early colorectal cancer quality and rules for a good …...early colorectal cancer quality and rules...
TRANSCRIPT
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Early colorectal cancer Quality and rules for a good pathology reportHistoprognostic factors
Pr Frédéric Bibeau, MD, PhD
Head, Pathology department
CHU de Caen,
Normandy University,
France
ESMO preceptorship, Barcelona, 20.10.17
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Quality and rules of a good pathology report
Simple but rigourous
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Reporting proforma for colorectal resection specimen
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Early colorectal cancer (CRC)
Useful histopronostic factors
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Micrometastaticdisease
Adjuvantchemotherapy
Useful histopronostic factors
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- Tumour
- Depth of invasion
- Distant extension
- Margins
Useful histopronostic factors
Content
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- Tumour
- Depth of invasion
- Distant extension
- Margins
Useful histopronostic factors
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Colorectal cancer (CRC): heterogeneous disease
Different histologic types
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CRC histologic types
Adenocarcinoma
Mucinous
Signet ring cells
Medullary
Lieberkühnian micropapillary
Serrated
adenosquamous
Small cells
Carcinoma
90%
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Mucinous
Signet ring cells
Medullary CD3+
Tumour Microenvironment
Crohn-like reaction
Lymphocytic infiltrate
MSI histologic features
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CRC grading
Low grade (well, moderatly differenciated)
High grade (poorly/indifferenciated)
modulation according to MSI status
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- Tumour
- Depth of invasion
- Distant extension
- Margins
Useful histopronostic factors
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Tis T1 T2 T3 T4
MUCOSA
SUB-MUCOSA
MUSCULARIS
SUB-SEROSA -->SEROSA -->
pT
pN
pM
Muscularis Muscosae -->
N0 : no positive lymph node (LN)N1 : 3 positive LNN2 : ≥ 4 positive LN
M0 : No distant metastasisM1 : Distant metastasis
Organe infiltrationand / or visceral
peritoneal perforation
pTNM classification
TNM UICC 2016 8th Classification
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Serosal involvement
Gross examination +++
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Serosal involvement
8th TNM UICC 2016 classification
pT4a
Frankel et al. Mod Pathol 2015
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pT4a
Frankel et al. Mod Pathol 2015
Serosa involvement +
reactive phenomenons ✻
pT3
✻Mesothelial Hyperplasia , inflammation, erosion, ulceration
<1mm
Serosal involvement
8th TNM UICC 2016 classification
Deeper block levels
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pT4a
Frankel et al. Mod Pathol 2015
8th TNM UICC 2016 classification
Serosal involvement
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Tumour budding
Invasion front
Wang LM, Am J Surg Path 2009
optionnal
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Tumor budding Score (0,785 mm2)
(Hot Spot method , X 20)
HE staining
1 (Budd 1) < 5 Faible
2 (Budd 2) 5-10 Intermédiaire
3 (Budd 3) ≥ 10 Elevé
Tumour budding
Recommandations AJCC 8th edition, Bern International Consensus Lugli et al, Modern Path 2017
optionnal
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Galon et al. Cancer Res 2007
Immune adaptative microenvironment
optionnal
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Prognostic impact of immune response
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Immune adaptative microenvironnement
optionnal
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- Tumour
- Depth of invasion
- Distant extension
- Margins
Useful histopronostic factors
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Tis T1 T2 T3 T4
MUCOSA
SUB-MUCOSA
MUSCULARIS
SUB-SEROSA -->SEROSA -->
pT
pN
pM
Muscularis Muscosae -->
N0 : no positive lymph node (LN)N1 : 3 positive LNN2 : ≥ 4 positive LN
M0 : No distant metastasisM1 : Distant metastasis
Organe infiltrationand / or visceral
peritoneal perforation
TNM UICC 2016 8thClassification
pTNM classification
Adjuvant
chemotherapy
N+
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Recommendations > 12But… More = Better
Distant extension: lymph nodes
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Nx Lymph node status not asessable
N0 No positive regional lymph node
N1 Metastase(s) in 1-3 regional lymph node(s)
• N1a
• N1b
• N1c
1 positive lymph node
➢ 2-3 positive regional lymph node
➢ Tumour deposits, satellites, in the sub-serosa or peri-rectal or
peri-colic non peritonised tissue, without regional metastatic
lymph node
N2 ≥ 4 or more positive regional lymph nodes
• N2a
• N2b
• ≥ 4-6 regional positive lymph nodes
• ≥ 7 regional positive lymph nodes
TNM UICC 2016 8thClassification
Distant extension : tumour deposits
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Pericolic or -rectal tissu location
Puppa et al. Modern Pathol 2007
Distant extension : tumour deposits
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Recommendations for interprétation(F.A.Q*)
- N1c only if negative lymph node
- No N1c if positive lymph node
- Do not add tumour deposits to positive lymph node
- Do not modify T stage
*Frequently Asked Question
Distant extension : tumour deposits
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Nagtegaal et al. J Clin Oncol 2017 35:1119-1127
Impact of « tumour deposits »
N+/TD+: Next TNM classification (9th edition) ?
