Low expression of Bax predicts poor prognosis in resected non-small cell lung cancer patients with non-squamous histology.

OBJECTIVE: The present study evaluated the prognostic significance of apoptosis-related proteins p53, Bax and galectin-3 in patients with non-small cell lung cancer (NSCLC) treated with surgical resection.
METHODS: We investigated the expression of these proteins and their association with clinicopathologic characteristics including disease-free survival (DFS) and overall survival (OS) in 205 NSCLC patients who underwent surgical resection (Stage I, 97; II, 46; IIIA, 45; IIIB, 17) using immunohistochemistry. Eighty-eight patients (43%) received adjuvant treatment (chemotherapy: 8, radiotherapy: 24, both: 56).
RESULTS: High expressions of Bax, p53 and galectin-3 were observed in 48 (23%), 81 (40%) and 105 (51%) patients, respectively. Low expression of Bax was significantly associated with male gender, squamous cell histology and low expression of galectin-3. Five-year DFS and OS of total patients were 37 and 46%, respectively. High expressions of p53 and galectin-3 were not associated with poor DFS or OS, and no significant correlation existed between low expression of Bax and outcome of patients. However, in patients with non-squamous histology (108 patients), low expression of Bax was a significant independent predictor of poor DFS (P = 0.017) and OS (P = 0.037). In addition, in patients with Stage II or III disease, low expression of Bax significantly correlated with poor DFS (P = 0.004). It was also the most significant independent poor prognostic factor second only to a large primary tumor size in Stage II or III patients with non-squamous histology.
CONCLUSIONS: Low expression of Bax was significantly associated with poor prognosis in resected NSCLC patients with non-squamous histology.

INTRODUCTION

Lung cancer is the most common malignancy in many countries and it has become the number one cause of cancer death in Korea, surpassing gastric cancer (1,2). Majority of lung cancer patients has non-small cell type, in which surgical resection is still the mainstay of the curative treatment (2). However, the prognosis of patients with non-small cell lung cancer (NSCLC) is still poor despite surgical treatment (2,3). Recently, several phase III trials demonstrated improved survival with adjuvant chemotherapy, especially in patients with Stage II or III disease (4–7). Therefore, the determination of parameters that may identify those patients who would benefit from adjuvant chemotherapy, and those who would not, has strong clinical implications. Apoptosis-related proteins are important candidates for such parameters, because apoptosis is the predominant mechanism in which chemotherapy and radiotherapy kill the cancer cells (8). Among several proteins involved in apoptosis, the fine interplay between the anti-apoptotic members of the Bcl-2 family and the death-promoting members such as Bax and p53 has been suggested as the most important process (8). BH3-only proteins or p53 directly or indirectly activate the Bax protein, which permeabilizes the mitochondrial outer membrane, leading to the activation of downstream apoptosis signaling pathways (8,9). In addition, galectin-3, which belongs to a family of the galactoside-binding protein-3, and is structurally and functionally similar to Bcl-2, is known to protect cells from apoptosis by various stimuli (10). Therefore, genetic defects in these proteins may not only result in intrinsic biologic aggressiveness, but also lead to resistance to the cytotoxic effects of chemotherapy and radiotherapy (8,11–13). We evaluated the prognostic significance of apoptosis-related proteins p53, Bax and galectin-3 in NSCLC patients treated with surgical resection with or without adjuvant treatment.

PATIENTS AND METHODS

Patients

Two hundred and five patients who underwent resection of primary NSCLC at Ajou University Medical Center between September 1996 and December 2002 were eligible to be included in this retrospective study. Patients with a history of cancer from a non-pulmonary origin were included if the disease was cured. Exclusion criteria included patients with history of previous lung cancer, a Stage IV disease and those treated preoperatively with either chemotherapy or radiotherapy. Before operation, each patient underwent the following staging procedures: chest radiography, chest computed tomography (CT) scan and hematologic and biochemical profiles. The American Joint Committee on Cancer staging was used for post-operative pathologic staging of the patients (14). This research protocol was approved by the Institutional Review Board of the Ajou University Medical Center, Suwon, Korea.

Chemotherapy

In the majority of patients in Stage II or III, adjuvant chemotherapy was performed according to the discretion of physicians. Although adjuvant chemotherapy regimens were not uniformly applied, all, except three, patients received cisplatin-based chemotherapy (gemcitabine, tegracil and gemcitabine/carboplatin, respectively). The most commonly administered regimen (24 patients) consisted of two cycles of etoposide/cisplatin chemotherapy followed by concurrent chemoradiotherapy with cisplatin. In this regimen, etoposide 100 mg/m2/day (Days 1–3) and cisplatin 20 mg/m2/day (Days 1–4) were administered every 3 weeks, while concurrent chemoradiotherapy consisted of radiotherapy with cisplatin 20 mg/m2/day for 4 days during Weeks 1 and 4 of radiotherapy.

