The Centers for Disease Control and Prevention recommended booster shots of the Pfizer COVID-19 vaccine at least six months after a second dose in the following groups:
The CDC recommendations state that people ages 18 to 49 with underlying medical conditions and people ages 18 to 64 who are at risk of COVID-19 exposure due to their work or living arrangements “may receive a booster shot” of the Pfizer vaccine “based on their individual benefits and risks.”
The CDC’s Sept. 24 recommendations align with the Pfizer booster shot authorizations from the U.S. Food and Drug Administration (FDA) released on Sept. 22.
President Joe Biden confirmed in a speech on Sept. 24 that eligible individuals who received their second dose of the Pfizer vaccine in March or earlier can receive a booster dose of the vaccine now, free of charge.
The CDC and FDA did not release recommendations about the Moderna vaccine or the single-dose Johnson & Johnson vaccine. Moderna announced that a booster shot of its COVID-19 vaccine improved protection against the delta variant in a press release on Sept. 1. Johnson & Johnson released a statement on Sept. 21 sharing that data from a phase 3 study demonstrated the benefits of a booster vaccine dose.
Both companies have submitted data on booster shots to the FDA for review.
A COVID-19 vaccine booster is administered when someone developed adequate immunity after the initial vaccine doses, but that immunity has decreased over time.
However, an additional dose of the vaccine may be recommended for those who did not develop an adequate immune response after the two-dose vaccination series.
The FDA amended the Pfizer and Moderna vaccines’ emergency use authorizations on Aug. 12 to allow a third vaccine dose for certain immunocompromised individuals. The new recommendations from the FDA and CDC do not change this eligibility. There is not yet guidance from the FDA or CDC on additional doses for immunocompromised people who received the Johnson & Johnson vaccine.
Individuals defined as immunocompromised include people in cancer treatment, people who received a stem cell transplant in the last two years, people who are organ donor recipients and taking immunosuppressive drugs, people taking high-dose steroids or other immunosuppressive drugs, as well as those with certain other health conditions.
The CDC did not release a comprehensive list of every condition or treatment that would make a person immunocompromised. Instead, the agency recommends individuals consult their doctors to determine if a third dose is appropriate for them.
The CDC recommends a third dose of the COVID-19 vaccine for moderately to severely immunocompromised people at least 28 days after their second vaccination with the Pfizer or Moderna vaccine.
Many medications used to treat lung cancer have negative effects on the immune system. This means that a person can be immunocompromised while undergoing cancer treatment, especially chemotherapy or immunotherapy. Immunotherapy medications for lung cancer include:
Chemotherapies used to treat lung cancer include:
The American Lung Association recommends receiving a COVID-19 vaccination two to three weeks before beginning lung cancer treatment with chemotherapy or immunotherapy. This gives the immune system time to develop a response to the COVID-19 vaccine and make antibodies against it. These guidelines do not apply to other lung cancer treatments, such as targeted therapies, because the medications work differently than chemotherapy or immunotherapy.
If you believe you are immunocompromised, ask your doctor whether an additional dose of a COVID-19 vaccine would be beneficial to you.
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