Advances in the European Validation Study of the Oxford Classification of IgA Nephropathy (VALIGA)

Similar documents
Prof. Rosanna Coppo Director of the Nephrology, Dialysis and Transplantation Department Regina Margherita Hospital Turin, Italy. Slide 1.

IgA Nephropathy: Morphologic Findings Associated with Disease Progression and Therapeutic Response A Working Group Approach

The Oxford IgA nephropathy clinicopathological classification is valid for children as well as adults

Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults

Classification of Glomerular Diseases and Defining Individual Glomerular Lesions: Developing International Consensus

Nephrology Grand Rounds. Mansi Mehta November 24, 2015

Atypical IgA Nephropathy

Increased C4 and decreased C3 levels are associated with a poor prognosis in patients with immunoglobulin A nephropathy: a retrospective study

Article. The Use of the Oxford Classification of IgA Nephropathy to Predict Renal Survival

Dr. Ghadeer Mokhtar Consultant pathologists and nephropathologist, KAU

Journal of Nephropathology

MOLECULAR PREDICTORS OF OUTCOME Ondrej Viklicky, Prague, Czech Republic. Chair: Daniel Abramowicz, Brussels, Belgium Rosanna Coppo, Turin, Italy

Case Report Corticosteroids in Patients with IgA Nephropathy and Severe Chronic Renal Damage

Henöch Schönlein Purpura nephritis and management. Licia Peruzzi

Validation of the Oxford classification of IgA nephropathy in cohorts with different presentations and treatments

The CARI Guidelines Caring for Australasians with Renal Impairment. Specific management of IgA nephropathy: role of tonsillectomy GUIDELINES

Secondary IgA Nephropathy & HSP

1st ERA-EDTA CME course in Cyprus. Recent breakthroughs in immunonephrology and inherited kidney diseases with emphasis on hematurias

CHAPTER 2 PRIMARY GLOMERULONEPHRITIS

Prof. Armando Torres Nephrology Section Hospital Universitario de Canarias University of La Laguna Tenerife, Canary Islands, Spain.

IgA Nephropathy - «Maladie de Berger»

Random forest can accurately predict the development of end-stage renal disease in immunoglobulin a nephropathy patients

Prof. Franco Ferrario Nephropathology Unit Department of Pathology San Gerardo Hospital Università Milan Bicocca Monza, Italy.

CLINICAL PROFILE AND SHORT TERM OUT COMES IN PATIENTS OF IGA NEPHROPATHY. Victoria Hospital Campus, Republic of India, Bengaluru, India

The response of the Oxford classification to steroid in IgA nephropathy: a systematic review and meta-analysis

The CARI Guidelines Caring for Australasians with Renal Impairment. Membranous nephropathy role of steroids GUIDELINES

Spontaneous remission of nephrotic syndrome in patients with IgA nephropathy

Title: A novel differential diagnostic model based on multiple biological parameters for immunoglobulin A nephropathy

IgA-Nephropathy: an update on treatment Jürgen Floege

The CARI Guidelines Caring for Australasians with Renal Impairment. Specific management of IgA nephropathy: role of steroid therapy GUIDELINES

CHAPTER 2. Primary Glomerulonephritis

Case Presentation Turki Al-Hussain, MD

Pathologic Predictors of Renal Outcome and Therapeutic Efficacy in IgA Nephropathy: Validation of the Oxford Classification

IgA nephropathy in Greece: data from the registry of the Hellenic Society of Nephrology

29th Annual Meeting of the Glomerular Disease Collaborative Network

Dr Ian Roberts Oxford. Oxford Pathology Course 2010 for FRCPath Illustration-Cellular Pathology. Oxford Radcliffe NHS Trust

Current treatment recommendations in children with IgA nephropathy Selçuk Yüksel

Faculty/Presenter Disclosure

Lupus Nephritis. Ingeborg Bajema

Validation of the Oxford classification of IgA nephropathy for pediatric patients from China

Donor Quality Assessment

Epidemiological Profile, Clinicopathological Correlation and Treatment response in adult

