HIV viral load testing in the era of ART. Christian Noah Labor Lademannbogen, Hamburg

Similar documents
Tools to Monitor HIV Infection in 2013 and Beyond.

Professor Anna Maria Geretti

Innovative diagnostics for HIV, HBV and HCV

Introduction. Abstract. Key words. Diego Ripamonti 1, Andrew Hill 2, Erkki Lauthouwers 3, Yvon van Delft 4 and Christiane Moecklinghoff 5 1

It takes more than just a single target

Low-Level Viremia in HIV

QUANTITATIVE HIV RNA (VIRAL LOAD)

Management of patients with antiretroviral treatment failure: guidelines comparison

Persistent low-level HIV-1 RNA between 20 and 50 copies/ml in antiretroviral-treated patients: associated factors and virological outcome

Resistance Analyses of Integrase Strand Transfer Inhibitors within Phase 3 Clinical Trials of Treatment-Naive Patients

QUANTITATIVE HIV RNA (VIRAL LOAD)

Professor Jonathan Weber

Determinants of residual viraemia during combination HIV treatment: Impacts of baseline HIV RNA levels and treatment choice

2 nd Line Treatment and Resistance. Dr Rohit Talwani & Dr Dave Riedel 12 th June 2012

Introduction: Table/Figure Descriptions:

Clinical Case. Prof.ssa Cristina Mussini

Rajesh T. Gandhi, M.D.

When to start: guidelines comparison

Središnja medicinska knjižnica

Virologic and Immunologic Monitoring

DNA Genotyping in HIV Infection

Antiretroviral Treatment Strategies: Clinical Case Presentation

The next generation of ART regimens

Technical Bulletin No. 161

BHIVA Workshop: When to Start. Dr Chloe Orkin Dr Laura Waters

Pediatric HIV Cure Research

HBV PUBLIC HEALTH IMPLICATIONS

Virological suppression and PIs. Diego Ripamonti Malattie Infettive - Bergamo

PAEDIATRIC HIV INFECTION. Dr Ashendri Pillay Paediatric Infectious Diseases Specialist

Somnuek Sungkanuparph, M.D.

IAS 2013 Towards an HIV Cure Symposium

2/10/2015. Switching from old regimens. HIV treatment revision: As simple as old versus new? What is an old regimen? What is an old regimen?

Didactic Series. CROI 2014 Update. March 27, 2014

Virological Tools and Monitoring in the DAA Era

Case # 1. Case #1 (cont d)

Resistance to Integrase Strand Transfer Inhibitors

Switching ARV Regimens: Managing Toxicity and Improving Tolerability; Switches & Class-Sparing Approaches

Micropathology Ltd. University of Warwick Science Park, Venture Centre, Sir William Lyons Road, Coventry CV4 7EZ

MDR HIV and Total Therapeutic Failure. Douglas G. Fish, MD Albany Medical College Albany, New York Cali, Colombia March 30, 2007

Management of ART Failure. EACS Advanced HIV Course 2015 Dr Nicky Mackie

New HIV Tests and Algorithm: A change we can believe in

Dr Marta Boffito Chelsea and Westminster Hospital, London

Updates to the HHS Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents Living with HIV Updated October 17, 2017

Evolving HIV Treatment Paradigms What we need to know

HIV-HBV coinfection: Issues with treatment in 2018

Immunologic Failure and Chronic Inflammation. Steven G. Deeks Professor of Medicine University of California, San Francisco

0% 0% 0% Parasite. 2. RNA-virus. RNA-virus

Virologic Outcomes of HIV-Infected Children Undergoing a Single-Class Drug Substitution from LPV/r- to EFV-Based cart: A retrospective cohort study.

ART Treatment. ART Treatment

HIV Basics: Clinical Tests and Guidelines

Roger Shapiro, MD, MPH Harvard TH Chan School of Public Health Botswana-Harvard Partnership May 2018

Report Back from CROI 2010

Qué aporta el laboratorio a la terapia del VHC en 2015?

Laboratory for Clinical and Biological Studies, University of Miami Miller School of Medicine, Miami, FL, USA.

Resistance Workshop. 3rd European HIV Drug

Tunisian recommendations on ART : process and results

Clinical skills building - HIV drug resistance

HIV Treatment Update. Awewura Kwara, MD, MPH&TM Associate Professor of Medicine and Infectious Diseases Brown University

HIV immunological and virological monitoring tools. Pascale Ondoa 5th INTEREST workshop Dar es Salam Thursday 12th, 2011

Effect of 24 Week Intensification with a CCR5-Antagonist on the Decay of the HIV-1 Latent Reservoir

Anumber of clinical trials have demonstrated

VIKING STUDIES Efficacy and safety of dolutegravir in treatment-experienced subjects

Crafting an ART Regimen for Initiation or Salvage: Are NRTI s Necessary?

