Esophageal Cancer Staging
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The American Joint Committee on Cancer (AJCC) tumor/node/metastasis (TNM) classification system for esophageal and esophagogastric junction cancer is provided below, along with histologic grade and anatomic/prognostic groups for squamous cell carcinoma and adenocarcinoma. [1, 2]
The T indicator is related to the extent of tumor invasion. The T stage (Table 1) has a direct impact on the patient’s stage, the likelihood of metastatic nodal disease, and outcome. [3] The location of the primary tumor does not have a direct correlation with prognosis, but influences management decisions, especially for non-metastatic disease, including surgical planning, consideration of neoadjuvant therapy, and determining radiation fields.
Positron emission tomography–computed tomography (PET-CT) has limited use in the T staging of esophageal cancers; however, it can demonstrate signs of adjacent organ infiltration. Endoscopic ultrasonography (EUS) is the imaging modality of choice for the evaluation of T staging. [4] Advanced (T4) disease is more accurately identified than early (T1) disease [5]
EUS can also be used to evaluate regional lymph nodes, allowing for N staging, especially with use of fine needle aspiration (FNA). CT and PET are inadequate for staging celiac and mediastinal lymph nodes. [6, 7, 8, 9] However, CT and EUS together can increase the accuracy of regional lymph node evaluation. [6, 10]
For T and N staging, EUS has good sensitivity and specificity. [5, 6]
PET-CT is extremely useful for the detection of metastatic disease that may not be identifiable with other imaging modalities. Diagnostic-quality CT images are also useful for additional information in case of uncertainties in the PET images. Fused images are also extremely useful, again, in the localization of subtle metastases and also for guiding a potential percutaneous biopsy.
PET-CT is the gold standard for evaluation of treatment with regard to quantifying metastatic disease response. This becomes particularly important as metabolic response to chemotherapy can often outstrip physical change in the tumor. Metabolic response has been seen to correlate with the histopathologic response, and the 3-year survival is far better in responders than in nonresponders (70% vs. 35%, respectively, in a study of esophageal junction adenocarcinoma). [11]
Histopathologic staging after surgical or endoscopic resection (Table 5) and postneoadjuvant therapy (Table 6) can be used for prognostication and guiding further management. [12]
Table 1. TNM Classification (Open Table in a new window)
Primary tumor (T)
TX
Primary tumor cannot be assessed
T0
No evidence of primary tumor
Tis
High-grade dysplasia,* defined as malignant cells confined by the basement membrane
T1
Tumor invades lamina propria, muscularis mucosae, or submucosa
T1a
Tumor invades lamina propria or muscularis mucosae
T1b
Tumor invades submucosa
T2
Tumor invades muscularis propria
T3
Tumor invades adventitia
T4
Tumor invades adjacent structures
T4a
Resectable tumor invading pleura, pericardium, azygos vein, diaphragm, or peritoneum
T4b
Unresectable tumor invading other adjacent structures, such as the aorta, vertebral body, and trachea
*High-grade dysplasia includes all noninvasive neoplastic epithelial lesions formerly called carcinoma in situ; that term is no longer used for columnar mucosae anywhere in the gastrointestinal tract.
Regional lymph nodes (N)
NX
Regional lymph node(s) cannot be assessed
N0
No regional lymph node metastasis
N1
Metastasis in 1-2 regional lymph nodes
N2
Metastasis in 3-6 regional lymph nodes
N3
Metastasis in 7 or more regional lymph nodes
Distant metastasis (M)
M0
No distant metastasis
M1
Distant metastasis
Table 2. Histologic grade (Open Table in a new window)
Histologic grade (G)
GX
Grade cannot be assessed—stage grouping as G1
G1
Well differentiated
G2
Moderately differentiated
G3
Poorly differentiated or undifferentiated*
*If undifferentiated with glandular component, stage as G3 adenocarcinoma; if undifferentiated with squamous cell component, or tumor remains undifferentiated after further testing, group as G3 squamous cell carcinoma.