Enterprise Interest None

Reducing proteinuria

Nephrotic syndrome minimal change disease vs. IgA nephropathy. Hadar Meringer Internal medicine B Sheba

Interventions to reduce progression of CKD what is the evidence? John Feehally

Dr Michael Rayment Chelsea and Westminster Hospital, London

Glomerular pathology in systemic disease

SCOTTISH REAL BIOPSY REGISTRY: SURVEY OF NATIVE KIDNEY BIOPSY IN SCOTLAND 2015

C1q nephropathy the Diverse Disease

Journal of Nephropathology

The CARI Guidelines Caring for Australasians with Renal Impairment


Design and Analysis of a Cancer Prevention Trial: Plans and Results. Matthew Somerville 09 November 2009

Dr. Mehmet Kanbay Department of Medicine Division of Nephrology Istanbul Medeniyet University School of Medicine Istanbul, Turkey.

Glomerular tip adhesions predict the progression of IgA nephropathy

Acute renal failure that is associated with macroscopic

Dr Ian Roberts Oxford. Oxford Pathology Course 2010 for FRCPath Illustration-Cellular Pathology. Oxford Radcliffe NHS Trust

Who is a migrant? 12/10/2018. HIV and migrants. Heterogeneous groups of persons with different migration drivers

The improvement of renal survival with steroid pulse therapy in IgA nephropathy

Management and treatment of glomerular diseases KDIGO Controversies Conference Part 1

Classification of Glomerular Diseases and Defining Individual Glomerular Lesions: Developing International Consensus

Epidemiology of kidney diseases in children

Progress Report of the activities of the Working Group «Hypertension and the Kidney»

Out of date SUGGESTIONS FOR CLINICAL CARE (Suggestions are based on level III and IV evidence)

What Are the Targets in CKD-MBD?

Clinicopathologic Characteristics of IgA Nephropathy with Steroid-responsive Nephrotic Syndrome

The CARI Guidelines Caring for Australasians with Renal Impairment. Specific management of IgA nephropathy: role of fish oil

The organs of the human body were created to perform ten functions among which is the function of the kidney to furnish the human being with thought.

Current levels and recent trends in health inequalities in the EU: Updates from the EU Report

Case 3. ACCME/Disclosure. Laboratory results. Clinical history 4/13/2016

Steroid Resistant Nephrotic Syndrome. Sanjeev Gulati, Debashish Sengupta, Raj K. Sharma, Ajay Sharma, Ramesh K. Gupta*, Uttam Singh** and Amit Gupta

Zhao Y Y et al. Ann Intern Med 2012;156:

What s hiding behind IgA nephropathy?

The most widespread type of glomerulonephritis is IgA

Case # 2 3/27/2017. Disclosure of Relevant Financial Relationships. Clinical history. Clinical history. Laboratory findings

Saudi Arabia February Pr Michel KOMAJDA. Université Pierre et Marie Curie Hospital Pitié Salpétrière

SELECTED ABSTRACTS. All (n) % 3-year GS 88% 82% 86% 85% 88% 80% % 3-year DC-GS 95% 87% 94% 89% 96% 80%

The CARI Guidelines Caring for Australasians with Renal Impairment. Blood Pressure Control role of specific antihypertensives

Corticosteroids in IgA Nephropathy: A Retrospective Analysis from the VALIGA Study

GSK Medicine: Study Number: Title: Rationale: Phase: Study Period: Study Design: Centres: Indication: Treatment: Objectives:

Approach to Glomerular Diseases: Clinical Presentation Nephrotic Syndrome Nephritis

Summary of Results for Laypersons

Chronic renal histological changes at implantation and subsequent deceased donor kidney transplant outcomes: a single-centre analysis

Palliative nursing care of children and young people across Europe

WCPT COUNTRY PROFILE December 2017 SWEDEN

Association of glomerular C4d deposition with morphologic variables of Oxford classification in IgA nephropathy patients; a preliminary study

