Around 1,300 people a year are diagnosed with gallbladder cancer in the UK, most of them women and most over 75. Half are diagnosed as emergencies. This page follows the NHS route from suspicion to treatment, names the specialist hepatobiliary centres, lists what the NHS funds today with the NICE and SMC decisions behind it, the genomic tests to ask for, the trials open in the UK, and where England, Scotland, Wales and Northern Ireland differ.
How the cancer usually comes to light, then the national standards that time each step. The standards are England's unless the four-nations section says otherwise.
Many gallbladder cancers are found when the gallbladder is removed for stones and the pathologist finds a tumour, or on a scan done for another reason. The pathology report's T stage then decides whether a second, wider operation is offered; that decision belongs to a specialist HPB team, not the local surgical unit.
Sources: NHS England service specification 2260: HPB, primary liver, secondary liver, perihilar biliary tract and gallbladder cancers (September 2024) (2024-09); British Society of Gastroenterology guidelines for the diagnosis and management of cholangiocarcinoma (Gut 2023;73:16-46) (2023-12-07)
NICE NG12 tells GPs to consider an urgent direct-access ultrasound scan for gall bladder cancer in people with an upper abdominal mass consistent with an enlarged gall bladder (recommendation 1.2.10), and to refer anyone aged 40 and over with jaundice on a suspected cancer pathway (1.2.4). In England 17 percent of gallbladder cancers diagnosed in 2019 came through an urgent suspected cancer referral.
Sources: NICE NG12: suspected cancer, recommendations by site (gall bladder cancer 1.2.10; jaundice 1.2.4) (2015); Cancer Research UK: gallbladder cancer statistics (2026-09-24)
Half of gallbladder cancers in England (2019) were diagnosed after an emergency presentation, typically jaundice, pain or a blocked bile duct needing a stent. The emergency team should hand the case to the specialist HPB MDT before any treatment decision.
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24); NHS England service specification 2260: HPB, primary liver, secondary liver, perihilar biliary tract and gallbladder cancers (September 2024) (2024-09)
The clock starts when the GP refers on the suspected cancer pathway, a screening or other route flags cancer, or (in Wales) at the point of suspicion. From 1 October 2023 England no longer measures the old two-week wait to first appointment; the 28-day Faster Diagnosis Standard replaced it.
Sources: NICE NG12: suspected cancer, recommendations by site (gall bladder cancer 1.2.10; jaundice 1.2.4) (2015); NHS England: changes to cancer waiting times standards from 1 October 2023 (2023-10-01)
NHS England's Faster Diagnosis Standard applies to urgent suspected cancer, breast symptomatic and screening referrals. For HPB cancers NHS England's timed pathway asks teams to complete the diagnostic process within 21 days where possible, because these cancers are aggressive.
Sources: NHS England: changes to cancer waiting times standards from 1 October 2023 (2023-10-01); NHS England: 2025/26 priorities and operational planning guidance (2025-01); NHS England: implementing a timed HPB cancer diagnostic pathway
The specialist HPB MDT (Level 3 in NHS England's model) takes every treatment decision for gallbladder cancer, including incidental cancers found after cholecystectomy and recurrences, with surgery and oncology present. It must preserve tissue for molecular profiling and consider trial recruitment for every patient.
Sources: NHS England service specification 2260: HPB, primary liver, secondary liver, perihilar biliary tract and gallbladder cancers (September 2024) (2024-09)
Applies to first and subsequent treatments: surgery, chemotherapy with immunotherapy, radiotherapy or a stent as definitive palliation.
Sources: NHS England: changes to cancer waiting times standards from 1 October 2023 (2023-10-01)
The headline standard for the whole route. Monthly trust-level performance is published by NHS England; HPB pathways often run long because tissue diagnosis needs an endoscopy or biopsy and surgery needs fitness assessment.
Sources: NHS England: changes to cancer waiting times standards from 1 October 2023 (2023-10-01); NHS England: 2025/26 priorities and operational planning guidance (2025-01); NHS England: cancer waiting times statistics
Curative surgery (re-resection of the liver bed and lymph nodes after an incidental finding, or a planned radical cholecystectomy) is done only at the specialist centre. Chemotherapy and immunotherapy may be given at a local cancer unit, but the specialist MDT keeps the decision and receives the outcome.
