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Resistance in the age of Integrases
Case presentation
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Patient JJ 53yo MSM DSP since diagnosis of HIV and subsequent health issues Diagnosed HIV+ve 5/2002 on presentation with PJP SVH Sydney CD4 Nadir at diagnosis 20 4%, VL /2002 Cigs: 30/day for years, now ex smoker ETOH : Nil Normotensive Substances : nil Not sexually active for years due to ill health Social: Cares for long term chaotic ex partner who has significant crystal addiction and subsequent mental health issues. Also HIV +ve Lives on the Gold Coast but wishes to continue HIV care in Brisbane Returned to Brisbane in September from Sydney
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Past Medical History 2-6/2018 – AIN 1 4/2018 – Moderate OSA
3/2017 – BMI 34 – secondary to inactivity, ill health, steroids post transplant 2015 – Revaccinations post transplant 2014 onwards – monthly IVIG infusions 07/07/2014 – AML : Bone Marrow stem cell transplant Sydney CMV reactivation during treatment 09/04/ AML- Chemotherapy remission 12/2013, relapse 04/2014 19/07/ Lumbar back pain - Large disc protrusion L4/5- chronic LBP 13/10/ Hypertriglyceridaemia 2007 – Hypogonadism – testosterone nadir Declines testosterone 2010 – GORD – persisting on endoscopy 2017 2010 – Severe COPD Chronic diarrhoea - colonoscopy surveillance – polyps 2008 – Persistent pulmonary nodules. CT surveillance thought to be benign granulomas – Anal SCC –chemotherapy, radiotherapy. Colostomy during therapy then reversed. Follow up normal until AIN in 2017 HIV infection
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Sulfonamide antibiotics Vancomycin Gentamycin Bactrim Medications
Allergy History Sulfonamide antibiotics Vancomycin Gentamycin Bactrim Medications Panadol Osteo 665 mg Modified release tablets [96 x2] Pantoprazole Tablets 20 mg Tablets [30] Onbrez Breezhaler Powder for inhalation 150 mcg Powder for inhalation [30] – LABA HLAB5701 – no record HIV CORECEPTOR TROPISM GENOTYPE Specimen Type: Plasma X4 Viruses: Detected Use of CCR5 antagonists not indicated
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Antiretroviral History
Abacavir/Lamivudine/Zidovudine- Trizivir Trizivir + Nevirapine /2010 Abacavir/Lamivudine + Nevirapine AZT ceased during chemotherapy for Anal SCC Nevirapine then ceased due to potential for induced metabolism of exogenous testosterone for hypogonadism Raltegravir, Abacavir/Lamivudine (variable adherence and viral escape 2015 due to medical conditions and social circumstances) 2/ /2016 Etravirine, Darunavir/r, Dolutegravir, Truvada based on GRA 10/2017-2/2018 Darunavir/r, TAF/FTC, Etravirine (initially minimal nausea but then recurred. Has ceased all meds again due to side effects) Suppressed VL and improving CD until AML relapse Adherence generally good ( Viral escape once in 2011 related to poor adherence) Supressed virus 3/ /2016 but significant nausea, vomiting so self ceased 12/16
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HIV Monitoring 26/07/2018 CD4: 230 (10%) VL:12325
02/04/2018: CD4: 340 (16%) CD8: 1400 (65%) VL: 1758 5/2/ VL: <40 08/01/2018: CD4: 350 (14%) CD8: 1650 (64%) VL: <40 16/10/2017 CD4: 350 (10%) CD8: 2370 (70%) VL: 28007 22/09/2017 CD4: 390 (13%) CD8: 2150 (71%) VL: 38000 18/09/ CD4: 480 (16%) CD8: 1950 (66%) VL: 5040 21/08/2017 CD4: 490 (15%) CD8: 2250 (67%) VL <40 26/06/ CD4: 480 (16%) CD8: 2090 (69%) VL: <40 29/05/ CD4: 440 (16%) CD8: 1870 (70%) VL: <40 03/04/ Cd4: 470 (11%) CD8: 3170 (75%) VL: 66890 06/03/ Cd4: 350 (15%) Cd8: 1600 (69%) VL: 33978 12/12/ CD4: 450 (18%) CD8: 1760 (68%) 14/11/ Cd4: 500 (16%) CD8: 2060 (67%) VL: <40 17/10/ CD4: 490 (18%) CD8: 1830 (67%) VL: <40 19/09/ CD4: 400 (13%) CD8: 2300 (73%) VL: <40 23/08/ CD4: 500 (14%) CD8: 2700 (75%) VL: ND 30/05/ CD4: 360 (13%) CD8: 2070 (73%) VL: <40 11/04/ CD4: 350 (13%) CD8: 1930 (74%) VL: <40 14/03/ CD4: 310 (12%) CD8: 1940 (76%) VL: 57 15/02/ VL: 19592 18/01/ CD4: 360 (12%) CD8: 2310 (76%) VL: 39770 21/12/ CD4: 400 (12%) CD8: 2590 (75%) VL: 12561 23/11/ CD4: 430 (13%) CD8: 2520 (74%) VL: 2145 04/11/ CD4: 350 (11%) CD8: 610 (78%) VL: 53000
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HIV GENOTYPE RESISTANCE 4/12/15 Stanford HIV subtype: D (PR 94