A Multicenter Study of the Predictive Value of Crescents in IgA Nephropathy

Journal of Nephropathology

WCPT COUNTRY PROFILE December 2017 HUNGARY

Clinicopathologic Correlation in IgA Nephropathy

February 20, 2019 MANAGEMENT CALL TO DISCUSS PHASE 2 PHOENIX RESULTS AND CKD PROGRAM UPDATES

Transcription:

Advances in the European Validation Study of the Oxford Classification of IgA Nephropathy (VALIGA) One of the major aims of the IWG is to facilitate European Nephrologists interested in the area of immune-mediated diseases to establish networks and perform collaborative studies. In June 2009 an application was presented, on behalf of the IWG, for the first ERA-EDTA Research Call, which was awarded among the first 3 projects accepted for funding (May 2010). The study started in June 2010 and was planned to last 18 months, thus ending December 2011. The scientific project started from the publication of a breakthrough report produced by an International Consensus Group based on a retrospective analysis of 265 adults and children with IgA nephropathy from four continents focused on prognostic information provided by renal biopsy. According to this Oxford Classification of IgA Nephropathy, four pathological features (mesangial hypercellularity, segmental glomerulosclerosis, endocapillary hypercellularity, and tubular atrophy/interstitial fibrosis) predict renal outcome independently from all clinical indicators at the time of biopsy and during follow up (Kidney Int 2009;76:534-45; Kidney Int 2009;76:546-56 and Kidney Int Kidney 2010;77:921-7). The limited number of patients and their heterogeneous origin indicated a need for validation studies involving larger cohorts of patients. VALIGA was planned to investigate European IgA nephropathy patients also in order to gather results complementary to those from similar studies in North America and Asia, allowing a global perspective on the value of these factors to predict the clinical outcome of patients with IgA Nephropathy. VALIGA INITIAL ASSESSMENT. The study entry criteria include biopsy-proven IgA Nephropathy with long follow-up or rapidly progressive course with renal biopsy material available for reviewing and scoring according to the new classification. Renal biopsies are to be scored by the local pathologist and centrally reviewed in Oxford. Complete clinical data at renal biopsy and during the follow-up are provided by local nephrologists to the coordinating center. Statistical analysis will be performed by the Canadian experts who participated also in the steering committee of the initial Oxford Study. The initial assessment included 25 Centres of Nephrology and Renal Pathology, from 9 European Countries, which had agreed, in June 2009 during the first submission, on providing clinical data and renal biopsy material for the reviewing process according to the Oxford Classification for IgA Nephropathy. A total of 500 cases were forecasted. Since this was a project proposed by the IWG it was publicized during its Symposium in Munich and published on the IWG website. Since then several other centres asked to participate in this study, and since this was actually the original aim of the IWG, they were all accepted. PRESENT ADVANCEMENT. At July 2011 the VALIGA Study includes 52 Centers of Nephrology and Renal Pathology from 13 European Countries (Croatia, Czech Republic, Estonia, Germany, Greece, Italy, Poland, Portugal, Spain, Sweden, The Netherlands, Turkey, United Kingdom) with a total of 1227 cases enrolled. 886 cases are completed (both clinical spreadsheets and pathology scoresheet review were received) of which 742 renal biopsy slides were sent to Oxford for review. Taking into consideration the increase in the number of centres, cases and the amount of work involved, the deadline for the termination of the VALIGA project has been postponed from December 2011 to December 2012. At this point, each Clinical and Pathology Center in Europe which sent clinical spreadsheets and pathology scoresheets have to be thanked for the work done. Laura Morando, PhD who is taking care of the clinical data-base in Turin is doing a terrific work and should be thanked. Prof Ian Roberts is going to have a very hard work in reviewing the

pathology slides which are arriving in Oxford and DR Stéphan Troyanov (Montreal) will do the hard final statistical work. This multicenter, multinational study supported by the ERA-EDTA Working Group of Immunonephrology will provide information beyond the validation of the Oxford classification of IgAN, aiming at detecting for each lesion the point of no return when no treatment is effective. But beside the scientific result, the enthusiastic participation of so many centers in Europe for a spontaneous study, is a valuable result for the scientific community of Nephrologists Prof. Rosanna Coppo, Nephrology, Dialysis and Transplantation Unit, Regina Margherita Children s University Hospital, Torino, Italy