Sources: NHS England service specification 2260: HPB, primary liver, secondary liver, perihilar biliary tract and gallbladder cancers (September 2024) (2024-09)
At diagnosis of advanced disease the team should request the biliary panel (FGFR2 and NTRK fusions, IDH1, mismatch repair or MSI) and HER2 testing, so that a second-line option is known before it is needed.
Sources: NHS Genomics Education Programme, GeNotes: patient with biliary tract cancer (reviewed 24 February 2025) (2025-02-24); NHS England: National Genomic Test Directory
24 centre entries across 4 nations, with what each offers for this cancer. The service model note below says what happens only at a specialist centre and what can be given closer to home under its MDT.
In England, surgery for gallbladder cancer is a specialised service commissioned by NHS England under service specification 2260 (September 2024). A specialist HPB cancer service must serve a catchment of at least two million people and perform at least 150 liver operations a year for cancer (75 of them major), hold a weekly specialist MDT with surgery and oncology present, take every treatment decision including for incidental cancers found at cholecystectomy, preserve tissue for molecular profiling and build trial recruitment into its work. Local hospitals (Levels 1 and 2) do the first scans and give palliative care under the centre's guidance. The English trust list comes from the National Pancreatic Cancer Audit's HPB specialist centre table, which also covers pancreatic and periampullary cancer; gallbladder surgery sits with the same HPB teams in most trusts, so confirm with your Cancer Alliance which centre takes your referral. Scotland, Wales and Northern Ireland run their own networks (listed above from Pancreatic Cancer UK and AMMF). The Getting It Right First Time programme has no gallbladder or hepatobiliary workstream: its specialty list runs from pancreatic cancer to lower gastrointestinal cancer with nothing for the liver or bile ducts, so its pancreatic cancer national report (November 2025), which carries a Liverpool case study on centralising HPB oncology, is the nearest GIRFT review of these services.
Sources: NHS England service specification 2260: HPB, primary liver, secondary liver, perihilar biliary tract and gallbladder cancers (September 2024) (2024-09); NHS England: service specification, HPB liver, biliary tract and gallbladder cancers (2024-09); National Pancreatic Cancer Audit 2025, methodology supplement, Table 7: trust codes for HPB specialist centres (2025-11); Pancreatic Cancer UK: your local specialist centre (covers pancreatic, liver, gallbladder and bile duct cancers) (2025-11); AMMF: UK centres with cholangiocarcinoma expertise (2023-03); GIRFT: pancreatic cancer national specialty report (November 2025); no gallbladder report exists (2025-11)
By line of treatment: England's NICE decision (which binds Wales and is adopted in Northern Ireland) and Scotland's SMC decision, each with its reference and date. Generic medicines were never appraised and are funded through national chemotherapy protocols.
| Line | Treatment | England (NICE) | Scotland (SMC) | Wales and Northern Ireland |
|---|---|---|---|---|
| After surgery (adjuvant) | Capecitabine for six months (BILCAP) BILCAP was a UK trial; capecitabine is the only adjuvant treatment with a randomised trial behind it. | NHS England Routinely available: a generic medicine never appraised by NICE, given under national SACT protocols; the BSG guideline recommends it | SMC Not appraised (generic); used under regional protocols | Wales: As England. NI: As England. |
| Advanced, first line | Gemcitabine and cisplatin with durvalumab (TOPAZ-1) | NICE TA9442024-01-10 Recommended within its marketing authorisation, with a commercial arrangement; on the Cancer Drugs Fund list as routine commissioning (Section B, Blueteq form DUR2, funded from 9 April 2024), not managed access | SMC SMC25822023-11-13 Accepted for use within NHSScotland (end of life and orphan equivalent process) | Wales: Follows NICE TA944. NI: Follows NICE TA944. |
| Advanced, first line (alternative) | Gemcitabine and cisplatin with pembrolizumab (KEYNOTE-966) Durvalumab is the funded immunotherapy partner across the UK. | NICE TA9662024-04-24 Not available: appraisal terminated because Merck Sharp and Dohme made no evidence submission | Wales: Not available (no NICE recommendation). NI: Not available. | |
| Advanced, second line (no target) | FOLFOX (oxaliplatin, fluorouracil, folinic acid) after gemcitabine-cisplatin (ABC-06) | NHS England Routinely available: generic medicines under national SACT protocols; the ABC-06 trial was UK-run | SMC Not appraised (generics); used under regional protocols | Wales: As England. NI: As England. |
