Yesterday’s post was not really about Avastin, but about medical journalism and how patients’ voices are handled by the media.
L. Husten, writing on a Forbes blog, cried that the press fawned, inappropriately, over patients’ words at the FDA hearing last week, and that led him to wonder why and if journalists should pay attention to what people with illness have to say, even if their words go against the prevailing medical wisdom.
There’s a fair amount of controversy on this. For sake of better discussion in the future, I think it best to break it up into 3 distinct but inter-related issues:
1. About health care journalism and patients’ voices:
A general problem I perceive (and part of why I started blogging) is how traditional medical journalists use patients’ stories to make a point. What some of my journalism professors tried to teach me, and most editors I’ve dealt with clearly want, is for the reporter to find a person with an illness, as a lead, and then tell about the relevant news, and provide some expert commentary – with at least one person speaking on each “side” of the issue, of course – and then end the story with some bit about the patient and the future.
I argue that this form of medical journalism reduces the patient to an object, used by the story-teller in order to capture the reader’s attention. So, with exceptions and always with the person’s consent, I prefer to offer my own story, from my perspective, so as not to use the patient as a vehicle or literary device.
So it appears that Husten is OK with using patients’ voices to tell a story (and sell papers/clicks?), but not with presenting their views unfiltered if they don’t mesh with the party line or a particular point an editor wants to make. This lies at the center of the journalism issue.
(As an aside, a few recent published studies have found value in analyses of patient-reported symptoms, unfiltered even by their doctors.)
2. About Avastin:
My opinion on this is that quite a few breast cancer and other patient advocates, including a National Breast Cancer Coalition representative who spoke at the FDA hearing, have “taken the hit” on this particular issue because they need to appear rational. The argument is that the data show Avastin doesn’t work and is often harmful, so it shouldn’t be FDA-approved for women with metastatic BC.
For a BC advocacy group, it may not be worth pushing for a drug that helps only around 5% of patients. The problem is there’s no biomarker for Avastin responsiveness, because this drug doesn’t target a particular genetic marker. (Rather it works by cutting the blood supply, which could vary even within a particular patient’s mets in different organs.) So the only way to test if Avastin works in a patient is to give the drug, with informed consent, and see how it goes. Unlike, say, a bone marrow transplant, which runs in the range of hundreds of thousands of dollars and, once done, is irreversible, you can give one dose of Avastin and stop it, or two and stop it, if it doesn’t work or it is not well-tolerated.
I don’t think Avastin is more toxic than many or even most cancer drugs. Its side effects have been heavily pushed by the media and public health/epidemiology academics who want to make a point about evidence based medicine (EBM).
3. About evidence-based medicine: I’m in favor of EBM, especially in principle. The problem is that published medical data is too-often flawed and also, that some patients are, really, outliers.
*This blog post was originally published at Medical Lessons*