PROSTABLOG NZ: The final report from a two-year NZ Parliamentary investigation into prostate cancer detection and treatment has been released by the Health Select Committee. READ MORE>
Posts Tagged ‘Health Select Committee’
Posted in Uncategorized, tagged blood test, blood tests, cancer screening, catheter, digital diagnosis, digital examination, Health Select Committee, Mark von Dadleszen, mass screening for prostate, medical checkups, Ministry of Health, NZ Health Select Committee, NZ Parliamentary inquiry into prostate cancer, Paul Hutchison, prostablog, prostate, PROSTATE CANCER, Prostate Cancer Foundation of NZ, prostate cancer inquiry, prostate cancer screening, prostate testing, prostate treatment debate, prostate-specific antigen, PSA, PSA test, Screening debate on April 2, 2011| 3 Comments »
PROSTABLOG NZ: Exact meaning of the word “encourage” will be pivotal in the continuing New Zealand saga on how best to prevent prostate cancer.
“We will be encouraging men to go to their GPs to discuss options…including whether or not they should have a PSA test,” says the chairman of Parliament’s inquiry into prostate cancer, Paul Hutchison, in today’s Dominion Post newspaper (see below).
In the same story, his statement is welcomed by Prostate Cancer Foundation of NZ president Mark von Dadelszen: “…we would certainly applaud that move.”
What they both mean by the term “encourage” is about to become the focus of a debate that has churned around in global prostate cancer politics since PSA testing became commonly available in the early 1990s.
First question: how does “encouraging” men to be tested differ from a national screening programme (which Hutchison signals will be rejected in the inquiry report due in a matter of weeks)?
A national screening programme presumably involves the Ministry of Health spending millions promoting tests to the general populace, as it does with breast and cervical cancers.
Such programmes “encourage” people to get along to their doctor and have the tests.
How will men be encouraged? Not with a lot of advertising, it seems.
So how, exactly?
By training barbers to spread the word to their clients, as has been tried in the US?
By sending doctors into communities to talk about risks and options, as the Foundation did last year when it flew a team to the Chathams?
By leaving it to the Foundation to publicise the disease and urge men to act, as happens now?
Whatever approach the Health Select Committee is about to recommend, it needs to deal with a mammoth in the waiting rooms – the Ministry of Health instruction to GPs that they must not raise the topic of PSA and rectal examination until the patient does or unless they spot symptoms obviously related to what is often a symptomless disease.
This is the real crux of the dilemma the Select Committee has presumably been wrangling with since its first public hearings in September, 2009.
What instruction will it recommend the Government give to the Ministry, whose staff and advisers adamantly oppose any widening of the availability of PSA testing?
Up to now, men have been the subject of a mild but just as deadly form of Russian roulette when it comes to being diagnosed.
Take my own case.
Over the past 30 years, I’ve been under the care of four GPs. The first never mentioned prostate cancer (to be fair, I was under 50); the second (mid 1990s) refused to consider PSA tests because to him they were unproven; the third insisted on it without my bidding; and my current one responded readily to my request for tests (saying Ministry instructions forbade him raising the matter unless I spoke up first!).
Anecdotal evidence suggests the Ministry’s obfuscation is becoming increasingly irrelevant – for some people, anyway.
The Foundation’s awareness campaigns have been effective, if I judge by the number of male acquaintances now being diagnosed early and successfully treated.
However, I suspect there are dangerous class factors at play here.
Me and my mates are okay because we have been blessed by education, higher socio-economic status, media awareness and access to health provision.
I fear for those who don’t. The Ministry’s stubbornness condemns them to an uncertain fate.
National prostate screening rejected
Dominion Post April 2, 2011
A PARLIAMENTARY inquiry into prostate cancer screening will not be recommending a national screening programme despite pressure from cancer survivors to do so.
The Prostate Cancer Foundation has backed the committee’s approach, but a former patient says the decision is disappointing.