| Second line, FGFR2 fusion or rearrangement | Pemigatinib The licence and the NICE wording say cholangiocarcinoma; FGFR2 fusions are found mainly in intrahepatic cholangiocarcinoma and are uncommon in gallbladder cancer. Ask the MDT how a gallbladder tumour with an FGFR2 fusion would be handled. | NICE TA7222021-08-25 Recommended within its marketing authorisation for cholangiocarcinoma after systemic therapy, with a commercial arrangement; CDF list Section B (routine commissioning, form PEMIG1, funded from 24 September 2021) | Wales: Follows NICE TA722. NI: Follows NICE TA722. | |
| Second line, FGFR2 fusion or rearrangement (alternative) | Futibatinib | NICE TA10052024-09-11 Recommended for previously treated advanced cholangiocarcinoma with an FGFR2 fusion or rearrangement, with a commercial arrangement; CDF list Section B (routine commissioning, form FUT1, funded from 12 December 2024) | Wales: Follows NICE TA1005. NI: Follows NICE TA1005. | |
| Second line, IDH1 R132 mutation | Ivosidenib IDH1 mutations are also concentrated in intrahepatic cholangiocarcinoma. | NICE TA9482024-01-31 Recommended for advanced cholangiocarcinoma with an IDH1 R132 mutation after one or more systemic treatments, with a commercial arrangement; CDF list Section B (routine commissioning, form IVO1, funded from 30 April 2024) | Wales: Follows NICE TA948. NI: Follows NICE TA948. | |
| Second line, HER2-positive (IHC 3+) | Zanidatamab (HERIZON-BTC-01) The most relevant targeted option for gallbladder cancer, where HER2 over-expression is commoner than in the bile ducts. Needs HER2 immunohistochemistry on the tumour. Not yet on the CDF list version read (1.365, June 2025, which predates TA1153); check the current list for its Blueteq form. | NICE TA11532026-05-07 Recommended for HER2-positive (IHC 3+) unresectable or metastatic biliary tract cancer after at least one line of systemic treatment, with a commercial arrangement | SMC Under consideration: full submission listed, publication date to be confirmed | Wales: Follows NICE TA1153. NI: Follows NICE TA1153. |
| Any line, MSI-high or mismatch repair deficient | Pembrolizumab alone after prior therapy | NICE TA9142023-09-20 Recommended for unresectable or metastatic biliary cancer with high MSI or MMR deficiency that has progressed after at least one prior therapy; CDF list Section B (routine commissioning, forms PEMB27 and PEMB28 for biliary tract cancer, funded from 19 December 2023; not funded at ECOG performance status 2) | SMC SMC25892024-01-15 Accepted for use within NHSScotland for MSI-H or dMMR biliary cancer after at least one prior therapy | Wales: Follows NICE TA914. NI: Follows NICE TA914. |
| Any line, NTRK fusion | Entrectinib or larotrectinib (tumour-agnostic) NTRK fusions are rare in any biliary cancer; the test is bundled with the FGFR2 panel. | NICE TA630 and TA644 · CDF2020 Recommended through the Cancer Drugs Fund for NTRK fusion-positive solid tumours when there are no satisfactory treatment options (larotrectinib TA630, entrectinib TA644); CDF list Section A (managed access): larotrectinib form LAR1a from 21 April 2020, entrectinib form ENT1a from 25 June 2020 | SMC Larotrectinib accepted; check the SMC for entrectinib | Wales: Follows NICE. NI: Follows NICE. |
NICE has published six technology appraisals on biliary tract cancer medicines and terminated one; the topic page lists them all. A NICE recommendation binds NHS England and NHS Wales to fund the medicine within 90 days for the appraised indication; Northern Ireland adopts NICE appraisals through its Department of Health; Scotland decides separately through the Scottish Medicines Consortium. Several of the licences say cholangiocarcinoma rather than gallbladder cancer, so eligibility for a gallbladder tumour with the same mutation is a question for the MDT. The National Cancer Drugs Fund list records which medicines sit in managed access (Section A) and which NHS England funds routinely (Section B), each with the Blueteq form a clinician completes. Version 1.365 (6 June 2025) was read in full: every biliary medicine NICE has recommended sits in Section B, and only the tumour-agnostic NTRK inhibitors remain in the Fund itself. The list page returned a bot challenge (HTTP 202) and the current version (1.406, 6 August 2026, according to the third-party Chemotherapy Updates tracker) has an address that could not be guessed (HTTP 404), so zanidatamab's entry should be checked on the page.