Quantification of HBV, HCV genotype and HIV subtype panels

Reduced Drug Regimens

Pediatric HIV Update NORTHWEST AIDS EDUCATION AND TRAINING CENTER

ID Week 2016: HIV Update

Supervised Treatment Interruption (STI) in an Urban HIV Clinical Practice: A Prospective Analysis.

GESIDA 2018 ANTIRETROVIRAL TREATMENT MAINTENANCE STRATEGIES AND BLOOD TELOMERE LENGTH CHANGE

HIV replication and selection of resistance: basic principles

Sysmex Educational Enhancement and Development No

Hepatitis B Case Studies

Analysis of HIV-1 Resistance Mutations from various Compartments of the Peripheral Blood in Patients with Low-Level Viremia

Definitions of antiretroviral treatment failure for measuring quality outcomes

HIV AND LUNG HEALTH. Stephen Aston Infectious Diseases SpR Royal Liverpool University Hospital

What is the Virologic Support for Two-Drug Regimens?

Supplemental Digital Content 1. Combination antiretroviral therapy regimens utilized in each study

PROVIDING EXCELLENT PRIMARY CARE FOR PATIENTS LIVING WITH HIV

Update on HIV Drug Resistance. Daniel R. Kuritzkes, MD Division of Infectious Diseases Brigham and Women s Hospital Harvard Medical School

Antiretroviral Therapy During Pregnancy and Delivery: 2015 Update

REASONS FOR DISCONTINUATION OF DUAL THERAPY WITH DOLUTEGRAVIR AND RILPIVIRINE

Diagnostic Methods of HBV and HDV infections

Scaling Up Routine Viral Load in Resource Limited Settings. MSF experience in Zimbabwe

Clinical Management of Resistance. AMJ Wensing, MD, PhD

Interpreting quantitative HBV, HCV and HIV-1 nucleic acid testing

Can HIV be cured? (how about long term Drug free remission?)

AIDS Research and Therapy. Open Access RESEARCH

Time taken to reach undetectable viral loads in therapy-naïve HIV patients commencing ART

CROI 2017 Review: Novel ART Strategies

Treatment of HIV-1 in Adults and Adolescents: Part 2

First line ART Rilpirivine A New NNRTI. Chris Jack Physician, Durdoc Centre ethekwini

Treatment strategies for the developing world

OPPORTUNISTIC INFECTIONS. Institute of Infectious Diseases, Pune India

Dr Melanie Rosenvinge

Genotypic Resistance Testing in Routine Care in South Africa:

Changes in cellular HIV DNA levels during the MONET trial: 144 Weeks of darunavir/ritonavir monotherapy versus DRV/r + 2NRTIs

Evaluating an enhanced adherence intervention among HIV positive adolescents failing 2 nd line treatment

Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents

ITREMA is a collaborative project between several universities in The Netherlands and South Africa and Ndlovu Care Group.

Early Antiretroviral Therapy in Newborns: Opportunities and Challenges. Ellen Gould Chadwick MD Northwestern University Feinberg School of Medicine

Transcription:

HIV viral load testing in the era of ART Christian Noah Labor Lademannbogen, Hamburg 1

Life expectancy of patients on ART Data from the UK Collaborative HIV Cohort (UK CHIC) Requirements: Early diagnosis Timely initiation of ART Adherence Periodic monitoring Successfully treated HIV patients have the chance of a normal life expectancy May et al. (2014), AIDS, 28, 1193-1202 2

HIV monitoring CD4 cell count Lymphocyte differentiation Marker of overall immune function Predictor of disease progession Urgency to initiate ART Indication for prophylaxis against opportunistic infection Viral load PCR Marker of treatment success and adherence Monitoring of the efficacy of ART Detection of virologic failure Selection of antivirals Substances/combinations not recommended >100000 copies/ml: Rilpivirin Abacavir/Lamivudine + Efavirenz or Atazanavir/r Darunavir/r+Raltegravir Risk of transmission 3

Monitoring intervals DAIG/DÖAG 2015 EACS 2015 Viral load pre ART: 2-3 months at ART initiation/switch: more frequent if suppressed: 2-4 months 3-6 months at ART initiation/switch: more frequent CD4 cells same as viral load 3-6 months every 12 months if stable on ART CD4 >350; VL <LOD IAS 2014 at least every 3 months 4 weeks after ART initiation at least every 3 months at least every 6 months if stable on ART CD4 >350; VL <LOD >1 year optional if stable on ART CD4 >500; VL <LOD >2 years DHHS 2016 every 3-4 months 2-8 weeks after ART start/switch every 6 months (adherence, immunologically stable, <LOD >2 years) every 3-6 months first 2 years on ART, CD4 <300, viremia every 12 months after 2 years on ART, VL <LOD, CD4 >300 optional CD4 >500 4

