Advances in Lung Cancer
Vol.3 No.1(2014), Article ID:43134,5 pages DOI:10.4236/alc.2014.31003

Five-Year Survivors of Non-Small Cell Lung Cancer Patients with Positive Pleural Lavage Cytology

Masaki Tomita*, Takanori Ayabe, Eiichi Chosa, Kunihide Nakamura

Department of Surgery II, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan

Email: *mtomita@med.miyazaki-u.ac.jp

Copyright © 2014 by authors and Scientific Research Publishing Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY).

http://creativecommons.org/licenses/by/4.0/

Received 12 December 2013; revised 10 January 2014; accepted 18 January 2014

ABSTRACT

Background: The pleural lavage cytology (PLC) for non-small cell lung cancer (NSCLC) patients has been reported as a significant prognostic factor. The aim of this study is to clarify the clinicopathological characteristics of 5-year survivors of patients with positive PLC. Methods: Among 401 resected NSCLC patients, 30 (7.48%) patients with positive PLC were reviewed retrospectively. Results: Only 7 of 30 patients (23.3%) survived more than 5-year. There were no differences in age, gender, histology, pT status and pN status between 5-year survivors and non-survivors. On the other hand, the serum carcinoembryonic antigen (CEA) level was significantly higher in non-survivors. Among these 5-year survivors, 4 of 7 patients died of NSCLC recurrences more than 5 years after surgery. Remaining 3 patients survived without cancer recurrences. Interestingly these 3 survivors had not received any adjuvant therapies after surgery. Conclusion: None of the 5-year survivor with positive PLC had high serum CEA level. Furthermore 5-year survival did not equal to cure in NSCLC patients with positive PLC.

Keywords:Pleural Lavage Cytology Positive; Non-Small Cell Lung Cancer; 5-Year Survivor

1. Introduction

Pleural lavage cytology (PLC) is the microscopic study of cells obtained from saline instilled into and retrieved from the chest cavity (in patients without preoperative pleural effusion) during surgery for non-small cell lung cancer (NSCLC). Since its first use in 1958 [1] , several studies, including meta-analytical studies, have clearly demonstrated a link between the presence of malignant cells in PLC and poor prognosis [2] -[11] . These concluded that positive PLC is a strong prognostic factor for survival.

However, some patients with positive PLC can survive more than 5-year. Therefore, in the present study, we examined the clinical characteristics of 5-year survivor with PLC positive NSCLC patients.

2. Patients and Methods

Consecutive NSCLC patients who had undergone surgical resection and pleural lavage cytology from 2000 through 2007 at University of Miyazaki Hospital were included in this study. There were 462 NSCLC patients who received complete resection. Following patients were excluded: 7 died of other diseases, 11 were lost to follow-up and 43 were not performed PLC. Therefore remaining 401 NSCLC patients were included in this study. PLC was performed as described before [8] Briefly, immediately following thoracotomy and prior to any further manipulation of the pulmonary parenchyma, the pleural cavity was carefully washed with 200 ml of physiologic saline solution. The fluid was irrigated over the visceral and parietal pleura. The fluid was placed in a glass bottle containing heparin and centrifuged at 1500 rpm for 5 minutes. The sediment was stained using Giemsa and Papanicolaou methods. Cytologic results were divided into two categories: negative and positive. Papanicolaou classes I, II, and III were regarded as negative; classes IV and V were considered positive. The PLC positive patients were included in this study.

Pathological (p) tumor-node-metastasis (TNM) staging was recorded in all patients based on the 7th edition of the American Joint Committee on Cancer (AJCC)/Union for International Cancer Control (UICC) classification. Follow-up information, including cause of death, was ascertained through a review of clinic notes and direct or family contact. Fischer’s exact test with Yates’ correction was used to correlate clinicopathological parameters. The survival curves of the patients were plotted by using the Kaplan-Meier method and analyzed using the log-rank test. Cox regression hazard model was used for univariate analysis. Statistical calculations were conducted with JMP (SAS Institute Inc. Cary, NC, USA) and values of p less than 0.05 were accepted as being significant.

3. Results

Positive PLC findings were present in 30 of 401 patients. The baseline characteristics of PLC positive patients are summarized in Table 1. There were 20 men and 10 women. Among PLC positive patients, there were only 7 of 30 patients who survived more than 5 years. The comparison of the clinicopathological characteristics between 5-year survivors and others was shown in Table 1. We failed to find any differences in age, gender, histology, pT status and pN status between 5-year survivors and non-survivors. Moreover postoperative adjuvant therapy was not related to 5-year survival. On the other hands, the serum carcinoembryonic antigen (CEA) level was significantly different between 5-year survivors and non-survivors. Figure 1 showed the survival curve based on serum CEA level. Preoperative high serum CEA level was found to be a significant prognostic factor in patients with positive PLC (p < 0.0001). The 5-year survival rate was 0% for patients with a high serum CEA level and positive PLC.