Health select committee chairman Paul Hutchison said the inquiry, which has been running since May 2009, was not due to report back for another few weeks, but when it did, it would not advocate screening.
There was still controversy over whether blood tests for prostate-specific antigens led to fewer prostate cancer deaths, he said.
Heightened levels of prostate specific antigen – PSA – can indicate the presence of prostate cancer. However, early detection can result in aggressive and unpleasant treatment of tumours that would never have grown or created ill-health.
The inquiry has heard from a huge number of prostate cancer survivors, many of whom asked for a screening programme for all men aged 50 and older.
Dr Hutchison could not go into detail about the committee’s findings but said there were two main conclusions.
‘‘We will not be recommending a PSA screening programme. However, we will be encouraging men to go to their GPs to discuss options … including whether or not they should have a PSA test.
‘‘Those are the two points that are loud and clear.’’
Prostate Cancer Foundation president Mark von Dadelszen said the organisation did not support a national screening programme because of ‘‘issues’’ with the PSA test.
‘What it does advocate is that men should be encouraged to have screening tests . . . we would certainly applaud that move.’’
Napier farmer Duncan McLean, who has just got the all-clear five years after being diagnosed with prostate cancer, said encouragement was good but the committee should recommend a full screening programme.
Mr McLean, 57, had his prostate gland removed in 2006 after several years of increasingly high PSA readings, followed by a biopsy that confirmed the cancer.
‘‘PSA testing is essential. I’m alive today because of it. It’s really disappointing they’re not [recommending screening].’’
Fears about over-treatment were ‘‘bollocks’’, he said. ‘‘You don’t leap in and go under the surgeon’s knife – I was monitored for three years before I had surgery.’’
International research on the matter is split, with several largescale studies under way.
The results of a 20-year Swedish study, published yesterday in the British Medical Journal, found screening did not significantly reduce prostate cancer deaths but the risk of overdetection and unnecessary treatment was considerable.
However, another Swedish study found death from prostate cancer more than halved among men who were screened.
Posted in SELECT COMMITTEE INQUIRY, tagged American Cancer Society, Australian Cancer Council, Cancer Society, digital diagnosis, digital examination, Health Select Committee, Health Select Committee inquiry, large randomised trials, Ministry of Health, National Health Committee, NZ Guidelines Group, NZ prostate cancer inquiry, Parliamentary Health Select Committee inquiry, prostablog, prostate, prostate blog, PROSTATE CANCER, prostate cancer inquiry, prostate cancer screening, prostate-specific antigen, PSA, PSA test, Royal NZ College of General Practitioners, Screening debate, UK Cancer Research Council, Urological Society of Australia and New Zealand on September 12, 2010| Leave a Comment »
PROSTABLOG NZ: It’s almost a year since the first hearings were held by the NZ Parliament’s Health Select Committee inquiry into the early detection and treatment of prostate cancer.
The obvious question now is when will it report back.
Since it published its terms of reference in August last year, the committee has received 33 submissions, four of them from the influential health lobby group, the NZ Guidelines Group, whose last submission was made in December.
This document made it clear that the group – an independent incorporated society originally set up by the government in 1996 – is opposed to population-based PSA screening.
To save one life, up to 41 men could incur significant harm.
It bases this view on its assessment of numerous NZ and international studies, including two large randomised trials (one European, the other American) that were reported last year.
Here are some of the last pages of the group’s December, 2009, submission (RCT = random controlled trial):
This also appears to be the main thrust of submissions on PSA testing from other health authorities (although the Guidelines Group is at pains to stress it is independent from the Ministry of Health).
Another “official” organisation, the National Health Committee, said in its submission (August 26, 2009) that it has seen nothing to change its 2005 advice to the MOH that population-based PSA screening is not an acceptable option.
However, it did favour targeted screening of high-risk groups, such as men with a family history of prostate cancer.
