Resource impact summary report

Resource impact summary report

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.

  • 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.

  • 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.

Table 1 Population expected to be eligible for zanidatamab in England  
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

Table 2 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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