Comparison of FISH, CpG-stimulation, chromosomal microarray and mate pair sequencing in 20 patients with CLL or lymphoma

Similar documents
Use of MYC, BCL2 and BCL6 FISH for investigations of high grade B cell lymphoma

CLL Complete SM Report

Test Utilization: Chronic Lymphocytic Leukemia

PhenoPath. Diagnoses you can count on B CELL NON-HODGKIN LYMPHOMA

Addressing the challenges of genomic characterization of hematologic malignancies using microarrays

MYC Translocations In Multiple Myeloma Involve Recruitment Of Enhancer Elements Resulting In Over- Expression and Decreased Overall Survival

Chronic Lymphocytic Leukemia FISH Panel. Impact on Diagnosis

Non-Hodgkin lymphomas (NHLs) Hodgkin lymphoma )HL)

Follicular Lymphoma: the WHO

Chronic Lymphocytic Leukemia Mantle Cell Lymphoma Elias Campo

UTILIZATION OF A SNP MICROARRAY FOR CHRONIC LYMPHOCYTIC LEUKEMIA: EFFICACY, INFORMATIVE FINDINGS AND PROGNOSTIC CAPABILITIES

CLL & SLL: Current Management & Treatment. Dr. Isabelle Bence-Bruckler

Initial Diagnosis and Treatment 81 Male

Objectives. Morphology and IHC. Flow and Cyto FISH. Testing for Heme Malignancies 3/20/2013

Molecular Markers. Marcie Riches, MD, MS Associate Professor University of North Carolina Scientific Director, Infection and Immune Reconstitution WC

Gray Zones and Double Hits Distinguishing True Burkitt Lymphoma from Other High-Grade B-NHLs Burkitt Lymphoma Burkitt-Like Lymphoma DLBCL Patrick Tres

7 Omar Abu Reesh. Dr. Ahmad Mansour Dr. Ahmad Mansour

Your single-source laboratory solution. FISH Probe Library

Short Telomeres Predict Poor Prognosis in Chronic Lymphocytic Leukemia

CLL: disease specific biology and current treatment. Dr. Nathalie Johnson

(Fully automated FISH Analysis for B-cell Chronic Lymphocytic Leukemia: a faster alternative to manual double scoring)

Classification of Hematologic Malignancies. Patricia Aoun MD MPH

Lymphoma/CLL 101: Know your Subtype. Dr. David Macdonald Hematologist, The Ottawa Hospital

2013 AAIM Pathology Workshop

The patient had a mild splenomegaly but no obvious lymph node enlargement. The consensus phenotype obtained from part one of the exercise was:

CLL & SLL: Current Management & Treatment. Dr. Peter Anglin

Template for Reporting Results of Biomarker Testing of Specimens From Patients With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Abstract. Hematopathology / Improved Cytogenetics in Lymphoma. Key Words: Cytogenetics; B-cell lymphoma; CpG-oligonucleotide DSP30

Volume 7, Issue 1 January 2012

Pathology of the indolent B-cell lymphomas Elias Campo

Molecular Advances in Hematopathology

Patterns of Lymphoid Neoplasia in Peripheral Blood. Leon F. Baltrucki, M.D. Leon F. Baltrucki, M.D. Disclosure

The role of cytogenomics in the diagnostic work-up of Chronic Lymphocytic Leukaemia

Canadian College of Medical Geneticists (CCMG) Cytogenetics Examination. May 4, 2010

Hematopathology Service Memorial Sloan Kettering Cancer Center, New York

Defined lymphoma entities in the current WHO classification

HIGH GRADE B-CELL LYMPHOMA DAVID NOLTE, MD (PGY-2) HUSSAM AL-KATEB, PHD, FACMG DEBORAH FUCHS, MD

CCND1-IGH Fusion-Amplification and MYC Copy Number Gain in a Case of Pleomorphic Variant Mantle Cell Lymphoma

From Morphology to Molecular Pathology: A Practical Approach for Cytopathologists Part 1-Cytomorphology. Songlin Zhang, MD, PhD LSUHSC-Shreveport

Aggressive B-cell Lymphomas Updated WHO classification Elias Campo

CLL Biology and Initial Management. Gordon D. Ginder, MD Director, Massey Cancer Center Lipman Chair in Oncology

CLL Ireland Information Day Presentation

Citation International Journal of Hematology, 2013, v. 98 n. 4, p The original publication is available at

