by: Rosemary Mathis, Director of SANE VAX, INC.
(NaturalNews) All drugs are associated with some risks of adverse reactions and vaccines are no exception. In weighing risks versus benefits, one has to keep in mind that vaccines represent a special category of drugs since they are generally given to healthy individuals. If there are uncertain benefits from a vaccine, only a small level of risk of harmful effects may be acceptable. If the benefits are certain, then a greater risk of side effects may be tolerated. Here I review the current evidence which indicates that the former case applies to Gardasil, the quadrivalent human papillomavirus (qHPV) vaccine:
Merck promoted Gardasil primarily as a vaccine against cervical cancer, rather than promoting it as a vaccine against HPV infection or sexually transmitted diseases.
According to recent reports published in two highly respected scientific journals, Nature Biotechnology and Journal of American Medical Association (JAMA):
"Most genital infections are asymptomatic and resolve spontaneously, but the virus can persist and cause precancerous lesions that can become malignant over the subsequent 20-30 years." (Nature Biotechnology, 2007 2)
"So how should a parent, physician, politician, or anyone else decide whether it is a good thing to give young girls a vaccine that partly prevents infection caused by a sexually transmitted disease (HPV infection), an infection that in a few cases will cause cancer 20 to 40 years from now? (JAMA, 2009 3).
The fact is that malignant cervical cancer takes decades to develop and yet the longest clinical trial on Gardasil was only four years in duration. In other words, Gardasil was never shown to prevent cervical cancer [emphasis added]. Furthermore, in all clinical trials conducted by Merck the cervical intraepithelial neoplasia (CIN) 2/3 precancerous lesion was used as the efficacy endpoint for evaluating the Gardasil. What is the problem with using the CIN 2/3 lesion as the standard for efficacy? First, if the marketing claim for Gardasil is that the vaccine "protects against cervical cancer" then cervical cancer should have been used as the endpoint for efficacy, not a surrogate marker such as a CIN 2/3 precancerous lesion [emphasis added]. Second, in the natural course of cervical cancer, only a small fraction of the CIN 2 lesions will progress to CIN 3 lesions and only a small fraction of CIN 3 lesions will eventually progress to cervical cancer. Furthermore, even CIN 3 lesions are heterogeneous (there are early small lesions and old advanced lesions and we do not know what proportion of the small lesions, which serve as clinical endpoints in current studies, would persist to become large, advanced CIN3 lesions). Therefore, in any female population (and that includes those who have undergone Gardasil clinical trials) there are many more CIN 2 lesions than a combination of CIN 3 lesions and cervical cancers. As a result, the vast majority of the "CIN 2/3 or worse" cases used for evaluation of efficacy, and listed in Merck's report to FDA Vaccines and Related Biological Products Advisory Committee (VRBPAC Background Document on Gardasil HPV Quadrivalent Vaccine 8), must have been CIN 2 lesions.
In a review of the literature from 1950-1992, it was noted that 60 percent of CIN 1 lesions regressed, 30% persisted, 10 percent progressed to CIN 3, and only 1 percent progressed to invasive cancer. The corresponding approximations for CIN 2 were 40 percent, 40 percent, 20 percent, and 5 percent, respectively. The likelihood of CIN 3 regressing was 33 percent and that of progressing to invasive cancer was greater than 12 percent.
The author of the study, Andrew G Ostor, MD, from the Departments of Obstetrics and Gynaecology and Pathology, University of Melbourne noted:
"It is obvious from the above figures that the probability of an atypical epithelium becoming invasive increases with the severity of the atypia, but does not occur in every case. Even the higher degrees of atypia may regress in a significant proportion of cases. As morphology by itself does not predict which lesion will progress or regress, future efforts should seek factors other than morphological to determine the prognosis in individual patients."
The above remark leads us to a third reason why a surrogate morphological marker is not an adequate endpoint for assessing the efficacy of cervical cancer vaccines:
"CIN 2 is not a true biologic entity but an equivocal diagnosis of pre-cancer, representing an admixture of HPV infection and pre-cancer. The existence of CIN 2 biopsy results as a clinical entity may be the consequence of the inaccuracies of colposcopy and colposcopically directed biopsy, which could result in less than-perfect representation of the underlying disease state."
Furthermore, the same report by the National Cancer Institute (NCI 9) states that:
"That CIN2 is the least reproducible of all histopathologic diagnoses may in part reflect sampling error."
Finally, according to second report by the NCI 10:
"Approximately 40 percent of undiagnosed CIN 2 will regress over two years." (this also precisely corroborates the findings of the study by Ostor)
Gardasil is marketed as the vaccine that prevents cervical cancer. This statement is incorrect. Based on the above NCI findings, we can conclude that the data presented in the VRBPAC Background Document on Gardasil HPV Quadrivalent Vaccine 8 only supports the claim that Gardasil can prevent "an equivocal diagnosis of pre-cancer, representing an admixture of HPV infection and pre-cancer" – about half of which are self-reversing to normal cases and not reflect actual cervical cancer.