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Nx Lymph node status non assessable
N0 No positive regional lymph node
N1 Metastase(s) in 1-3 regional lymph node(s)
• N1a
• N1b
• N1c
1 positive lymph node
➢ 2-3 positive regional lymph node
➢ Tumour deposits, satellites, in the sub-serosa or peri-rectal or
peri-colic non peritonised tissu without regional metastatic lymph
node
N2 ≥ 4 or more positive regional lymph nodes
• N2a
• N2b
• ≥ 4-6 regional positive lymph nodes
• ≥ 7 regional positive lymph nodes
TNM UICC 2017 8thClassification
Distant extension : N+ subdivision
3 vs 6 months CT ?
Clinical trials stratification
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Liebig et al J Clin Oncol 2010Mori et al. Histopathology 2009 Harris et al, Am J Surg Path 2008
Lymphatic invasion Venous invasion Perineural invasion
Distant extension : VELIPI*
*Venous emboli and lymphatic and perineural invasion
L category V category
8th TNM UICC 2016 classification
Pn1 category
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Extra-mural venous invasion
30%: frequent underestimation ?
Nagtegaal et al. histopathology 2015
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Perineural invasion
DFS CSS
OS
Knijn et al. Am J Surg Path 2015
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- Tumour
- Depth of invasion
- Distant extension
- Margins
Useful histopronostic factors
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Margins
Distal ans proximal
very rarely positive
Circumferential (Rectum)
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- Tumour
- Depth of invasion
- Distant extension
- Margins
Useful histopronostic factors
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Molecular profileMicrosatellite instability (15%)
Immunohistochemistry Molecular biology
Favorable prognosis in CCR stage II
Normal DNA
MSI tumour
Less or
supple-
mentary
nucleotides
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• Impact of KRAS et BRAF mutations
• Poor prognosis in stage III CRC (MSS)*
• Not used as prognostic factors in 2017…
• Stratification for clinical trials ?
• MSI, RAS, BRAF status for all CRC, tomorrow ?
*Taieb et al JAMA Oncol 2016
Molecular profile
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Cellule tumorale circulante (CTC)
ADN tumoral circulant (ADN ct)
MicroARN (miRNA)
Adapted from Diaz et al J Clin Oncol 2014; 32:579-86
Perspectives: liquid biopsyMinimal residual disease Tie J, sci Transl Med 2016
Pierre Laurent-Puig
lecture +++
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Perspectives
- Treatment for particular stage II ?- No treatment for certain stage III ?
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Take home messages
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- pTNM
- Grade
- VELIPI
- MSI
Early CRC in 2017
Useful histopronostic factors for treatment
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- pTNM
- Grade
- VELIPI
- MSI
N+ (including N1c= tumour dep.) adjuvant CT
Stage III
Early CRC in 2016
Useful histopronostic factors for treatment
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- pTNM
- Grade high (poor differenciation)
- VELIPI +
- MSI -
N0 pT4 (serosa +), <12 N
Adjuvant CT
(Multidisciplinaryteam discussion)
Stage II
Early CRC in 2016
Useful histopronostic factors for treatment
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Differenciation (Grade)
Extension- Tumour (pT)- Lymph node (pN)
Margins- Distal/proximal - Circumferential
(Rectum)
Histologic type
OMS
Vasculo-lymphatic and perineural invasions
Lymphatics Veins Nerves
Pathology report key elementsMultidisciplinary board
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• www.sfpathol.org
• www.ecancer.fr
Reporting proforma for colorectal cancer
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Translationnal research
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Back up slides
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Goldstein et al. Am J Surg Pathol 2002
Distant extension: lymph nodes
Recommendations > 12But…
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Tougeron et al. Modern Path 2009.