Advances in the European Validation Study of the Oxford Classification of IgA Nephropathy (VALIGA)

1th submission: July 2009 2nd submission: September 2009 Result of the selection: May 2010 Funding provided: June 1th, 2010 For Office Use Only YEAR OF CALL: 2009 Application No: Name of Applicant: Approved Denied Amount granted: Name of Applicant: First name: Rosanna Last name: Coppo ERA-EDTA SUPPORTED RESEARCH APPLICATION FORM Endorsed by the ERA-EDTA working group of Immunonephrology EUROPEAN VALIDATION STUDY OF THE OXFORD CLASSIFICATION OF IGA NEPHROPATHY (VALIGA)

International IgA Nephropathy Network & Renal Pathology Society

Consensus Classification of IgAN (265 cases) 206 adults 59 children

Age and Geographical Origin of Study Cohort of 265 Cases of IgA Nephropathy Adults Children Total 206 59 Asia 48 14 Europe 73 21 North and South America 85 24 CP1333770-5

Oxford study Enrolment criteria: 1) likely progressive IgAN (proteinuric patients) 2) follow-up > 1 year in order to allow calculation of e-gfr decline Focus on the most common form of mildly severe IgAN in which markers of disease progression are needed Excluded from enrolment in Oxford study 1) Non proteinuric likely non progressive IgAN 2) Rapidly progressive forms (severely crescentic)

International Consensus on clinico-pathological Classification of IgAN: Oxford Classification Mesangial hypercellularity score Endocapillary hypercellularity Segmental MEST combination glomerular sclerosis Tubular atrophy/interstitial fibrosis M0/M1 E0/E1 S0/S1 T0/T1/T2 At univariate analysis the variables are significantly correlated with the outcome (e-gfr decline and doubling of Cr or ESRF) These features maintain their independent predictive value also when the multivariate analysis considers - Clinical data at renal biopsy (e-gfr, MAP, UP) - Clinical data at follow-up (UP and MAP during time)

Results from the Oxford study A systematic approach was developed to produce a histological scoring scheme in IgA nephropathy A small number of lesions have been identified that are both reproducible and independent predictors of patient outcome. Recommendations were made for standardised reporting of renal biopsies in IgA nephropathy. The findings of this study require validation in other patient groups.

VALIDATION STUDY IS NEEDED in order to Validate or modify Oxford criteria in a pan European cohort (> 500 cases) Investigate the effect of additional features which had enrollment bias in the first study (rapidly progressive and non progressive cases) Investigate the combined prognostic value of adding clinical data to biological scores (e.g. proteinuria at renal biopsy or during follow-up). detect for each lesion the most effective treatment and the point of no return when no treatment is effective.

RETROSPECTIVE ANALYSIS OF RENAL BIOPSIES (REVIEWED ACCORDING TO OXFORD CLASSIFICATION) AND OUTCOME IN IgAN IgAN (dominant or codominant IgA) children and adults, regardless of treatment given 8 or more glomeruli at least 3 measurements of creatinine, proteinuria and blood pressure, the first of which should be within 3 months of the date of renal biopsy and the last at the end of the follow-up Patients having progressed to ESRD regardless of the duration of follow-up or Patients with a follow-up longer than 1 year. Excluded: Henoch-Schönlein nephritis, and IgAN with relevant comorbid conditions such as diabetes or tumors.

