Treatment Approach for Tumors in HIV Patients
HIV-infected patients with tumors should receive standard cancer therapy appropriate for their tumor type while maintaining antiretroviral therapy (ART), with treatment decisions guided by a multidisciplinary team including an oncologist and HIV specialist. 1
General Management Principles
HIV Management During Cancer Treatment
- HIV screening: All patients with cancer should be screened for HIV 1
- Antiretroviral therapy:
- ART should be initiated or continued during cancer treatment 1
- ART interruptions should be avoided due to risk of immunologic compromise, opportunistic infections, and death 1
- Continuation of ART improves tolerance of cancer treatment, response rates, and survival 1
- Pretreatment plasma viral load should be checked and cancer therapy should be administered when viral load is undetectable 1
Collaborative Care
- All HIV patients with cancer should be co-managed by an oncologist and HIV specialist 1
- Consultation with HIV pharmacist and oncology pharmacist is recommended to manage drug interactions 1
- Cancer treatment should not be delayed for HIV workup when possible 1
Specific Considerations for Cancer Treatment
Immunotherapy Considerations
- HIV-infected individuals with tumor types that are candidates for immunotherapy should be considered for cancer treatment 1
- For anti-PD-1/PD-L1 therapy:
Chemotherapy Considerations
- Standard chemotherapy regimens should be used but may require modifications:
- Consider dose reduction in early cycles if CD4+ T cell count is <100 cells/μL 1
- Growth factor support is strongly recommended for all regimens in HIV patients 1
- For AIDS-related Kaposi's sarcoma, paclitaxel 135 mg/m² IV over 3 hours every 3 weeks or 100 mg/m² IV over 3 hours every 2 weeks is recommended 2
- For HIV patients receiving paclitaxel:
Infection Prophylaxis
Required/Strongly Recommended Prophylaxis
Pneumocystis jirovecii pneumonia (PJP) prophylaxis:
Herpes simplex virus/Varicella zoster virus prophylaxis:
Gram-negative infection prophylaxis:
Mycobacterium avium complex (MAC) prophylaxis:
Additional Prophylaxis to Consider
- Antifungal prophylaxis during periods of prolonged neutropenia (≥7 days) 1
Monitoring During Treatment
- More frequent HIV viral load testing (e.g., monthly for first 3 months, then every 3 months) 1
- Consider measuring CD4+ T cell count more frequently in patients receiving cancer treatments anticipated to cause lymphopenia 1
- Monitor for drug interactions between ART and cancer therapy 1
- High index of suspicion for opportunistic infections, including early testing for fungal and cytomegalovirus infections 1
Special Considerations
Antiretroviral Drug Interactions
- Avoid if possible:
Imaging Interpretation
- Interpretation of diagnostic and staging imaging may be complicated by increased incidence of non-malignant lesions 1
- PET/CT-guided therapy is feasible but care should be taken to recognize potential confounding factors (non-malignant causes for PET-avid regions) 1
- MRI is the optimal method for staging CNS lymphomas, but cerebral opportunistic infections may mimic lymphoma in HIV patients 1
Common Pitfalls to Avoid
- Delaying cancer treatment unnecessarily - Cancer treatment should not be delayed for HIV workup when possible 1
- Interrupting ART during cancer treatment - This increases risk of opportunistic infections and death 1
- Failing to provide adequate prophylaxis - HIV patients receiving cancer therapy need comprehensive infection prophylaxis 1
- Overlooking drug interactions - Always check for interactions between cancer therapy and ART 1
- Misinterpreting imaging findings - Non-malignant lesions may be mistaken for cancer spread or recurrence 1
- Underutilizing growth factors - Myeloid growth factor support should be strongly considered even for regimens with low risk of febrile neutropenia 1