molecular testing of lung carcinoma testing... · 2018-03-16 · response in lung adenocarcinoma...
TRANSCRIPT
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Molecular testing of lung carcinoma
Los Angeles Society Of Pathologists January 25, 2014
Sanja Dacic, MD, PhD
University of Pittsburgh Medical Center
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OUTLINE
Clinical testing for predictors of therapy
response
EGFR, ALK, other
Role of surgical pathologists in targeted
therapies
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Treatment of advanced NSCLC
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EGFR
EML4/ALK
BRAF
Her2
VEGFR
ADENOCA
FGFR1
DDR2
IGF-R
Same as
ADC
SQC NSCLC-NOS
Platinum based therapies
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Diagnosis of lung carcinoma
Before 2005.
Small cell carcinoma vs. non-small cell
carcinoma
From 2005- present
Small cell carcinoma vs. non-squamous cell
carcinoma
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EGFR mutations and EGFR- TKI responders
N Engl J Med 2004; 350:2129-39
Women; never smokers
Adenocarcinoma
Non-squamous carcinoma
Pretreatment
Posttreatment
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Genetic alterations in lung
adenocarcinoma
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KRAS
EGFR
ALK
NF1
METexon14
HER2-mut
BRAF
PI3KCA
MET amp
AKT
MAP2KI
ROS1
KIF5B-RET
HRAS
NRAS
WT
KRAS
EGFR
ALK
WT
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COMMON QUESTIONS
What assay to choose?
What type of sample to send for molecular
analysis?
What histologic subtype of NSCLC should
be tested?
What is the future of molecular testing?
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Iressa Pan-Asian Study (IPASS)
EGFR-Mutation-Positive EGFR-Mutation-Negative
Mok TS et al. NEJM 2009;361:947-957
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Frequency of EGFR mutations
10 Modified from Shigematsu et al. Int J Cancer 2006;118:257-262.
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CAP/IASLC/AMP
recommendation
Multiple test platforms are acceptable for EGFR mutation testing
A mutation method must be at least as sensitive as Sanger sequencing
EGFR mutation analysis should capture all mutations that individually account for 1% or more of mutant case
Assay for the T790M should have sensitivity in the 1-5%
range
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DETECTION OF EGFR
ABNORMALITIES
Immunohistochemistry
FISH/CISH
Detection of mutations
DNA sequencing or other mutation detection
techniques
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EGFR IHC
IHC for total EGFR
Not acceptable
IHC for phosphorylated EGFR
Limited experience, unreliable
IHC for mutant forms of EGFR
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EG
FR
IH
C
EG
FR
exo
n 1
9 d
el
IHC
H
&E
Courtesy of Lucian Chirieac, MD, Brigham and Women’s Hospital
EGFR MUTATION SPECIFIC ANTIBODIES
Clin Cancer Res 2009;15(9):3023-3028
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EGFR exon 19 and L858R mutation
specific antibodies
Antibody
Sensitivity (%) Specificity (%)
Exon 19
15 bp 100 98.8
<15 bp 74.2 98.8
Exon 21 95.2 98.8
Brevet et al. JMD 2010; 12:169-176.
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CAP/IASLC/AMP
recommendation
EGFR IHC is NOT recommended test for EGFR
TKI treatment selection
Mutant EGFR allele-specific IHC is too
insensitive to be used as a stand alone assay for
EGFR-TKI treatment selection
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Response to Crizotinib in ALK-Positive Tumors
Kwak EL et al. N Engl J Med 2010;363:1693-1703.
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ALK and fusion products in NSCLC
18 JCO 2009;27 (26):4232-35.
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ROS1 rearrangements
19
Bergethon et al., JCO 2012; 30(8): 863-70, 2012; Takeuchi et al., Nat Med 2012; 18(3): 378-81.
ROS1 positive
UPMC
ROS1 negative
UPMC
receptor tyrosine
kinase of the insulin receptor
family
6q22
2% lung ADC
Young, never smokers
Respond to crizotinib
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METHODS OF DETECTION
Classical cytogenetics
FISH
Immunohistochemistry
RT-PCR
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ALK- FISH
Diagn Mol Pathol 2004; 13(4):197-206
Dept of Pathology UPMC
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ALK-IHC
CLONE PROVIDER SPECIFICITY
(%)
SENSITIVITY
(%)
D5F3
Rabbit monoclonal
Ventana Medical System, Inc.