There was yet another important oversight in assessing the efficacy of Gardasil. Most cervical cancers are believed to be linked to infection with genital HPV types 6, 11, 16, and 18 2 3 11. According to NCI, the only reliable HPV genotyping method is a "PCR system with short target sequences" or alternatively, "'sentinel-base' genotyping by PCR." Ironically, these HPV genotyping methods were never used to determine the HPV type associated with precancerous lesions in the clinical trials for evaluation of the efficacy of Gardasil to prevent type-specific HPV infections.
2) Cervical cancer is a rare disease in developed countries which invalidates the recommendations for universal immunization with any HPV vaccine. The incidence of cervical cancer has dropped substantially since implementation of regular Pap screening procedures. Currently, in the US, the death rate from cervical cancer (2.4/100,000 women) is lower than the rate of reported serious adverse events, including death, from Gardasil (3.34/100,000 doses distributed)
The severity of cervical cancer should not be undermined. Advanced cervical cancer is a deadly disease, especially in areas where the resources and infrastructure to fully implement
Papanicolaou (Pap) smear tests are limited such as Latin America, Africa, India and South Asia. In the past four decades, industrialized countries such as the US, have cut cervical cancer mortality and incidence rates by 74 percent largely through the use of the Pap smear 2.
Thus, as noted by Diane Harper, MD, Professor and Vice Chair, Obstetrics and Gynecology, Community and Family Medicine and Informatics and Personalized Medicine, who conducted the phase 2 and phase 3 trials for Gardasil, authoring their publications, in developed countries such as the US, which have regular Pap screening programs in place, the HPV vaccine will do little to decrease the already very small cancer rate. In fact, Harper noted that if women who are vaccinated stop going for Pap smears, the incidence rate for cervical cancer would increase.
Based on L1-encoded virus-like particles, Gardasil should protect against the HPV genotypes 16 and 18, which are thought to account for 70 percent of cervical cancers. Since Gardasil does not even claim to protect against all cases of cervical cancer but only those "caused by HPV strains 16 & 18", it does not replace the need for a regular pap smear.
More crucially, however, for deciding whether a risk of adverse effects from the HPV vaccine is worth taking, much depends on the perceived benefit from the vaccine relative to that risk. If benefits are indeed substantial, then many individuals would be willing to accept the risk. However, if the benefit of the vaccine has not been demonstrated and is in fact only speculative, and if a majority of those women who are persistently infected with HPV are not likely to develop cancer providing they are adequately screened, then most reasonably they will only be willing to accept very small risk of harm from the vaccine. Data from clinical safety trials argue against small risks from Gardasil vaccination. In a paper published in JAMA, Slade et al. (2009) 11 report that from June 1, 2006, through December 31, 2008, the US Vaccine Adverse Event Reporting System (VAERS) received 424 reports of adverse reaction following receipt of Gardasil amongst which, 772 (6.2 percent) were serious, including 32 deaths. Given the overall reporting rate of 53.9 reports per 100, vaccine doses distributed, the estimated rate of reported serious adverse events from Gardasil is 3.34/100 doses distributed. This rate is higher than the death rate from cervical cancer in the US which stands at 2.4/100 women (according to CDC statistics, 15).
Harper poses an important question 14:
"Would a parent accept such a rate of serious adverse events if the same cancer prevention can occur with continued Pap screening? Is there any acceptable level of risk of serious adverse events, including death, to prevent genital warts?" [emphasis added]
The later claim was in reference to one of the vaccine's other claimed benefits.
3) Most HPV infections are benign and resolve spontaneously without causing cervical cancer
According to Harper 16:
"70 percent of all HPV infections resolve themselves without treatment within a year. Within two years, the number climbs to 90 percent. Of the remaining 10 percent of HPV infections, only half will develop into cervical cancer."
These numbers are consistent with those above quoted from Nature Biotechnology:
"Most genital infections are asymptomatic and resolve spontaneously, but the virus can persist and cause precancerous lesions that can become malignant over the subsequent 20-30 years."
In addition, in a recent JAMA editorial, Charlotte Haug, MD, PhD, emphasized:
"The virus does not appear to be very harmful because almost all HPV infections are cleared by the immune system. In a few women, the HPV infection persists, and some women may develop precancerous cervical lesions and eventually cancer. It is currently impossible to predict in which women this will occur and why. Likewise, it is impossible to predict exactly what effect vaccination of young girls and women will have on the incidence of cervical cancer 20 to 40 years from now."
Thus, again, there appears to be little rationale in support of universal immunization with any HPV vaccine.
(Note from SaneVax: Are the benefits of Gardasil vaccination worth the risks? Take a good look at the following in-depth study, then decide for yourself.)