The NHC is aware that since providing its advice in 2005, clinical practice has found
that targeted screening for men at high risk of prostate cancer appears to be useful
and potentially cost effective. These are men who have a family history of prostate
or related cancers.
The Royal NZ College of General Practitioners – presumably speaking on behalf of doctors on the frontline – said in its submission it would go along with the NZ Guidelines Group’s views.
It did make a couple of pleas, however, calling for up-to-date information to hand out to patients, and for treatment to be available to all:
It is important that inequities in access relating to follow up after positive
screening results, and for symptomatic men, are identified and eliminated.
The Cancer Society agreed with the Guidelines Group, and backed this up by quoting from selected organisations in other Western countries.
Most agencies around the world have some form of recommendation that decisions for screening for prostate cancer should be made on an individual basis and in consultation with a medical professional:
The Australian Cancer Council states that:
“In the absence of direct evidence showing a clear benefit of population based screening for prostate cancer, a patient centred approach for individual decisions about testing is recommended. Screening discussions and decisions should always include and take into account, age and other individual risk
factors such as a family history of the disease” (Cancer Council Au 2005).
The American Cancer Society states that:
“The American Cancer Society (ACS) does not recommend routine testing for prostate cancer at this time. ACS believes that doctors should discuss the pros and cons of testing with men so each man can decide if testing is right for him. If a man chooses to be tested, the tests should include a PSA blood test and
DRE (digital rectal exam) yearly, beginning at age 50, for men at average risk who can be expected to live at least 10 more years.” (American Cancer Society 2009).
The UK Cancer Research Council states:
“in the UK, there is no national screening programme for prostate cancer because trials have not yet shown clear evidence that screening will reduce deaths from this disease. Also, many men diagnosed with
prostate cancer have very slowly growing cancers that will never cause any symptoms or problems in their lifetime. So at the moment there is no clear benefit in diagnosing prostate cancer early and it may actually cause harm for some men.”(Cancer Research UK 2009).
Urological Society of Australia and New Zealand states:
“Individual men aged 50 to 70 years with at least a 10 year life expectancy should be able to be screened by annual DRE and PSA testing, after appropriate counselling regarding the potential risks and benefits of investigations and the controversies of treatment.”(Urological Society ANZ 1999).
The majority of submissions – from prominent medical practitioners, prostate cancer lobby groups and patients – urged the committee to recommend PSA testing, if not on a population (all men) screening basis, then at least as a service offered routinely by GPs, without men having to ask (the current MOH policy).
Posted in NZ Media coverage, tagged Brachytherapy, catheter, Health Select Committee, LDR brachytherapy treatment, Mark Ebrey, prostablog, prostate, prostate blog, PROSTATE CANCER, Sunday magazine, Sunday Star-Times on September 5, 2010| 1 Comment »
PROSTABLOG NZ: Kiwi prostate cancer campaigner Mark Ebrey sent this supportive note today about my small appearance in the Sunday Star-Times‘ magazine feature about people who reveal all on the web:
“I see you got an honorable mention in the Sunday magazine today. Well done.
I’ve got a petition currently before the Health Select Committee considering whether to review the LDR brachytherapy treatment option.
You will be interested to know I had the implant a month ago yesterday and to date – absolutely no side effects whatsoever, other than the pain over heart where the $24,000 bill is.
Am beginning to wonder about a disease I had no symptoms for, and treatment with no side effects – have I actually been conned?”
Posted in PROSTATE CANCER, Screening debate, tagged blood test, blood tests, digital diagnosis, digital examination, digital rectal examination, Dr Paul Hutchison, Health and Disability Commissioner, Health Select Committee, medical checkups, NZ Parliament, PCF president Barry Young, prostablog, prostate, prostate blog, PROSTATE CANCER, Prostate Cancer Foundation of NZ, prostate cancer inquiry, prostate cancer screening, prostate-specific antigen, PSA, PSA test, PSA tests denied, Screening debate on September 25, 2009| Leave a Comment »
PROSTABLOG NZ: The NZ Health Select Committee has asked the NZ Prostate Cancer Foundation to send any cases it knows about of men being declined prostate cancer tests by doctors to the Health and Disability Commissioner.
