TY - JOUR
T1 - Cancer risk and use of protease inhibitor or nonnucleoside reverse transcriptase inhibitor-based combination antiretroviral therapy: The D:A:D study
T2 - Journal of Acquired Immune Deficiency Syndromes
AU - Bruyand, M.
AU - Ryom, L.
AU - Shepherd, L.
AU - Fatkenheuer, G.
AU - Grulich, A.
AU - Reiss, P.
AU - De Wit, S.
AU - Darminio Monforte, A.
AU - Furrer, H.
AU - Pradier, C.
AU - Lundgren, J.
AU - Sabin, C.
AU - Torres, Ferran
N1 - Cited By :31
Export Date: 17 February 2022
CODEN: JJASF
Correspondence Address: Bruyand, M.; INSERM, case 11, 146 rue Léo Saignat, France; email: [email protected]
Chemicals/CAS: proteinase inhibitor, 37205-61-1; Protease Inhibitors; Reverse Transcriptase Inhibitors
Funding details: 5U01AI042170-10, 5U01AI046362-03
Funding details: National Institute of Allergy and Infectious Diseases, NIAID, U01AI042170, U01AI046362, U01AI069907
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Accessed July 29, 2014
PY - 2015/4
Y1 - 2015/4
N2 - Background: The association between combination antiretroviral therapy (cART) and cancer risk, especially regimens containing protease inhibitors (PIs) or nonnucleoside reverse transcriptase inhibitors (NNRTIs), is unclear. Methods: Participants were followed from the latest of D:A:D study entry or January 1, 2004, until the earliest of a first cancer diagnosis, February 1, 2012, death, or 6 months after the last visit. Multivariable Poisson regression models assessed associations between cumulative (per year) use of either any cART or PI/NNRTI, and the incidence of any cancer, non-AIDS-defining cancers (NADC), AIDS-defining cancers (ADC), and the most frequently occurring ADC (Kaposi sarcoma, non-Hodgkin lymphoma) and NADC (lung, invasive anal, head/neck cancers, and Hodgkin lymphoma). Results: A total of 41,762 persons contributed 241,556 person-years (PY). A total of 1832 cancers were diagnosed [incidence rate: 0.76/100 PY (95% confidence interval: 0.72 to 0.79)], 718 ADC [0.30/100 PY (0.28-0.32)], and 1114 NADC [0.46/100 PY (0.43-0.49)]. Longer exposure to cART was associated with a lower ADC risk [adjusted rate ratio: 0.88/year (0.85-0.92)] but a higher NADC risk [1.02/year (1.00-1.03)]. Both PI and NNRTI use were associated with a lower ADC risk [PI: 0.96/year (0.92-1.00); NNRTI: 0.86/year (0.81-0.91)]. PI use was associated with a higher NADC risk [1.03/year (1.01-1.05)]. Although this was largely driven by an association with anal cancer [1.08/year (1.04-1.13)], the association remained after excluding anal cancers from the end point [1.02/year (1.01-1.04)]. No association was seen between NNRTI use and NADC [1.00/year (0.98-1.02)]. Conclusions: Cumulative use of PIs may be associated with a higher risk of anal cancer and possibly other NADC. Further investigation of biological mechanisms is warranted. © 2015 Wolters Kluwer Health, Inc. All rights reserved.
AB - Background: The association between combination antiretroviral therapy (cART) and cancer risk, especially regimens containing protease inhibitors (PIs) or nonnucleoside reverse transcriptase inhibitors (NNRTIs), is unclear. Methods: Participants were followed from the latest of D:A:D study entry or January 1, 2004, until the earliest of a first cancer diagnosis, February 1, 2012, death, or 6 months after the last visit. Multivariable Poisson regression models assessed associations between cumulative (per year) use of either any cART or PI/NNRTI, and the incidence of any cancer, non-AIDS-defining cancers (NADC), AIDS-defining cancers (ADC), and the most frequently occurring ADC (Kaposi sarcoma, non-Hodgkin lymphoma) and NADC (lung, invasive anal, head/neck cancers, and Hodgkin lymphoma). Results: A total of 41,762 persons contributed 241,556 person-years (PY). A total of 1832 cancers were diagnosed [incidence rate: 0.76/100 PY (95% confidence interval: 0.72 to 0.79)], 718 ADC [0.30/100 PY (0.28-0.32)], and 1114 NADC [0.46/100 PY (0.43-0.49)]. Longer exposure to cART was associated with a lower ADC risk [adjusted rate ratio: 0.88/year (0.85-0.92)] but a higher NADC risk [1.02/year (1.00-1.03)]. Both PI and NNRTI use were associated with a lower ADC risk [PI: 0.96/year (0.92-1.00); NNRTI: 0.86/year (0.81-0.91)]. PI use was associated with a higher NADC risk [1.03/year (1.01-1.05)]. Although this was largely driven by an association with anal cancer [1.08/year (1.04-1.13)], the association remained after excluding anal cancers from the end point [1.02/year (1.01-1.04)]. No association was seen between NNRTI use and NADC [1.00/year (0.98-1.02)]. Conclusions: Cumulative use of PIs may be associated with a higher risk of anal cancer and possibly other NADC. Further investigation of biological mechanisms is warranted. © 2015 Wolters Kluwer Health, Inc. All rights reserved.
KW - antiretroviral therapy
KW - cancer
KW - HIV
KW - risk
KW - nonnucleoside reverse transcriptase inhibitor
KW - proteinase inhibitor
KW - RNA directed DNA polymerase inhibitor
KW - adult
KW - anus cancer
KW - Article
KW - cancer diagnosis
KW - cancer incidence
KW - cancer mortality
KW - cancer risk
KW - female
KW - head and neck cancer
KW - highly active antiretroviral therapy
KW - Hodgkin disease
KW - human
KW - human cell
KW - invasive anal cancer
KW - Kaposi sarcoma
KW - lung cancer
KW - major clinical study
KW - male
KW - nonhodgkin lymphoma
KW - priority journal
KW - prospective study
KW - adverse effects
KW - follow up
KW - HIV Infections
KW - incidence
KW - middle aged
KW - Neoplasms
KW - procedures
KW - risk assessment
KW - Adult
KW - Antiretroviral Therapy, Highly Active
KW - Female
KW - Follow-Up Studies
KW - Humans
KW - Incidence
KW - Male
KW - Middle Aged
KW - Prospective Studies
KW - Protease Inhibitors
KW - Reverse Transcriptase Inhibitors
KW - Risk Assessment
UR - https://www.scopus.com/pages/publications/84925089152
U2 - 10.1097/QAI.0000000000000523
DO - 10.1097/QAI.0000000000000523
M3 - Article
C2 - 25763785
SN - 1944-7884
VL - 68
SP - 568
EP - 577
JO - Journal of acquired immune deficiency syndromes (1999)
JF - Journal of acquired immune deficiency syndromes (1999)
IS - 5
ER -