STRATEGIE THERAPEUTIQUE JL Meynard Hôpital Saint-Antoine 75012 PARIS.

Slides:



Advertisements
Similar presentations
Monica Gandhi MD, MPH Associate Professor and Women’s HIV Clinic provider, HIV/AIDS Division San Francisco General Hospital/ UCSF Safe Poz Love, U.S. Positive.
Advertisements

1 The START Trial: On the Shoulders of SMART 5 years after SMART INSIGHT Satellite Session WAC, Washington DC, July 2012.
Slide 1 of 11 From CB Hicks, MD, at Chicago, IL: May 20, 2013, IAS-USA. IAS–USA Charles B. Hicks, MD Professor of Medicine Duke University Medical Center.
Comparison of INSTI vs PI  FLAMINGO  GS  ACTG A5257.
N ORTHWEST AIDS E DUCATION AND T RAINING C ENTER CROI 2015: What’s New in Hepatitis? Nina Kim, MD Associate Professor of Medicine Division of Allergy &
HIV Early Treatment Project Groups 1 and 2 n Among HIV-infected participants in sub-Saharan Africa, does initiation of antiretroviral treatment (ART) at.
N ORTHWEST A IDS E DUCATION AND T RAINING C ENTER HIV and Non Hodgkin Lymphoma Virginia C. Broudy, MD September 25, 2014 Presentation prepared by: Presenter.
VBWG IDEAL: The Incremental Decrease in End Points Through Aggressive Lipid Lowering Study.
START study: UK-CAB July2015 Community feedback: START study Simon Collins HIV i-Base
Semuloparin for Thromboprophylaxis in Patients Receiving Chemotherapy for Cancer Agnelli G et al. N Engl J Med 2012;366(7): George D et al. Proc.
IAS–USA When to Start Antiretroviral Therapy Constance A. Benson, MD Professor of Medicine University of California San Diego FINAL: Presented.
Jorge A. Tavel, MD On behalf of the STALWART Protocol Team of the INSIGHT Network 5 th IAS Conference on HIV Pathogenesis, Treatment and Prevention
Copyright ©2011 Merck & Co., Inc., Whitehouse Station, New Jersey, USA, All Rights Reserved IAS 2011_ Abstract # WEPDB0102 Sustained Efficacy and Tolerability.
Nguyen ML, Sumbry A, Reddy D, Harvey K, Gunthel C, Wang W, Tsui C, Ziemer D, del Rio C, Young JL Increased Incidence of Non AIDS-related Malignancies and.
HIV and serious non-AIDS conditions Five Years after the SMART Study, a Paradigm Shifting Trial INSIGHT Symposium XIX International AIDS Conference Washington.
HIV i-Base: SMART Study & CROI Feedback UK-CAB - Feb 2006 UK-CAB 24 February 2006 CROI Feedback: SMART Study Simon Collins.
Introductory talk D Costagliola.
Enrollment and Outcomes Fan Fan Hou, et al. N Engl J Med 2006;354:
Switching ARVs in Virologically Suppressed Patients.
Maintenance therapy with Trizivir® after 6 months induction with Trizivir® plus either efavirenz or lopinavir/r in naïve patients. Trizefal study J. Mallolas*
Arthritis Advisory Committee March 4, 2003 Update on the Safety of TNF Blockers Li-ching Liang, M.D. FDA / CBER/ OTRR Arthritis Advisory Committee March.
Head-to-Head Comparison of Obinutuzumab (GA101) plus Chlorambucil (Clb) versus Rituximab plus Clb in Patients with Chronic Lymphocytic Leukemia (CLL) and.
Clinical development programme for Second-Line treatment Anton Pozniak World AIDS Conference, July 2014.
Joel E. Gallant, MD, MPH Medical Director, Specialty Services Southwest CARE Center Santa Fe, New Mexico State-of-the-ART in Antiretroviral Management.
Time to Secondary Resistance (TSR) After Interruption of Imatinib: Updated Results of the Prospective French Sarcoma Group Randomized Phase III Trial on.
Strategies for Management of Antiretroviral Therapy Study Wafaa El-Sadr and James Neaton for the SMART Study Team.
Lenalidomide Maintenance After Stem-Cell Transplantation for Multiple Myeloma: Follow-Up Analysis of the IFM Trial Attal M et al. Proc ASH 2013;Abstract.
FRENCH high-resolution studies - Breast cancer: 1990, 1997, 2003, 2010 ? - Colorectal cancer: 1990, 1995, 2000, 2005, 2010 ? - Prostate cancer: 1995,
Mok TS, Wu SL, Thongprasert S, et al. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma. N Engl J Med. 2009;361: Gefitinib Superior.
July 19-22, 2015 Vancouver, Canada Highlights of IAS 2015 CCO Official Conference Coverage of the 8th IAS Conference on HIV Pathogenesis, Treatment, and.