The request comes after PCF president Barry Young told the first day of the committee’s hearings into prostate cancer that GPs are doing this in NZ and it may be responsible for some men not being diagnosed in time for treatment.
The foundation already has ample evidence of this problem, says Barry Young, but this invitation by Health Select Committee chairman Dr Paul Hutchison is a chance for all NZ men who have faced this problem to speak out.
If you or someone you know has been declined a request for a PSA test or digital rectal examination by a GP in NZ, please email details to the PCF at:
Or PHONE: 0800 477 678
NZ prostate inquiry first day: battle lines drawn between prostate community and medical bureaucrats
Posted in PROSTATE CANCER, Screening debate, SELECT COMMITTEE INQUIRY, tagged Barry Young, cancer research, Dr Jim Vause, Eric Roy, Health Select Committee, NZ Guidelines Group, NZ Ministry of Health, NZ prostate inquiry, Professor Brett Delahunt, Professor Cindy Farquhar, prostablog, prostate, prostate blog, PROSTATE CANCER, Prostate Cancer Foundation of NZ, prostate cancer medical professionals, Prostate cancer patients, prostate cancer screening, prostate treatment debate, PSA, PSA tests, public medical system, rectal exams, Screening debate, Steve Caldwell, tobacco lobby, vested interests in prostate cancer, Vietnam on September 24, 2009| Leave a Comment »
PROSTABLOG NZ: The battle lines were drawn at yesterday’s first hearing of the NZ Parliamentary inquiry into prostate cancer – “vested interests” versus those who guard the country’s public medical system.
The former group, apparently, comprises prostate cancer patients and some medical professionals who operate in the field of prostate cancer; the latter, the NZ Guidelines Group, a committee from the medical fraternity and bureaucracy on whom the Ministry of Health relies for expert advice on health policy.
According to the Guidelines Group, the vested interests (a term they used at today’s hearing before the Health Select Committee) must be excluded from the process of deciding how or whether prostate cancer testing should be funded and implemented.
This proposition alarmed some members of the select committee, who asked if the reference to “vested interests” referred to drug companies or other commercial interests who might benefit from prostate screening and testing.
The Guidelines Group – represented by chair Professor Cindy Farquhar, chief executive Steve Caldwell and a Nelson GP, Dr Jim Vause – seemed reluctant to spell out exactly what they meant, but when pressed conceded it was, in part, people who suffer from the disease being discussed.
It was a crucial moment at yesterday’s hearing, a three-hour session during which the committee of MPs heard evidence from mostly those in the “vested interests” corner – prostate survivors and their medical advocates.
It threw into sharp relief the attitude of those whose opposition to screening and testing have influenced the government’s position on prostate cancer for more than a decade, a decade during which medical science has moved rapidly to outflank some of their views.
The battleground was forcefully defined from the start of the hearings, when Prostate Cancer Foundation president Barry Young (see video) gave a passionate outline of what he termed the unnecessary loss of men’s lives because of confused communications between the Ministry of Health, GPs and patients.
He and Professor Brett Delahunt – an eminent Wellington pathologist who specialises in urology – claimed earlier attempts (in 2004) by the NZ Guidelines Group to produce policy on prostate cancer testing were a fiasco, which dishonestly misrepresented the outcome as the consensual work of the specialists involved (who included Delahunt).
The MPs were taken aback by these claims and will provide the Guidelines Group with a recording of what Young and Delahunt said so the group can respond (interestingly, the Guidelines people were last up today, so they didn’t attend the earlier submissions to hear what was said).
All the submissions yesterday were effective.
