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Chronic therapy of cardiovascular disease

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Atenolol vs Losartan. 9193 patients. Age 55-80 years. Previously treated or untreated hypertension ... Atenolol 80.9 mm Hg. Losartan 81.3 mm Hg. B Dahlof et al. ... – PowerPoint PPT presentation

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Title: Chronic therapy of cardiovascular disease


1
Chronic therapy of cardiovascular disease
  • Eric J Topol MD Provost and Chief Academic
    Officer Chairman, Department of Cardiovascular
    Medicine The Cleveland Clinic Foundation Clevela
    nd, Ohio
  • Robert M Califf MD Professor of
    Medicine Associate Vice Chancellor for Clinical
    Research Director, Duke Clinical Research
    Institute Duke University Medical
    Center Durham, North Carolina

2
LIFE and OVERTURE/OCTAVE
  • LIFE
  • Losartan Intervention For Endpoint Reduction in
    Hypertension
  • OVERTURE
  • Omapatrilat Versus Enalapril Randomized Trial of
    Utility in Reducing Events
  • OCTAVE
  • Omapatrilat Cardiovascular Treatment Assessment
    Versus Enalapril

3
LIFE Inclusion criteria
  • Atenolol vs Losartan
  • 9193 patients
  • Age 55-80 years
  • Previously treated or untreated hypertension
  • Systolic BP 160-200 mm Hg or diastolic BP 95-115
    mm Hg
  • ECG LVH
  • Primary composite endpoint of cardiovascular
    morbidity and mortality, defined as stroke, MI,
    or cardiovascular death

4
LIFE Event rate
p0.021
13
11
p0.491
p0.001
p0.206
7
5
4
4
5
4
ACC 2002
5
LIFE Implications
  • Beta-blockade had been on such a high pedestal
    and now this puts the sartans in a whole other
    light
  • "I'm a little bit stunned about the results,
    not knowing exactly how to change practice."
  • Topol

6
LIFE Expectations
  • Investigators expected the primary beneficial
    effect to be on the heart as a result of the
    animal data
  • "The trial was done extremely well and measured
    the right things, but the result was unexpected.
    The benefit was in the direction the
    investigators had postulated but not for the
    outcome reason they had thought."
  • Califf

7
LIFE Head-to-head clinical trials
  • As we get head-to-head trials, interpreting them
    will be very complicated.
  • "The Evidence-Based Medicine Mafia has been
    extremely high on beta-blockers , and I
    haven't lost any enthusiasm for beta-blockers
    from this trial but I've gained a lot of respect
    for ARBs and their potential to produce benefit."
  • Califf

8
LIFE Blood pressure follow-up (4.8 years)
Atenolol
Losartan
Atenolol 145.4 mm Hg
Systolic
Losartan 144.1 mm Hg
mm Hg
Losartan 81.3 mm Hg
Diastolic
Atenolol 80.9 mm Hg
Study Month
B Dahlof et al. Lancet 2002359995-1003
9
LIFE Blood pressure
  • The real role of blood pressure can be difficult
    to determine
  • We don't have any information about the pulse
    wave, which is potentially important
  • "Nor do we have quite yet the full sense of the
    distribution of blood pressure effects in the
    population or across time."
  • Califf

10
LIFE How generalizable?
  • This trial had an overwhelmingly white patient
    population. Can we generalize to the more
    heterogeneous population you would find in
    general practice?
  • Topol
  • "I wouldn't abandon the fundamental principles
    that you treat blood pressure with a low-dose
    thiozide diuretic and in someone who has a risk
    of MI you err toward beta-blocker and an ACE
    inhibitor."
  • Califf

11
LIFE Not cheap
  • These are exciting new drugs with real potential
    but they are not cheap
  • "For people who can take an ACE inhibitor and
    who don't cough and feel fine and can get them
    at a lower price, I'm all for that."
  • Califf

12
LIFE Stroke belt
Source CDC
13
LIFE Applying the data
  • There could be a genetic component to the stroke
    belt, making the LIFE data difficult to
    generalize
  • "I've been using ARBs a fair amount, this will
    make me feel even better about using them more
    often but to make a radical change in the
    fundamental approach to blood pressure based on
    one trial, I think would be a mistake."
  • Califf

