Skip to main content

Radioligand therapy · London

Lutetium-177 PSMA therapy, private in London.

A targeted radioligand for metastatic castration-resistant prostate cancer. Lu-177 PSMA-617 (Pluvicto) is delivered as up to six cycles by a therapy-trained nuclear medicine team in a licensed London unit, with PSMA-PET selection before cycle one.

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

Why patients choose us

  • 01

    A licensed nuclear medicine unit, not a general oncology day-case

    Lutetium-177 PSMA-617 (Pluvicto) needs a specific radiopharmacy licence, a shielded delivery suite and a therapy-trained nuclear medicine team. We match you to units that hold all three.

  • 02

    PSMA-PET first, then treatment

    Every candidate has a 68Ga-PSMA or 18F-DCFPyL PET-CT reviewed before cycle one. No PSMA-avid disease, no Pluvicto. An honest read either way.

  • 03

    Independent, and free

    We are paid by no centre, so the recommendation on where to have your six cycles is impartial and costs you nothing.

Indicative pricing

What private Lutetium-177 PSMA costs in London.

Indicative ranges across our partner London units. Send your scans and letters and we quote firm figures across two or three centres.

In short

Per cycle in London: £22,000 to £38,000. Full six-cycle course: £130,000 to £220,000.

Item Indicative range
Second-opinion review of scans, PSA and prior treatment £350–£600
68Ga-PSMA-11 or 18F-DCFPyL PET-CT (eligibility scan) £2,400–£3,600
Lutetium-177 PSMA-617 (Pluvicto), per cycle £22,000–£38,000
Full 6-cycle course (drug, admin, imaging, review) £130,000–£220,000
Mid-treatment PSMA-PET response scan £2,400–£3,600
MDT eligibility review and treatment planning £450–£800

Prices vary by centre, by radiopharmacy sourcing, by whether the eligibility PSMA-PET is bundled, and by the number of cycles actually completed. Where NHS access via NICE TA1000 fits, we say so.

What it is

A small molecule that finds prostate cancer, carrying a radiation warhead.

Radioligand therapy delivers targeted radiation from inside the bloodstream, at cellular range. It is a very different mechanism from external beam radiotherapy or systemic chemotherapy.

  • The ligand: PSMA-617

    A small molecule that binds tightly to prostate-specific membrane antigen (PSMA), a protein expressed on the surface of most prostate cancer cells and their metastases.

  • The isotope: lutetium-177

    A beta-emitting radioisotope with a short tissue range (around 2 mm) and a 6.7-day half-life. Ideal for cellular-range irradiation with limited off-target dose.

  • The combination: Pluvicto

    Chemically linked, PSMA-617 delivers Lu-177 directly to PSMA-expressing metastases anywhere in the body. Non-PSMA tissue receives a much lower dose.

The evidence

VISION 2021, and NICE TA1000 in 2023.

Lu-177 PSMA-617 is not experimental. It is a licensed, NICE-approved treatment with a phase III trial behind it.

VISION trial (NEJM 2021)

831 patients with post-taxane mCRPC, PSMA-avid on 68Ga-PSMA-PET.

Lu-177 PSMA-617 plus standard care improved overall survival by around 4 months compared with standard care alone (median 15.3 vs 11.3 months) and improved radiographic progression-free survival (8.7 vs 3.4 months). Objective response rate 30 per cent versus 2 per cent.

NICE TA1000 (May 2023)

Recommended on the NHS for PSMA-positive mCRPC after 2 or more prior treatments.

NICE approved lutetium (177Lu) vipivotide tetraxetan for adults with PSMA-positive hormone-relapsed metastatic prostate cancer who have had at least one androgen receptor pathway inhibitor and taxane chemotherapy. Private access mirrors this population.

The course

Six cycles, six weeks apart - with PSMA-PET at the start and midway.

One team from first message to end-of-course review, including the eligibility PSMA-PET, the six-cycle schedule and the mid-treatment response scan.

  1. 01

    Before

    You send your recent scans and letters

    A short, confidential form. Most recent PSA, prior treatments (abiraterone or enzalutamide, docetaxel, cabazitaxel), current PSMA-PET if you have one, bloods and renal function.

