HPV Vaccine Comparison: Gardasil 9, Cervarix, and Cervavac
Current U.S. Availability and FDA Approval Status
As of January 2017, Gardasil 9 (9-valent HPV vaccine) is the only HPV vaccine available in the United States, making it the sole option for HPV vaccination in this country. 1
Historical Context of U.S.-Approved Vaccines
Until 2017, three HPV vaccines were available or licensed in the United States 1:
- Cervarix (bivalent, 2vHPV) – GlaxoSmithKline product targeting HPV types 16 and 18, licensed for use in females only 1
- Gardasil (quadrivalent, 4vHPV) – Merck product protecting against HPV types 6,11,16, and 18, licensed for both females and males 1
- Gardasil 9 (9-valent, 9vHPV) – Merck product licensed in December 2014, now the exclusive U.S. vaccine 1
Cervavac is not FDA-approved or available in the United States – it appears to be a vaccine product used in other countries (likely India based on naming conventions), but it has no FDA approval status and is not part of U.S. vaccination guidelines. 2
Key Differences Between the Vaccines
HPV Type Coverage
Gardasil 9 provides the broadest protection, covering nine HPV types compared to the more limited coverage of earlier vaccines 1:
Gardasil 9 (9vHPV): Types 6,11,16,18,31,33,45,52, and 58 1, 2
Cervarix (2vHPV): Types 16 and 18 only 1
Original Gardasil (4vHPV): Types 6,11,16, and 18 1
FDA Approval and Licensing
Gardasil 9 received progressive FDA approvals 1:
- December 2014: Initially licensed for females ages 9-26 years and males ages 9-15 years 1
- December 2015: Extended to males through age 26 years 1
- October 2016: FDA approved the 2-dose schedule for persons ages 9-14 years 1
- October 2018: Extended approval to adults ages 27-45 years 2
Cervarix and original Gardasil were previously FDA-approved but are no longer distributed in the United States as of January 2017 1
Dosing Schedules for U.S. Vaccination
The dosing schedule depends on age at first dose, not the specific vaccine product 1, 2:
Two-Dose Schedule (Ages 9-14 Years at First Dose)
- Recommended for immunocompetent adolescents who initiate vaccination before their 15th birthday 1, 2
- Dose 1: Day 0 1, 2
- Dose 2: 6-12 months after first dose (minimum interval 12 weeks) 1, 2
- Longer intervals (closer to 12 months) produce stronger immune responses than shorter intervals 1, 2
- Younger adolescents (9-14 years) generate significantly higher antibody titers than older individuals receiving three doses, supporting the two-dose regimen 1, 2
Three-Dose Schedule (Ages ≥15 Years at First Dose)
- Required for all persons who initiate vaccination at age 15 years or older 1, 2
- Dose 1: Day 0 1, 2
- Dose 2: 1-2 months after first dose (minimum interval 4 weeks) 1, 2
- Dose 3: 6 months after first dose (minimum interval 12 weeks after dose 2) 1, 2
Special Populations Requiring Three Doses
- All immunocompromised persons require a three-dose schedule regardless of age at initiation 2
- This includes HIV-positive individuals, solid organ transplant recipients, and those on immunosuppressive medications 2
Clinical Recommendations for U.S. Practice
Routine Vaccination Age
Administer HPV vaccination routinely at age 11-12 years, though it can be started as early as age 9 years 1, 2:
- Vaccination before sexual debut provides maximum protection 1, 2
- Approximately 24% of adolescents report sexual intercourse by 9th grade and 58% by 12th grade 1, 2
- Nearly 60% of males acquire HPV infection within 2 years after sexual initiation 2
Catch-Up Vaccination
- Recommended for all persons through age 26 years who are not adequately vaccinated 2
- Shared clinical decision-making for adults ages 27-45 years 2
Important Clinical Considerations
- No prevaccination testing (HPV DNA, antibody, or Pap testing) is required before vaccination 2
- Prior HPV exposure, history of genital warts, abnormal Pap tests, or positive HPV tests are NOT contraindications to vaccination 2
- The vaccine protects against HPV types not yet acquired, even in sexually active individuals 1, 2
- Cervical cancer screening must continue regardless of vaccination status, as vaccines do not protect against all oncogenic HPV types 1, 2
Series Interruption
- If the vaccine series is interrupted, continue from where you left off—do NOT restart the series 2
- The critical determining factor is the age when the first dose was given, not when subsequent doses are administered 2
- There is no maximum time interval between doses 2
Common Pitfalls to Avoid
- Do not delay vaccination waiting for "optimal" timing—complete the series before sexual debut when possible 2
- Do not administer booster doses to individuals who completed their primary series—no booster is recommended regardless of which vaccine was used 5, 6
- Do not switch from 4vHPV or 2vHPV to 9vHPV after completing the original series—this is not recommended or cost-effective 6
- Do not skip cervical cancer screening in vaccinated women—screening remains essential 2, 5, 6
- Observe patients for 15 minutes post-vaccination due to syncope risk in adolescents 2
Comparative Immunogenicity Data (Historical Context)
While no longer clinically relevant for U.S. practice, historical studies showed 3, 4:
- Cervarix induced 3-9 fold higher peak neutralizing antibody titers to HPV 16/18 than original Gardasil 3
- Cervarix demonstrated sustained high antibody titers for at least 10 years 7
- Cervarix showed superior cross-protection against HPV types 31,33, and 45 compared to Gardasil 3, 4
- Both vaccines provided >90% efficacy in preventing CIN 2+ disease caused by HPV 16/18 in baseline-negative women 3
However, these comparisons are now academic since only Gardasil 9 is available in the United States.
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