Three prostate survivors – one a former medic with the NZ army in Vietnam – gave different perspectives on their experiences, and were questioned closely by the MPs on what they think the committee can do to meet the challenges.
The most affecting presentation came from Kim Cook (Mary on this blogsite), whose story about partner Brian’s saga with advanced prostate cancer deeply affected those listening to her by teleconference.
Veteran MP Eric Roy (right) could be seen wiping tears from his eyes, and most in the room were not far removed from such a show of emotion.
Kim’s efforts to empower herself in the face of a seemingly implacable medical profession were accorded great respect by the committee.
As second man up, Barry Young told the committee that “some members of the medical profession have not distinguished themselves at all” in the way they have dealt with prostate cancer.
“The attitude of some members has indeed led to the death of men in this country,” he said. These were men who had been refused the option of PSA tests or rectal exams or both.
When men came to the foundation in desperation in such circumstances, the foundation’s advice was for them to find another GP.
“We need an education programme not only for the public but for the medical profession as well.”
He was critical of the process used by the Ministry of Health to formulate its policies on prostate cancer screening.
He described an earlier instance when he and prominent prostate specialists were invited on to a Ministry-funded committee to investigate research and best practice.
When it was completed, the committee was disbanded and to his alarm the Ministry’s advisors declined to have the resulting policy peer-reviewed.
“None of us recognised a single paragraph of the policy report that was produced. I can understand why GPs are confused.”
Later, he was asked by Eric Roy why some GPs were not offering screening.
“I think it’s because they are confused. Even the information given to urologists is less than clear. We need to remove the ambiguity – from the medical profession, from the Ministry of Health.”
Brett Delahunt (left) was even more condemnatory of the Ministry’s policy advice process, describing the last instance by the NZ Guidelines Group in 2004 as a “fiasco”.
He was invited onto that review committee late in the procedure and went to its last two meetings.
He felt his views and those of other specialists involved were largely ignored.
“The recommendations of the Guidelines Group [for GPs not to recommend PSA testing to asymptomatic male patients] were not a consensus. They were inflicted on the committee after the meetings.”
The problem with such a policy was that in most cases, by the time men showed symptoms, the cancer had spread and metastasised, which meant it was too late to treat them: “If you wait for symptoms to occur you’ve left it too long.”
The PSA (prostate-specific antigen) was the most sensitive of all cancer markers. The false negative rate was “quite low” if the procedures were properly handled.
What the clinician should look for is change in the level of PSA. If the level began to double in less than a year, the approach should be aggressive.
He believes it is now possible to tell the difference between indolent and aggressive tumours.
He described the confusion initially caused when researchers used data including the early use of the Gleason score (for cancer aggression) which once included grades 1 and 2.
It has since been found that samples showing such low scores were not cancers at all (so the Gleason scale no longer includes them), but treatment and mortality data used to compare trends had been muddied as a result.
He said other governments (Canada, US and some in Europe) show a much more positive approach than New Zealand’s to screening and to making men aware of the dangers of slow-growing prostate cancer.
Evidence of the success of opportunistic screening (as opposed to population-based) was now overwhelming.
Chair Paul Hutchison (right) asked for elaboration about Delahunt’s Guidelines Group comments, saying he was under the impression the group was independent and very anxious to take an evidence-based approach.
Delahunt: “That’s fair – but the evidence base was out of date.” He also said he became a member only through accident, after a colleague in Australia mentioned to him the process was under way and asked why he was not part of it.
He said when the group’s guidelines were published his name was listed on the document, something he objected to, since he disagreed with its negative tenor: “There was an element of dishonesty in the Guidelines Group thanking us for the work done.”
Challenged by MP Ruth Dyson (left) on what she perceived to be an allegation the medical profession was deliberately not doing its best, Delahunt said he did not believe anyone went out of their way to deter men from being diagnosed.
His assertion was that some men with the potential to have the diagnosis and cure were missing out.