Among these 5-year survivors, 4 of 7 patients had recurrences and died of NSCLC at 66, 75, 78 and 101 months after surgery (shown in CEA normal group of Figure 1). Among these 4 patients, 3 patients were detected brain metastasis at 4 year, 5.5 year, 6 year after surgery, and other 1 patient had meningeal carcinomatosis at 4.5 year after surgery. The Remaining 3 of 7 5-year survivors were alive without cancer recurrences. Interestingly our 3 survivors had not received any adjuvant therapies after surgery.

Although the number of patients in the present study is small, we also examined univariate analysis. The result of univariate analysis (Table 2) also showed the prognostic significance of serum CEA level. Other factors did not related to patients’ survival for patients with positive PLC.

4. Discussion

The present result showed that the ratio of positive PLC patients was 7.48% (30/401). The frequency of positive results in the literature varies according to amount of solution used, timing of the procedure, and the center, but in general is less than 10% in the larger published series [2] -[11] .

The 5-year survival rate was 23.3% for the patients with positive PLC, and the survival curve was similar to

Table 1. The baseline clinicopathological factors.

CEA: carcinoembryonic antigen.

Table 2. Univariate analysis.

CI: confidence interval; CEA: carcinoembryonic antigen.

Figure 1. Survival of patients based on their preoperative serum CEA.

that for patients with advanced disease. Kondo and colleagues [2] reported that patients with positive PLC showed survival equal to that in patients with stage IIIB or IV. Our result was similar to these findings. The reason for poor survival of patients with positive PLC has been largely unknown. It is considered that positive PLC might be a possible indicator of the initial stage of carcinomatous pleuritis. However Satoh and colleagues [10] analyzed recurrence patterns in patients with positive PLC results and reported that 72% had distant metastasis. Therefore positive PLC might reflect not only initial stage of carcinomatous pleuritis but also systemic disease.

We also showed that positive PLC patients with high serum CEA level had poorer survival. The CEA is one of the most common serum tumor markers in NSCLC patients. Many authors reported that NSCLC patients with a high serum CEA concentration have a poor prognosis [12] . Some previous studies examined the CEA level in pleural lavage fluid, and reported to be useful as prognostic markers of NSCLC after surgery [9] [13] [14] . However there were few reports about the combined examination of PLC findings and serum CEA level. In the present study, the 5-year survival rate was 0% for patients with a high serum CEA level and positive PLC. Kawachi and colleagues [11] also reported the similar results and they concluded that positive PLC alone may not be a contraindication for surgical resection, but patients who are complicated with a high CEA level preoperatively should receive special attention since no long-term survivors were observed.

It is generally accepted that 5-year survival is the most commonly used benchmark for long-term survival in NSCLC and has, at times, been equated with cure [15] . In our series, 4 of 7 patients with 5-year survivor had recurrences and died of NSCLC more than 5-year after surgery. Thus the 5-year survival rate of positive PLC NSCLC was 23.3%, but 5-year survival without recurrences was only 10.0%. This indicates that 5-year survival did not equal to cure in positive PLC NSCLC patients. Therefore long-term (more than 5-year) follow-up after resection should be performed.

Since the prognosis of patients with positive PLC is poor, several previous studies concluded that adjuvant systemic therapy may be necessary to improve outcome for patients with positive PLC [2] -[10] . However, to our knowledge, there are no data whether adjuvant systemic therapy might improve the prognosis of patients with positive PLC. Among 5-year survivors of positive PLC patients in our series, there were only 3 patients who survived without any recurrences. Interestingly these 3 survivors had not received any adjuvant therapies. However we do not believe that it denies the usefulness of adjuvant therapies. In our series, we did not perform the adjuvant therapies based on the PLC findings. Therefore our series are not suitable to examine the usefulness of the adjuvant therapies for positive PLC patients. In addition, the number of patients was quite small. Further clinical studies will be necessary to evaluate the efficacy of adjuvant therapy for positive PLC patients. An active form (deletion type of exon19 or mutation type of exon21) of Epidermal Growth Factor Receptor-Tyrosine Kinase (EGFR-TK) is well known to be predictive factor on the response to EGFR-TKI such as gefinitib and erlotinib [16] . In our series, we examined EGFR mutation for 7 of 30 patients, and we found that only 2 patients had EGFR mutation. These 2 patients received EGFR-TKI, and they died at 32 and 101 months after surgery. There is a possibility that EGFR-TKI might be also an effective drug for patients with both EGFR mutation positive and PLC positive.

5. Conclusion

In conclusion, none of the 5-year survivors with positive PLC had high serum CEA level. Furthermore 5-year survival did not equal to cure in PLC positive NSCLC patients.

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NOTES

*Corresponding author.