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Published on: September 25, 2018
Anti-PD-1/PD-L1 immunotherapy in patients with solid organ transplant, HIV or hepatitis B/C infection
Martin Tio1, Rajat Rai1, Ogochukwu M Ezeoke2
1Melanoma Institute Australia, Sydney, Australia.
Background:
Anti-programmed cell death protein 1/programmed death ligand 1 (PD-1/PD-L1) immunotherapy is now routinely used to treat several cancers. Clinical trials have excluded several populations, including patients with solid organ transplant, HIV infection and hepatitis B/C infection. We examined the safety outcomes of these populations treated with anti-PD-1/PD-L1 treatment in a multicentre retrospective study.
Methods:
Patients from 16 centres with advanced cancer and solid organ transplant, HIV infection or hepatitis B/C infection were included. Demographic, tumour, treatment, toxicity and outcome data were recorded.
Results:
Forty-six patients were included for analysis, with a median age of 60 years, and the majority of patients diagnosed with melanoma (72%). Among six patients with solid organ transplants, two graft rejections occurred, with one resulting in death, whereas two patients achieved partial responses. There were four responses in 12 patients with HIV infection. In 14 patients with hepatitis B, there were three responses, and similarly, there were three responses in 14 patients with hepatitis C. There was no unexpected toxicity in any viral infection group or an increase in viral load.
Conclusion:
Patients with HIV or hepatitis B/C infections treated with anti-PD-1/PD-L1 immunotherapy may respond to treatment without increased toxicity. Given the risk of graft rejection in solid organ transplant patients and also the potential for response, the role of anti-PD-1/PD-L1 immunotherapy needs to be carefully considered.
Insights
Anti-PD-1/PD-L1 immunotherapy shows potential in patients with HIV or hepatitis B/C infections, with no increased toxicity. However, solid organ transplant recipients face graft rejection risks, requiring careful consideration for this cancer treatment.
Area of Science:
- Oncology
- Immunotherapy
- Infectious Diseases
Background:
- Anti-programmed cell death protein 1/programmed death ligand 1 (PD-1/PD-L1) immunotherapy is a standard cancer treatment.
- Clinical trials have historically excluded patients with solid organ transplant, HIV, or hepatitis B/C infections.
- This study investigates the safety and efficacy of PD-1/PD-L1 inhibitors in these underrepresented patient groups.
Purpose of the Study:
- To evaluate the safety outcomes of PD-1/PD-L1 immunotherapy in patients with solid organ transplants, HIV, or hepatitis B/C infections.
- To assess treatment response rates in these specific patient populations.
- To identify any unexpected toxicities or changes in viral load associated with immunotherapy.
Main Methods:
- A multicentre retrospective study included 46 patients with advanced cancer.
- Patients had either solid organ transplants, HIV infection, or hepatitis B/C infection.
- Demographic, tumor, treatment, toxicity, and outcome data were collected and analyzed.
Main Results:
- Among 6 solid organ transplant patients, 2 experienced graft rejection (1 fatal), and 2 had partial responses.
- In 12 HIV-infected patients, 4 achieved responses.
- 14 patients with hepatitis B and 14 with hepatitis C each showed 3 responses, with no unexpected toxicity or increased viral load.
Conclusions:
- PD-1/PD-L1 immunotherapy can be safely administered to patients with HIV or hepatitis B/C infections, showing potential for treatment response without increased toxicity.
- The risk of graft rejection in solid organ transplant recipients necessitates careful consideration of PD-1/PD-L1 immunotherapy, despite potential treatment benefits.
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