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Ann Thorac Surg 1999;68:326-330
© 1999 The Society of Thoracic Surgeons
a Department of Thoracic Surgery, Hyogo Medical Center for Adults, Hyogo, Japan
Address reprint requests to Dr Tsubota, Department of Thoracic Surgery, Hyogo Medical Center for Adults, Kitaohji-cho 13-70, Akashi City 673, Hyogo, Japan
e-mail: n-tsubo{at}sanynet.ne.jp
| Abstract |
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Methods. Of 1,002 consecutive patients who underwent operation for primary lung cancer between June 1984 and December 1996, we reviewed the medical record of 889 patients who underwent complete resection for nonsmall cell lung cancer.
Results. We considered 89 patients (10.0%) to have synchronous ipsilateral PM. After reclassification to the former staging system revised in 1992, 5 patients were classified as stage I, 29 as stage IIIA, 48 as stage IIIB, and 7 as stage IV. In the new staging system revised in 1997, 48 patients were recategorized as stage IIIB, and 41 as stage IV. The 5-year survival of patients without PM (49.5%) was significantly better than that of patients with PM in primary-tumor lobe (29.6%, p = 0.002) or in nonprimary-tumor ipsilateral lobe (23.4%, p = 0.0002). Although the survival of patients with stage IV cancer without PM was significantly worse than that of patients with the new (1997) stage IV cancer with PM (p = 0.02), it was similar to that of patients with the former (1992) stage IV cancer with PM. The survival of PM patients with N0 or N1 disease was significantly better than that of PM patients with N2 or N3 disease (p = 0.001). Furthermore, in patients with the new (1997) stage IIIB cancer, the survival of N0 disease was better than that of N2 disease (p = 0.007).
Conclusions. Inasmuch as the prognosis of nonsmall cell carcinoma in patients with PM strongly correlated with N factor rather than PM factor, N factor should be reflected in a staging designation. We therefore consider the new TNM classification for PM reclassified in 1997 to be less acceptable for surgical-pathologic staging than the revision in 1992.
| Introduction |
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In 1992, the Union Internationale Contre le Cancer and American Joint Committee on Cancer revised the TNM classification for lung cancer with PM by upgrading T factor as a local progression instead of M factor. Briefly, T factor was upgraded by a single unit if PM was located at the primary lobe, or was determined as T4 if PM occurred in the other lobes of the ipsilateral lung [5, 6]. However, the 1997 recommendations for staging have included new rules, namely that satellite tumors within the primary-tumor lobe of the lung should be classified T4 and that ipsilateral PM in a distant, that is nonprimary-tumor, lobe of the lung should be classified M1 [7] (Table 1). In this study, our goal is to see whether the new staging system might be adequate through surgical-pathologic findings and postoperative prognoses of patients with synchronously detected and resected ipsilateral PM lesions.
