The
FDA-approved cervical cancer vaccine "Gardasil," has been
debated for a number of reasons including its cost of $360
(plus the cost of doctors visits to get the shots) and the
fact that it is approved for young girls and the moral and
sexual implications associated with this. Up until recently,
however, no one challenged the vaccine on the grounds of its
presumed safety and efficacy. The fact that it is FDA
approved was considered prima facie evidence that the
vaccine is both safe and effective. We must remember,
however, that the FDA that approved Gardasil is an agency
with countless conflicts of interest that has approved drugs
and vaccines that were later found to be dangerous or deadly
such as Vioxx and RotaShield.
When
Cancer Monthly began looking at the research that enabled
this "cervical cancer vaccine" to receive FDA approval we
were astounded to find that this approval was not based on
the vaccine's actual prevention of cervical cancer.
Instead a surrogate was used - precancerous lesions. We were
pleased to see a recent article in the Wall Street Journal
(WSJ) that echoed these same issues - "Questions on Efficacy
Cloud a Cancer Vaccine" April 16, 2007; Page A1. The WSJ
stated, "The Food and Drug Administration didn't ask its
panel of experts advising on Gardasil to rule on whether the
vaccine specifically prevented the cancer itself."
Cancer Not Measured
How
effective is Gardasil in decreasing the incidence of
cervical cancer? 100%? 50%? No one really knows because this
question has not yet been answered. As of today, the
Gardasil vaccine has never been proven to decrease the
actual incidence of cervical cancer. In the studies
that led to the vaccine's approval, the incidence of
cervical cancer was not measured. Instead CIN (cervical
intraepithelial neoplasia) 2/3 and AIS (adenocarcinoma in
situ) were used as the surrogate markers for prevention of
cervical cancer because according to the vaccine's insert "CIN
2/3 and AIS are the immediate and necessary precursors of
squamous cell carcinoma and adenocarcinoma of the cervix,
respectively." While this is true it is also true that
CIN 2/3 and AIS usually do not lead to cancer. For
example, according to published data, CIN2 only leads to
invasive carcinoma 5% of the time and CIN3 only leads to
invasive carcinoma 12% of the time.1
HPV Alone Insufficient to Cause Cancer
In
addition, Gardasil is targeted against Human Papilloma Virus
(HPV) (types 6, 11, 16, and 18). However, during discussions
at the FDA it was admitted that HPV alone is
insufficient to cause cancer. Dr. Elizabeth Unger of
the Centers for Disease Control stated, "So it is
believed that infection alone is insufficient to cause
cancer, and additional factors are required for
neoplasia. There are certainly lots of questions about HPV
infection…"2 This point is echoed in the medical
text book Cancer:
Principles & Practice of Oncology whose editors
include Dr. Vincent DeVita, Jr. who was President of the
National Cancer Institute and Dr. Steven Rosenberg, Chief of
Surgery at the National Cancer Institute. According to this
text, "HPV infection is not sufficient for cervical
carcinogenesis…"3
HPV the Correct Target?
This is
of course quite rational. If HPV alone caused cervical
cancer than the number of cases in the U.S. would be the
same as the number of women with HPV infections. Since only
a relatively small percentage of HPV infected women get
cervical cancer this raises the question whether a vaccine
against HPV is the right target at all? In fact, according
to the text Cancer: Principles & Practice of Oncology, "In most
studies, HPV status was not a strong independent
prognosticator of outcome in cervical cancer patients;
however there appears to be a trend for HPV-negative tumors
to do worse …those tumors containing HPV DNA tend to be of
an early stage and low grade."4
This suggests that if the goal is to reduce
deaths from cervical cancer the target should not be HPV at
all because
the tumors without HPV actually "do worse."
Concern at the FDA
Obviously
a vaccine designed to prevent cervical cancer should have
measured cervical cancer during testing, but it did not.
During meetings at the FDA, Dr. Karen Goldenthal of the FDA
discussed this very point. She said, "Now, here is some
advantages of cervical cancer as an endpoint. Clearly the
major concern is cervical cancer. This would be viewed as
very, very definitive data, and it may be easier to identify
any unanticipated vaccine associated problems."5
Nonetheless, the FDA did not require that the actual
number of cervical cancers be measured. As a result
we now have an FDA approved "cervical cancer vaccine" that
is yet unproven to reduce or prevent cervical cancer.
Leap of Faith
As quoted
in the Wall Street Journal article, Scott Emerson, a
professor of biostatistics at the University of Washington
who sat on the FDA advisory committee, says he's not
persuaded the vaccine is worth the billions of dollars
likely to be spent on it in coming years. "I do believe that
Gardasil protects against HPV 16 and 18, but the effect it
will have on cervical-cancer rates in this country is
another question entirely…There is a leap of faith
involved," Dr. Emerson said.
End
Notes
(1)
Arends MJ, et al., Aetiology, pathogenesis, and pathology of
cervical neoplasia. J Clin Pathol. 1998 Feb;51(2):96-103.
Available here:
http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=500501&blobtype=pdf
(2) Dr. Beth Unger. See Minutes from: FDAVaccines and
Related Biological Products Advisory Committee, November 28,
2001, p. 21 available here:
http://www.fda.gov/ohrms/dockets/ac/cber01.htm#Vaccines%20&%20Related%20Biological
(3) Vincent T. Devita, Jr., et al., editors, Cancer
Principles & Practice of Oncology, 6th edition, volume2, p.
1523
(4) Vincent T. Devita, Jr., et al., editors, Cancer
Principles & Practice of Oncology, 6th edition, volume2, p.
1523
(5) Dr. Karen Goldenthal. See Minutes from: FDAVaccines and
Related Biological Products Advisory Committee, November 28,
2001, p. 83 available here:
http://www.fda.gov/ohrms/dockets/ac/cber01.htm#Vaccines%20&%20Related%20Biological