May 29 - June 2, 2015 Borealis-1: Apatorsen + Gemcitabine/Cisplatin for Pts With Advanced Bladder Cancer CCO Independent Conference Highlights of the 2015.
Slideset on: Patel P, Hanson DL, Sullivan PS, et al. Incidence of types of cancer among HIV-infected persons compared with the general population in the.
Nuovi paradigmi della HAART Antonella Castagna IRCCS San Raffaele Nuove associazioni terapeutiche in HIV, tra efficacia e sostenibilita Catania, 9 novembre.
HAART Initiation Within 2 Weeks of Seroconversion Associated With Virologic and Immunologic Benefits Slideset on: Hecht FM, Wang L, Collier A, et al. A.
Initiation of Antiretroviral Therapy in Early Asymptomatic HIV Infection The INSIGHT START Study Group Ben Andres Oct 15, 2015.
Efavirenz Use Not Associated With Depressive Episodes, According to Analysis of Randomized Clinical Trial Outcomes Slideset on: Journot V, Chene G, De.
Dr. William P. Howlett Matthew P. Rubach, MD Dr. Neema W. Minja Department of Internal Medicine, KCMC KCMC/Duke Collaboration HIV in Tanzania: Current.
Changes in Cancer Mortality among HIV-Infected Patients : The Mortalité 2005 Survey Fabrice Bonnet, Christine Burty, Charlotte Lewden, Dominique Costagliola,
Problems of HIV Infection in the HAART Era Akihiko Suganuma M.D. Tokyo Metropolitan Komagome Hospital Department of Infectious Diseases.
Slideset on: Gathe J, da Silva BA, Cohen DE, et al. A once-daily lopinavir/ritonavir-based regimen is noninferior to twice-daily dosing and results in.
Diego Ripamonti - Malattie Infettive - Bergamo Simposio HOT TOPICS Hot topics in HIV 2015.
Slideset on: Emery S, Neuhaus JA, Phillips AN, et al. Major clinical outcomes in antiretroviral therapy (ART)-naive participants and in those not receiving.
ACTG 5142: First-line Antiretroviral Therapy With Efavirenz Plus NRTIs Has Greater Antiretroviral Activity Than Lopinavir/Ritonavir Plus NRTIs Slideset.
First-Line Treatment of HIV Infection With Either NNRTI- or PI-Based Regimens Effective for Long-term Disease Control Slideset on: MacArthur RD, Novak.
Increased risk of suicidal behaviour with use of efavirenz: Results from the START Trial Alejandro Arenas-Pinto, Birgit Grund, Shweta Sharma, Esteban Martinez,
Who Benefited Most From Immediate Treatment in START A Subgroup Analysis JM Molina, B Grund, F Gordin, I Williams, M Schechter, M Losso, M Law, E Ekong,
Phase 3 Treatment-Naïve and Treatment-Experienced
Novel Antiretroviral Studies and Strategies
Comparison of INSTI vs INSTI
COMPLICATIONS INFECTIONS OPPORTUNISTES
Dolutegravir plus Rilpivirine as Maintenance Dual Therapy SWORD-1 and SWORD- 2: Design
Presented at the American Diabetes Association
ELOQUENT-2: Elotuzumab + Len/Dex in R/R MM
Imperative of Test and Treat
ASPEN: Prolonged PFS With Sunitinib vs Everolimus in Nonclear-Cell RCC CCO Independent Conference Highlights of the 2015 ASCO Annual Meeting* May 29 -
1.
Higher rate of antiretroviral therapy reinitiation among HIV-HBV coinfected patients in the episodic arm of the SMART study Dore G.1, Soriano V.2, Neuhaus.
Slide set on: McCarthy PL, Owzar K, Hofmeister CC, et al
SOCRATES Trial design: Patients with acute ischemic stroke were randomized in a 1:1 fashion to receive either ticagrelor 180 mg load + 90 mg BID or aspirin.
ESPAC-4: Adjuvant Gemcitabine/ Capecitabine Improves 5-Yr Survival vs Gemcitabine Alone in Resected Pancreatic Ductal Carcinoma CCO Independent Conference.
Intensification with INSTI
Presented by: Daniel Poe Sana Safeer March 24, 2016
Adult Guidelines Pretoria, Saturday 17th February 2018
When to START During an OI
HOPE-3 Trial design: Patients without known cardiovascular disease, and with an intermediate risk of cardiovascular events, were randomized in a 2 x 2.
Comparison of INSTI vs INSTI
Intensification with INSTI
Switch to DTG-containing regimen
A prospective, randomized, Phase III trial of NRTI-, PI-, and NNRTI-sparing regimens for initial treatment of HIV-1 infection – ACTG 5142 Riddler S.A.,
Dolutegravir in PEPFAR
Presentation transcript:

STRATEGIE THERAPEUTIQUE JL Meynard Hôpital Saint-Antoine PARIS

clinicaloptions.com/hiv Highlights of IAS 2015 START: Immediate vs Deferred Therapy for Asymptomatic, ART-Naive Pts  International, randomized trial  Composite primary endpoint: any serious AIDS-related (AIDS-related death or AIDS- defining event) or non-AIDS–related event (non-AIDS–related death, CVD, end-stage renal disease, decompensated liver disease, non-AIDS–defining cancer)  Mean follow-up: 3 yrs; median baseline CD4+ cell count: 651 cells/mm 3 ; median baseline HIV-1 RNA: 12,759 copies/mL  Median CD4+ cell count at initiation of ART for deferred group: 408 cells/mm 3 Immediate ART ART initiated immediately following randomization (n = 2326) INSIGHT START Study Group. N Engl J Med. 2015;[Epub ahead of print]. Lundgren J, et al. IAS Abstract MOSY0302. Deferred ART Deferred until CD4+ cell count ≤ 350 cells/mm 3, AIDS, or event requiring ART (n = 2359) HIV-positive, ART-naive adults with CD4+ cell count > 500 cells/mm 3 (N = 4685) Study closed by DSMB following interim analysis

clinicaloptions.com/hiv Highlights of IAS 2015 START: 57% Reduced Risk of Serious Events or Death With Immediate ART  4.1% vs 1.8% in deferred vs immediate arms experienced serious AIDS or non-AIDS–related event or death (HR: 0.43; 95% CI: ; P <.001) Cumulative Percent With Event Mo Deferred ART Immediate ART INSIGHT START Group. N Engl J Med. 2015;[Epub ahead of print]. Lundgren J, et al. IAS Abstract MOSY0302. Reproduced with permission.

clinicaloptions.com/hiv Highlights of IAS 2015 START: Primary Endpoint Components With Immediate vs Deferred ART Endpoint Immediate ART (n = 2326) Deferred ART (n = 2359) HR (95% CI) P Value NRate/100 PYN Serious AIDS-related event ( ) <.001 Serious non-AIDS–related event ( ).04 All-cause death ( ).13 Tuberculosis ( ).008 Kaposi’s sarcoma ( ).02 Malignant lymphoma ( ).07 Non-AIDS–defining cancer ( ).09 CVD ( ).65 INSIGHT START Group. N Engl J Med. 2015;[Epub ahead of print]. Lundgren J, et al. IAS Abstract MOSY0302.