  2. 02

    Before

    We come back with a recommendation

    Within one working day: whether Lu-177 PSMA fits now, whether you need a PSMA-PET first, or whether radium-223 or a trial route is a better call. Indicative cost per cycle and for the full course.

  3. 03

    Before

    PSMA-PET and MDT sign-off

    68Ga-PSMA-11 or 18F-DCFPyL PET-CT to confirm PSMA-avid metastases, plus bloods, GFR and salivary-gland assessment. MDT confirms VISION-style eligibility before cycle one is booked.

  4. 04

    On the day

    Cycle day at the nuclear medicine unit

    Arrival, cold saline hydration, ice packs to the parotids, then a slow IV infusion of 7.4 GBq Lu-177 PSMA-617 over 20 to 30 minutes. A few hours of observation and post-therapy SPECT/CT imaging.

  5. 05

    On the day

    Home the same day with radiation advice

    Written aftercare on hydration, toilet hygiene, distance from young children and pregnant women for a few days, and a 24/7 contact number. You go home the same day in the UK.

  6. 06

    After

    PSA, bloods and repeat cycles every 6 weeks

    PSA and full blood count before each cycle. Six cycles at six-weekly intervals is the standard course, with a mid-treatment PSMA-PET around cycle 2 or 3 to check response.

  7. 07

    After

    End-of-course review and next line

    A restaging PSMA-PET after cycle 6, a treatment summary letter to your oncologist and GP, and a conversation about what comes next: maintenance, a trial, or a different systemic option.

Full course window: around 30 weeks. Per cycle: 7.4 GBq. Interval: 6 weeks.

Who it is for

When Lu-177 PSMA is the right next step - and when it is not.

The eligibility criteria we work to, plus the signals that mean lutetium is abandoned in favour of a trial, cabazitaxel, or a different systemic option.

  • Metastatic castration-resistant prostate cancer

    Disease progression on continuous ADT with a castrate testosterone, radiologically confirmed on CT, MRI or bone scan.

  • Post-taxane chemotherapy

    Progression after or intolerance of docetaxel and, in most cases, cabazitaxel. This is the licensed VISION-trial population.

  • Post abiraterone or enzalutamide

    Progression on at least one androgen receptor pathway inhibitor. Most candidates have had both by the time Pluvicto is discussed.

  • PSMA-avid disease on PSMA-PET

    At least one lesion with uptake above liver background, and no dominant PSMA-negative disease on the eligibility scan.

  • ECOG 0 to 2 and adequate organ function

    Well enough for a six-cycle course. Haemoglobin, platelets, neutrophils, GFR and liver enzymes within VISION-trial thresholds.

  • Not suitable if dominant PSMA-negative disease

    Visceral lesions that light up on FDG-PET but not PSMA-PET suggest de-differentiated disease that will not respond. We say so.

  • Not suitable if marrow reserve is exhausted

    Heavy prior radium-223, wide-field external beam or platinum chemotherapy can leave the marrow too fragile for six lutetium cycles.

  • Red flag: cord compression or uncontrolled pain

    Impending cord compression, uncontrolled bone pain or acute renal obstruction is a hospital admission, not a private booking. Ring 999 or go to A&E.

Options and sequence

Lu-177 PSMA sits in a sequence - not on its own.

Lutetium usually comes after abiraterone or enzalutamide and docetaxel, before or in place of cabazitaxel, and ahead of actinium-225 PSMA in trial settings. The eligibility scan is a PSMA-PET.

  • Lutetium-177 PSMA-617 (Pluvicto)

    The Novartis product used in the VISION trial and licensed by the MHRA and EMA. 7.4 GBq per cycle, six cycles at six-weekly intervals. The current UK standard.

  • Lutetium-177 PSMA-I&T

    An alternative Lu-177 PSMA ligand used in academic centres and the SPLASH and ECLIPSE trials. Broadly comparable pharmacology, different licensing status in the UK.

  • 68Ga-PSMA-11 PET-CT

    The classical eligibility scan. Half-life 68 minutes, generator-produced, widely available in UK PET centres. Uptake pattern determines candidacy for lutetium.

  • 18F-DCFPyL (piflufolastat) PET-CT

    Fluorine-18 PSMA tracer with a longer half-life and higher-resolution images. Equally accepted for VISION-style eligibility where available.