Translocations and clonality detection in lymphoproliferative disorders by capturebased Next-generation sequencing

Association for Molecular Pathology Promoting Clinical Practice, Basic Research, and Education in Molecular Pathology

Risk Stratification in Childhood Leukemia

Recent advances in the genetics & biology of lymphoma

Oncology Cytogenetics Diagnostic Service - User Guide 2014

We Can Cure Chronic Lymphocytic Leukemia with Current / Soon to be Approved Agents: CON ARGUMENT

WBCs Disorders 1. Dr. Nabila Hamdi MD, PhD

HEMATOPATHOLOGY SERVICES

Genomic complexity and arrays in CLL. Gian Matteo Rigolin, MD, PhD St. Anna University Hospital Ferrara, Italy

REAL LIFE AMBULATORIALE E STUDI CLINICI RANDOMIZZATI NELLA PROGRAMMAZIONE TERAPEUTICA DELLA LEUCEMIA LINFATICA CRONICA.

Molecular Diagnosis. Nucleic acid based testing in Oncology

Template for Reporting Results of Biomarker Testing of Specimens From Patients With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Investigation and Management of Chronic Lymphocytic Leukemia. James Johnston

MED B Form CLL. Johannes Schetelig. London 09/April/

Nucleic Acid Testing - Oncology. Molecular Diagnosis. Gain/Loss of Nucleic Acid. Objectives. MYCN and Neuroblastoma. Molecular Diagnosis

Multiple Copy Number Variations in a Patient with Developmental Delay ASCLS- March 31, 2016

BTK Inhibitors and BCL2 Antagonists

INDIVIDUALIZED MEDICINE

GP CME. James Liang Consultant Haematologist. Created by: Date:

Reporting cytogenetics Can it make sense? Daniel Weisdorf MD University of Minnesota

Fluorescence in-situ Hybridization (FISH) ETO(RUNX1T1)/AML1(RUNX1) or t(8;21)(q21.3;q22)

Infections and nonmicrobial inflammatory stimuli can cause leukocytosis (as seen in Lab 1) as well as lymph node enlargement (lymphadenopathy).

Do acgh analysis have a place in routine cytogenetic workup in leukemia/cancer? - A single institution experience. Cambridge, April 9 th 2013

Small, mature-appearing appearing

Pathology #07. Hussein Al-Sa di. Dr. Sohaib Al-Khatib. Mature B-Cell Neoplasm. 0 P a g e

Methods used to diagnose lymphomas

UnitedHealthcare Pharmacy Clinical Pharmacy Programs

CLL what do I need to know as an Internist in Taimur Sher MD Associate Professor of Medicine Mayo Clinic

Lymphoma: What You Need to Know. Richard van der Jagt MD, FRCPC

Integrated Diagnostic Approach to the Classification of Myeloid Neoplasms. Daniel A. Arber, MD Stanford University

LES CAHIERS CERBA. Recommendations for the diagnosis and interpretation of blood lymphocytosis

Low-grade B-cell lymphoma

Generating Spontaneous Copy Number Variants (CNVs) Jennifer Freeman Assistant Professor of Toxicology School of Health Sciences Purdue University

Collected: , PM Sent: , PM Received: , PM Preliminary: , PM. Notification Status: COMPREHENSIVE DIAGNOSIS

Outline. Chromosomal analysis FISH. Chromosomal abnormalities in cancer. Clinical application of cytogenetics. Procedure Nomenclature

The 1 World Congress on Controversies in Hematology (COHEM) Rome, September 2010

The Challenges of Precision Medicine: New Advances in Molecular Diagnostic Testing- Impact for Healthcare

Clinical Genomics. Ina E. Amarillo, PhD FACMGG

Flow cytometric analysis of B-cell lymphoproliferative disorders

Hematopathology Case Study

GENETIC MARKERS IN LYMPHOMA a practical overview. P. Heimann Dpt of Medical Genetics Erasme Hospital - Bordet Institute

Lymphoma Update: Lymphoma Update: What s Likely to be New in the New WHO. Patrick Treseler, MD, PhD University of California San Francisco

LINFOMA B (INCLASIFICABLE) CON RASGOS INTERMEDIOS ENTRE LINFOMA DE BURKITT Y LINFOMA B DIFUSO DE CÉLULAS GRANDES.