14
LIFE New onset diabetes
8
Intention-to-Treat
7
Atenolol
6

Losartan
5
Proportion of patients with first event ()
4

3

2

Adjusted Risk Reduction 25, p0.001
1

0
6
18
24
30
36
42
48
54
60
66
0
12

Study Month
Dahlof et al. Lancet 2002359995-1003
15
LIFE Lifestyle changes
  • Walking 4 times a week for 30 minutes a day
    would be more effective than losartan
  • "But the changes in lifestyle are hard to come
    by. Unfortunately, our society relies too much
    on some pill and potion rather than the
    discipline of exercise and diet."
  • Topol

16
LIFE Start with ARBs for hypertension?
  • Maybe we could start with ACE inhibitors or ARBs
    in a newly diagnosed hypertensive patient
  • Patients successfully on beta-blockers shouldn't
    be switched
  • These patients are hypertensives with serious
    left-ventricular hypertrophy and have already
    tried diuretic therapy and failed
  • This may all be rendered moot by advances in
    genomics, proteonomics, and tailored
    therapy Topol

17
LIFE Multiple drugs
  • The average person with real systolic
    hypertension will require 2.6 drugs at maximal
    FDA levels to get their pressure below 140
  • The ARB option is well-tolerated, making it very
    attractive
  • ALLHAT does not include ARBs, but should give us
    the first real evidence about what drug you
    should start with
  • Califf

18
LIFE The pocketbook
  • We have to balance what we need to do and the
    pocketbook
  • Economic factors get in the way of proper
    treatment
  • "It's difficult to take someone who feels fine
    and has not had a stroke and convince them that
    they should take not one, and not two, but
    three drugs that cost 2 or 3 bucks a day
    apiece."
  • Califf

19
LIFE DPP
11.0
7.8
4.8
Diabetes Prevention Program Research Group. N
Engl J Med 2002346(6)393-403
20
LIFE Obesity
19.8
18.9
17.9
15.3
12.0
Source CDC
21
LIFE NAVIGATOR
  • Nateglinide And Valsartan in Impaired Glucose
    Tolerance Outcomes Research
  • Nateglinide (60mg before main meals) vs valsartan
    (160mg daily) vs placebo
  • gt 60 000 patients screened for impaired glucose
    tolerance (IGT)
  • 7500 subjects to be enrolled
  • 600-800 centers in 40 countries
  • Age gt 50 with at least 1 CV risk factor

22
LIFE Outpatient cardiology
  • Outpatient cardiology is really a metabolic
    clinic we're seeing the classic lifestyle
    problems
  • It is hoped we can integrate the diabetologists'
    understanding of glucose management
  • "We're going to see much attention to focused
    metabolic clinics run by major cardiovascular
    centers."
  • Califf

23
LIFE Marinating the blood vessels
  • Jay Cohn advocates we abandon measuring blood
    pressure we should focus on getting patients on
    effective doses of drugs
  • "The concept of marinating blood vessels with
    the right doses of drugs as opposed to trying to
    hit these targets, which have never really been
    proven to be correct, might be the way to go."
  • Califf

24
LIFE Diabetes prevention
  • Diabetes prevention has been seen in 3 rigorous
    trials there is a theme
  • "I think it's more than just marinating the
    blood vessels. There must be an
    anti- inflammatory effect that's afforded by
    working on this neurohumoral axis of ACE and
    ARBs and I think it's fascinating."
  • Topol

25
Topol 2 thumbs up for LIFE
  • "Very provocative trial. I love to see trials
    where you get a surprise finding, shake the
    bushes. It's good for the field."
  • "I hope this one does get the interest it
    deserves in the cardiovascular community."
  • Topol

26
OVERTURE and OCTAVE
  • "OVERTURE and OCTAVE were supposed to be the
    big trials to validate omapatrilat as a
    cornerstone of heart failure and hypertension
    therapy. And I guess that didn't exactly turn out
    to be the case."
  • Topol

27
OVERTURE Background
  • Omapatrilat vs enalapril for heart failure
  • An ACE-NEP inhibitor (works through angiotension
    converting enzyme and the neutral endopeptidase)
  • More effective than straight ACE inhibitor in
    lowering systolic blood pressure
  • Two phase 2 trials both trended to mortality
    reduction
  • Califf

28
OVERTURE Event rate
HR0.91p0.024
HR0.93p0.187
HR0.93p0.233
HR0.94p0.339
primary endpoint
Packer et al. ACC 51st Annual Scientific Session.
29
OVERTURE Negative perception
  • Most portrayals seem overly negative
  • "If your expectation was that omapatrilat was
    going to have to be way better than ACE
    inhibitor then it's definitely a negative. If
    your expectation was that we could
    make a modest incremental improvement, it may
    not have knocked omapatrilat out of the box,
    at least in the field of heart failure."
  • Califf