  • Radium-223 (Xofigo)

    An alpha-emitter bone-seeker for symptomatic bone-only mCRPC. Complementary to lutetium rather than a substitute, and used earlier in the sequence for bone-dominant disease.

  • Actinium-225 PSMA (trial)

    An alpha-emitter PSMA ligand under trial evaluation for Lu-177 non-responders. Higher tumour cell kill per decay, higher xerostomia risk. Not routinely commissioned.

  • Cabazitaxel

    Second-line taxane chemotherapy. The TheraP trial compared it head-to-head with lutetium; both remain valid post-docetaxel options with different toxicity profiles.

  • Second-opinion review

    A specialist review of your PSMA-PET, CT, bloods and prior treatment history to confirm whether Pluvicto is the right next step, or whether a trial or different agent fits better.

Where in London

A short list of London units, licensed for Lu-177 PSMA.

Radioligand therapy needs a specific radiopharmacy licence. In London that means a small group of centres: University College London Hospital Private, Royal Marsden Private, Guy's and St Thomas' Private, and HCA London Bridge Nuclear Medicine.

Selection criteria

How we pick a London unit for your six cycles.

A licensed London nuclear medicine therapy suite set up for Lu-177 PSMA infusion
Licensed radiopharmacy · London
  • Nuclear medicine units with a specific radiopharmacy licence for Lu-177 PSMA-617

  • On-site 68Ga-PSMA-11 or 18F-DCFPyL PET-CT for eligibility and response scans

  • Uro-oncology MDT with genitourinary oncologist, nuclear medicine physician and clinical nurse specialist

  • Trial access to actinium-225 PSMA and next-generation ligands when lutetium is no longer working

Side effects and safety

What to plan for - honestly.

Radioligand therapy is generally better tolerated than chemotherapy, but it is not side-effect free. The things worth planning for are dry mouth, cumulative fatigue, bloods before every cycle and simple radiation precautions for a few days.

  • Dry mouth (xerostomia) in 40 to 50 per cent

    The commonest side effect. PSMA is expressed in salivary glands, so they take a dose. Ice packs during infusion, sugar-free gum and pilocarpine sprays help. Usually mild to moderate and reversible.

  • Fatigue during the course

    Cumulative fatigue is common by cycles 4 to 6. It settles within a few weeks of finishing. Plan lighter weeks around each cycle and stay well hydrated.

  • Nausea and altered taste

    Mild nausea in the 24 to 48 hours after each cycle. A single dose of ondansetron before the infusion is usually enough. Metallic taste for a few days is common.

  • Cytopenias (anaemia, thrombocytopenia)

    Marrow suppression is dose-limiting. Grade 3 or 4 anaemia in around 13 per cent and thrombocytopenia in around 8 per cent in VISION. Bloods before every cycle.

  • Renal impairment

    PSMA is expressed in the proximal tubule, so kidneys take a dose. GFR is checked before each cycle. Clinically relevant renal impairment is uncommon at 7.4 GBq x 6.

  • Radiation precautions for a few days

    Frequent toilet flushing, careful hand hygiene, sleeping alone for a night or two and keeping distance from young children and pregnant women for the first few days after each cycle.

  • Fertility and contraception

    Lu-177 PSMA is not for men who might father a child during or shortly after treatment. Effective contraception is advised for at least 14 weeks after the last cycle.

  • Rare late effects

    Second malignancy, including therapy-related myelodysplasia, is a rare late risk documented in radioligand therapy series. Long-term follow-up remains important.

  • Red flags after discharge

    Fever above 38C, unexplained bruising or bleeding, breathlessness, reduced urine output or severe back pain: call the unit or go to A&E the same day.

Outcomes and reporting

What good looks like. Read the last line first.

In VISION, 46 per cent of Lu-177 PSMA patients had a PSA fall of more than 50 per cent. Median overall survival was 15.3 months versus 11.3 months on standard care alone.

A UK genitourinary oncologist reviewing PSMA-PET and PSA response after Lu-177 PSMA-617

A quiet reminder

Radioligand reports are dense and can read coldly. We translate them for you.

If you would like us to talk you through the cycle summary or the mid-treatment PSMA-PET before your review, just ask.