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| Material and methods |
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All cancers were staged using the criteria of the International Staging System for Lung Cancer [1, 2, 57], and staging was based on data obtained from imaging, bronchoscopy, invasive diagnostic techniques, operative findings, and pathologic examination. Careful intraoperative staging at the time of surgical resection was performed by dissecting intrapulmonary, hilar, and mediastinal nodes. The TNM subsets are used as follows: T1 N0 M0 or T2 N0 M0, stage I; T1 N1 M0 or T2 N1 M0, stage II; T3 N0 M0, T3 N1 M0, T3 N2 M0, T1 N2 M0, T2 N2 M0, or T3 N2 M0, stage IIIA; T4 N1 M0, T4 N2 M0, T4 N3 M0, T1 N3 M0, T2 N3 M0, or T3 N3 M0, stage IIIB; T1 N1 M1, T1 N2 M1, T1 N3 M1, T2 N1 M1, T2 N2 M1, T2 N3 M1, T3 N1 M1, T3 N2 M1, T3 N3 M1, T4 N1 M1, T4 N2 M1, or T4 N3 M1, stage IV. The changes of the TMN classification for PM are shown in Table 1. According to the TNM system revised in 1992 [5, 6], PM in the ipsilateral lung was alternatively included in T factor, instead of M1 in the TNM classification produced in 1986 [1, 2]. If PM was located in the primary lobe, T factor was upgraded by a single unit, and if PM was done in the other lobes of the ipsilateral lung, it was determined as T4. Furthermore, the latest revision in 1997 proposed that satellite tumors within the primary-tumor lobe should be classified T4 and PM in nonprimary-tumor lobes should be classified M1 [7]. On the other hand, PM in the contralateral lung, which was considered as distant metastasis, was included in M1 disease. In the ipsilateral lung, including the lobe in which the primary lesion was located, the presence of PM was first checked macroscopically by close palpation during operation. Postoperatively, surgeons, radiologists, and pathologists together checked satellite nodules macroscopically and by palpation in the fixed specimen sliced 1 cm in thickness. Suspicious nodules were evaluated microscopically in detail. Histologic typing was done according to the World Health Organization classification [10]. All cases of bronchioloalveolar carcinoma were excluded just because of the question of multicentricity of those primary cancers. Generally, the histopathology of adenomatous hyperplasia and atypical adenomatous hyperplasia is similar to that of PM of adenocarcinoma. We therefore paid attention to excluding adenomatous hyperplasia and atypical adenomatous hyperplasia. All patients underwent a surgical resection of the main and metastatic pulmonary lesions with a dissection of hilar and mediastinal lymph nodes. In patients with stage IV cancer, the distant metastatic lesions were treated with surgical resection or radiotherapy. All patients had a chest roentgenogram, a history, and a physical examination made at the follow-up visit, which took place at least twice a year. All deaths including the operative death were presumed to be associated with lung cancer, and the analysis included all types of death. The final date for evaluation was December 31, 1997. Overall follow-up ranged from 12 to 163 months, with a median of 69 months.
Cumulative survival rates were calculated by the Kaplan-Meier estimation using the date of pulmonary resection as the starting point and the date of death or last follow-up as the end point, and differences in survival were determined by log-rank analysis. A multivariate analysis of independent prognostic factors was performed with Coxs proportional hazards regression model.
| Results |
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Pneumonectomy including sleeve procedure was performed in 7 patients, lobectomy including sleeve technique in 69, and segmentectomy including partial resection in 13. Regarding N classification, 32 patients had N0 disease; 17, N1 disease; 33, N2 disease; and 7, N3 disease. Concerning staging of 800 patients without PM (pm0), 400 were classified as stage I, 109 as stage II, 196 as stage IIIA, 72 as stage IIIB, and 23 as stage IV (Table 2). Reclassification of patients with PM is shown in Table 2. In the 1986 staging system, all the patients with PM belonged to stage IV. After reclassification of the patients with PM to the 1992 staging system, 5 patients were classified as stage I, 29 as stage IIIA, 48 as stage IIIB, and 7 as stage IV. In the 1997 staging system, 48 patients were recategorized as stage IIIB, and 41 as stage IV.
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| Comment |
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Miller [12] and Barsky and associates [13] raised the possibility that adenocarcinoma with bronchioloalveolar features of PM might represent multifocal bronchioloalveolar carcinoma rather than PM. The reason for an excellent survival of these cases raises questions about the biologic behavior of bronchioloalveolar carcinoma as compared with other types of adenocarcinoma. Therefore, we excluded all cases of bronchioloalveolar carcinoma from this study. Nakajima and coworkers [14] stated in their detailed histopathologic study that 30% of PM lesions might be adenomatous or atypical adenomatous hyperplasias, and patients with such lesions also exhibited a long postoperative survival. It is hard to distinguish adenomatous hyperplasia or atypical adenomatous hyperplasia from PM when the main lesion was well-differentiated adenocarcinoma. Indeed, atypical adenomatous hyperplasia has been regarded as a precancerous lesion, and its morphology is very similar to that of the peripheral part of well-differentiated adenocarcinoma. We demonstrated no significant differences in survival between PM patients with well-differentiated adenocarcinoma and those with a more poorly differentiated one, supporting little chance for a contamination of adenomatous hyperplasia or atypical adenomatous hyperplasia.