Sources: NICE: all guidance on biliary tract cancers (2026-09-24); NHS England: national Cancer Drugs Fund list; NHS England: National Cancer Drugs Fund list, version 1.365 (6 June 2025), the latest version whose PDF could be downloaded (2025-06-06); Scottish Medicines Consortium: medicines advice, cholangiocarcinoma (2026-09-24)
The NHS position of every approved product is on the NHS coverage page; the same decisions by country are on funding verdicts by country.
National Genomic Test Directory entries with their codes, what a result opens, and how the request is made. Ask at diagnosis of advanced disease, not at progression.
| Target | Code | Test | What a positive result opens | How to get it |
|---|---|---|---|---|
| FGFR2 fusion or rearrangement | M220.1 | Multi-target NGS panel for structural variants (NTRK1, NTRK2, NTRK3, FGFR2) on formalin-fixed tumour | Pemigatinib (TA722, SMC2399) or futibatinib (TA1005, SMC2661) after first-line treatment | Your oncologist or the MDT requests it through the regional Genomic Laboratory Hub using the Test Directory code; an existing biopsy or surgical specimen is usually enough. Sources: NHS Genomics Education Programme, GeNotes: patient with biliary tract cancer (reviewed 24 February 2025) (2025-02-24); NHS England: National Genomic Test Directory |
| NTRK1, NTRK2, NTRK3 fusions | M220.1 | Same structural-variant panel as FGFR2 | Entrectinib or larotrectinib (TA644, TA630, Cancer Drugs Fund) | Comes with the FGFR2 request; no separate sample. Sources: NHS Genomics Education Programme, GeNotes: patient with biliary tract cancer (reviewed 24 February 2025) (2025-02-24) |
| IDH1 R132 mutation | M220.6 | Multi-target NGS panel for small variants including IDH1 | Ivosidenib (TA948, SMC2664) after one or more systemic treatments | Requested alongside M220.1; the GeNotes page notes the result can also aid diagnosis. Sources: NHS Genomics Education Programme, GeNotes: patient with biliary tract cancer (reviewed 24 February 2025) (2025-02-24) |
| Mismatch repair deficiency or MSI-high | M220.5 | Microsatellite instability testing (or mismatch repair immunohistochemistry in pathology) | Pembrolizumab alone (TA914, SMC2589); a positive result also prompts a Lynch syndrome conversation | Mismatch repair IHC is done by the pathology lab; MSI testing (M220.5) where IHC is not done. Sources: NHS Genomics Education Programme, GeNotes: patient with biliary tract cancer (reviewed 24 February 2025) (2025-02-24) |
| HER2 (ERBB2) over-expression | pathology | HER2 immunohistochemistry, with in-situ hybridisation for equivocal results, on the tumour block | Zanidatamab for IHC 3+ disease after one line (TA1153) | Not a Test Directory code: ask the MDT to request HER2 IHC from histopathology, as for breast or stomach cancer. NICE TA1153 (May 2026) makes this the test most likely to change a gallbladder cancer plan. Sources: NICE TA1153: zanidatamab (2026-05-07) |
| Whole genome sequencing | M232 | Whole genome sequencing of tumour and blood for any solid tumour once standard-of-care testing and treatment are exhausted | Trial matching, for example SAFIR-ABC10, and rare targets | Needs fresh-frozen tumour and a blood sample, so it is best planned before surgery or biopsy; a record of discussion form is required. Sources: NHS Genomics Education Programme, GeNotes: patient with biliary tract cancer (reviewed 24 February 2025) (2025-02-24) |
| DPYD variants (before capecitabine or fluorouracil) | M220.3 | Germline DPYD hotspot test on a blood sample | Dose adjustment or avoidance of fluoropyrimidines (capecitabine after surgery, FOLFOX second line) to prevent severe toxicity | Requested before the first dose; no record of discussion form needed. Sources: NHS Genomics Education Programme, GeNotes: patient with biliary tract cancer (reviewed 24 February 2025) (2025-02-24) |