HIV GENOTYPE RESISTANCE 4/12/15 Stanford HIV subtype: D (PR 94.9%) B (RT 96.2%): SUBTYPE B HIV Viral Load .....: copies/mL Protease Inhibitor Resistance Mutations: PI Major Resistance Mutations PI Minor Resistance Mutations L10I Other Mutations I15V E35D M36I R41K L63T I93L Protease Inhibitors ...: ATV/r Susceptible DRV/r Susceptible FPV/r Susceptible IDV/r Susceptible LPV/r Susceptible NFV/r Susceptible SQV Susceptible TPV/r Susceptible Reverse Transcriptase Resistance Mutations: NRTI Resistance Mutations M184MV NNRTI Resistance Mutations Other Mutations V21I V60I K122E T128IT I142V G196E E203D R211K NRTIs NNRTIs 3TC High-Level Resistance RPV Susceptible ABC Low-Level Resistance EFV Susceptible AZT Susceptible NVP Susceptible D4T Susceptible ETR Susceptible DDI Potential Low-Level Resistance FTC High-Level Resistance TDF Susceptible Comments "RTPOS184VI NRTI": M184V/I cause high-level resistance to 3TC and FTC and low-level resistance to DDI and ABC. However, M184V/I are not contraindications to continued treatment with 3TC or FTC because they increase susceptibility to AZT, TDF and D4T and are associated with clinically significant reductions in HIV-1 replication. In combination with K101E or E138K, M184I synergistically reduces RPV susceptibility. "PRPOS10IV PIMinor": L10I/V are polymorphic, PI-selected accessory mutations that reduce PI susceptibility of increase the replication of viruses with other PI-resistance mutations.
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HIV INTEGRASE RESISTANCE 4/12/15 Stanford HIV Subtype: B (IN 95
HIV INTEGRASE RESISTANCE 4/12/15 Stanford HIV Subtype: B (IN 95.1%) HIV Viral Load......: copies/mL Integrase Inhibitor Resistance Mutations: Integrase Major Resistance Mutations N155H Integrase Accessory Mutations T97A Other Mutations E11D A21T V31I C40CY D41N K71R A91T S119R T125A V201I I208L S230N L234I D256E R284G Integrase Inhibitors Dolutegravir..: Low-Level Resistance Elvitegravir..: High-Level Resistance Raltegravir ..: High-Level Resistance Comments: "INPOS155H Major": N155H is a nonpolymorphic mutation selected in patients receiving RAL and EVG. Alone, it reduces RAL susceptibility 15-fold and EVG susceptibility 30-fold. Susceptibility is further reduced when N155H occurs in combination with E92Q and other primary or accessory INI-reistance mutations. N155H has been selected by DTG in RAL-experienced patients but does not reduce DTG susceptibility by itself. "INPOS97A Accessory": T97A is a polymorphic accessory INI-resistance mutation that, depending on subtype, occurs in 1% to 5% of viruses from untreated persons. It is selected by RAL and EVG. Alone, it has minimal effect on any INI susceptibility but in combination with Y143C/R it markedly reduces RAL susceptibility. "INPOS230N None": S230N is a polymophism that is not associated with reduced INI susceptibility. HIV CORECEPTOR TROPISM GENOTYPE Specimen Type: Plasma X4 Viruses: Detected
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4/11/11
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HIV INTEGRASE RESISTANCE 27/10/17
Stanford HIV subtype: B (3.86) HIV Viral load......: copies/mL Protease Inhibitor Resistance Mutations: PI Major Resistance Mutations PI Minor Resistance Mutations: Other Mutations L10I I15V E35D M36I R41K L63T I93L Protease Inhibitors....: ATV/r Susceptible DRV/r Susceptible FPV/r Susceptible IDV/r Susceptible LPV/r Susceptible NFV/r Susceptible SQV/r Susceptible TPV/r Susceptible Reverse Transcriptase Resistance Mutations: NRTI Resistance Mutations NNRTI Resistance Mutations Other Mutations V21I V60I K122E I142V G196E E203D R211K NRTIs NNRTIs 3TC Susceptible RPV Susceptible ABC Susceptible EFV Susceptible AZT Susceptible NVP Susceptible D4T Susceptible ETR Susceptible DDI Susceptible FTC Susceptible TDF Susceptible Comments: PRPOS10IV Other: L10I/V are polymorphic, PI-selected accessory mutations that increase the replication of viruses with other PI-resistance mutations.
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Integrase Inhibitors Dolutegravir. : Susceptible Elvitegravir
Integrase Inhibitors Dolutegravir..: Susceptible Elvitegravir..: Potential Low-Level Resistance Raltegravir...: Potential Low-Level Resistance Comments: INPOS97A Accessory: T97A is a polymorphic accessory mutation that, depending on subtype, occurs in 1% to 5% of viruses from untreated persons. It is selected by RAL and EVG. Alone, it has minimal effects on INI susceptibility but in combination with other primary resistance mutations, particularly Y143C/R, it synergistically reduces susceptibility to EVG and RAL. INPOS230N Other: S230N is a polymorphism that is not associated with reduced INI susceptibility.
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Options Aim for viral suppression Limit adverse events Which Integrase
Which PI Which NNRTI/NRTI Biktarvy + Prezcobix + Rilpivirine Dolutegravir bd + Descovy + Prezcobix + Rilpivirine
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