Table 3. Squamous cell carcinoma location (Open Table in a new window)
X
Location unknown
Upper
Cervical esophagus to lower border of azygos vein
Middle
Lower border of azygos vein to lower border of inferior pulmonary vein
Lower
Lower border of inferior pulmonary vein to stomach, including gastroesophageal junction
Table 4. Clinical stage groups (Open Table in a new window)
Stage Group
cT
cN
cM
Squamous cell carcinoma
0
Tis
N0
M0
I
T1
N0–1
M0
II
T2
N0–1
M0
T3
N0
M0
III
T3
N1
M0
T1–3
N2
M0
IVA
T4
N0–2
M0
T1–4
N3
M0
IVB
T1–4
N0–3
M1
Adenocarcinoma
0
Tis
N0
M0
I
T1
N0
M0
IIA
T1
N1
M0
IIB
T2
N0
M0
III
T2
N1
M0
T3–4a
N0–1
M0
IVA
T1–4a
N2
M0
T4b
N0–2
M0
T1–4
N3
M0
IVB
T1–4
N0–3
M1
Table 5. Pathologic stage groups (Open Table in a new window)
Stage group
pT
pN
pM
Grade
Location
Squamous cell carcinoma
0
Tis
N0
M0
N/A
Any
IA
T1a
N0
M0
G1, X
Any
IB
T1b
N0
M0
G1–3, X
Any
T1a
N0
M0
G2–3
Any
T2
N0
M0
G1
Any
IIA
T2
N0
M0
G2–3, X
Any
T3
N0
M0
Any
Lower
T3
N0
M0
G1
Upper/middle
IIB
T3
N0
M0
G2–3
Upper/middle
T3
N0
M0
GX
Any
T3
N0
M0
Any
X
T1
N1
M0
Any
Any
IIIA
T1
N2
M0
Any
Any
T2
N1
M0
Any
Any
IIIB
T4a
N0–1
M0
Any
Any
T3
N1
M0
Any
Any
T2–3
N2
M0
Any
Any
IVA
T4a
N2
M0
Any
Any
T4b
N0–2
M0
Any
Any
T1–4
N3
M0
Any
Any
IVB
T1–4
N0–3
M1
Any
Any
Adenocarcinoma
0
Tis
N0
M0
N/A
IA
T1a
N0
M0
G1, X
IB
T1a
N0
M0
G2
T1b
N0
M0
G1–2, X
IC
T1
N0
M0
G3
T2
N0
M0
G1–2
IIA
T2
N0
M0
G3, X
IIB
T1
N1
M0
Any
T3
N0
M0
Any
IIIA
T1
N2
M0
Any
T2
N1
M0
Any
IIIB
T4a
N0–1
M0
Any
T3
N1
M0
Any
T2–3
N2
M0
Any
IVA
T4a
N2
M0
Any
T4b
N0–2
M0
Any
T1–4
N3
M0
Any
T1–4
N0–3
M1
Any
N/A = not applicable; X = not defined
Table 6. Postneoadjuvant therapy staging (Open Table in a new window)
Stage Group
ypT
ypN
ypM
I
T0-2
N0
M0
II
T3
N0
M0
IIIA
T0-2
N1
M0
IIIB
T4a
N0
M0
T3
N1
M0
T0-3
N2
M0
IVA
T4a
N1-2, X
M0
T4b
N0-2
M0
T1-4
N3
M0
IVB
T1–4
N0–3
M1
[Guideline] NCCN Clinical Practice Guidelines in Oncology. Esophageal and Esophagogastric Junction Cancers. National Comprehensive Cancer Network. Available at http://www.nccn.org/professionals/physician_gls/pdf/esophageal.pdf. Version 4.2017 — October 13, 2017; Accessed: February 7, 2018.
American Joint Committee on Cancer. Esophagus and Esophagogastric Junction. Amin MB, Edge S, Greene F, Byrd DR, Brookland RK, et al, eds. AJCC Cancer Staging Manual. 8th edition. New York, NY: Springer; 2016.
DeMeester SR. Adenocarcinoma of the esophagus and cardia: a review of the disease and its treatment. Ann Surg Oncol. 2006 Jan. 13 (1):12-30. [Medline].
Bruzzi JF, Munden RF, Truong MT, Marom EM, Sabloff BS, Gladish GW, et al. PET/CT of esophageal cancer: its role in clinical management. Radiographics. 2007 Nov-Dec. 27 (6):1635-52. [Medline].
DaVee T, Ajani JA, Lee JH. Is endoscopic ultrasound examination necessary in the management of esophageal cancer?. World J Gastroenterol. 2017 Feb 7. 23 (5):751-762. [Medline]. [Full Text].
ASGE Standards of Practice Committee., Jue TL, Sharaf RN, Appalaneni V, Anderson MA, Ben-Menachem T, et al. Role of EUS for the evaluation of mediastinal adenopathy. Gastrointest Endosc. 2011 Aug. 74 (2):239-45. [Medline].
