hep-druginteractions.org) GPP 8.3.1 We recommend starting ART in HIV-positive patients with
KS. 1A We recommend starting ART in HIV-positive patients with non-Hodgkin lymphoma (NHL). 1B We suggest starting ART in HIV-positive patients with cervical cancer. 1C We recommend starting ART in HIV-positive patients who are commencing radiotherapy or chemotherapy for cervical cancer. 1D 8.3.2 We suggest starting ART in HIV-positive patients with non-AIDS-defining malignancies (NADMs). 2C We recommend starting ART in HIV-positive Ku-0059436 ic50 patients who are commencing immunosuppressive radiotherapy or chemotherapy for NADMs. 1C 8.3.3 We recommend that potential pharmacokinetic interactions between ARVs and systemic anticancer therapy be checked before administration (with tools such as: http://www.hiv-druginteractions.org). GPP We suggest avoiding ritonavir-boosted ART in HIV-positive PI3K Inhibitor Library mouse patients who are to receive cytotoxic chemotherapy agents that are metabolized by the cytochrome P450 (CYP450) enzyme system. 2C We recommend against the use of ATV in HIV-positive patients who are to receive irinotecan. 1C We suggest avoiding ARV agents in HIV-positive patients who are to receive cytotoxic chemotherapy agents that have overlapping toxicities. 2C 8.4.2 We recommend patients with symptomatic HIV-associated NC disorders start ART irrespective
of CD4 lymphocyte count. 1C 8.4.3 We recommend patients with HIV-associated NC disorders start standard combination ART regimens. 1C 8.4.4 In patients with ongoing or worsening NC impairment despite ART we
recommend the following best practice management: GPP • Reassessment for confounding conditions. • Assessment of cerebrospinal fluid (CSF) HIV RNA, CSF HIV genotropism and genotyping of CSF HIV RNA. • In subjects with detectable CSF HIV RNA, modifications Etofibrate to ART should be based on plasma and CSF genotypic and genotropism results. 8.5.1 We recommend patients with HIVAN start ART immediately irrespective of CD4 cell count. 1C We recommend patients with end-stage kidney disease who are suitable candidates for renal transplantation start ART irrespective of CD4 cell count. 1C 8.5.2 We recommend against the use of ARV drugs that are potentially nephrotoxic, in patients with stages 3–5 chronic kidney disease (CKD) if acceptable alternative ARV agents are available. GPP We recommend dose adjustment of renally cleared ARV drugs in patients with reduced renal function. GPP 8.6.4 We suggest avoiding: ABC, FPV/r and LPV/r in patients with a high cardiovascular disease (CVD) risk, if acceptable alternative ARV drugs are available. 2C 8.7.2 We recommend therapy-naïve HIV-positive women who are not pregnant start ART according to the same indicators as in men (see Section 4: When to Start) 1A 8.7.