STAR ABSTRACT Staging lung cancer Philippe Grenier MD In non-small cell lung cancer (NSCLC), radical surgical resection is considered to represent therapy most likely to offer cure. This is usually only possible if there is no involvement of unresectable structures and no distant metastases. In advanced disease, par- ticularly in the presence of distant metastases, cure is usually not possible and palliative chemotherapy and radiotherapy is considered the most appropriate therapeutic strategy. In small cell lung cancer (SCLC) treatment consists of chemotherapy with or without additional radiother- apy. In selected cases of disease limited to one hemithorax: radical surgery in combination with chemo- and/or radiotherapy may provide curative treatment. The aim of staging procedures is to determine the extent of the disease and, thus, select the most appropriate treatment. For this purpose it is important to reliably detect local tumor extent (T stage: Tl-T4) as well as the presence or absence of lym- phatic (N stage: NO-N3) and hemato- geneous (M stage: MO, Ml) metas- tases (Table 1). Staging system Revisions in stage grouping of the TNM subsets in the international sys- tem for staging lung cancer were made 1997, to provide greater speci- ficity for identifying patient groups with similar prognoses and treatment options. Patients who are likely to benefit from surgical resection are those with localized disease. Only stages I, II and IlIA can be considered as technically resectable (Table 2). Patients considered as definitely unre- sectable are those having distant metastases (Ml), controlateral or sub- clavian lymph node metastases (N3) or tumor classified T4. The local extent of tumor affects the extent of surgery required for rad- ical resection. Generally, a tumor sur- Table I. TNM description for staging lung cancer (1) TX Primary tumor cannot be assessed or cannot be visualized despite presence of malignant cells in sputum or bronchial wash- ings TO No evidence of primary tumor Tis Carcinoma in situ Tl 'Iumor s 3 cm surrounded by lung or visceral pleura; without bronchoscopic evidence of infiltration of main bronchus T2 Tumor> 3 cm / infiltration of main bronchus> 2 cm to carina / infiltration of visceral pleura / obstructive pneumonitis or atelectasis extending to the hilum but not involving entire lung T3 Infiltration of main bronchus < 2 cm to carina / infiltration of parietal or mediastinal pleura, chest wall, pericardium, diaphragm / obstructive pneumonitis or atelectasis of entire lung T4 Infiltration of heart, great vessels,trachea, esophagus, vertebral body / malignant pleural or pericardial effusion / satellite tumor nodules within the same lobe NX Regional lymph nodes cannot be assessed NO No regional lymph node metastases Nl Metastasis to ipsilateral intrapulmonary, peribronchial or hilar lymph nodes N2 Metastasis to ipsilateral mediastinal and/or subcarinallymph nodes N3 Metastasis to contralateral hilar, contralateral mediastinal, ipsi- or contralateral scalene or supraclavicular lymph node metas- tases (note: cervical or abdominal lymph node metastases are considered Ml) MX Presence of distant metastases can not be assessed MO No distant metastases Ml Distant metastases (brain, adrenal, skeleton etc.), lymphatic distant metastases (cervical and abdominal lymph nodes), satellite tumor nodules in other lobes 14 SA JOURNAL OF RADIOLOGY • December 2002 STAR ABSTRACT TableII. Stagegrouping - TNM subsets (1) StagelA Tl NO MO StageI B T2 NO MO StageIIA Tl Nl MO StageII B T2 Nl MO T3 NO MO StageIII A T3 Nl MO Tl-3 N2 MO StageIII B T4 NO-2 MO Tl-4 N3 MO StageIV Tl-4 NO-3 Ml rounded by aerated lung with no invasion of the main bronchus (Tl) can be resected by lobectomy, whereas infiltration of the main bronchus, chest wall, diaphragm or medi- astinum requires more aggressive surgery (pneumonectomy or sleeve resection, resection of chest wall, diaphragm etc.) which is associated with higher morbidity and mortality. Infiltration of structures that are either unresectable (heart) or in which resection is usually associated with higher morbidity or mortality (esophagus, brachial plexus, spine, aorta, superior vena cava etc.) are usu- ally considered inoperable, particular- ly in view of the usually poor survival associated with these degrees of tumor extent. Other features do not affect resectability but reflect a more extensive tumor spread such as the presence of satellite tumor nodules in the same lobe. As treatment options in small cell lung cancer are more limited a simpli- fied staging system is often used in clinical practice (Table 3). Tumour extent CT continues to playa major role in preoperative staging of non-small cell lung cancer for selecting those TableIII. Staging of small celllung cancer (VeteransAdministration Lung Cancer Study Group) (2) Verylimited disease (VLD) StageI and II Limited disease (LD) Primary tumor limited to one hemithorax Ipsilateralhilar,mediastinalor supraclavicularlymph node metastases Contralateralmediastinallymph node metastases Atelectasis Paralysisof recurrent or phrenic nerve Smallpleural effusionwith no malignant cells Extensivedisease I (EDI) Contralateralhilar or supraclavicularlymph