Cell Signaling Technology,
Danvers, MA
75-99
91-100
5A4
Rabbit monoclonal
Novocastra, New Castle, UK
87.5-98
100
ALK1 M7195
Mouse monclonal
Dako, Carpinteria, CA
91-99
64-100
CCR 2010; JCP 2010; JTO 2011, 2012, 2013; Ann Oncol 2012, Mod Pathol 2013, Plos One 2013
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IHC ASSAY IMPLEMENTATION
CHALLENGES
Tissue quality and quantity
Antibody clone
IHC protocol (antigen retrieval method,
detection system)
Interpretation criteria
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ALK IHC agreement with FISH
Agreement Between IHC and
FISH
Agreement Rate n/N (%) 95% CI Overall Percent Agreement 92/98 ( 93.9) 87.3, 97.2
Positive Percent Agreement 39/43 ( 90.7) 78.4, 96.3
Negative Percent Agreement 53/55 ( 96.4) 87.7, 99.0
WCLC , Sydney 2013
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CAP/IASLC/AMP
recommendation
A commercial break-apart FISH assay
developed by Abbott Molecular is recommended
DAKO ALK1 antibody is not reliable for ALK
rearrangement screening
RT-PCR is not currently recommended as a first-
line diagnostic method for ALK fusion status
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WHAT TYPE OF TISSUE
SAMPLE SHOULD BE TESTED?
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SAMPLE FOR EGFR/ALK
TESTING
Sample processing
Primary vs. metastatic tumor
Selecting a block for analysis
Multiple primary lesions
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SAMPLE PROCESSING
ACCEPTABLE fixatives
– 10% neutral-buffered formalin (NBF)
– Alcohol (70% ethanol)
UNACCEPTABLE fixatives
– Heavy metal fixatives (e.g. Zenker’s, B5, AZF, B plus)
– Acidic solutions (Bouin’s solution, bone decalcifying
solutions)
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SAMPLE PROCESSING CAP/IASLC/AMP recommendation
Specimen should be fixed in 10% NBF for
no less than 6 hours and no more than 48
hours before processing
Cell block is recommended for cytology
specimens
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Paraffin-embedded tissue sample: Core biopsy or FNA cell block
preparation
Level 1: Hematoxylin & Eosin
Level 6: Hematoxylin & Eosin
Levels 7-17
H&E and unstained slides Mutation
testing EGFR/KRAS
Levels 18-23
H&E and FISH (ALK, ROS, RET,
MET)
Level 24: Hematoxylin & Eosin
(core biopsies only)
Levels 25-26
Immunohistochemistry
Level 27
Negative control for
immunohistochemistry
Pathologist
Pathologist
Pathologist
Levels 2-5
Immunohistochemistry
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WHAT TUMOR SAMPLE TO TEST
PRIMARY TUMOR OR METASTASES ?
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Heterogeneity of EGFR mutations
Intratumor heterogeneous population of both EGFR mutated and non-
mutated cancer cells, resulting in a reduced response to gefitinib
(Taniguchi K. et al Cancer Sci 2008; 99:929; Nakano H. Lung Cancer
2008; 60:136)
Discrepancy in EGFR mutations between primary tumors and
metastatic lymph nodes, suggesting tumor heterogeneity at the
molecular level during the process of metastasis (Park S. JTO
2009;4:809; Schmid K. CCR 2009; 15:4554; Chang YL. Ann Surg
Oncol 2011; 18:543)
Discrepancy in EGFR mutations between primary and recurrent
NSCLC
Role of chemotherapy (Bai H. JCO 2012 ;30:3077)
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The distribution of the EGFR mutations
Yatabe Y et al. JCO 2011;29:2972-2977
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EGFR mutation and amplification
EGFR mutation +/
amplification -
EGFR mutation +/
amplification +
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Pseudoheterogeneity of EGFR mutations in lung
adenocarcinoma
Yatabe Y et al. JCO 2011;29:2972-2977
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Cell 2012; 150:1121.
