IHC Panel Selection by Tumor Type (ASCO/CAP)
IHC Panel Selection by Tumor Type (ASCO/CAP): IHC Panel Selection → Morphologic Category → Carcinoma Panel → Breast Cancer Predictive → IHC Reporting.
Interactive Decision Tree
Algorithm Steps
- ▶Start
IHC Panel Selection
Choose appropriate panel based on differential
- ◆Decision
Morphologic Category
Initial classification by H&E
- Carcinoma (epithelial)
- Sarcoma (mesenchymal)
- Melanoma
- Lymphoma/Leukemia
- Neuroendocrine
- Undifferentiated/Unknown
- ●Action
Carcinoma Panel
Determine primary site
- CK7/CK20 pattern
- TTF-1 (lung, thyroid)
- CDX2 (GI)
- PAX8 (kidney, gynecologic)
- GATA3 (breast, urothelial)
- PSA/NKX3.1 (prostate)
- Napsin-A (lung adenocarcinoma)
- ●Action
Breast Cancer Predictive
Required biomarkers
- ER (threshold ≥1%)
- PR (threshold ≥1%)
- HER2 (IHC 0, 1+, 2+, 3+)
- If HER2 2+: FISH reflex
- Ki-67 (prognostic)
- ●Action
IHC Reporting
Standardized reporting
- Clone and vendor
- Percentage positive (when applicable)
- Intensity (weak, moderate, strong)
- Pattern (nuclear, cytoplasmic, membranous)
- Interpretation and differential
- ●Action
Colorectal Cancer Markers
Lynch and predictive
- MMR panel: MLH1, MSH2, MSH6, PMS2
- If MLH1 loss: BRAF V600E IHC or MLH1 methylation
- Consider HER2 for metastatic
- PDL1 if MSI-H
- ●Action
Lung Cancer Markers
Predictive and diagnostic
- TTF-1, Napsin-A (adenocarcinoma)
- p40, CK5/6 (squamous)
- PDL1 (TPS for pembrolizumab)
- ALK, ROS1 IHC (reflex to FISH)
- Consider molecular panel (NGS)
- ●Action
Carcinoma Unknown Primary
Systematic approach
- CK7+/CK20-: Lung, breast, ovary, pancreatobil
- CK7-/CK20+: Colorectal
- CK7+/CK20+: Upper GI, pancreas, urothelial
- CK7-/CK20-: RCC, HCC, SCC
- Site-specific markers to narrow
- ●Action
Melanoma Panel
Confirm melanocytic origin
- S100 (sensitive)
- SOX10 (sensitive)
- Melan-A/MART-1 (specific)
- HMB-45 (specific)
- PRAME (distinguish from nevi)
- Ki-67 (prognostic)
- ●Action
Sarcoma Panel
Subtype classification
- SMA, desmin (smooth/skeletal muscle)
- S100, SOX10 (nerve sheath)
- CD34 (DFSP, SFT)
- MDM2 (liposarcoma)
- TLE1 (synovial sarcoma)
- STAT6 (solitary fibrous tumor)
- ●Action
Neuroendocrine Panel
Confirm and grade
- Synaptophysin (sensitive)
- Chromogranin (specific)
- INSM1 (sensitive)
- Ki-67 (grading)
- TTF-1 (lung NET)
- CDX2 (midgut)
Guideline Source
ASCO/CAP IHC Guidelines and WHO Classification
Clinical Safety Information
Clinical Decision Support — Not a Substitute for Clinical Judgment
Individual patient factors may require deviation from these recommendations.
Known Limitations
- IHC interpretation requires clinical correlation
- Panels are suggestions, not exhaustive
- Sensitivity/specificity varies by antibody clone
- Quality control essential
- Molecular testing increasingly supplements IHC
Applicable Regions
AU: RCPA IHC recommendations
UK: RCPath IHC standards
US: ASCO/CAP biomarker guidelines
Next steps
Finish the workflow by opening the most relevant calculator, then convert the session into a live account when you are ready.
Related Resources
Frequently Asked Questions
What is the IHC Panel Selection by Tumor Type (ASCO/CAP)?
The IHC Panel Selection by Tumor Type (ASCO/CAP) is a diagnostic clinical algorithm for Pathology. It provides a structured decision tree to guide clinical decision-making, based on ASCO/CAP IHC Guidelines and WHO Classification.
What guideline is the IHC Panel Selection by Tumor Type (ASCO/CAP) based on?
This algorithm is based on ASCO/CAP IHC Guidelines and WHO Classification (DOI: 10.1200/JCO.2016.68.6757).
What are the limitations of the IHC Panel Selection by Tumor Type (ASCO/CAP)?
Known limitations include: IHC interpretation requires clinical correlation; Panels are suggestions, not exhaustive; Sensitivity/specificity varies by antibody clone; Quality control essential; Molecular testing increasingly supplements IHC. Individual patient factors may require deviation from these recommendations.
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