The TNM classification of patients with ipsilateral PM is difficult, because of the small number of patients identified for end result studies. Several reports that led to the current rules for classifying patients with PM may provide insight into the complexity of developing internationally acceptable rules for classification. Deslauriers and associates [11], in the first published study of the influence of satellite nodules on prognosis, showed that satellite nodules, which they considered a manifestation of local disease, had a deleterious effect on prognosis and recommended that they be classified as T3. Actually, patients with nonsmall cell carcinoma with PM have a better prognosis than those with other types of distant metastasis if a surgical resection is possible [3, 4]. These data suggested that PM might be an intrathoracic disease if no distant metastasis or invasion to the neighboring structures was observed, supporting that the incidence of PM in the ipsilateral lung was alternatively included in the T factor instead of M factor. On the other hand, Naruke and colleagues [15] supported a new rule in 1997 that the satellite tumor within the primary-tumor lobe should be classified T4 and ipsilateral PM in nonprimary-tumor lobe should be classified M1. As a result of these studies, the American Joint Committee on Cancer and the Union Internationale Contre le Cancer revised the TNM classification of lung cancer with ipsilateral PM in 1992 [5, 6] and in 1997 [7]. In our study, we evaluated the prognosis of patients with nonsmall cell carcinoma with ipsilateral PM to investigate the appropriateness of the TNM classification. The prognosis of our patients with PM was comparable with that of subgroups in the same stage revised in 1992 rather than in the same stage revised in 1997 or before 1992. Analysis showed that the prognosis of patients with nonsmall cell carcinoma strongly correlated with N factor as compared with PM factor, supporting that N factor rather than PM factor should be reflected in a designation of the TNM staging system. In patients with PM who underwent resection, the ones with N0 or N1 disease did better at 5 years than those with N2 disease, confirming that nodal status is the best predictor of survival in resected lung cancer. According to the 1997 staging system, no significant difference was observed between the survival of patients with stage IIIB cancer with PM and those with stage IV cancer with PM. That was the reason that N factor would be utterly ignored in the 1997 staging system. Based on surgical-pathologic staging and the postoperative survival data, we consider the new classification for PM to be less acceptable than that revised in 1992. Naruke and coworkers [15] revealed that 5-year survival for all patients were stage I, 68.5%; stage II, 46.9%; stage IIIA, 26.1%; stage IIIB, 9.0%; and stage IV, 11.2%, and that 5-year survival rates for patients with pm1 and pm2 were 17.8% and 8.3%, respectively. Although the survival of all their patients grouped by stage was similar to that of our series (stage I, 67.2%; stage II, 49.4%; stage IIIA, 30.4%; stage IIIB, 16.7%; and stage IV, 10.8%), the survival of their patients with PM was much worse compared with that of ours (pm1, 29.6% and pm2, 23.4%) which was comparable with that of the studies by Shimizu and associates [16], Yoshino and coworkers [17] and Fujisawa and colleagues [18]. This significant difference in survival may be because of closer attention to detect PM lesion during and after the operation, which would affect stage bias. Although we discovered ipsilateral PM lesions in 10.0% of total patients, Naruke and associates [15] only found them in 5.9%. Checking for the presence of PM lesions by palpation during operation and in the fixed specimen sliced thinly after operation might provide the difference.
Because these repeated modifications of the TNM staging system are certain to be a source of confusion to many, we must give attention to collecting significantly more data to confirm any classification rule. We could regard nonsmall cell carcinoma with ipsilateral PM as representing rather locally advanced disease than systematic disease. With some certainty we can therefore recommend that patients with satellite lesions should be considered for surgical resection unless otherwise contraindicated.
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