Monitoring intervals DAIG/DÖAG 2015 EACS 2015 IAS 2014 DHHS 2016 Viral load pre ART: 2-3 months at ART initiation/switch: more frequent if suppressed: 2-4 months every 3 months 3-6 months at ART initiation/switch: more frequent baseline before ART every 1-2 months after at least every 3 months 4 ART weeks initiation after ART until initiation suppression consider lower frequency (every 6 months) if <LOD >2 years every 3-4 months 2-8 weeks >350 after CD4 ART cells start/switch every adherence 6 months (adherence, immunologically stable, <LOD >2 years) CD4 cells same as viral load 3-6 months every 12 months if stable on ART CD4 >350; VL <LOD at least every 3 months at least every 6 months if stable on ART CD4 >350; VL <LOD >1 year optional if stable on ART CD4 >500; VL <LOD >2 years every 3-6 months first 2 years on ART, CD4 <300, viremia every 12 months after 2 years on ART, VL <LOD, CD4 >300 optional CD4 >500 5

Future role of CD4 cell count in HIV monitoring Metaanalysis (13 studies) 20000 virologically suppressed patients Proportion of an unexplained, confirmed CD4 decline: 0,4 % (95 % CI 0,2-0,6) No adverse events among patients experiencing CD4 declines Ford et al. 2015; JIAS 18:20061 6

Definition of treatment response Viral load [copies/ml] Limit of detection (LOD) 0 1 2 3 4 5 6 Months after ART initiation 7

Definition of treatment response Cobas Amplicor (Roche Diagnostics) defined by a technical cutoff: 50 copies/ml 8

Limits of detection: the Roche history Cobas Amplicor Cobas Ampliprep/Taqman Cobas 6800 400 (1995) ultrasensitive 50 (1998) Version 1 40 (2005) Version 2 20 (2009) 20 copies/ml (2015) 9

Platforms for viral load measurement Roche COBAS Ampliprep/Taqman Siemens VERSANT kpcr Molecular System Abbott m2000rt Real Time PCR System 20 Kopien/ml Roche Cobas 6800 37 Kopien/ml Qiagen QIAsymphony RGQ 40 Kopien/ml 20 Kopien/ml 34 Kopien/ml 10

Definition of optimal treatment response Viral load [copies/ml] DAIG/DÖAG 2015 EACS 2015 <50 after 3-4 months after 6 months if viral load was high at baseline <50 after 6 months Limit of detection (LOD) IAS 2014 <LOD (<20-75) after 6 months 0 1 2 3 4 5 6 Months after ART initiation DHHS 2016 <LOD (<20-75) after 6 months 11

Treatment failure? Viral load [copies/ml] 99 0 1 2 3 4 5 6 Months after ART initiation 12

Treatment failure? No, just a blip... Viral load [copies/ml] Blip = transient viremia 0 1 2 3 4 5 6 Months after ART initiation 13

Biological causes of blips Infections Vaccination Syphilis: 27,6 % viremic during active infection Palacios R (2007), J Acquir Immune Defic Syndr 44(3), 356-359. Tuberculosis: 5-160 fold increase of viral load during active infection Goletti D (1996), J Immunol 157(3), 1271-1278 Influenza: 20,6 % viremic 2-4 weeks after vaccination Kolber MA (2002), AIDS 16(4), 537-542. Tetanus 100 % viremic after vaccination Stanley SK (1996) N Engl J Med 334(19), 1222-1230. Pneumococi Vigano A (1998), AIDS Res Human Retroviruses 14(9), 727-734. 14

Technical causes of blips 1. Pre-analytical errors proviral DNA avoid hemolysis Plasma should be separated from cells within 24 h after blood withdrawal 2. Assay variation 15

Definition of the limit of detection (LOD) Viral load detected with a probability of 95 % Example: COBAS AmpliPrep/COBAS Taqman HIV-1-Test, v. 2,0 LOD 20 copies/ml Concentration [copies/ml] Replicates Positive Detection (WHO standard) rate [%] 60 40 30 20 15 10 5 0 126 186 126 126 59 126 125 126 126 185 125 124 53 108 66 0 100 99 99 98 90 86 53 0 PROBIT 95 % analysis: 16,5 copies/ml 95 %.confidence interval: 14,3-19,8 16

Target not detected negative 130 patients 3TC/d4T + LPV/r ornfv mit 3TC und d4t als Backbone <50 copies/ml within 24 weeks <50 copies/ml after 60 weeks After 2 years: No significant drop of the viral load After 60 weeks: 83 % of the patients viremic Single Copy PCR LOD 1 copy/ml After 7 years: 77 % of the patients viremic Median 3,34 copies/ml After treatment intensification (Raltegravir): No significant drop of the viral load Median 3,1 copies/ml Maldarelli F et al. (2007), PLoS Pathogens, 3(4), 46 Palmer S et al. (2008) PNAS, 105 (10), 3879 Gandhi RT et al. (2010). PLoS Medicine 7(8), e1000321 17

