|
|
||||||||
Ann Thorac Surg 2007;83:419-424
© 2007 The Society of Thoracic Surgeons
a Division of Thoracic Surgery, Department of Surgery, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taipei, Taiwan
c Division of Experimental Surgery, Department of Surgery, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taipei, Taiwan
b Division of Thoracic Surgery, Department of Surgery, Mackay Memorial Hospital, Taipei, Taiwan
Accepted for publication July 26, 2006.
* Address correspondence to Dr Wen-Hu Hsu, Division of Thoracic Surgery, Department of Surgery, Taipei Veterans General Hospital, and National Yang-Ming University School of Medicine, No 201, Section 2, Shih-Pai Rd, Taipei, Taiwan. (Email: whhsu{at}vghtpe.gov.tw).
| Abstract |
|---|
|
|
|---|
METHODS: In this study, we looked at 163 female patients with stage I NSCLC. Patient charts were reviewed to collect patient data, including the age of the patient, tumor location, tumor size, visceral pleural invasion, the stage of disease, and the preoperative serum CEA level. The cutoff value of serum CEA level was 6.0 ng/mL. The significance of preoperative CEA level in the prognosis of female patients with stage I NSCLC was evaluated.
RESULTS: Among the 163 female patients with stage I NSCLC, 47 patients (28.8%) had abnormal preoperative serum CEA level (>6 ng/mL). Diagnosis of adenocarcinoma and bronchoalveolar carcinoma accounted for 83.4% of these 163 female patients. In-hospital mortality was encountered in 1 patient. Univariate analysis of survival in the other 162 female patients with stage I NSCLC showed that age, stage, tumor size, and preoperative CEA level were prognostic factors. Visceral pleural invasion had no impact on the prognosis of these patients. Multivariate analysis revealed that tumor size and preoperative CEA level were independent prognostic factors in female patients with stage I NSCLC.
CONCLUSIONS: Preoperative serum CEA level and tumor size are independent prognostic factors in female patients with stage I NSCLC. In contrast, visceral pleural invasion was not associated with the prognosis. Importantly, these results suggest that female patients with abnormally high preoperative CEA level and tumor size larger than 3 cm may need a thorough preoperative evaluation and careful postoperative follow-up to rule out occult metastasis of early NSCLC.
| Introduction |
|---|
|
|
|---|
Patients with NSCLC were evaluated for markers including carcinoembryonic antigen (CEA). Although CEA is mainly associated with adenocarcinoma of the gastrointestinal tract, elevated levels of CEA have been reported in about 35% to 60% of patients with NSCLC, showing higher sensitivity in adenocarcinoma of lung and in advanced stages [510]. Sawabata and colleagues [11] have suggested that the serum CEA level might be a useful predictor of survival for patients with clinical stage I NSCLC, and that a persistently high CEA level after surgery is a particularly strong indicator of a very poor prognosis. Evaluation of serum CEA level is also useful for monitoring the response to postoperative chemotherapy and detecting whether there is cancer relapse [12]. The significance of the preoperative CEA serum level in female patients with lung cancer is still unclear.
In addition, visceral pleural invasion was adopted as a specific description in the TNM classification of the International Union Against Cancer (UICC) staging system in the mid-1970s and has remained unchanged [13]. The new International System for staging lung cancer defined tumors with invasion of visceral pleura as T2. However, several authors have pointed out that visceral pleural invasion does not affect the outcome in stage I NSCLC. In this study, we conducted a retrospective review to investigate the prognostic significance of the preoperative CEA level and visceral pleural invasion on female patients with stage I NSCLC.
| Patients and Methods |
|---|
|
|
|---|
From January 1995 to December 2002, among 336 consecutive female patients undergoing surgical treatment for NSCLC at Taipei Veterans General Hospital, pathologic diagnosis of stage I NSCLC was made in 163 female patients. Patients who had preoperative chemotherapy or radiotherapy were excluded in this study. The clinical data including the age of the patient, tumor location, tumor size, visceral pleural invasion, the stage of disease, and preoperative serum CEA level were collected by chart review. Patients either underwent radical mediastinal lymphadenectomy (the majority underwent this procedure) or mediastinal node sampling according to the surgeons preference. In cases in which pleural effusion was present, a sample was collected and sent for cytologic examination. Patients with malignant pleural effusion were not included in the study.
Blood samples for CEA measurement were obtained 2 weeks before pulmonary resection. Carcinoembryonic antigen levels were measured using an immunoradiometric assay (ELSA2-CEA) obtained from CIS Bio International (Gif-Sur-Yvette, Cedex, France). The cutoff value of serum CEA level was 6.0 ng/mL. The pathologic stage was determined using the new TNM system for lung cancer [13]. Zero time was defined as the date of pulmonary resection, and the terminal event was the death attributable to cancer. All other deaths resulting from other than cancer or unknown causes were treated as withdrawals in the cumulative survival analyses. Survival curves were calculated by the KaplanMeier method, and comparison was performed by log-rank test. Multivariate analysis was performed using the Cox proportional hazard model. Probability values of less than 0.05 were considered significant.
| Results |
|---|
|
|
|---|
|
|
|
|
|
| Comment |
|---|
|
|
|---|
On the contrary, the American Thoracic Society and the European Respiratory Society jointly published their clinical guidelines for pretreatment evaluation of NSCLC in 1997 and stated: "... Unfortunately, none [ie, no serum tumor marker] appears sufficiently sensitive and has a high enough specificity to add to our ability to reliably detect occult disease or influence disease management. The routine measurement of any of these substances in the screening, staging, or evaluation of disease progression is not recommended" [15]. Similarly, the 2006 guidelines of the National Comprehensive Cancer Network of NSCLC do not include preoperative CEA as a pretreatment evaluation [16].