clinicaloptions.com/hiv Highlights of IAS 2015 START: Cancer Events With Immediate vs Deferred ART Cancer Event, n Immediate ART (n = 2326) Deferred ART (n = 2359) Total1439 Kaposi’s sarcoma111 Lymphoma, NHL + HL310 Prostate cancer23 Lung cancer22 Anal cancer12 Cervical or testis cancer 12 Other types*49 Time to Cancer Event Cumulative % With Event Mo *Immediate ART: squamous cell carcinoma, plasma cell myeloma, bladder cancer, fibrosarcoma. Deferred ART: gastric adenocarcinoma, breast cancer, ureteric cancer, malignant melanoma, myeloid leukemia, thyroid cancer, leiomyosarcoma, liver cancer, squamous cell carcinoma of head and neck. INSIGHT START Group. N Engl J Med. 2015;[Epub ahead of print]. Lundgren J, et al. IAS Abstract MOSY0302. Reproduced with permission. Deferred ART Immediate ART Rate/100 PY: immediate, 0.20; deferred, 0.56 (HR: 0.36; 95% CI: ; P =.001)

clinicaloptions.com/hiv Highlights of IAS 2015 START: Primary Endpoint Events by Latest CD4+ Cell Count Latest CD4+ count > 500 cells/mm 3 Immediate ART Deferred ART Primary events, % (n/N) 88 (37/42) 59 (57/96) Rate/100 PY Immediate ARTDeferred ART Percent of Follow-up Time Latest CD4+ Cell Count (cells/mm 3 ) (4.7) No. of Pts With Events (Rates/100 PY) 3 (0.8) 6 (0.4) 11 (0.6) 20 (0.6) 5 (1.8) 34 (2.0) 34 (1.5) 9 (0.6) 14 (1.1) < ≥ 800 < ≥ 800 INSIGHT START Group. N Engl J Med. 2015;[Epub ahead of print]. Lundgren J, et al. IAS Abstract MOSY0302. Reproduced with permission.

clinicaloptions.com/hiv Highlights of IAS 2015 TEMPRANO: Immediate or Deferred ART Initiation ± IPT for African Pts  Randomized, controlled, unblinded, multicenter (Ivory Coast), 2 x 2 factorial Pts with HIV infection and CD4+ cell count < 800 cells/mm 3 who did not meet WHO criteria for initiating ART* (N = 2056) Immediate ART † (n = 515) Immediate ART † + IPT ‡ (n = 518) Deferred ART § (n = 511) Deferred ART § + IPT ‡ (n = 512) *WHO criteria evolved during the study (updates 2006, 2010, 2013). † ART initiated immediately following randomization. ‡ IPT = 300 mg daily isoniazid initiated 1 mo after enrollment and terminated 7 mos after enrollment. § Deferred until meeting WHO criteria for initiating ART. TEMPRANO ANRS Study Group. N Engl J Med. 2015;[Epub ahead of print].  Pts in the treatment arms well matched at baseline –First-line ART primarily EFV + TDF/FTC (68% to 71%) or LPV/RTV + TDF/FTC (22% to 24%)  Median duration of follow-up: 29.9 mos

clinicaloptions.com/hiv Highlights of IAS 2015 TEMPRANO: Immediate vs Deferred ART Initiation and IPT Delivery for African Pts TEMPRANO ANRS Study Group. N Engl J Med. 2015;[Epub ahead of print]. Mos From Randomization Cumulative Probability of Death or Severe HIV-Related Illness (%) Deferred ART Deferred ART + IPT Immediate ART Immediate ART + IPT 30-Mo Probability, %

Conclusion Bénéfice clairement démontré d’une introduction précoce des antirétroviraux Bénéfice déjà démontré d’une réduction du risque de transmission du VIH sous tt ARV efficace Nécessité d’un dépistage précoce et d’un large accès aux ARV