Research Group Coordinating center: Coppo R, Turin, Italy Steering committee group: Coppo R, Feehally J, Roberts I, Cook T, Cattran D, Troyanov S (core group of the Oxford classification) Pathology review center: Roberts I (Oxford, UK) Statistical analysis center: Troyanov S, Cattran D (Montreal and Toronto, Canada)

Phase I: Patients enrolment Clinical nephrology centers List of patients with IgA nephropathy meeting the enrolment criteria List sent to renal pathology centers Renal pathology centers Check availability of renal biopsy material for review June 2011: Phase I completed LIST OF ENROLLED CASES SENT TO THE COORDINATING CENTER

Done by nephrologists Clinical dataset Demographics including date of birth, gender, ethnicity, date of biopsy. Clinical parameters collected within 3 months of date of biopsy (table 3) and during follow up (table 4) including: systolic and diastolic BP, weight, height, serum creatinine and 24hr urine protein or UP/UCr Treatment modalities. June 2011: Phase I completed

Phase II: Clinical data collection and renal biopsy scoring Clinical nephrology centers Renal pathology centers Clinical data spreadsheet filled-in SPREADSHEETS SENT TO THE COORDINATING CENTER Renal biopsies scored by the local pathologists blinded to the clinical data June 2011: Phase II on the way

Pathology scoresheet Prepared by pathologist PAS stained RB according to the Oxford Classification the cut-off will be mesangial hypercellularity score : 0.5 (equivalent to 50% of glomeruli showing mesangial hypercellularity); segmental glomerulosclerosis, endocapillary hypercellularity and extracapillary proliferation: present or absent; tubular atrophy/interstitial fibrosis: absent/mild (0-25%), moderate (26-50%), severe(>50%).

Phase II: Clinical data collection and renal biopsy scoring SCORED BIOPSIES SLIDES SENT TO THE PATHOLOGY REVIEW CENTER June 2011: Phase II on the way

Phase III: Renal biopsy review Pathology review center (Oxford) Renal biopsy slides reviewed, blinded to clinical data and local scoring June 2011: Phase III on the way SCORESHEETS SENT TO THE COORDINATING CENTER

Phase IV: Data collection Coordinating center June 2011: Phase IV on the way Insure clinical and pathologic spreadsheets and scoresheets completeness, communicating with each center as necessary DATABASE SENT TO STATISTICAL ANALYSIS CENTER

Phase V: Statistical analysis and publication Statistical center Data analysis Steering committee Data analysis Manuscript writing Phase IV has to be done

Database management: Laura Morando (Turin, Italy) Statistical analysis will be performed by the Statistical Analysis Centers (Montreal and Toronto, Canada). Data analysis will be overseen by the steering committee (core group of the Oxford classification: Coppo R, Feehally J, Roberts I, Cook T, Cattran D, Troyanov S)

Pathology data analysis Reproducibility for each pathology variable will be assessed using intraclass correlation coefficient (ICC) which was adopted for the work leading to Oxford classification Continuous pathological variables will be categorized according to the rate of e-grf decline (dichotomized in 2 groups by the median value) using receiver operating characteristic (ROC) curves

Clinical data analysis Three clinical outcomes will be studied to address the predictive value of pathology variables: [a] the rate of renal function decline (slope of egfr); [b] survival from a 50% reduction in renal function, or ESRD; [c] proteinuria during follow up [as a surrogate outcome measure].

Statistical analysis Survival analysis using Cox regression will be performed to test the association between each pathological finding and a combined event (50% reduction in renal function or ESRD, to increase the rate of events and permit a valid multivariate analysis) multivariate Cox regression will be performed. Interactions with age, ethnicity and immunosuppressive treatment will be investigated.

1th submission: July 2009 2nd submission: September 2009 Result of the selection: May 2010 Funding provided: June 1th, 2010 For Office Use Only YEAR OF CALL: 2009 Application No: Name of Applicant: Approved Denied Amount granted: Name of Applicant: First name: Rosanna Last name: Coppo ERA-EDTA SUPPORTED RESEARCH APPLICATION FORM On behalf of the ERA-EDTA working group of Immunonephrology EUROPEAN VALIDATION STUDY OF THE OXFORD CLASSIFICATION OF IGA NEPHROPATHY (VALIGA)

North America 187 cases (adults and children) 4 centers form North America Korea 273 cases 1 center

EUROPEAN VALIDATION STUDY OF THE OXFORD CLASSIFICATION OF IGA NEPHROPATHY VALIGA 26 Centers of Nephrology and Renal Pathology from 9 European Countries (Spain, France, United Kingdom, Italy, Germany, Sweden, Poland, Netherlands, Turkey) have agreed on June 2009 upon providing clinical data and renal biopsy material available for the reviewing process according to the Oxford Classification for IgAN. A total of 500 cases was forecasted.