The significance of serum CEA levels had also been discussed in several studies. In the report by Icard and colleagues [17], 152 patients with lung cancer and a CEA level greater than 10 ng/mL were enrolled in a study to investigate the prognostic significance of preoperative CEA level. The authors found a critical unfavorable CEA level of prognostic significance of 30 ng/mL. The increase of preoperative CEA levels was associated with the severity of disease [17]. Recently, Okada and coauthors [18] reported their experience with 1,000 consecutive resections for stage I lung cancer and concluded that perioperative measurement of serum CEA concentrations yields information valuable for detecting patients at high risk of poor survival. However, the difference of the prognostic significance of CEA level between sexes was not mentioned in these studies. Elevated levels of serum CEA have been observed in patients with nonmalignant disease such as chronic bronchitis, emphysema, or colitis [19, 20].
Cigarette smoking and aging are also associated with increased serum CEA level [21, 22]. Cigarette smoking is a major risk of lung cancer, and only approximately 3% of lung cancers occur in nonsmokers in the Western world [23]. In contrast, in Taiwan, the majority of women with lung cancer are nonsmokers [24]. In our study, only 7.6% of female patients with stage I lung cancer had smoking history in our study. In addition, up to 83.4% of our patients had adenocarcinoma or bronchioalveolar carcinoma.
This study investigated the relationship between serum CEA levels and early NSCLC in female patients with stage I disease. Patients with more advanced stages of NSCLC were ruled out for the purposes of this study to minimize factors such as cigarette smoking and prognosis stratification across early and advanced stages of tumor. The results showed that preoperative CEA level is a prognostic factor in female patients with stage I NSCLC.
We did not look at the significance of CEA level in nonsmoking men as most of the male patients in our series had a smoking history. It is still unknown whether the CEA level is also a prognostic factor in male patients with squamous cell carcinoma. The possible absence of the correlation between CEA level and the prognosis of patients with squamous cell carcinoma could be related to the fact that squamous cell carcinoma is more often related to smoking history than adenocarcinoma.
Our findings suggest that even when the patients with an abnormally elevated preoperative serum CEA level had complete resection for pathologically confirmed stage I NSCLC, the prognosis was worse than the patients with normal preoperative serum CEA level. This may have been related to the tumor burden or failure to eradicate all pulmonary disease even though curative resection was apparently performed. Several studies have shown that a preoperative CEA level higher than 50 ng/mL always indicates a higher frequency of metastasis even after surgical resection [17, 18, 25]. In addition, Icard and colleagues [17] reported that patients with preoperative CEA level greater than 50 ng/mL died within 2 years. In our study, 7 female patients with a preoperative CEA level greater than 50 ng/mL had a limited median survival of 16.6 months. Only 1 patient was still alive 56.4 months after operation.
Although the T2 classification includes tumors of any size with invasion of the visceral pleura, several studies have failed to establish visceral pleura invasion as a significant prognostic factor for NSCLC [2628]. Whether the extent of visceral pleural invasion by tumor affects the outcome is unknown. The Japan Lung Cancer Society classifies the visceral pleural invasion as follows: p0, tumor with no pleural involvement beyond its elastic layer; p1, tumor that extends beyond the elastic layer of the visceral pleura but is not exposed on the pleural surface; p2, tumor that is exposed on the pleural surface but does not involve adjacent anatomic structures; and p3, tumor that involves adjacent anatomic structure [29]. The Society classifies a p2 tumor of any size as T2 and a p1 tumor of 3 cm or less as T1.
In contrast, the UICC TNM system classification describes only tumors with visceral pleural invasion as T2. In our study, we followed the definition of the UICC TNM system for staging NSCLC and found that visceral pleural invasion was not a prognostic factor in female patients with stage I NSCLC. In patients with T1 size tumors, survival between the patients without visceral pleural and the patients with visceral pleural invasion (stage T2) was not significantly different. The result was the same in patients with T2 size tumors.
In conclusion, preoperative CEA serum level and tumor size are independent prognostic factors in female patients with stage I NSCLC. Visceral pleural invasion was not associated with the prognosis. Importantly, these results suggest that female patients with abnormally elevated preoperative CEA level or tumor size larger than 3 cm may need a thorough preoperative evaluation and careful postoperative follow-up to rule out occult metastasis of early NSCLC.
| Acknowledgments |
|---|
|
|
|---|
| References |
|---|
|
|
|---|
Related Article
This article has been cited by other articles:
![]() |
H. Igai, N. Matsuura, S. Tarumi, S. S. Chang, N. Misaki, S. Ishikawa, and H. Yokomise Prognostic factors in patients after lobectomy for p-T1aN0M0 adenocarcinoma Eur J Cardiothorac Surg, March 1, 2012; 41(3): 603 - 606. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Igai, N. Matsuura, S. Tarumi, S. S. Chang, N. Misaki, T. Go, S. Ishikawa, and H. Yokomise Clinicopathological study of p-T1aN0M0 non-small-cell lung cancer, as defined in the seventh edition of the TNM classification of malignant tumors Eur J Cardiothorac Surg, June 1, 2011; 39(6): 963 - 967. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. B. Putnam Jr Invited commentary Ann. Thorac. Surg., February 1, 2007; 83(2): 424 - 424. [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |