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The upcoming TNM staging Hussein Elkhayat,MD CardioThoracic surgery , Assiut University Assiut,Egypt

New TNM staging for lung cancer

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Page 1: New TNM staging for lung cancer

The upcoming TNM staging

Hussein Elkhayat,MD CardioThoracic surgery , Assiut UniversityAssiut,Egypt

Page 2: New TNM staging for lung cancer

Pulmonary emergencies !

Page 3: New TNM staging for lung cancer

History of CANCER staging

Dr. Pierre Denoix, 1912–1990. Surgical oncologist at the Institut Gustave-Roussy, Paris

From 1929 the lead was taken by the Radiological Sub-Commission of the Cancer Commission of the League of Nations Health Organization.

IT WAS ALL ABOUT COMMON LANGUAGE

Page 4: New TNM staging for lung cancer

TNM Classification of Malignant Tumours 1968

T0 for cases in which one could find no evidence of the primary tumor, T1 for tumors confined to a segmental bronchus or to a segment of one lobe, T2 in which tumor was confined to a lobar bronchus or one lobe, T3 in which tumor was involving the main bronchus or more than one lobe,

and T4 for tumors extending beyond the lung. The N descriptors were NX, N0 and N1, in which there was “enlargement” of

“intrathoracic” lymph nodes on “clinical, radiological or endoscopic evidence.” These intrathoracic lymph nodes were further divided in to “hilar” or “peripheral” nodes Is this enough !

Page 5: New TNM staging for lung cancer

The 7th TNM

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HOW THEY DO IT !

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The Principles of the TNM System

1. To aid the clinician in the planning of treatment 2. To give some indication of prognosis 3. To assist in evaluation of the results of treatment 4. To facilitate the exchange of information between treatment centres 5. To contribute to the continuing investigation of human cancer

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What’s next to T N M

cTNM pTNM If there is doubt concerning the correct T, N, or M category to which a

particular case should be allotted, then the lower (i.e., less advanced) category should be chosen.

In the case of multiple simultaneous tumours in one organ, the tumour with the highest T category should be classified and the multiplicity or the number of tumours should be indicated in parentheses, e.g., T2 (m) or T2 (5).

Isolated Tumour Cells

Page 9: New TNM staging for lung cancer

Isolated Tumour Cells

N0 No regional lymph node metastasis histologically, no examination for isolated tumour cells(ITC)

pN0(i–) No regional lymph node metastasis histologically, negative morphological findings for ITC

pN0(i+) No regional lymph node metastasis histologically, positive morphological findings for ITC

pN0(mol–) No regional lymph node metastasis histologically, negative non-morphological findings for ITC

pN0(mol+) No regional lymph node metastasis histologically, positive non- morphological findings for ITC

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Histopathological Grading

GX Grade of differentiation cannot be assessed G1 Well differentiated G2 Moderately differentiated G3 Poorly differentiated G4 Undifferentiated

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Additional Descriptors

The suffix m the presence of multiple primary tumours at a single site y Symbol. In those cases in which classification is performed during or

following initial multimodality therapy, The ycTNM r Symbol. Recurrent tumours, when classified after a disease-tree

interval, are identified by the prefix r. a Symbol. The prefix a indicates that classification is first determined at

autopsy.

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Optional Descriptors

L – Lymphatic Invasion LX Lymphatic invasion cannot be assessed L0 No lymphatic invasion L I Lymphatic invasion

V – Venous Invasion VX Venous invasion cannot be assessed V0 No venous invasion VI Microscopic venous invasion V2 Macroscopic venous invasion

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C-Factor

certainty factor, reflects the validity of classification according to the diagnostic methods employed. Its use is optional.

Cl Evidence from standard diagnostic means (e.g., inspection, palpation, and standard radiography, intraluminal endoscopy for tumours of certain organs)

C2 Evidence obtained by special diagnostic means (e.g., radiographic imaging in special projections, tomography, computerized tomography [CT], ultrasonography, lymphography, angiography; scintigraphy; magnetic resonance imaging [MRI]; endoscopy, biopsy, and cytology)

C3 Evidence from surgical exploration, including biopsy and cytology C4 Evidence of the extent of disease following definitive surgery and pathological examination

of the resected specimen C5 Evidence from autopsy Ex. T3C2, N2C1, M0C2.

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Residual Tumour (R) Classification RX Presence of residual tumour cannot be assessed R0 No residual tumour R1 Microscopic residual tumour R2 Macroscopic residual tumour

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Definitions for T,N,M Descriptors

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N Subclassification

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Node stations

Note station 3 The AJCC, UICC and IASLC recommend that

at least 6 nodes are removed during surgical resection, 3 from N1 and 3 from N2 stations (i.e. a representative node from each station) for accurate staging

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M Descriptor

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Patterns of Disease and TNM Classification of Patients with Lung Cancer with Multiple Pulmonary Sites of Involvement

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5-year survival (%)

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pT2a1v1(3)(c3)N1(c4)M1a(contra nod)(c5)-R0

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CASE study

• 69 yrs old male pt• Cancer larynx from 8 yrs • Operated for total laryngectomy with permanent tracheostomy• Receive postoperative adjuvant chemotheryapy and

radiotherapy • Esophageal stricture with frequent endoscopic dilatation • Accidentally discovered left upper lung zone opacity • CT scan left upper lobe mass with no detectable LNs.• Oncolgist consultation suggest it is a second primary NOT a

mets and recommend surgical treatment • PFT : !!!

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VATS 2 ports LUL

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What we need to do ?

Multidisciplinary team approach Low dose CT scan for males ,<55yrs and smoker MSCT scan with contrast AND REPORT ! Biopsy when suspected ;Bx, radiologically guided, EUBS,

Mediastinoscopy, VATS ,Thoracotomy Re-CT scan after treatment Multidisciplinary team approach Multidisciplinary team approach Multidisciplinary team approach

THANK YOU