
Review and go-ahead
A doctor or nurse reviews your results and symptoms. If platelets or liver tests are not right, the dose may be delayed.
A delay is a safety step, not a setback.Preparing and giving the drip
The pharmacy makes up your dose. A nurse places a small tube in a vein, or uses your port, and runs the drip through a pump.
Watching and going home
You stay for a period of observation, then receive your next date and any medicines to take home.
Before you leave
- Confirm the date of your next cycle
- Check when your next heart scan is due
- Keep the number to call if you feel unwell
Across the course
What the fourteen cycles look like
Words you will hear
The vocabulary, in plain language
- Infusion
- Medicine given slowly into a vein through a drip.
- Cannula
- A thin, soft tube placed in a vein in your hand or arm for the drip, removed before you go home.
- Port
- A small device placed under the skin of the chest, giving easy access to a vein over many months.
- Observation period
- Time spent in the unit after the drip so staff can watch for any reaction.
- Infusion reaction
- Chills, fever, flushing, breathlessness or a racing heart during or soon after the drip.
- Echocardiogram
- An ultrasound scan of the heart that measures how well it pumps.
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Have a question about your situation?
Call the helpline or leave your details, and someone will help you arrange a consultation at the CION centre nearest you. One helpline serves every CION centre.
Being straight with you
Honest realities of treatment days
The drip itself is short, but the whole visit often is not. Being prepared helps you manage the day.
Waiting is part of it
Blood results and pharmacy preparation can take longer than expected, especially on busy days.
Plans can change on the day
If your blood tests or symptoms are not right, your dose may be postponed. This can be frustrating, but it protects you.
Fourteen visits is a long commitment
Most of a year of three-weekly visits affects work, travel and family life. It is reasonable to feel worn down at times.
What this page cannot tell you
It cannot tell you the exact routine at your hospital, or how you personally will feel after each dose. Your unit can explain their process.
Getting ready
How to prepare for your visit
A little preparation the day before makes infusion days calmer and more comfortable.
What to bring
Your appointment card, a list of all your medicines and supplements, water, a light snack, something to read or listen to, and a warm layer, as units can feel cool.
Eating and drinking
There is usually no need to fast. Eat a normal light meal and drink fluids unless your unit tells you otherwise.
Clothing
Wear loose sleeves that roll up easily, or a top that opens at the front if you have a port.
Questions to jot down
Note any symptoms since your last dose, such as bruising, nosebleeds, tingling or breathlessness, so you remember to mention them.
During the drip
What to tell the nurse straight away
Most infusions pass without any problem. Reactions are most likely during the first dose, and nurses are trained to deal with them quickly.
Signs of a reaction
Tell the nurse at once if you feel hot, flushed, shivery, breathless, dizzy, or notice a racing heartbeat or chest tightness. The drip can be slowed or paused.
Problems at the drip site
Pain, stinging, redness or swelling around the cannula can mean the medicine is leaking under the skin. Say so immediately so the drip can be stopped and checked.
After you get home
Mild tiredness, headache or nausea over the next few days is common. Call your team for fever, bleeding that will not stop, or breathlessness.
Commonly believed
What people assume about infusion days
It is given as a day-care treatment, and most people go home the same day.
If the first goes well, later infusions usually run faster with a shorter wait.
Fasting is not usually needed; a light meal and fluids are generally fine.
A delayed dose is a routine safety step, and treatment usually continues soon after.
Questions we are asked
Common questions about T-DM1 infusion days
How long will I be at the hospital?
The first visit often takes most of the day, because the drip runs slowly and you are observed afterwards. Later visits are usually shorter. Waiting for blood results and pharmacy preparation adds time, so plan for a few hours even once treatment is routine.
Do I need a port?
Not always. Many people have T-DM1 through a cannula placed in the arm at each visit. If you already have a port from earlier chemotherapy, it is often used. If finding a vein has been difficult, your team may suggest keeping or placing one for the course.
Can someone come with me?
Most units welcome one companion, especially for the first visit, although space can be limited. A companion can help with questions and the journey home. Check your unit's current policy before you travel.
Can I drive home afterwards?
Many people feel well enough to travel independently after later visits. For your first infusion, arranging a lift is sensible in case you feel tired or have a reaction. If you ever feel dizzy or unwell after treatment, do not drive.
Will I be given medicines before the drip?
Routine pre-medicines are not always needed with T-DM1. Some units offer anti-sickness medicine, and if you have had a reaction before, you may be given medicines to reduce the chance of another. Your team will explain what applies to you.
What if my blood tests are not good enough on the day?
Your dose may be postponed, often by about a week, until platelets or liver tests recover. Sometimes the next dose is lowered. This is a common and routine decision. You will be given a new date and told whether any extra tests are needed.
Why is a heart scan needed?
HER2 treatments can weaken the heart's pumping strength in some people. A scan before starting, then every few months, checks for this early. If the pumping strength falls, your team may pause treatment and review your heart before deciding how to continue.
Can I have radiotherapy on the same days?
After surgery, radiotherapy is often given during the same months as T-DM1. The daily radiotherapy sessions and the three-weekly drip are usually coordinated between your teams. Ask them how to plan the appointments so they fit together.
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Sources
- European Medicines Agency — Kadcyla: product information
- Macmillan Cancer Support — Trastuzumab emtansine (Kadcyla)
- Cancer Research UK — Trastuzumab emtansine (Kadcyla)
This page is general information, not a prescription. Do not change or stop any treatment based on what you read here. If anything is worrying you, contact your own treating team — or call our helpline and we will help you reach the right specialist.