at least 5 probes standard 8 probes (13, 15, 16, 18, 21, 22, 15, X, Y) at least 5 probes standard 8 probes (13, 15, 16, 18, 21, 22, X, Y)

Outlines. Disclosures. Updates on B-cell Chronic Lymphoproliferative Disorders of the Blood and Bone Marrow

Defining Actionable Novel Discoveries, Annotating Genomes, and Reanalysis in Cancer A Laboratory Perspective

September 04, 2008

Chronic Lymphocytic Leukaemia and Its Challenges for Insurers

Session 5. Pre-malignant clonal hematopoietic proliferations. Chairs: Frank Kuo and Valentina Nardi

Case Report Parotid gland follicular lymphoma lacking both cytoplasmic and surface light chains: a rare case

Management of CLL in the Targeted Therapy Era

CYTOGENETICS INTRODUCTION SPECIAL INSTRUCTIONS ON SAMPLE COLLECTION AND HANDLING

The Lymphomas. An overview..

TEST MENU TEST CPT CODES TAT. Chromosome Analysis Bone Marrow x 2, 88264, x 3, Days

Georg Hopfinger 3. Med.Abt and LBI for Leukemiaresearch and Haematology Hanusch Krankenhaus,Vienna, Austria

Transcription:

Comparison of FISH, CpG-stimulation, chromosomal microarray and mate pair sequencing in 20 patients with CLL or lymphoma Stephanie Smoley Cancer Genomics Consortium August 9 th, 2017 2016 MFMER slide-1

Chronic Lymphocytic Leukemia (CLL)/ Small Lymphocytic Lymphoma (SLL) Disorder of the B-lymphocytes Most common form of adult leukemia/lymphoma in Western countries average age at diagnosis 71 years male:female ratio 2:1 Highly variable clinical course survival ranging 2-20 years 2016 MFMER slide-2

CLL staging Rai Stage Risk Characteristics Survival (years) 0 Low lymphocytosis >13 I Intermediate lymphocytosis plus lymphadenopathy 8 II Intermediate lymphocytosis plus hepatomegaly or splenomegaly w/ or w/o lymphadenopathy 5 III High lymphocytosis plus anemia w/ or w/o hepatomegaly, splenomegaly or lymphadenopathy 2 IV High lymphocytosis plus thrombocytopenia 1 Rai et al., Blood 1975 2016 MFMER slide-3

Dohner Classification 17p- Nl/+12 11q- 13q- FISH abnormality 17p- 32 11q- 79 +12 114 Normal 111 13q- 133 Median Survival (months) Dohner et al., NEJM 2000 Shanafelt et al., J Clin Oncol 2006 2016 MFMER slide-4

Why is prognostication so important? No cure has been found For asymptomatic patients watch and wait Many patients with CLL aren t healthy enough for treatment Targeted therapy 17p deletions Evolution 2016 MFMER slide-5

Cytogenetic testing for CLL FISH Limited targets ~30% are normal CpG stimulated karyotype Whole genome Low resolution Chromosomal microarray Whole genome High resolution Cannot detect rearrangements Mate Pair Sequencing Whole genome High resolution CNV and rearrangements 2016 MFMER slide-6

20 Test Patients RFR CLL or lymphoma Not all patients were confirmed to have CLL Chosen based on suitability for mate pair testing Highly enriched for IGH rearrangements 2016 MFMER slide-7

FISH vs. MPseq (n=20) 1* 15 4 15 matched 1 case w/ FISH advantage: MPseq missed a low level 13q-, (*but identified the BCL2 partner as IGL) 4 cases w/ MPseq advantage: 2 reclassified 13q-x1 to 13q-x2 1 identified the IGH partner as BCL11A 1 identified a CCND1/IGH not visible by FISH testing FISH exceeds MPseq FISH & MPseq match MPseq exceeds FISH 2016 MFMER slide-8

CpG vs. MPseq (n=19) 1* 16 2 16 match 1 case w/ CpG advantage MPseq missed low level add(18), (*but identified the IGH partner as BCL11A) 2 cases w/ MPseq advantage detected 13q- and identified the IGH partner as BCL11A add(14) characterized as BCL11A/IGH CpG exceeds MPseq CpG & MPseq match MPseq exceeds CpG 2016 MFMER slide-9

Example #1 CpG advantage Referrred for testing CLL FISH 11q- (77%) IGH separation (95.5%) 2016 MFMER slide-10