EUROPEAN VALIDATION STUDY OF THE OXFORD CLASSIFICATION OF IGA NEPHROPATHY VALIGA at June 2011 52 Centers of Nephrology and Renal Pathology from 13 European Countries (Croatia, Czech Republic, Estonia, Germany, Greece, Italy, Poland, Portugal, Spain, Sweden, The Netherlands, Turkey, United Kingdom) have enrolled their patients.

VALIGA Duration: 18 months: end December 2012 Update July 2011: 1227 cases sent (both initial and follow-up clinical spreadsheets) 886 pathology scoresheets received 742 renal biopsy slides sent to Oxford for review

ITALY: completed cases sent to Oxford: 241 completed cases, slides to be reviewed by I.Roberts: 103 120 100 80 60 40 20 0 Rome+Lazio Milan + Lombardi a Rome & Latium 6 Center Turin & Piedmont 12 Centers Milan & Lombardy 5 Centers Bari & Puglia 1 Center Modena Modena & Emilia 1 Center Verona & Veneto 1 Center others to be completed 290 to be completed

80 70 60 SWEDEN: completed cases sent to Oxford: 83 42 41 40 39 SPAIN: completed cases sent to Oxford: 78 50 40 30 20 10 0 Stockholm Stochkolm Uppsala Uppsala Nord 38 37 36 35 34 33 Madrid Madrid Barcelona Barcelona 2 centers Nord

THE NETHERLANDS: completed cases sent to Oxford: 35 25 20 15 10 Nord 25 20 15 10 GREECE: completed cases sent to : 33 Thessaloniki Patras To be completed: Ioannina 5 5 0 Nijmegen Nijmegen Lieden Leiden Thessaloniki 0 Thessaloniki Patras To be completed: Ioannina Patras To be completed: Ioannina: 25

25 20 15 10 5 TURKEY: completed cases sent to Oxford: 43 Nord 0 Istanbul Ankara Ankara Warsaw 31 30 29 28 27 26 25 24 23 POLAND: completed cases sent to Oxford: 31 WarsowTo to be completed be completed: Katowice and Warsaw: 26 Warsow to be completed

OTHER COUNTRIES: completed cases sent to Oxford: Total completed cases: 147 Estonia (Tartu) Germany Croatia (Zagreb) (Aachen) To be completed (UK): 53

Completed cases sent to Oxford

To be completed Italy UK Poland Greece Portugal Spain Sweden

N Cases Completed cases sent to Oxford adults and children <18 years old 600 400 200 0 adults childre n

Follow-up 1 to 20 years Follow up duration 1000 800 600 400 200 0 total n of cases Follow up > 1 year Dialysis before 1 year

Clinical data 350 300 250 200 150 100 50 0 First Creat>1.5 Last Creat>1.5 Dialysis

Proposed therapy for IgAN ACEI and/or ARB + steroids (pulses i.v.more effective than oral) + azathioprine/cyclophosphamide in progressive forms Dialysis and Transplantation Proteinuria and GFR reduction are likely not to be the only markers to early select treatment options for individual patients with IgAN ACEI and/or ARB: increased up to the highest tolerated dose CRF ESRD GFR reduction controls Proteinuria > 1 g Proteinuria < 1 g Macroscopic microscopic hematuria

This multicenter, multinational study supported by the ERA-EDTA Working Group of Immunonephrology will provide information beyond the validation of the Oxford classification of IgAN, aiming at detecting for each lesion the point of no return when no treatment is effective. But beside the scientific result, the enthusiastic participation of so many centers in Europe for a spontaneous study, is a valuable result for the scientific community of Nephrologists

VALIGA: a good platform to launch the Immunonephrology WG of ERA-EDTA Many thanks to all the 52 participating Centers from 13 European Countries!!!