Precision of viral load assays (Roche) 15 runs 3 lots 3 replicates Viral load log10/ml Charge 1 Total SD (log) Charge 2 Total SD (log) Charge 3 Total SD (log) Charge 1-3 Total -SD (log) Total VC der Log- Normalverteilung (%) 2 3 4 5 6 7 0,19 0,07 0,07 0,04 0,10 0,11 0,16 0,09 0,07 0,05 0,09 0,12 0,17 0,07 0,06 0,07 0,10 0,14 0,17 0,08 0,07 0,06 0,10 0,13 41 20 16 15 25 33 Example: Viral load 10 2 /ml = 100 copies/ml 10 2,17 /ml = 148 copies/ml 10 1,83 /ml = 68 copies/ml 18

Precision of viral load assays (Siemens) 19

Precision of viral load assays (Abbott) 20

Comparison of viral load assays Results from over 4000 paired plasma samples Roche Taqman Version 1+2 Roche Amplicor Abbott RealTime J Clin Microbiol (2014). 52(2), 517-523 Overall good correlation (0,90-0,97) Low level viremia <200: 0,45-0,85 21

Assay variation Residual viremia <LOD Ability of commercial assays to detect HIV RNA <LOD Inaccurate quantification at low levels Overquantification of residual viremia = Blip 22

Treatment failure? Viral load [copies/ml] 99 0 1 2 3 4 5 6 Months after ART initiation 23

Treatment failure? Maybe yes, maybe no... Viral load [copies/ml] Resistance development persistent viremia low-level very-low-level high-level 0 1 2 3 4 5 6 Months after ART initiation 24

Risk factors for persistent viremia ADHERENCE Interactions Pharmacogenomics Stage of infection high baseline VL low CD4 cell count CDC state Very low level viremia overall conflicting data most cases multifactorial no one factor is determinative Regimen PI>NNRTI Duration of suppression <50 Ryscavage R. et al. (2014), AAC, 58(7), 3585-3598 25

How to manage viremia? Which viral load is predictive for treatment failure? Viral load level Persistence 26

Significance of persistent low-level viremia Data from 18 cohorts including 17902 patients No LLV 93,8 % LLV 50-199 3,5 % LLV 200-499 2,7 % Virologic failure (VL 500 copies/ml): 1903 patients (10.6 %) No LLV 1745 (10,4%) LLV 50-19949 (7,9 %) LLV 200-499 109 (22,6 %) 91,7 % of patients with VF without any previous LLV LLV 200-499 strongly associated with VF (adjusted HR 3,97) LLV 50-199 weakly associated with VF No association with VF: type of regimen duration of LLV Vandenhende 2015, CROI, Poster 1014 27

Significance of low-level viremia (LLV) LLV is common: blips: 70-82 % persistent LLV: 18-24 % high level viremia: 6-9 % Persistent LLV associated with an increased risk of resistance 19 % resistance mutations at first LLV (50-1000) Risk correlated with viral load level Median VL in patients evolving resistance: 472 copies/ml vs. 369 copies/ml in patients not evolving resistance (p=0,067) Ryscavage R. et al. (2014), AAC, 58(7), 3585-3598 28

Definition of treatment failure DAIG/DÖAG 2015 EACS 2015 IAS 2014 Detectable viral load >50 copies/ml (confirmed) Drop of <2 log10 after 4 weeks Detectable viral load 6 months after ART start Detectable viral load >50 copies/ml (confirmed) Depending on assay limit could be higher or lower Detectable viral load 6 months after ART start Detectable viral load >50 copies/ml (confirmed) Detectable viral load >200 copies/ml DHHS 2016 Detectable viral load >200 copies/ml (confirmed) 29

Management of viremia Confirmation Assessment of factors leading to suboptimal response Adherence (TDM?) Interactions (TDM?) Infections Vaccinations Pre-analytic issues (incl. sample confusion)... 30

Management of viremia VL 50-500 (=low-level viremia) Confirmation within 4 weeks VL <50 (=very low-level viremia): No clinical relevance Regular follow-up 3 months later VL >500: Virologic failure Resistance test Switch regimen as soon as possible No resistance mutations: assess adherence (again?) a) Not confirmed: Blip No clinical relevance Regimen with low genetic resistance barrier: consider shorter follow-up interval b) Confirmed: 50-200 Weak association with virologic failure Regular Follow-up 3 months later Consider resistance test (optional) 200-500 Predictive for virologic failure Resistance test Switch of regimen No resistance mutations: assess adherence (again?) 31

32