Abstract:Human immunodeficiency virus (HIV) chronically infected patients are at increased risk of developing non-Hodgkin lymphoma compared with the general population. Highly active antiretroviral therapy has had a dramatic effect on the natural history of HIV infection, reducing the incidence of acquired immunodeficiency syndrome-related non-Hodgkin lymphoma and improving overall survival. However, problems related to adherence to treatment, frequently experienced during adolescence, may increase the risk of acquired… Show more
“…Treatment outcomes were not reported. This study echoes a previous report from Italy, describing two cases of Burkitt lymphoma in AYALHIV who were chronically exposed to high-levels HIV viremia [23]. These two case series support the concerns of longer term oncogenic risk for the current generation of perinatally infected AYALHIV following prolonged viremia due to late diagnosis, and low rates of viral suppression due to previous inferior ART regimens, suboptimal dosing, non-adherence and the evolution of resistance [22].…”
Although data are sparse, the increased cancer risk for AYALHIV is the cause for concern and must be modified by improving global access and uptake of antiretroviral therapy, human papilloma virus (HPV) and hepatitis B virus (HBV) vaccination, screening for hepatitis B and C infection, and optimized cancer screening programs. Education aimed at reducing traditional modifiable cancer risk factors should be embedded within multidisciplinary services for AYALHIV.
“…Treatment outcomes were not reported. This study echoes a previous report from Italy, describing two cases of Burkitt lymphoma in AYALHIV who were chronically exposed to high-levels HIV viremia [23]. These two case series support the concerns of longer term oncogenic risk for the current generation of perinatally infected AYALHIV following prolonged viremia due to late diagnosis, and low rates of viral suppression due to previous inferior ART regimens, suboptimal dosing, non-adherence and the evolution of resistance [22].…”
Although data are sparse, the increased cancer risk for AYALHIV is the cause for concern and must be modified by improving global access and uptake of antiretroviral therapy, human papilloma virus (HPV) and hepatitis B virus (HBV) vaccination, screening for hepatitis B and C infection, and optimized cancer screening programs. Education aimed at reducing traditional modifiable cancer risk factors should be embedded within multidisciplinary services for AYALHIV.
“…NADC incidence in PLWH is two times higher than in the general population, despite the use of ART [93]. In addition, in the past few years, an increase in the number of NADCs has been recorded, while ADC cases are decreasing but still reported [94,95].…”
Section: Non-aids Co-morbidities In Plwhmentioning
Despite effective antiretroviral therapy (ART), people living with HIV (PLWH) still present persistent chronic immune activation and inflammation. This condition is the result of several factors including thymic dysfunction, persistent antigen stimulation due to low residual viremia, microbial translocation and dysbiosis, caused by the disruption of the gut mucosa, co-infections, and cumulative ART toxicity. All of these factors can create a vicious cycle that does not allow the full control of immune activation and inflammation, leading to an increased risk of developing non-AIDS co-morbidities such as metabolic syndrome and cardiovascular diseases. This review aims to provide an overview of the most recent data about HIV-associated inflammation and chronic immune exhaustion in PLWH under effective ART. Furthermore, we discuss new therapy approaches that are currently being tested to reduce the risk of developing inflammation, ART toxicity, and non-AIDS co-morbidities.
“…18,19 For AYALWH, this is anecdotally supported by a report on two vertically infected 15year-olds in Italy who were diagnosed with Burkitt lymphoma after prolonged exposure to HIV viremia. 20 Compared to other age groups, AYALWH have higher rates of non-adherence to antiretroviral treatment and, thus, of virologic failure. 2 This may put AYALWH at particularly high risk of developing HIV-related hematologic malignancies.…”
Section: Discussionmentioning
confidence: 99%
“…We classified cancers based on the International Classification of Diseases for Oncology, 3 rd Edition (ICD-O-3), recoded for AYA. 9 We categorised cancers into the following groups 10 : leukaemia (AYA recode 01-04), non-Hodgkin lymphoma (05), Hodgkin lymphoma (06), central nervous system (CNS) and other intracranial and intraspinal neoplasms (07-16), osseous & chondromatous neoplasms (17)(18)(19)(20), Kaposi sarcoma (24), soft tissue sarcomas other than Kaposi sarcoma (21)(22)(23)25), germ cell and trophoblastic neoplasms (26)(27)(28), melanoma and skin carcinomas (29,30), carcinomas (31-48), and miscellaneous specified and unspecified neoplasms and unclassified cancers (49-56, 99). We further divided the non-Hodgkin lymphomas into their most common subtypes: Burkitt lymphomas (ICD-0-3 morphology code 9687) and diffuse large B-cell lymphomas (ICD-0-3 morphology code 9680 or 9684), with a separate category for other non-Hodgkin lymphomas.…”
Section: Inclusion Criteria and Definitionsmentioning
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