In England the National Genomic Test Directory sets which tests the NHS funds and the seven Genomic Laboratory Hubs run them; the codes above are those GeNotes lists for cholangiocarcinoma, reviewed 24 February 2025. Scotland requests through its four regional laboratories and the Scottish Genomic Test Directory; Wales through the All Wales Medical Genomics Service; Northern Ireland through the Regional Molecular Diagnostics Service in Belfast. Turnaround times are set by each Genomic Laboratory Hub, and only two publish them: North Thames gives a national target of 42 days for core and cancer NGS panels against a current 56 to 64 days (correct as of 1 September 2025), and East Genomics publishes the national target range of 3 to 84 days by test category without current figures. Central and South's solid tumour page carries no turnaround statement, the South West hub's site is being decommissioned, and the North West, North East and Yorkshire and South East hub addresses did not resolve on the check date. Ask the MDT what the local turnaround is before a treatment decision waits on a result.
Sources: NHS England: National Genomic Test Directory; NHS Genomics Education Programme, GeNotes: patient with biliary tract cancer (reviewed 24 February 2025) (2025-02-24); GeNotes: genomic testing in the devolved nations (reviewed 6 August 2026) (2026-08-06); North Thames Genomic Medicine Service: our turn-around times (correct as of 1 September 2025) (2025-09-01); East Genomics: service turnaround times (target range by category, no current figures) (2026-09-24)
Match a report to targets and drugs on the biomarker matrix.
Registered trials with UK sites, from the ISRCTN registry and the sponsors' pages, with the setting each is for. Eligibility is decided by the trial team.
Patients are profiled and offered one of seven targeted therapies matched to the result; about 800 participants worldwide.
Registry or sponsor page →Early-phase; eligibility is by tumour type and prior treatment.
Registry or sponsor page →ISRCTN is the UK registry; searches for gallbladder, biliary tract cancer and cholangiocarcinoma were run through its public API on the check date. Trials registered only on ClinicalTrials.gov with UK sites appear on the trial records linked from the cancer page. The NIHR's Be Part of Research site lets you search by condition and postcode and register interest; it could not be read automatically here, so open it directly.
Sources: ISRCTN registry search: gallbladder; NIHR Be Part of Research: gallbladder cancer
Run through the National Cancer Research Network and led from Manchester and London, ABC-02 randomised 410 people with advanced biliary tract cancer, including gallbladder cancer, to gemcitabine alone or gemcitabine with cisplatin. The combination lengthened survival and became the first-line standard everywhere; TOPAZ-1 and KEYNOTE-966 later added immunotherapy on top of it rather than replacing it.
Sources: Valle et al, Cisplatin plus gemcitabine versus gemcitabine for biliary tract cancer (ABC-02), NEJM 2010 (2010-04-08); ISRCTN82956140: ABC-02
Led from Southampton, BILCAP randomised 447 people who had had their biliary cancer removed to capecitabine tablets for six months or observation. Median survival was longer with capecitabine in the pre-specified analysis, and the trial made adjuvant capecitabine the standard offered after gallbladder cancer surgery in the UK and in international guidelines. The UK HPB Research Collaborative Group's CAPBIL study (2026) is the real-world check: it pooled 516 gallbladder cancer operations from 24 UK centres between 2014 and 2022 and found no survival benefit from adjuvant therapy once patients were propensity-matched, while its companion paper on 285 incidental cancers found that those who completed adjuvant chemotherapy lived longer. How far BILCAP's result carries to gallbladder cancer in particular is therefore an open question for ACTICCA-1 and ARTEMIDE-Biliary01 to settle.