Example #1 46-47,XY,t(2;14)(p15;q32),del(11)(q22q23),add(18)(q21)[cp10] 2016 MFMER slide-11

Example #1 ATM IGH CpG - 46-47,XY,t(2;14)(p15;q32),del(11)(q22q23),add(18)(q21)[cp10] 2016 MFMER slide-12

Example #1 SERTAD2 SERTAD2 IGH locus IGH locus 2016 MFMER slide-13

Example #1 2016 MFMER slide-14

Example #1 BCL11A/IGH 2016 MFMER slide-15

Example #2 MPseq advantage Referred for testing CLL CpG - 46,XY,t(5;6)(q13;q23)[10]/46,XY[10] FISH 13q-x1 (56%) 2016 MFMER slide-16

Example #2 CpG - 46,XY,t(5;6)(q13;q23)[10]/46,XY[10] FISH 13q-x1 (56%) 2016 MFMER slide-17

Example #2 CN=1.4 CN=0.8 CpG - 46,XY,t(5;6)(q13;q23)[10]/46,XY[10] FISH 13q-x1 (56%) 2016 MFMER slide-18

Example #2 Abbott Molecular D13S319 probe 2016 MFMER slide-19

Example #3 MPseq advantage Referred for testing CLL/SLL Flow cytometry indicative of follicular lymphoma or marginal zone lymphoma FISH for CCND1/IGH, CCND2, MYC and 7qwere all negative FISH showed ~90% 17p- 2016 MFMER slide-20

Example #3 46,XX,+3,add(3)(p11)x2,t(5;20)(p13;q11.2),-13 2016 MFMER slide-21

Example #3 CpG - 46,XX,+3,add(3)(p11)x2,t(5;20)(p13;q11.2),-13 MPseq 46,XX,+3,add(3)(q10)x2,t(5;13)(q11.2;q22.1),t(11;14)(q13.3;q32.33) 2016 MFMER slide-22

Example #3 CpG - 46,XX,+3,add(3)(p11)x2,t(5;20)(p13;q11.2),-13 MPseq 46,XX,+3,add(3)(q10)x2,t(5;13)(q11.2;q22.1),t(11;14)(q13.3;q32.33) 2016 MFMER slide-23

Example #3 CpG - 46,XX,+3,add(3)(p11)x2,t(5;20)(p13;q11.2),-13 MPseq 46,XX,+3,add(3)(q10)x2,t(5;13)(q11.2;q22.1),t(11;14)(q13.3;q32.33) 2016 MFMER slide-24

Example #3 CCND1 CCND1 IGH locus IGH locus 2016 MFMER slide-25

Example #3 t(11;14)(q13.3;q32.33) Atlas of Genetics & Cytogen 2016 MFMER slide-26

chr11 chr14 t(11;14)(q13.3;q32.33) 2016 MFMER slide-27

chr11 chr14 Abbott CCND1 D-FISH probe Abbott IGH-XT D-FISH probe t(11;14)(q13.3;q32.33) 2016 MFMER slide-28

Abbott CCND1 D-FISH probe Insertional translocation Abbott IGH-XT D-FISH probe t(11;14)(q13.3;q32.33) 2016 MFMER slide-29

Conclusions: No single method provides all information FISH is more sensitive for follow-up and MRD MPseq is a useful diagnostic tool detecting more than any other method: Variant translocations (BCL11A, IGK, IGL) More accurately classifies heterozygous vs homozygous 13q deletions Novel changes 2016 MFMER slide-30

Acknowledgements: Genomics Lab: Umut Aypar, PhD Linda Baughn, PhD Patricia Greipp, DO Katherine Geiersbach, MD Nicole Hoppman, PhD Robert Jenkins, MD, PhD Hutton Kearney, PhD Rhett Ketterling, MD Beth Pitel, MS Jeannette Rustin William Sukov, MD Erik Thorland, PhD Daniel Van Dyke, PhD Bioinformatics: Eric Klee, PhD Saranya Sankaranarayan, MS Satwica Yerneni Biomarker Discovery: Athanasios (Saki) Gaitatzes, MS Sarah Johnson, MS James Smadbeck, PhD George Vasmatzis, PhD Clinical Genome Sequencing Lab: Joseph Blommel, MS Lisa Peterson 2016 MFMER slide-31

Questions? I think you should be more explicit here in step two 2016 MFMER slide-32