Keith J.Kaplan, MD Geoffrey L. Turner, MD PhD Grace E. Kronauer
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Quantitative Image Analysis Quantitative Image Analysis of HER2 Immunohistochemistry of HER2 Immunohistochemistry Compared with Manual Compared with Manual Pathologist Analysis in Pathologist Analysis in Breast Cancer Breast Cancer A Pilot Study A Pilot Study Keith J.Kaplan, MD Geoffrey L. Turner, MD PhD Grace E. Kronauer Northwestern University Feinberg School of Medicine Johns Hopkins University
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Quantitative Image Analysis of HER2 Immunohistochemistry Compared with Manual Pathologist Analysis in Breast Cancer A Pilot Study. Keith J.Kaplan, MD Geoffrey L. Turner, MD PhD Grace E. Kronauer Northwestern University Feinberg School of Medicine Johns Hopkins University. Background – HER2. - PowerPoint PPT Presentation
Transcript of Keith J.Kaplan, MD Geoffrey L. Turner, MD PhD Grace E. Kronauer
Quantitative Image Analysis of Quantitative Image Analysis of HER2 Immunohistochemistry HER2 Immunohistochemistry
Compared with Manual Compared with Manual Pathologist Analysis in Breast Pathologist Analysis in Breast
CancerCancerA Pilot StudyA Pilot StudyKeith J.Kaplan, MD
Geoffrey L. Turner, MD PhDGrace E. Kronauer
Northwestern University Feinberg School of Medicine
Johns Hopkins University
Background – HER2Background – HER2 Human epidermal growth factor receptor
2 gene ERBB2 (commonly referred to as HER2) is amplified in approximately 18% to 20% of breast cancers.
HER2 overexpression is associated with clinical outcomes in patients with breast cancer.
HER2 status is also predictive for several systemic therapies.
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BackgroundBackground Several studies have now shown that agents
that target HER2 are remarkably effective in both the metastatic and adjuvant settings. Trastuzumab (Herceptin; Genentech, South San Francisco, CA), a humanized monoclonal antibody, improves response rates, time to progression, and even survival when used alone or added to chemotherapy in metastatic breast cancer. Active as a single agent. Approve for the treatment of metastatic disease.
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BackgroundBackground HER2 testing should be routinely
performed in patients with a new diagnosis of invasive breast cancer. However, the best method to assess HER2 status, in regards both to the type of assay used and the optimal method to perform each assay, remains controversial. IHC with reflex of 2+ to FISH Overexpression by IHC (3+) or amplification
by FISH considered positive result4
BackgroundBackground Several assays have been used for HER2 determination
in tissue. US Food and Drug Administration regulations also allow pathology laboratories to develop and implement so called “home brew assays” using US Food and Drug Administration–approved analyte specific reagents.
While some assays have been carefully validated, others, especially “home brew assays,” have not. Prospective substudies from two of the adjuvant randomized trials of trastuzumab versus nil have demonstrated that approximately 20% of HER2 assays performed in the field (at the primary treatment site's pathology department) were incorrect when the same specimen was re-evaluated.
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BackgroundBackground Such a disorganized practice and high rate of
inaccuracy, for such an important test that dictates a critically effective yet potentially life-threatening and expensive treatment, is not acceptable.
Trastuzumab therapy is not without its drawbacks. Therapy recommended for 12 months The drug cost of 52 weeks of trastuzumab in the
community setting in the United States is approximately $100,000 based on average sales price (www.accc-cancer.org).
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BackgroundBackground Associated with a small risk of serious
cardiac toxicity. Approximately 5% to 15% of patients develop
cardiac dysfunction, Approximately 1% to 4% develop significant
cardiac events (including symptomatic congestive heart failure) while taking trastuzumab.
Taken together, the significant benefits coupled with the high cost and potential cardiotoxicity of trastuzumab demand accurate HER2 testing.
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Archives of Pathology and Laboratory Medicine: Vol. 131, No. 1, pp. 18–43.
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Archives of Pathology and Laboratory Medicine: Vol. 131, No. 1, pp. 18–43.