Tumor heterogeneity revisited by deep
sequencing
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HIGH CONCORDANCE BETWEEN
PRIMARY TUMORS AND METASTASES
Vignot S. JCO 2013; 31(17); 2167
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PRIMARY TUMOR VS. METASTASES
CAP/IASLC/AMP recommendation
The choice of primary vs. metastatic tumor
should be based on the sample qualities (tumor
content and preservation)
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MULTIPLE PRIMARY LESIONS
CAP/IASLC/AMP recommendation
Both separate primary tumors should be
tested if tissue available
Testing of multiple areas of a single
primary tumor is not recommended
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EGFR inhibitor acquired resistance
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EGFR T790M +/-
amplification 50%
Her2 amplification
12%
MAPK1 amplification 5%
PIK3CA 5%
MET amplification 4%
SCLC transformation 6%
Unknown 15%
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CAN HISTOLOGIC SUBTYPE OF
LUNG ADENOCARCINOMA
PREDICT MUTATION PROFILE?
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MUTATION and MORPHOLOGY
43
EGFR/BRAF-PAPILLARY EGFR/BRAF-LEPIDIC
KRAS-MUCINOUS ALK-SOLID WITH SIGNET RING
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0
20
40
60
80
100
AC SOL BAC MUC PAP
PRIMARY HISTOLOGIC PATTERNS IN MIXED
SUBTYPE ADENOCARCINOMAS AND MUTATION
TYPE
EGFR+
KRAS+
EGFR-/KRAS-
AC- acinar; SOL-solid; BAC-bronchioloalveolar; MUC-mucinous; PAP-papillary
%
Dacic S. et al. Mod Pathol 2010;23(2):159-68.
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EGFR + predictor KRAS + predictor
Absence of solid growth pattern OR 0.024; 95% CI <0.001-0.825
P=0.0388
Mucinous growth pattern OR 3.938; 95% CI 1.574-9.852
P=0.001
MORPHOLOGIC PREDICTORS OF
MUTATIONAL PROFILE
Dacic S. et al. Mod Pathol 2010;23(2):159-68.
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WHAT ABOUT OTHER NSCLC WITH
GLANDULAR DIFFERENTIATION?
46
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KRAS/EGFR in adenosquamous
carcinoma and sarcomatoid carcinomas
47
H&E KRAS EGFR-FISH
Tochigi et al. AJCP 2011
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LARGE CELL CARCINOMA
48
ADC SQC
NULL
ADSQ
TTF-1
P40
Mucin
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Genetic Alterations in SQC
(mutations, amplifications)
Courtesy of Dr. Elisabeth Brambilla
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Gene expression subtypes of SQC
Nature 2012
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HISTOLOGY AND GENOTYPIC ANALYSIS
CAP/IASLC/AMP recommendation
All NSCLC that contain an
adenocarcinoma component, regardless of
histologic grade
Not recommended for pure squamous cell
carcinoma, small cell carcinoma or large
cell neuroendocrine carcinoma
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52 Seidel et al. Sci Transl Med Oct 30, 2013
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Genomic alterations and histology
53
Seidel et al. Sci Transl Med Oct 30, 2013
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Tissue collection/Fixation
Fixation/Tissue Processing
Pathologists review and report
EGFR mutation testing
ALK-FISH
Final report with tumor histology and mutation results
Biopsy 24 hrs
1-2 working days
(except IHC)
Molecular testing
Final report
Pathology
10 working days
Routine work up of lung adenocarcinomas
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WHAT IS NEXT?
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Next Generation Sequencing
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A RECENT CASE –SUCCESS STORY
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TTF-1 +/p40-
Point MutationFBXW7 p.R465HPre-treatment
Post-treatment
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HOW MUCH IS ENOUGH ?
Roychowdhury et al. Sci Transl Med 2011
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Obstacles in molecular testing
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Payers
Drug
companies
FDA
Physicians
Patent
owners
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What does a surgeon/oncologist
expect from a pathologist?
Close interactions, good communication, respect
Accuracy fast response
Integration of molecular profiling and diagnostic
work up of NSCLC
Team approach!
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SUMMARY
Molecular testing for predictors of targeted therapy
response in lung adenocarcinoma must include EGFR
mutation analysis for exons 19-21 and ALK-FISH
Testing for other molecular biomarkers in NSCLC is not
currently indicated for clinical management
Pathologist must make every effort to spare the tissue for
molecular testing after histologic diagnostic evaluation
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62 Thank you