Sources: Primrose et al, Capecitabine compared with observation in resected biliary tract cancer (BILCAP), Lancet Oncology 2019 (2019-05); ISRCTN72785446: BILCAP; McClements et al, surgical outcomes in gallbladder cancer: evidence from the UK nationwide CAPBIL study, HPB 2026 (2026-06-22); McClements et al, management of incidental gallbladder cancer in the nationwide CAPBIL study, British Journal of Surgery 2026 (2026-08-01)
ABC-06 was the first randomised trial of second-line treatment in biliary cancer. It compared FOLFOX plus active symptom control with active symptom control alone after gemcitabine-cisplatin, and showed a modest but real survival gain, which is why FOLFOX is the NHS's default second-line chemotherapy when no targetable change is found.
Sources: Lamarca et al, second-line FOLFOX chemotherapy versus active symptom control for advanced biliary tract cancer (ABC-06), Lancet Oncology 2021 (2021-05)
Each figure with its nation, period and the page it was read from. Survival figures are population averages and sit behind the usual disclosure.
Around 900 in women and 380 in men; less than 1 percent of all cancers.
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24)
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24)
Rates peak at ages 85 to 89 (13 percent of cases).
Sources: Cancer Research UK: gallbladder cancer incidence (2026-09-24)
Up by a third in the last decade; projected to rise a further 43 percent by 2038-2040, to about 3,100 cases a year.
Sources: Cancer Research UK: gallbladder cancer incidence (2026-09-24)
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24)
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24)
About 15 cases a year. The registries' own stage tables for Northern Ireland (2019-2023) and Wales (2020-2022) are below; NDRS blocks automated reading, so no England stage split is quoted.
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24)
22 percent had systemic anti-cancer therapy and 2 percent radiotherapy.
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24)
Averages across everyone diagnosed, often years ago. A median is the middle of a group: half the people counted lived longer than the figure shown, and some lived far longer. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
Sources: Cancer Research UK: gallbladder cancer survival (2026-09-24)
Averages across everyone diagnosed, often years ago. A median is the middle of a group: half the people counted lived longer than the figure shown, and some lived far longer. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24)
Sources: Cancer Research UK: gallbladder cancer statistics (2026-09-24)
Sources: Cancer Research UK: gallbladder cancer incidence (2026-09-24)
22 men and 54 women; 63 a year on average over 2018-2022 (66, 50, 63, 62, 76), summed from the WCISU counts by four-digit ICD-10 code, age band and sex.
Sources: Public Health Wales, WCISU: cancer incidence in Wales 2002-2022, data tables (counts by ICD-10 code, xlsx) (2026-02)
13 men and 40 women; 52 in each of 2023 and 2024 and 47 a year on average over 2021-2025, summed from the WCISU counts by ICD-10 code.
Sources: Public Health Wales, WCISU: cancer mortality in Wales 2002-2025, data tables (counts by ICD-10 code, xlsx) (2026-03)
Of the 159 cases with a known stage, 8 percent were stage I or II and 81 percent stage IV. Wales does publish stage for gallbladder cancer; an earlier version of this page said it did not.
Sources: Public Health Wales, WCISU: cancer incidence in Wales 2011-2022, stage data table (xlsx) (2026-02)
574 cases in 2019-2023, 115 a year, 335 of them in women; median age 76; European age-standardised rate 6.7 per 100,000. The registry groups the gallbladder with the extrahepatic bile ducts.
Sources: Northern Ireland Cancer Registry: gallbladder and biliary tract cancer data tables, 1993-2023 (xlsx, Tables 1, 4, 9, 11, 12 and 17) (2026-09-24)
199 deaths in 2019-2023, 40 a year; median age at death 79.
Sources: Northern Ireland Cancer Registry: gallbladder and biliary tract cancer data tables, 1993-2023 (xlsx, Tables 1, 4, 9, 11, 12 and 17) (2026-09-24)
Of cases with a known stage: I 8 percent, II 11 percent, III 28 percent, IV 53 percent (TNM 8 from 2018).
