Vaccine
Talk
(Egyptian Edition)
"Everything you need to know about
vaccines in Egypt"
(Egyptian Edition)
"Everything you need to know about
vaccines in Egypt"
Patients with cancer are at increased risk of vaccine-preventable infections due to both the underlying malignancy and the immunosuppressive effects of cancer treatment. Chemotherapy, radiotherapy, immunotherapy, biologic agents, and other immunosuppressive therapies can impair immune function, reduce vaccine responses, and increase susceptibility to severe infections.
Vaccination is an important component of comprehensive cancer care. Whenever possible, vaccines should be administered before treatment begins to maximize protection.
The optimal vaccination strategy depends on several factors, including:
People with cancer, particularly those with hematological malignancies or advanced disease, often experience significant immune dysfunction as a result of both their disease and treatment.
Patients receiving chemotherapy or radiation therapy for leukemia, lymphoma, multiple myeloma, or solid tumors should generally be considered immunocompromised.
Whenever feasible, all indicated vaccines should be administered before:
Vaccination during chemotherapy may be necessary in some situations, particularly when delaying vaccination would leave the patient vulnerable to infection.
Although vaccine responses may be suboptimal, inactivated vaccines remain safe and may provide meaningful protection.
Patients with severe neutropenia (absolute neutrophil count <0.5 × 10⁹/L) should generally defer vaccination until recovery to avoid confusion with treatment-related febrile episodes.
Influenza can cause significant morbidity and mortality in cancer patients, including:
Annual influenza vaccination is recommended for all cancer patients aged 6 months and older.
Recommended
Inactivated influenza vaccine (IIV)
Not recommended
Live attenuated influenza vaccine (LAIV)
Optimal timing includes:
Because influenza is seasonal, vaccination should not be unnecessarily delayed when protection is needed.
Family members and close contacts should also receive annual influenza vaccination to reduce the risk of transmission.
Patients receiving immune checkpoint inhibitors such as:
may have an increased risk of immune-related adverse events following influenza vaccination. The timing of vaccination should be discussed with the treating oncologist.
Patients with:
are at increased risk of invasive pneumococcal disease. Vaccination should ideally be administered before treatment begins.
Current recommendations favor the use of pneumococcal conjugate vaccines because they induce superior immune responses compared with polysaccharide vaccines.
Depending on age and local recommendations, vaccination may include:
Patients with hematological malignancies, functional asplenia, or other high-risk conditions may require individualized schedules.
Hepatitis B virus (HBV) reactivation is a recognized complication of chemotherapy and immunosuppressive therapy, particularly among patients receiving anti-CD20 therapies such as rituximab.
Immunity to tetanus, diphtheria, and pertussis may decline following cancer treatment. A booster dose of Tdap should be considered following completion of therapy according to age-appropriate recommendations.
HPV vaccination is recommended according to routine age-based schedules.
Immunosuppression is not a contraindication to HPV vaccination, although vaccine responses may be reduced.
Meningococcal vaccination is recommended for:
Patients with splenic dysfunction due to malignancy or splenic irradiation should follow recommendations for individuals with asplenia.
Hepatitis A vaccination is recommended for cancer patients with:
All immunocompromised adults with cancer aged 18 years and older are recommended to receive:
The vaccine is non-live and can be safely administered to immunocompromised patients.
Patients receiving:
may have impaired vaccine responses.
Live vaccines are generally contraindicated in patients with:
Live vaccines may be considered when:
Patients with anatomical or functional asplenia are at increased risk of overwhelming infection caused by encapsulated bacteria.
Whenever possible, vaccination should occur at least 2 weeks before elective splenectomy. Patients with persistent asplenia may require booster doses according to risk-based recommendations.
For more, please visit: Anatomic or Functional Asplenia
Patients who completed their primary vaccination schedule before cancer diagnosis generally retain some immune memory and can receive most recommended vaccines after recovery without routine pre-vaccination antibody testing.
For patients who are clinically well and in remission for at least 6 months after completion of therapy, the following booster vaccinations may be considered.
Children younger than 10 years
Individuals aged 10 years and older
Serologic testing for measles and rubella immunity should be performed 6–8 weeks after vaccination. Individuals who fail to seroconvert may require an additional dose.
For individuals who have not completed a recommended pneumococcal series:
Individuals with asplenia should receive MenACWY booster doses every 5 years if the risk remains.
For previously unvaccinated individuals:
Seronegative individuals may receive:
Vaccination should occur at least 6 months after completion of chemotherapy and only when adequate immune recovery has been achieved.