ASGE Standards of Practice Committee., Evans JA, Early DS, Chandraskhara V, Chathadi KV, Fanelli RD, et al. The role of endoscopy in the assessment and treatment of esophageal cancer. Gastrointest Endosc. 2013 Mar. 77 (3):328-34. [Medline].
van Vliet EP, Heijenbrok-Kal MH, Hunink MG, Kuipers EJ, Siersema PD. Staging investigations for oesophageal cancer: a meta-analysis. Br J Cancer. 2008 Feb 12. 98 (3):547-57. [Medline]. [Full Text].
Lerut T, Flamen P, Ectors N, Van Cutsem E, Peeters M, Hiele M, et al. Histopathologic validation of lymph node staging with FDG-PET scan in cancer of the esophagus and gastroesophageal junction: A prospective study based on primary surgery with extensive lymphadenectomy. Ann Surg. 2000 Dec. 232 (6):743-52. [Medline]. [Full Text].
Puli SR, Reddy JB, Bechtold ML, Antillon D, Ibdah JA, Antillon MR. Staging accuracy of esophageal cancer by endoscopic ultrasound: a meta-analysis and systematic review. World J Gastroenterol. 2008 Mar 14. 14 (10):1479-90. [Medline]. [Full Text].
Ott K, Weber WA, Lordick F, Becker K, Busch R, Herrmann K, et al. Metabolic imaging predicts response, survival, and recurrence in adenocarcinomas of the esophagogastric junction. J Clin Oncol. 2006 Oct 10. 24 (29):4692-8. [Medline].
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Primary tumor (T)
TX
Primary tumor cannot be assessed
T0
No evidence of primary tumor
Tis
High-grade dysplasia,* defined as malignant cells confined by the basement membrane
T1
Tumor invades lamina propria, muscularis mucosae, or submucosa
T1a
Tumor invades lamina propria or muscularis mucosae
T1b
Tumor invades submucosa
T2
Tumor invades muscularis propria
T3
Tumor invades adventitia
T4
Tumor invades adjacent structures
T4a
Resectable tumor invading pleura, pericardium, azygos vein, diaphragm, or peritoneum
T4b
Unresectable tumor invading other adjacent structures, such as the aorta, vertebral body, and trachea
*High-grade dysplasia includes all noninvasive neoplastic epithelial lesions formerly called carcinoma in situ; that term is no longer used for columnar mucosae anywhere in the gastrointestinal tract.
Regional lymph nodes (N)
NX
Regional lymph node(s) cannot be assessed
N0
No regional lymph node metastasis
N1
Metastasis in 1-2 regional lymph nodes
N2
Metastasis in 3-6 regional lymph nodes
N3
Metastasis in 7 or more regional lymph nodes
Distant metastasis (M)
M0
No distant metastasis
M1
Distant metastasis
Histologic grade (G)
GX
Grade cannot be assessed—stage grouping as G1
G1
Well differentiated
G2
Moderately differentiated
G3
Poorly differentiated or undifferentiated*
*If undifferentiated with glandular component, stage as G3 adenocarcinoma; if undifferentiated with squamous cell component, or tumor remains undifferentiated after further testing, group as G3 squamous cell carcinoma.
X
Location unknown
Upper
Cervical esophagus to lower border of azygos vein
Middle
Lower border of azygos vein to lower border of inferior pulmonary vein
Lower
Lower border of inferior pulmonary vein to stomach, including gastroesophageal junction
Stage Group
cT
cN
cM
Squamous cell carcinoma
0
Tis
N0
M0
I
T1
N0–1
M0
II
T2
N0–1
M0
T3
N0
M0
III
T3
N1
M0
T1–3
N2
M0
IVA
T4
N0–2
M0
T1–4
N3
M0
IVB
T1–4
N0–3
M1
Adenocarcinoma
0
Tis
N0
M0
I
T1
N0
M0
IIA
T1
N1
M0
IIB
T2
N0
M0
III
T2
N1
M0
T3–4a
N0–1
M0
IVA
T1–4a
N2
M0
T4b
N0–2
M0
T1–4
N3
M0
IVB
T1–4
N0–3
M1
Stage group
pT
pN
pM
Grade
Location
Squamous cell carcinoma
0
Tis
N0
M0
N/A
Any
IA
T1a
N0
M0
G1, X
Any
IB
T1b
N0
M0
G1–3, X
Any
T1a
N0
M0
G2–3
Any
T2
N0
M0
G1
Any
IIA
T2
N0
M0
G2–3, X
Any
T3
N0
M0
Any
Lower
T3
N0
M0
G1
Upper/middle
IIB
T3
N0
M0
G2–3
Upper/middle
T3
N0
M0
GX
Any
T3
N0
M0
Any
X
T1
N1
M0
Any
Any
IIIA
T1
N2
M0
Any
Any
T2
N1
M0
Any
Any
IIIB
T4a
N0–1
M0
Any
Any
T3