Asked by Green MP Kevin Hague who should make the decision about a screening programme, Delahunt said he was not proposing a national population-based programme. The need was to encourage opportunistic screening.
“This committee should tell the medical profession there is a need for more clearcut guidelines.”
Hutchison asked who would be in a position to achieve that.
Delahunt: “A balanced group could be appointed.”
Later, he added that some men were not getting a fair deal. Roughly the same number of men died from prostate cancer as women from breast cancer.
The Guidelines Group trio was last to speak (rather mysteriously “welcomed back” by the committee), with GP Jim Vause leading the committee through a series of PowerPoint slides.
These included simplified graphics illustrating what he perceived to be the main thrust of results from the two randomised studies: ie. that many men (more than 1400) need to be screened for prostate cancer before a single life is saved.
He did not mention that many more women (thousands) need to be screened for breast and cervical cancer before their single lives are saved.
Hutchison pointed out that there were known problems with the two trials. Vause said he would get to that later, but didn’t.
He showed that the NZ prostate cancer death rate has been stable since 1961, but that since the early to mid-1990s, the number of diagnoses has risen steeply.
He put that down largely to the prostate awareness programme (but Bret Delahunt would give a big share of the credit to the introduction of the PSA test in 1993).
He was at pains to warn of the risks of treatment – especially death.
A key slide shown to the committee said: “[There is a] need for presenting information free of bias from vested interests in an (sic) manner that a man can understand.”
He said he believed the key point in all this is informed consent.
Guidelines Group chair and surgeon Cindy Farquhar (right) said it was vital to have reliable evidence when introducing a new strategy.
This involved trade-offs between:
- benefits of intervention (in this case a screening programme to detect early prostate cancer);
- risk of the intervention (harms from the additional biopsies, downstream treatments);
- cost of intervention;
- patient preferences.
She mentioned the downside of “just doing it”, listing three examples from the past when such an approach proved disastrous.
Her last slide elaborated the Guideline Group’s processes:
- systematic approach;
- researchers with expertise in clinical studies, critical appraisal, combining studies, developing recommendations, grading evidence;
- developing guidelines – how to apply the international evidence to the NZ health sector.
The main message from her group was that its review of the two overseas studies (reported in the New England Journal of Medicine last March) was still going on and would not report until November.
Hutchison asked for an assurance that would be done on time, got it, and said the committee would look forward to hearing from the group once that had happened.
The MPs were impressive during yesterday’s hearing.
It was obvious they had done their reading. Their questions showed they have a sound grasp of the issues they must somehow try to resolve.
In the end, it came down to a couple of straight-forward questions:
- How can the confusion that seems to abound between patients and doctors over prostate cancer be resolved?
- What can be done to break through Kiwi males’ “I can tough it out” attitude to getting themselves checked out?
The committee made it clear that sorting out the vast morass of conflicting data about prostate cancer detection and treatment is not its job – it will probably recommend this be done by a truly independent group representing all stakeholders, “vested interests” and all.
The only thing everyone seems agreed on at this stage is that population-based mass screening of all men for prostate cancer is not a starter.
But neither is the status quo acceptable. Leaving men without symptoms out of the equation (the medical bureaucracy’s current stance) won’t do.
FOOTNOTE: Committee chair Dr Paul Hutchison said after the hearings that he would write to Barry Young and ask him to provide details to the Health and Disability Commissioner of any cases the foundation knows about of men being refused PSA tests by their GPs.
NEWS COVERAGE of the hearing
NZPA : Hundreds of men are unnecessarily dying of prostate cancer every year because doctors refuse to test them, a parliamentary select committee has been told. READ MORE>
TVNZ: New Zealand specialists say men as young as 40 should have regular prostate checks, because they believe waiting until 50 is just too risky. READ MORE>
RADIO NZ: Parliament’s health select committee has distanced itself from accusations some doctors are responsible for the deaths of hundreds of men from prostate cancer. READ MORE>