  1. 01 Header

    Cycle number, activity and route

    Which cycle of six, activity in GBq (typically 7.4), route and duration of infusion, and any dose reduction from the standard schedule.

  2. 02 Imaging

    PSMA-PET and post-therapy SPECT/CT

    Baseline PSMA-PET uptake pattern, mid-treatment response scan interpretation, and the post-therapy SPECT/CT showing where the dose actually went.

  3. 03 Response

    PSA and radiological response

    PSA trajectory across cycles, RECIST or PCWG3 response on cross-sectional imaging, and any new sites of disease that appeared during treatment.

  4. 04 Impression

    Plan for next cycle or next line

    Read this first: is the next cycle going ahead, is a dose reduction needed, are more cycles planned, or is it time to switch to a different systemic option or a trial?

Recognised by major UK insurers

BupaAXA HealthVitalityAvivaWPACignaHealixBupaAXA HealthVitalityAvivaWPACignaHealixBupaAXA HealthVitalityAvivaWPACignaHealix

Cover for Lu-177 PSMA varies by insurer and is normally case-by-case, pre-authorised, for the VISION-trial population. We check cover before you commit to cycle one.

Frequently asked

Everything we get asked about Lu-177 PSMA.

Quick answers on eligibility, PSMA-PET, side effects, insurance, timing and what comes after lutetium.

  • Am I eligible for lutetium-177 PSMA therapy on VISION criteria?

    The licensed population is metastatic castration-resistant prostate cancer that has progressed on at least one androgen receptor pathway inhibitor (abiraterone or enzalutamide) and at least one taxane chemotherapy (usually docetaxel), with PSMA-avid disease on a 68Ga-PSMA or 18F-DCFPyL PET-CT and adequate marrow, renal and hepatic function. NICE TA1000 broadly follows this. If you fall outside these criteria, a trial route may still be open to you.

  • Is a PSMA-PET scan essential before treatment?

    Yes. Every candidate has a PSMA-PET (68Ga-PSMA-11 or 18F-DCFPyL) reviewed before cycle one to confirm PSMA-avid metastases and rule out dominant PSMA-negative disease. Treating without it risks giving a course of radioligand therapy to disease that will not respond.

  • What are the main side effects to plan for?

    Dry mouth (40 to 50 per cent, usually mild), fatigue building through the course, mild nausea for a day or two after each cycle, and dose-limiting marrow suppression (anaemia and low platelets) picked up on pre-cycle bloods. Renal impairment is uncommon. Radiation precautions for young children and pregnant women apply for a few days after each cycle.

  • Does UK private medical insurance cover Lu-177 PSMA?

    Cover varies. Some insurers now fund Pluvicto for the licensed VISION-trial indication on a pre-authorised, case-by-case basis, especially since NICE TA1000. Others do not. We check cover with your insurer before you commit to cycle one, and we always quote the self-pay figure alongside for transparency.

  • How are the six cycles timed and can I have them all in one place?

    Standard schedule is 7.4 GBq every 6 weeks for up to 6 cycles, giving a total treatment window of around 30 weeks. You can complete all six at the same unit, or split between units if travel matters. Bloods and PSA are checked before each cycle, and a mid-treatment PSMA-PET is used to confirm response before continuing.

  • What comes after lutetium: is actinium-225 next?

    For patients who respond and then progress, options include a further short course of Lu-177, cabazitaxel if not already used, a PARP inhibitor if there is a homologous recombination repair mutation, or a clinical trial. Actinium-225 PSMA is being evaluated in trials for Lu-177 non-responders, with higher tumour cell kill per decay but a higher rate of severe xerostomia. It is not routinely commissioned in the UK yet.

Ready to be reviewed?

Send your PSA, scans and treatment history. We come back within a working day.

One private, confidential form. We check whether Lu-177 PSMA fits your case, whether you need a PSMA-PET first, and quote firm figures from two or three licensed London units.

Pulse Healthcare concierge

Send us your enquiry

A concierge service for UK private healthcare. We match you with the best vetted clinics and consultants in our network - they then contact you directly.

So we can match you to the right clinician close to you.

We reply to every enquiry within 24 hours (Mon–Fri). Confidential - your details are never shared outside our vetted consultant network.