Sources: Northern Ireland Cancer Registry: gallbladder and biliary tract cancer data tables, 1993-2023 (xlsx, Tables 1, 4, 9, 11, 12 and 17) (2026-09-24)
Averages across everyone diagnosed, often years ago. A median is the middle of a group: half the people counted lived longer than the figure shown, and some lived far longer. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
Sources: Northern Ireland Cancer Registry: gallbladder and biliary tract cancer data tables, 1993-2023 (xlsx, Tables 1, 4, 9, 11, 12 and 17) (2026-09-24)
Public Health Scotland's open data CSVs and its incidence and mortality Table 1 spreadsheets carry liver and intrahepatic bile ducts (C22) and pancreas (C25) but no C23 or C24 site, so no Scottish count exists to quote; the UK total from Cancer Research UK includes Scotland.
Sources: Public Health Scotland: cancer incidence in Scotland to December 2024 (Table 1 spreadsheet checked for a C23 site) (2026-08-18)
193 of 285 patients in CAPBIL; 97.9 percent of those resections took liver segments 4b and 5. Five-year disease-free survival 41.5 percent and overall survival 45.1 percent for the whole cohort.
Sources: McClements et al, management of incidental gallbladder cancer in the nationwide CAPBIL study, British Journal of Surgery 2026 (2026-08-01)
Median follow-up 25 months; T3 to T4 stage and nodal disease predicted worse survival; no survival benefit from adjuvant therapy after propensity matching.
Sources: McClements et al, surgical outcomes in gallbladder cancer: evidence from the UK nationwide CAPBIL study, HPB 2026 (2026-06-22)
Charities focused on this cancer, the general cancer charities, and the official schemes that help with costs. Each link goes to the organisation's own page.
More schemes by country on Assistance; costs of care on Costs.
Where England, Scotland, Wales and Northern Ireland run different rules for the same step.
| Topic | England | Scotland | Wales | Northern Ireland |
|---|---|---|---|---|
| Waiting-time standards Sources: NHS England: changes to cancer waiting times standards from 1 October 2023 (2023-10-01); NHS England: 2025/26 priorities and operational planning guidance (2025-01); Public Health Scotland: cancer waiting times, 1 January to 31 March 2026 (2026); Welsh Government: suspected cancer pathway quality report; NHS Wales Performance and Improvement: Suspected Cancer Pathway; Department of Health (Northern Ireland): cancer waiting times; Department of Health (Northern Ireland): cancer waiting time statistics, January to March 2026 (2026) | 28-day Faster Diagnosis Standard (75%, 80% by March 2026); 31 days from decision to treat (96%); 62 days from referral to first treatment (85%, planning target 75% by March 2026). | 62 days from urgent suspicion of cancer referral to first treatment and 31 days from decision to treat, both set at 95%; 72.2% met the 62-day standard in January to March 2026. | Single Suspected Cancer Pathway: 62 days from the point of suspicion to first definitive treatment, target 75% (the clock starts at suspicion, not referral). | 31 days from decision to treat (98%) and 62 days from urgent GP referral (95%); performance is published quarterly by the Department of Health. |
| Who decides drug funding Sources: NICE: all guidance on biliary tract cancers (2026-09-24); Scottish Medicines Consortium: medicines advice, cholangiocarcinoma (2026-09-24) | NICE technology appraisals; the Cancer Drugs Fund for managed access; NHS England commissions. | Scottish Medicines Consortium; five biliary medicines are accepted (pemigatinib, durvalumab, ivosidenib, futibatinib, pembrolizumab for MSI-high), pembrolizumab with chemotherapy was not recommended after a non-submission (SMC2683), and zanidatamab is pending. | Follows NICE appraisals; the All Wales Medicines Strategy Group appraises medicines NICE has not. | The Department of Health endorses NICE appraisals for the HSC. |
| Genomic testing route Sources: NHS England: National Genomic Test Directory; GeNotes: genomic testing in the devolved nations (reviewed 6 August 2026) (2026-08-06) | National Genomic Test Directory, seven Genomic Laboratory Hubs (codes M220.1, M220.5, M220.6, M232). | Scottish Genomic Test Directory; four regional laboratories in Aberdeen, Dundee, Edinburgh and Glasgow. | All Wales Medical Genomics Service. | Northern Ireland Regional Molecular Diagnostics Service, Belfast. |
