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Lutetium-177 PSMA therapy for advanced prostate cancer, delivered at a UK specialist centre.

A targeted radionuclide therapy - Lutetium-177 linked to a PSMA ligand - that seeks out PSMA-expressing prostate cancer cells and delivers radiation directly to them. NHS-funded for eligible patients under NICE TA1041 since March 2025.

A radiographer guides a patient onto the bed of an advanced 3 Tesla MRI scanner in a London imaging suite

Indicative pricing

What Lutetium-177 PSMA therapy costs in the UK.

NHS-funded for eligible patients under NICE TA1041. Private courses are possible in a small number of centres - indicative ranges below.

In short

NHS-funded via NICE TA1041; a private course runs roughly £45,000–£70,000.

Item Indicative range
Lutetium-177 PSMA - full course (NHS via NICE TA1041) NHS-funded
Lutetium-177 PSMA - full course (private) £45,000–£70,000
Lutetium-177 PSMA - single cycle (private) £9,000–£14,000
68Ga- or 18F-PSMA PET-CT (eligibility) £1,800–£2,800
PSMA PET-CT restaging (per scan) £1,800–£2,800
Uro-oncology consultation £300–£500

Prices vary by centre, by whether PSMA PET-CT is included, and by how many cycles are planned. Private availability is currently limited.

The problem

The right team, the right selection, the right conversation.

Lutetium-PSMA is a narrow, later-line treatment. The commonest mistakes are chasing it before eligibility is confirmed, or being told it will cure a disease it can only slow.

  • Not sure you qualify?

    NICE TA1041 needs both an ARPI and a taxane behind you, and PSMA-avid disease on PET-CT.

  • Worried about side effects?

    Dry mouth, dry eyes, fatigue and marrow effects are the honest realities. A specialist team walks you through them cycle by cycle.

  • Want it done at a proper centre?

    A nuclear medicine department licensed for Lutetium-177, working alongside uro-oncology and medical physics - not a generalist clinic.

When it helps

When Lutetium-PSMA is the right next step.

The situations we see most, plus the one red flag that means an emergency rather than an appointment.

  • mCRPC after ARPI and taxane

    Metastatic castration-resistant prostate cancer that has progressed after an androgen receptor pathway inhibitor and a taxane - the NICE TA1041 indication.

  • PSMA-avid disease on PET-CT

    PSMA PET-CT shows enough uptake - typically SUVmax >10 with disease at two or more sites - to make radioligand therapy worthwhile.

  • Rising PSA on current therapy

    Biochemical progression despite abiraterone, enzalutamide, apalutamide or darolutamide, with imaging or symptom progression.

  • Symptomatic bone metastases

    Painful, widespread PSMA-avid bone disease where systemic radioligand therapy may improve pain and quality of life.

  • Chemotherapy no longer tolerable

    Docetaxel or cabazitaxel has been used, or is no longer suitable, and further cytotoxic chemotherapy is not the right next step.

  • Preserved organ function

    Adequate bone marrow, kidney and liver function to safely receive four to six cycles of radionuclide therapy.

  • Shared decision-making

    You understand this is survival-extending, not curative - and want a specialist team to walk you through the trade-offs honestly.

  • Red flag: cord compression or fracture

    Sudden back pain with leg weakness, numbness or bladder trouble is a spinal cord emergency - same-day A&E, not a clinic booking.

Pathway options

Lutetium-PSMA is one option - not the only one.

What each option on the table actually involves - and which fits which pattern of disease.

  • Standard Lutetium-177 PSMA-617

    The VISION-trial regimen: 7.4 GBq IV every six weeks, up to six cycles, in a licensed nuclear medicine department.

  • PSMA PET-CT selection

    68Ga- or 18F-PSMA PET-CT to confirm PSMA expression and rule out dominant PSMA-negative disease before committing to therapy.

  • Dosimetry-guided planning

    Medical physics calculates dose to kidneys, salivary glands and marrow to keep therapy within safe organ limits.

  • Combination pathways (emerging)

    Trials combining Lutetium-PSMA with ARPIs, PARP inhibitors or immunotherapy - discussed if a suitable study is open at your centre.

  • Radium-223 alternative

    For bone-only disease where PSMA uptake is limited, radium-223 (Xofigo) may be a better fit - a separate radionuclide with a different profile.

  • Best supportive care

    Symptom control, palliative radiotherapy and specialist nurse input remain part of the plan regardless of whether radioligand therapy proceeds.

  • Clinical trial referral

    If you fall outside NICE TA1041 - for example pre-chemotherapy - a UK trial of Lutetium-PSMA earlier in the pathway may be an option.

  • Consultation only

    An honest second opinion on whether Lutetium-PSMA is realistic for your disease, or whether another line of treatment fits better.

Safety and side effects

What to expect between cycles - honestly.

Lutetium-PSMA is generally well tolerated for a cancer treatment, but the side-effect profile is real. What matters is knowing what is normal, what to watch for, and when to call.

  • Dry mouth is very common

    PSMA is expressed in the salivary glands, so 60–70% of patients notice xerostomia. For some it settles between cycles; for others it persists and needs long-term saliva substitutes.

  • Dry, gritty eyes

    Lacrimal glands also express PSMA. Dry eye is common - lubricating drops help and your team will screen for it at each cycle.

  • Fatigue is expected

    Most patients feel more tired for a week or two after each infusion. It usually improves before the next cycle.

  • Nausea, constipation and back pain

    Managed with anti-emetics, laxatives and simple analgesia. A short pain flare in the first few days is not unusual.