30
OVERTURE Event rate
HR0.91p0.024
In a head-to-head trial, how do you know either
is better than placebo? If you use the ACE
inhibitor mortality trial end point, you get a
nominally significant result Califf
31
OVERTURE Adverse events
Packer et al. ACC 51st Annual Scientific Session.
32
OVERTURE Shades of benefit
  • ACE inhibitors are generic now, making for an
    inexpensive reference standard
  • "You have some shades of benefit but its going
    to be an expensive alternative and the benefit
    is not assured. And angioedema is not
    exactly a nuisance, it's life- threatening."
  • Topol

33
OVERTURE Interpreting the data
  • "I think fundamentally, the most important
    point about the pragmatic interpretation of the
    data is that to replace an ACE inhibitor,
    you've got to really beat it. And this trial did
    not beat it."
  • Califf

34
OVERTURE The future
  • "For those more interested in research and its
    future implications, does this mean the death of
    the ACE/NEP combination? I don't think so. Yet."
  • Califf
  • "Unfortunately, though, for the expectations of
    the drug, which were far greater than validating
    it as an alternative, it was demonstrating its
    superiority, and it was far from that."
  • Califf

35
OVERTURE Before and after
  • "Going into the ACC I would have thought most
    people would say, ARBs, that's a yawner. You
    know, they're nice to have around, but so what?
    ACE/NEP, that's where the action is."
  • "Now after the ACC we say, Jeez, ARBs, they're
    phenomenal, and the ACE/NEP well, you know,
    you've got a drug that's maybe a little better
    but has the same side effects or worse."
  • Califf

36
OVERTURE Benefit of sartans
  • "This whole class has been kind of clouded by
    lack of data showing precise benefits."
  • "You're right, I think that was one of the
    major themes that came out of this meeting is
    that there were some big benefits that I guess
    were not fully expected."
  • Topol

37
OCTAVE Risk of angioedema
The OCTAVE Study Group. ACC 51st Annual
Scientific Session.
38
OCTAVE Pharmacogenetics
  • "This could be a great drug for managing blood
    pressure if you could just screen out the people
    who were gonna be getting angioedema. And that
    could be easily done by a SNP analysis."
  • "This could be one of the earliest applications
    of pharmaco- genetics."
  • Topol

39
OCTAVE At-risk patients
  • We need a way to identify the population at
    high-risk for angioedema
  • "Those who look on the rosy side say, 'Well,
    there's not been a death yet due to angioedema
    in the omaptrilat experience.' But the setting
    of a clinical trial is very different from the
    setting in a community health clinic where
    people with hypertension are being treated and
    sent out there."
  • Califf

40
OCTAVE Good blood pressure response
  • No one has seen the full data from OCTAVE
  • Blood pressure response was better with
    omapatrilat
  • If blood pressure effects are important in
    hypertension, this could be of benefit for those
    with the worst levels of systolic hypertension
  • Califf

41
OCTAVE How important is BP
  • "I'm uncertain how much of it is really a
    pressure effect."
  • A meta-analysis by Curt Furberg implies that 50
    of the benefit of any hypertensive drug is based
    purely on the blood pressure lowering
  • Califf

42
OCTAVE Benefits of low BP
  • I can't argue there is no benefit to lowering
    blood pressure per se
  • "I can bleed you into a trash can and lower
    your blood pressure and it doesn't mean its good
    for you."
  • "You've got to consider the full effects of a
    drug you're going to give people."
  • Califf

43
OCTAVE Screening
  • Omapatrilat is a potent drug, but it has a
    relatively infrequent serious side effect we
    could screen out
  • "Perhaps some day we'll see broad application
    but in a pharmacogenetic way. It only takes a
    few dollars to run a polymorphism and it could
    mean a very effective therapy in those patients
    who are not at risk."
  • Topol

44
OCTAVE Applying polymorphisms
  • "How are you going to get doctors to run a
    polymorphism test when they can't even give the
    drug in the first place?"
  • Califf

45
OCTAVE Genetics in cancer
  • Cancer specialists are ahead of cardiovascular
    specialists in using pharmacogenetics
  • Talking about specific genetic linkages used to
    design therapies
  • Omapatrilat is an attractive case because we know
    the pathway and it is easy to find SNPs in
    particular genes
  • By next year, it should be a "no-brainer"
  • Topol

46
OCTAVE The big issue
  • Getting the drugs to the people who benefit the
    most is the big issue
  • "Oftentimes I'm afraid that people just assume
    that operationalizing a concept is automatic.
    We've got a lot of work to do."
  • Califf
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