•Image analysis can be an effective tool for achieving consistent interpretation. However, a pathologist must confirm the image analysis result. Image analysis equipment, just as other laboratory equipment, must be calibrated and subjected to regular maintenance and internal quality control evaluation. Image analysis procedures must be validated before implementation. One issue identified during the panel discussion was lack of calibration of the optical microscopes used by pathologists, something which certainly contributes to interpretive variation. If pathologists use several different microscopes to read assays, a system of calibration of these instruments should be implemented to ensure consistent interpretation.
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Inconsistency of HER2 Test Raises Questions
J Natl Cancer Inst 2007;99(14)1064-1065.The tests that determine who gets the powerful breast cancer drug trastuzumab (Herceptin) may not be as reliable as previously thought, researchers reported at the annual meeting of the American Society of Clinical Oncology. That means some women who should be getting trastuzumab treatment are not, whileother women who will not benefit are unnecessarily exposed to a drug that can cause heart problems.
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Study DesignStudy Design Retrospectively reviewed 81 (81/122) breast
cancers newly diagnosed within 2006 and tested for HER2 by IHC with reflex FISH testing in equivocal (2+) cases (majority)
LIS searched for “FISH” and “HER2” in 2006 Whole slide scanned using ScanScope and
analyzed using membrane stain algorithm provided
Algorithms not “calibrated” or “standardized” to our laboratory. Slides not re-reviewed or IHCs re-scored Non-sequential cases from 10 pathologists Home-brewed assay
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MA – 1+ FISH non-amplified IA – 014
MA – 2+ FISH non-amplified IA – 1+15
MA – 2+ FISH non-amplified IA – 1+16
MA – 2+ FISH non-amplified IA – 1+17
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MA – 3+ FISH non-amplified IA – 3+
DB
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MA – 3+ FISH amplified IA – 3+20
ResultsResults IA more accurate than MA 68% (55/81)
IA 1+ compared with MA 2+ IHC FISH non-amplified in all cases
MA more accurate than IA 15% (12/81) 8/12 overscored 3+ IHC (1+ IHC MA) 8/8 FISH non-amplified 4/12 underscored 1+ IHC (3+ IHC MA) 3/4 FISH amplified
IA equivalent to MA 17% (14/81) 1+ to 3+ with majority (8/14) as 2+ IHC
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ResultsResults Scan time on order of a few minutes Processing time on order of 15 minutes
for whole slide 2 slides unable to be scanned Extra resources needed to incorporate
into workflow Retrieval of material, scanning, processing,
analyzing and reporting
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CaveatsCaveats Cases signed out prior to guidelines in
2007 Home-brewed assay used for IHC Using FISH as gold standard rather than
outcome Low threshold for calling indeterminate
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ConclusionsConclusions IA appears to be more accurate than MA in HER2
IHC, particularly for 2+ cases (FISH non-amplified)
Algorithms appeared to overscore or underscore a minority of cases, particularly 1+ IHC cases (FISH non-amplified)
Pilot study suggests a role for IA in 2+ cases to avoid unnecessary FISH testing in overscored cases
Cost and time required for WSI analysis may still be prohibitive for routine clinical use without added resources in the laboratory for IA.
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Order HER2
Perform IA
Transcribe Results
Sign out case
Office MolecularIA Workstation
Perform FISH?
ConclusionsConclusions CPT 88360 – Morphometric analysis, tumor
immunohistochemistry (eg, Her2/neu, estrogen/progesterone receptor), quantitative, semiquantitative, each antibody; manual PC+TC=$147.95
CPT 88361 – Morphometric analysis, tumor immunohistochemistry (eg, Her2/neu, estrogen/progesterone receptor), quantitative, semiquantitative, each antibody; using computer assisted technology 88361 PC+TC=$229.16 Δ(TC+PC)=$81.21
HER2 FISH 88368 PC+TC=$710.00
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AcknowledgmentsAcknowledgments Aperio Technologies, Inc. Laura Nottoli, Craig Fenstermaker,
Holger Lange Grace Kronauer Geoffrey Turner MD PhD Tracy Roberts
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