  • Bone marrow effects

    Anaemia and thrombocytopenia are the commonest blood changes. Grade 3–4 neutropenia or low platelets needing transfusion are less common but monitored at every cycle.

  • Kidney function is watched closely

    Hydration protects the kidneys during and after each infusion. Renal function is checked before every cycle and dosing adjusted if needed.

  • Radiation precautions for 24–48 hours

    Per UK MHRA and BNMS guidance: relative distancing from pregnant women, infants and young children for the first day or two after each infusion. The team writes it down for you.

  • Rare serious effects

    Pituitary or thyroid dysfunction, radiation-induced secondary malignancy and myelodysplastic syndrome are rare and typically delayed. They are part of the consent conversation.

  • Red flags between cycles

    Fever with low white cells, unusual bruising or bleeding, sudden weakness in the legs or bladder trouble - all reasons to call the acute oncology line the same day.

Reading your treatment notes

Your Lutetium-PSMA note in four parts. Read the last one first.

Whichever centre delivers your treatment, the letter your oncologist sends you keeps to the same shape.

A UK consultant uro-oncologist reviewing a patient’s Lutetium-PSMA treatment notes

A quiet reminder

Oncology language is precise and can read coldly - we translate it for you.

If you would like us to talk you through the note before your review, just ask.

  1. 01 Header

    Indication and eligibility summary

    Why Lutetium-PSMA was offered - mCRPC after ARPI and taxane - and confirmation you meet the NICE TA1041 criteria.

  2. 02 Technique

    Dose, cycle number and dosimetry

    The activity delivered (7.4 GBq per cycle), which cycle number this is, and the dosimetry to kidneys, salivary glands and marrow.

  3. 03 Findings

    PSA, bloods and imaging response

    PSA trend, FBC, renal and liver function, and how PSMA PET-CT restaging compares with your baseline.

  4. 04 Impression

    Plan for next cycle, precautions, review

    Read this first: whether to proceed to the next cycle, radiation precautions to follow at home, and when your oncologist wants to see you.

Recognised by major UK insurers

BupaAXA HealthVitalityAvivaWPACignaHealixBupaAXA HealthVitalityAvivaWPACignaHealixBupaAXA HealthVitalityAvivaWPACignaHealix

Insurer cover for Lutetium-PSMA varies and is evolving following NICE TA1041. Many eligible patients are treated on the NHS; private cover depends on your policy and indication.

Frequently asked

Everything we get asked about Lutetium-PSMA therapy.

Quick answers on eligibility, VISION outcomes, side effects and cost.

  • What is Lutetium-177 PSMA therapy (Pluvicto)?

    It’s a targeted radionuclide therapy for advanced prostate cancer. Lutetium-177, a beta-emitting radioactive isotope, is linked to a PSMA ligand (PSMA-617). The PSMA ligand binds to prostate cancer cells that express PSMA on their surface, delivering cytotoxic radiation directly to the tumour while largely sparing normal tissue.

  • Who is eligible under NICE TA1041?

    Adults with metastatic castration-resistant prostate cancer (mCRPC) that has progressed after an androgen receptor pathway inhibitor (abiraterone, enzalutamide, apalutamide or darolutamide) AND a taxane chemotherapy (docetaxel or cabazitaxel), whose disease is PSMA-positive on 68Ga- or 18F-PSMA PET-CT - typically SUVmax >10 with disease at two or more sites.

  • How well does it work?

    The VISION Phase 3 trial showed median overall survival of 15.3 months with Lutetium-PSMA plus standard care versus 11.3 months with standard care alone - a hazard ratio of 0.62, or a 38% reduction in the risk of death. Median radiographic progression-free survival was 8.7 months versus 3.4 months. Around 30–40% of patients have a PSA fall of more than 50%.

  • How much does it cost in the UK?

    Since March 2025 it is NHS-funded per NICE TA1041 in eligible specialist centres. Private courses currently cost roughly £45,000–£70,000 for a full four- to six-cycle programme, plus PSMA PET-CT scans (£1,800–£2,800 each) and consultations. Private availability is limited.

  • What is the treatment like?

    Four to six outpatient infusions of 7.4 GBq Lutetium-177 PSMA-617, given every six weeks in a licensed nuclear medicine department. You go home the same day with anti-emetics, hydration advice and short radiation precautions for the first 24–48 hours.

  • What are the side effects?

    The commonest are dry mouth, dry eyes, fatigue, mild nausea, constipation, back pain, and lower blood counts (anaemia and low platelets). Serious effects - grade 3–4 low counts, kidney impairment, secondary malignancy or MDS - are much rarer but part of the consent discussion.

  • Is Lutetium-PSMA a cure?

    No. It is survival-extending, not curative. It is offered as an advanced, later-line treatment in mCRPC to extend life and improve quality of life for the right patients.

  • Where in the UK is it delivered?

    A small number of specialist centres, including UCLH, The Royal Marsden and The Christie among others. Delivery requires a nuclear medicine department licensed for Lutetium-177 therapy, uro-oncology input and on-site medical physics.

  • Can I have Lutetium-PSMA before chemotherapy?

    Not under NICE TA1041 - the current NHS indication is after both an ARPI and a taxane. Earlier-line use is being studied in clinical trials, and referral to a UK trial may be an option in some cases.

  • When should I seek urgent medical help during treatment?

    Fever with low white cells, unusual bruising or bleeding, sudden back pain with leg weakness or bladder trouble, or heavy dehydration all warrant same-day contact with your acute oncology team or A&E.