| Where surgery happens Sources: NHS England service specification 2260: HPB, primary liver, secondary liver, perihilar biliary tract and gallbladder cancers (September 2024) (2024-09); Pancreatic Cancer UK: your local specialist centre (covers pancreatic, liver, gallbladder and bile duct cancers) (2025-11) | Specialised HPB cancer centres commissioned by NHS England under specification 2260 (catchment of at least two million; 150 liver operations a year). | Regional networks: Glasgow Royal Infirmary (West), Royal Infirmary of Edinburgh (South East), Aberdeen, Dundee and Inverness (North). | Morriston Hospital, Swansea for South Wales; North Wales patients go to Liverpool; some mid-Wales patients to Stoke-on-Trent. | One HPB service in the Belfast Trust. |
| Cancer statistics Sources: NDRS: Cancer Registration Statistics, England 2023; Cancer Research UK: gallbladder cancer statistics (2026-09-24); Public Health Scotland: cancer incidence in Scotland to December 2024 (Table 1 spreadsheet checked for a C23 site) (2026-08-18); Public Health Scotland: cancer mortality in Scotland, annual update to 2024 (Table 1 spreadsheet checked for a C23 site) (2026-07-14); Public Health Scotland open data: annual cancer incidence CSV (sites carried: liver C22 and pancreas C25; no gallbladder C23) (2026-09-24); Public Health Wales, WCISU: cancer incidence in Wales 2002-2022, data tables (counts by ICD-10 code, xlsx) (2026-02); Northern Ireland Cancer Registry: gallbladder cancer and other biliary cancer (ICD-10 C23-C24), official statistics 1993-2023 (2026-09-24) | National Disease Registration Service (NDRS): Cancer Registration Statistics, England, with counts by stage; its pages and downloads returned 403 to OnCo. | Public Health Scotland: gallbladder cancer is not a separately published site (its open data and Table 1 spreadsheets carry C22 and C25 only). | Welsh Cancer Intelligence and Surveillance Unit (Public Health Wales): counts by ICD-10 code and a stage table that includes gallbladder cancer (C23), as spreadsheets. | Northern Ireland Cancer Registry (Queen's University Belfast): gallbladder and biliary tract (C23-C24) tables with stage and survival, as a spreadsheet and factsheet. |
| Prescription charges Sources: NHS Business Services Authority: medical exemption certificates (five years for cancer, the effects of cancer or its treatment) (2026-09-24); NHS inform: prescription charges and exemptions (prescriptions in Scotland are free) (2026-01-07); Welsh Government: free prescriptions (2020-09-18); nidirect: help with health costs (all prescriptions dispensed in Northern Ireland are free of charge) (2026-09-24) | £9.90 an item unless exempt; anyone being treated for cancer or its effects gets a five-year medical exemption certificate, and everyone over 60 is exempt. | Free for everyone; no certificate needed (an EC92A form only for dispensing in England). | Free for everyone registered with a Welsh GP and dispensed in Wales; a WP92A medical exemption certificate covers cancer patients dispensing elsewhere in the UK. | Free for everyone; nothing to apply for. |
| Benefits under the special rules for end of life Sources: GOV.UK: get benefits if you're nearing the end of life (special rules) (2026-09-24); DWP: the Special Rules, how the benefit system supports people nearing the end of life (SR1 form, for clinicians) (2026-09-24); nidirect: benefits if you are nearing the end of life (2026-09-24); GOV.UK: Personal Independence Payment; GOV.UK: Attendance Allowance | PIP (under State Pension age) or Attendance Allowance (over it) fast-tracked at the higher rate, no assessment, when a clinician says 12 months or less; SR1 form. | Adult Disability Payment through Social Security Scotland instead of PIP; GOV.UK notes different special rules apply in Scotland. | As England (DWP). | The same 12-month test through the Department for Communities; if you live longer the benefit continues, with a review after three years. |
Named gaps, so a missing figure is never mistaken for a zero.