N1
M0
Any
Any
T2–3
N2
M0
Any
Any
IVA
T4a
N2
M0
Any
Any
T4b
N0–2
M0
Any
Any
T1–4
N3
M0
Any
Any
IVB
T1–4
N0–3
M1
Any
Any
Adenocarcinoma
0
Tis
N0
M0
N/A
IA
T1a
N0
M0
G1, X
IB
T1a
N0
M0
G2
T1b
N0
M0
G1–2, X
IC
T1
N0
M0
G3
T2
N0
M0
G1–2
IIA
T2
N0
M0
G3, X
IIB
T1
N1
M0
Any
T3
N0
M0
Any
IIIA
T1
N2
M0
Any
T2
N1
M0
Any
IIIB
T4a
N0–1
M0
Any
T3
N1
M0
Any
T2–3
N2
M0
Any
IVA
T4a
N2
M0
Any
T4b
N0–2
M0
Any
T1–4
N3
M0
Any
T1–4
N0–3
M1
Any
N/A = not applicable; X = not defined
Stage Group
ypT
ypN
ypM
I
T0-2
N0
M0
II
T3
N0
M0
IIIA
T0-2
N1
M0
IIIB
T4a
N0
M0
T3
N1
M0
T0-3
N2
M0
IVA
T4a
N1-2, X
M0
T4b
N0-2
M0
T1-4
N3
M0
IVB
T1–4
N0–3
M1
Anand D Patel, MD Hematologist/Oncologist, Ascension Wisconsin
Anand D Patel, MD is a member of the following medical societies: American College of Physicians, American Medical Association, Student National Medical Association
Disclosure: Nothing to disclose.
Prianka Bhattacharya, MD Fellow, Department of Hematology and Medical Oncology, Lankenau Medical Center
Prianka Bhattacharya, MD is a member of the following medical societies: American Society of Clinical Oncology, American Society of Hematology, National Society of Collegiate Scholars, Phi Beta Kappa
Disclosure: Nothing to disclose.
Thomas Oliver, DO Resident Physician, Department of Medicine, Lankenau Medical Center
Thomas Oliver, DO is a member of the following medical societies: American College of Physicians, American Medical Association, American Osteopathic Association, American Society of Clinical Oncology
Disclosure: Nothing to disclose.
Jessica Katz, MD, PhD, FACP Senior Medical Director, Immuno-Oncology, Oncology R&D, GlaxoSmithKline
Jessica Katz, MD, PhD, FACP is a member of the following medical societies: American College of Physicians, American Society of Clinical Oncology, American Society of Hematology
Disclosure: for: Currently employed at GSK.
Mary L Windle, PharmD Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference
Disclosure: Nothing to disclose.
Christopher D Braden, DO Hematologist/Oncologist, Chancellor Center for Oncology at Deaconess Hospital; Medical Director, Deaconess Hospital Outpatient Infusion Centers; Chairman, Deaconess Hospital Cancer Committee
Christopher D Braden, DO is a member of the following medical societies: American Society of Clinical Oncology, American Society of Hematology
Disclosure: Nothing to disclose.
N Joseph Espat, MD, MS, FACS Harold J Wanebo Professor of Surgery, Assistant Dean of Clinical Affairs, Boston University School of Medicine; Chairman, Department of Surgery, Director, Adele R Decof Cancer Center, Roger Williams Medical Center
N Joseph Espat, MD, MS, FACS is a member of the following medical societies: Alpha Omega Alpha, American Association for Cancer Research, American College of Surgeons, American Medical Association, American Society for Parenteral and Enteral Nutrition, American Society of Clinical Oncology, Americas Hepato-Pancreato-Biliary Association, Association for Academic Surgery, Central Surgical Association, Chicago Medical Society, International Hepato-Pancreato-Biliary Association, Pancreas Club, Sigma Xi, Society for Leukocyte Biology, Society for Surgery of the Alimentary Tract, Society of American Gastrointestinal and Endoscopic Surgeons, Society of Surgical Oncology, Society of University Surgeons, Southeastern Surgical Congress, Southern Medical Association, Surgical Infection Society
Disclosure: Nothing to disclose.
Terence D Rhodes, MD, PhD Medical Oncologist, Intermountain Medical Group
Terence D Rhodes, MD, PhD is a member of the following medical societies: American Association for Cancer Research, American Society of Clinical Oncology
Disclosure: Nothing to disclose.
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