2008 marks the 60th anniversary of the establishment of the National Health Service (the NHS) in the UK. While it has undoubtedly served the British public well in that time, the five part BBC1 series Dom’s on the Case continues the current trend for documentary programming which investigates inequalities with the NHS system, specifically geographical inequalities which arise from the so called ‘postcode lottery’.
Previous BioethicsBytes posts have highlighted resources which have examined this issue in detail (including The NHS Postcode Lottery: It Could Be You – Panorama and Herceptin: Wanting the wonder drug – Panorama), so here we highlight some additional issues raised within the third episode of Dom’s on the Case, which was first broadcast on BBC1 on Wednesday 24th September 2008, at 09.15. In this 45 minute programme, reporter Dom Littlewood highlights some of the inequalities which arise from differential prescription charging and access to drugs across the UK. While the programme’s tone may seem excessively negative – insofar as it presents only the perspectives of aggrieved patients and members of the public – it offers a number of short clips which provide concise descriptions of the various sources of inequality. Further it highlights the extreme measures that some patients feel forced to take in order to “beat the postcode lottery” (00:10:05) and access the drugs and treatment they feel they deserve.
Her-2: The Making of Herceptin, a Revolutionary Treatment for Breast Cancer – Bazell (1998)
September 4, 2008Bazell, R. (1998). "Her-2: The Making of Herceptin". New York: Random House.
In his interesting and insightful account of “the making” of Herceptin, Robert Bazell, shows how the creation of a new drug is not only a scientific process, but also a social endeavour involving patients, doctors, regulators, funders, politicians, activists and the media. This is particularly so when it comes to clinical trials for a new product, and Bazell’s description of this procedure for Herceptin (Trastuzumab) is detailed and would form an excellent resource for illustrating its complexities and/or discussing its complications.
While the book deals with much more than the clinical trials of Herceptin – including the sources of early interest in the Her-2/neu receptor in breast cancer and the collaborations that eventually brought the potential of this monoclonal antibody to the attention of Genentech’s management – this post focusses on the clinical trials that formed the basis for its licensing by the FDA (Food and Drug Administration) in the US and subsequent worldwide use as an adjuvant therapy in advanced (metastatic) breast cancer.
This post is accompanied by a BioethicsBytes Extended Commentary on the making of herceptin (available here), which discusses some additional bioethical issues raised in this post.
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