Cancer immunotherapy in special challenging populations: recommendations of the Advisory Committee of Spanish Melanoma Group (GEM).
Maria Gonzales CaoTeresa PuertolasMar RiveiroEva Muñoz-CouseloCarolina OrtizRoger ParedesDaniel PodzamczerJose Luis ManzanoJose MoltoBoris RevolloCristina CarreraLourdes MateuSara FancelliEnrique EspinosaBonaventura ClotetJavier Martinez-PicadoPablo CerezuelaAinara SoriaIvan Marquez-RodasMario MandalaAlfonso Berrocalnull nullPublished in: Journal for immunotherapy of cancer (2021)
Cancer immunotherapy based on the use of antibodies targeting the so-called checkpoint inhibitors, such as programmed cell death-1 receptor, its ligand, or CTLA-4, has shown durable clinical benefit and survival improvement in melanoma and other tumors. However, there are some special situations that could be a challenge for clinical management. Persons with chronic infections, such as HIV-1 or viral hepatitis, latent tuberculosis, or a history of solid organ transplantation, could be candidates for cancer immunotherapy, but their management requires a multidisciplinary approach. The Spanish Melanoma Group (GEM) panel in collaboration with experts in virology and immunology from different centers in Spain reviewed the literature and developed evidence-based guidelines for cancer immunotherapy management in patients with chronic infections and immunosuppression. These are the first clinical guidelines for cancer immunotherapy treatment in special challenging populations. Cancer immunotherapy in chronically infected or immunosuppressed patients is feasible but needs a multidisciplinary approach in order to decrease the risk of complications related to the coexistent comorbidities.
Keyphrases
- end stage renal disease
- clinical practice
- systematic review
- ejection fraction
- newly diagnosed
- chronic kidney disease
- mycobacterium tuberculosis
- antiretroviral therapy
- stem cells
- hiv positive
- hiv infected
- peritoneal dialysis
- cancer therapy
- quality improvement
- emergency department
- prognostic factors
- mesenchymal stem cells
- oxidative stress
- drug delivery
- drug induced