node metastases Infiltrationof chestwall Pleuraleffusion(exceptfor smalleffusionwith non malignant cells) Superiorvena cavasyndrome Metastasesto controlaterallung Extensivedisease II (EDII) Pleuriticcarcinomatosis Lymphangiticcarcinomatosis Distant metastases patients with localized disease who are likely to benefit from surgical resec- tion. Certain CT findings have been demonstrated as being diagnostic of unresectable disease. In many of these situations, biopsy proof of diagnosis is necessary but thoracotomy is not indicated. Although gross mediastinal invasion can be confidently diagnosed with CT, the contiguity of tumor with adjacent mediastinal structures is not equivalent to definite invasion. MR has the same limitations as CT in distinguishing tumor contiguity from tumor extension into mediasti- nal structures. Owing to its superior contrast res- olution, MR may demonstrate subtle chest wall invasion and be superior to CT in this regard. MR is also thought to be more accurate that CT in depict- ing chest wall invasion from superior sulcus tumor that commonly involves the vertebra posteriorly, and the sub- clavian vessels and brachial plexus 15 SA JOURNAL OF RADIOLOGY • December 2002 anteriorly. On the other hand, using helical scanning with thin collima- tion, bolus injection of contrast medi- um, and sagittal and coronal recon- structions, the anatomical environ- ment of the plexus may also be accu- rately assessed with CT. MR remains an alternative only in cases in which the CT findings are inconclusive and in those in which extension into the neural foramina and epidural space is suspected. Both CT and MR! cannot reliably differentiate between benign and malignant pleural and pericardial effusions. Presence of malignant pleural or pericardial effusion is best diagnosed by demonstration of malignant cells at aspiration. Nodal extent CT is very valuable in detecting mediastinal lymph node enlargement. Low sensitivity of CT is due to its inability to detect microscopic metas- STAR ABSTRACT tases within normal-sized lymph nodes. Low specificity arises from the frequent occurrence of enlarged hyperplastic nodes. Consequently, all patients with abnormal mediastinal lymph nodes on CT scans need lymph node resection or biopsy. MR has no superiority over CT and is not indicated in this regard. Positron emission tomography (PET) with F- 18 2 fluoro-2-deoxy-D-glucose (FDG) is more sensitive and specific than CT for nodal staging in lung can- cer. Mediastinoscopy has proven to be unnecessary in patients with CT evi- dence for stage I disease and a negative PET of the regional nodes. Increased FDG uptake in hilar and mediastinal lymph nodes can be used to direct surgical nodal sampling. The com- bined use of CT and PET to stage intrathoracic nodal metastases is not only clinically useful but also cost- effective. PET reduces the probability that a patient with unresectable medi- astinal nodal metastases will undergo an attempt at curative resection. Distant metastases In most institutions lung cancer patients undergo routine staging pro- cedures including chest radiographs, CT of the chest, abdomen and brain, bone scintigraphy and ultrasound examination of the abdomen. Because the adrenal glands are the most com- mon site for extrathoraeie metastases, CT examination should include the upper abdomen. An adrenal mass however may represent an incidental adenoma. Most incidental non- hyperfunctioning adrenal adenomas are less than 3 cm in diameter and of uniform low attenuation « 10 HU), because of their fat content. Routine unenhanced CT of the adrenal glands allows accurate prospective character- ization of many adrenal masses in patients with lung carcinoma. In institutions in which PET is readily available, this may be per- formed as the only additional exami- nation after CT, as it is the most accu- rate non-invasive imaging technique to confirm or exclude both lymph node and distant metastases (except for brain metastases) in a single exam- ination. Whole-Body FDG-PET improves the detection of extratho- racic disease and alters management in up to 40% of cases. Conclusion CT remains the imaging technique of choice in staging lung cancer. Despite its limitation, CT is indicated in order to determine the extent of the primary tumor, to evaluate the mediastinal space for the presence of nodal enlargement, and to screen metastatic disease in the adrenal glands. MR is only indicated as an additional examination in patients with superior sulcus tumor. Whole body PET is the best technique for screening both lymph node and dis- tant metastases. Suggested reading 1. Mountain CF. Revisions in the international system for staging lung cancer. Chest 1997; Ill: 1710-1717. 2. Stahel RA, Ginsberg R, Haveman K. Staging and prognostic factors in small cell lung cancer: a consensus report. Lung Cancer 1989; 5: 119- 124. 3. Parek BJ, Louie 0, Altorki N. Staging and the surgical management of lung cancer. In: "The radiologic clinics of north america. Lung can- cer': Henschke Cl, W.B. Saunders Company, Philadelphia, 2000, vol38, p 545-562. 4. Macari M, Rofsky NM, Naidich DP, Megibow AJ. 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