Distant extension: lymph nodes
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Gross examination +++
No magic number !More = better
Distant extension: lymph nodes
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TNM 5th edition
>3 mm
Lymph node
No residual lymph node
Tumour deposit
Smooth shape
Lymph node
Distant extension : tumour deposits
Frankel et al. Mod Pathol 2015
TNM 6th edition TNM 7, 8th edition
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Impact of « tumour deposits » (N1c)
P< 0.001
Jin et al. Am J Surg Path 2014
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Jin et al. Am J Surg Path 2014
P= 0.087
Impact of « tumour deposits » (N1c)
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Invasion front
Expansive InfiltrativeSvrcek et al. Cancero Dig. 2012
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TNM Classification of Malignant
Tumours - 8th edition
Changes between the 7th and 8th editions
“We unite the cancer community to reduce the global cancer
burden, to promote greater equity, and to integrate cancer
control into the world health and development agenda.”
December 2016
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Colon and Rectum
Definition of tumour deposit clarified
Tumour deposits (satellites) are discrete macroscopic or microscopic nodules of cancer in the
pericolorectal adipose tissue’s lymph drainage area of a primary carcinoma that are
discontinuous from the primary and without histological evidence of residual lymph node or
identifiable vascular or neural structures. If a vessel wall is identifiable on H&E, elastic or
other stains, it should be classified as venous invasion (V1/2) or lymphatic invasion (L1).
Similarly, if neural structures are identifiable, the lesion should be classified as perineural
invasion (Pn1). The presence of tumour deposits does not change the primary tumour T
category, but changes the node status (N) to N1c if all regional lymph nodes are negative
on pathological examination
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Colon and Rectum
• T and N categories Unchanged
M1 Distant metastasis
M1a Metastasis confined to one
organ (liver, lung, ovary,
non regional lymph node(s))
without peritoneal
metastases
M1b Metastasis in more than one
organ
M1c Metastasis to the
peritoneum with or without
other organ involvement
Stage Unchanged except for Stage IVA,
IVB, IVC as below
Stage IV Any T Any N M1
Stage IVA Any T Any N M1a
Stage IVB Any T Any N M1b
Stage IVC Any T Any N M1c
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Conclusion
New TNM
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Ratio tumeur/stroma
Mesker WE et al. Cell Oncol Cell Oncol. 2007;29(5):387-98. Cell Oncol. 2009;31(3):169-78
Huijbers A et al. Ann Oncol. 2013 Jan;24(1):179-85.
Pronostic défavorable
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Voie CIN Voie MSIVoie CIMP≈20 % 15- 20 %80-85 %
Syndrome de
Lynch
Tumeurs
festonnéesCarcinome classique
Cancer du
sujet âgé
Classification moléculaire CCR
Lieberkühnien Festonné Médullaire/ lymphocytes
Instabilité chromosomique Instabilité épigénétique Instabilité microsatellitaire
KRAS TP 53 BRAF
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Profil moléculaire CCR
- Corrélation morphologique?
- Intégration clinique ?
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RAS et BRAF WT
Mutation
KRAS exon 2
Mut KRAS
ex 3, 4
40%
Mut
NRAS
50%
RAS muté
HER-2
BRAF
10%
MSI
15%
Amplifications: 2,5%
Mutations: 1,9%
Courtoisie Astrid Lièvre
Penault-Llorca et al.ESMO 2016
Taieb et al. Jama Oncology 2016
Profil moléculaire CCR
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Individualisation pronostique par IHC ?
BRAF +muté
BRAF +muté
MSI
MSS
Toon et al. Modern Pathol 2014, Dalerba et al. N Eng J Med 2015
CDX2- CDX2+