Resource impact summary report
Resource impact summary report
Guidance recommendation
Financial and capacity resource impact
The key drivers of resource impact are that:
-
Zanidatamab has a longer average treatment duration than FOLFOX, the comparator treatment, and therefore requires additional IV administration appointments.
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Zanidatamab does not require a long-term implanted central venous access device for IV administration unlike FOLFOX that requires a PICC (peripherally inserted central catheter), Portacath or Hickman line. So zanidatamab requires less administration time, and will have fewer incidences of adverse events associated with having a central line than FOLFOX.
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Zanidatamab may have a higher relative dose intensity compared with FOLFOX because it is better tolerated.
The company has a confidential commercial arrangement. This makes zanidatamab available to the NHS at a discount. The size of the discount is commercial in confidence.
The payment mechanism for the technology is determined by the responsible commissioner and depends on whether the technology is classified as high cost.
Eligible population for zanidatamab
The eligible population is estimated to be about 65 people. The uptake is expected to be 90% by year 3. Because the population is small, we have not produced a resource impact template.
Table 1 shows the estimated eligible population for zanidatamab and the assumptions used to calculate the eligible population.
| Eligibility criteria | Proportion (%) | Eligible population |
|---|---|---|
|
Incidence of biliary tract cancer |
- |
4,531 |
|
Proportion diagnosed at advanced or metastatic stages |
79% |
3,580 |
|
Proportion having first-line treatment |
33.9% |
1,213 |
|
Proportion HER2-positive |
13.8% |
167 |
|
Proportion IHC3-positive |
77.5% |
130 |
|
Proportion having second-line treatment |
50.0% |
65 |
Based on: Cancer registration statistics 2023, Rethink Liver Cancer p7, AMMF online accessed 10.04.26 (PDF only), Blueteq data, Harding JJ et al. 2023 and clinical expert opinion.
Treatment options for the eligible population
The comparator treatment for the eligible population is FOLFOX, which is administered intravenously, and active symptom control, which includes a range of supportive measures.
Key information
| Time from publication to routine commissioning funding |
90 days |
|---|---|
| Programme budgeting category |
PBC 02X |
| Commissioner |
NHS England |
| Providers |
NHS Hospital trusts |
| Pathway position |
Second line |
About this resource impact summary report
This resource impact summary report accompanies the NICE technology appraisal guidance on zanidatamab for treating HER2-positive advanced biliary tract cancer after 1 or more lines of systemic treatment and should be read with it.
ISBN: 978-1-4731-9457-1
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