Economics of Cancer and CDF (RE) Flashcards

1
Q

What is the reason for fragmentation of the oncology market?

A

74% total sales 2011 were on personalised therapies
Developers are starting to focus on niche subsets for patients with genetic mutations making it harder for drugs to reach blockbuster status.

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2
Q

What are Biosimilars?

A

Like the ‘generic’

A biopharmaceutical drug designed to have active properties similar to one that has previously been licensed.

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3
Q

When are biosimilars available and why are they relevant?

A

Once the patent/licensing has run out the market opens up to smaller companies
On average the cost of the drug reduces by 20%

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4
Q

How has the cost of Tamoxifen varied?

A

In 2011, Tamoxifen (Nalvodex) cost about £1 per 20mg tablet.

Now, the cost of a generic Tamofixen tablet is 8p per 20mg.

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5
Q

What are the prices in the BNF?

A

Public prices; a purchasing pharmacist will have negotiated the price further for NHS use.

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6
Q

What is Kadcyla?

A

Trastuzumab emtansine

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7
Q

What is the financial story / controversy surrounding Kadcyla?

A

In the UK, Kadcyla was not recommended for use by the National Health Service by advisory body NICE, reportedly because an acceptable pricing agreement could not be reached with Roche. Originally it cost £5,900 a month. and NICE estimated it cost £166,000 per QALY (well over the usual maximum). It has been funded by the English NHS Cancer Drugs Fund but in January 2015 it was proposed to remove it from the approved list. After a secret discount was agreed by Roche the Cancer Drugs Fund will continue to fund it.

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8
Q

What are NICE technology appraisals?

A

Technology appraisal guidance are recommendations on NHS

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9
Q

What do NICE technology appraisals review?

A

Review available evidence for clinical and cost effectiveness in medicines, devices, diagnostic technique, surgical procedures and health promotion activities.

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10
Q

How is incremental cost calculated?

A

Total cost of proposal - total cost of comparator

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11
Q

How is incremental QALY calculated?

A

Total QALYs for proposal - total QALYs for comparator

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12
Q

What is the Markov Model designed to do?

A

To represent the disease progression of a cohort of patients (i.e. NSCLC )
The clinical pathway and decision making is aligned with UK clinical practice

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13
Q

What stages of disease are included in the Markov Model?

A

Pre-progression –> Post-progression–> Dead
We want to reduce the transition in patients from 1 to 2
The drug should maintain you at pre-progression.

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14
Q

What is the time frame allocated to ‘End of Life’ treatment?

A

Normally assigned to patient with less than 24 months
There must be sufficient evidence that the treatment offers an extension of life, the addition of atleast 3 months compared with NHS treatment

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15
Q

What is a QALY reweighted to in ‘End of Life’?

A

QALY threshold increased to £50,000 per QALY from £20,000

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16
Q

What is Blue Teq?

A

Scheme that pharmacists in hospitals work under to acquire/request CDF drugs.
Patient access scheme after companies have lowered the original price

Blueteq has a range of healthcare systems that address the needs within both the Public and Private sectors, ranging from the Individual Funding Request (IFR) suite through clinical systems to full patient and hospital management systems

17
Q

When was the Cancer Drugs Fund established?

A

In 2011, The Coalition outlined their “Programme for Government” and committed to the establishment of a CDF

18
Q

What is the fundamental problem with CDF?

A

£200m/year was bugeted for 3 years beginning April 2011
Recently the fund was increased to £280m/year in 2016

Overspending everywhere; reevaluation needed.

19
Q

What reasons mean that authorities in England could provide drugs that were not otherwise available on the NHS?

A

Drugs appraised by NICE and not recommended on the basis of cost effectiveness

Drugs recommended for restricted access

Drugs not, or not yet, appraised by NICE

20
Q

How is access to the CDF determined?

A

Based primarily on ranking of the drug treatment based on the strength and quality of evidence of clinical effectiveness

21
Q

How can clinicians and patients access drug treatments via the CDF?

A

The national CDF Cohort Priority List

More commonly, Individual CDF Requests (ICDFRs)

22
Q

Who can prescribe drugs on the CDF Cohort Priority List?

A

Oncology specialists;

EXAMPLE Pemetrexed in the maintenance of NSCLC

23
Q

Where will we go after the Cancer Drugs Fund?

A

The joint NHS and NICE England public consultation underway from April 2016
These proposals will maintain access to medicines while data is collected on how to provide treatment in future.