Radiotherapy

Radiotherapy was performed using 6- or 15-MV LINAC (CLINAC 2100CD, Varian Medical Systems, Palo Alto, CA, USA). Patients were treated with multiple portals, and a conformal isodose plan was created. The target volume was the bronchial stump, and ipsilateral hilar and mediastinal lymph nodes with a 1–2 cm margin. The primary tumor bed was included when there was chest wall invasion. The radiation dose to target volume was 50.4 Gy in 27–30 fractions, 5 days/week when corrections for inhomogeneity were not made. After inhomogeneity corrections were made, radiation of 54–60 Gy in 27–30 fractions were delivered to the target volume. Boost radiation of 10–15 Gy was required when the tumor cells were on the resection margins. The dose to the spinal cord did not exceed 45 Gy.

Evaluation

The patients were followed with chest radiography either with or without chest CT scan every 3 months for 2 years, then every 6 months for 3 years and yearly thereafter.

Construction of Tissue Microarray and Immunohistochemical Staining for Apoptosis-Related Proteins

Two representative areas were taken of all cases from paraffin tissue blocks after reviewing the hematoxylin–eosin-stained slides of the primary tumor. A total of 410 core tissue biopsies (diameter, 1.0 mm) were taken and arrayed into three new recipient paraffin blocks. Five-micrometer sections of these tissue array blocks were then cut, placed on charged poly-l-lysine–coated slides and used for immunohistochemical analysis.

Sections from the tissue array were deparaffinized in xylene and were rehydrated in graded alcohol and water. Endogenous peroxidase activity was blocked by treatment with 3% hydrogen peroxide for 10 min. Sections were treated with a protein-blocking solution and then with primary antibodies, including mouse anti-human monoclonal antibodies against p53 (DO-7, dilution 1:20) and galectin-3 (NCL-GAL3, dilution 1:100) (Novocastra Laboratories Ltd, Newcastle upon Tyne, UK), and rabbit anti-human polyclonal antibody against Bax (dilution 1:1000, DAKO, Carpinteria, CA, USA), for 1 h at room temperature. After rinsing several times in phosphate-buffered saline, the sections were incubated in biotinylated secondary antibody. Bound antibodies were detected by the streptavidin–biotin method with a Cap-Plus detection kit (Zymed Laboratories Inc, San Francisco, CA, USA). Slides were rinsed in phosphate-buffered saline, exposed to diaminobenzidine and counterstained with Mayer’s hematoxylin. The negative controls for these proteins were made by omitting the primary antibody during the process of immunohistochemical staining. For positive controls of p53 and Bax, a tissue section of colon adenocarcinoma known to have high expression of p53 and lymphocytes in the germinal center were used, respectively, while a tissue section of the tonsil was used as the positive control for galectin-3.

The slides were examined independently by two observers (JHH, JHK) blinded to both clinical and pathologic data. Expression of the apoptosis-related proteins was quantified using a visual grading system based on the extent of staining (percentage of positive tumor cells) (graded on a scale of 0–3; 0, 0–25%; 1, 26–50%; 2, 51–75%; 3, >75%) for p53, and the intensity of staining (graded on a scale of 0–3; 0, no staining; 1, weak staining; 2, moderate staining; 3, strong staining) for Bax and galectin-3, respectively. There was close agreement (>90%) in the evaluation of apoptosis-related proteins between both investigators. In case of disagreement, final grading was determined by consensus. Expression of apoptosis-related proteins was classified into high (Grade 2, 3) and low (Grade 0, 1) expressions (Fig. 1).

Figure 1.

Immunohistochemical staining of apoptosis-related proteins in non-small cell lung cancer (×400). (A) High expression of Bax: cytoplasmic staining (Grade 3 in the intensity). (B) Low expression of Bax (Grade 1 in the intensity). (C) High expression of p53: nuclear staining (Grade 3 in the extent). (D) High expression of galectin-3: cytoplasmic staining (Grade 3 in the intensity).

Statistical Analysis

Disease-free survival (DFS) and overall survival (OS) were calculated using the Kaplan–Meier method (15). DFS was defined as the time from the day of operation to a documented day of recurrence, development of a second primary cancer or death from any other cause. Data on patients who did not experience recurrence were censored at the last follow-up. OS was defined as the time from the day of operation to the time of death; data on survivors were censored at the last follow-up. The differences between the survival curves were tested using the log-rank test and the Wilcoxon test. The Cox proportional-hazards regression model was used to determine the joint effects of several variables on survival (16). The comparison of clinicopathologic characteristics was evaluated with the Fisher’s exact test. All statistical analyses were performed two-sided, with SPSS for Windows 12.0 software.

RESULTS

Patient Characteristics

The median age of 205 patients with NSCLC was 63 years (range: 30–78), and the median longest diameter of the primary tumor was 3.9 cm (1.2–12). Twenty-six patients (13%) were in Stage IA, 71 (35%) in IB, 7 (3%) in IIA, 39 (19%) in IIB, 45 (22%) in IIIA and 17 (8%) in IIIB. One hundred and fifty-eight male patients (99%) and seven female patients (16%) had a history of smoking (current or previous smoker). In terms of histologic type, 98% of patients with squamous cell carcinoma had a history of smoking, while 63% of adenocarcinoma patients and 74% of patients with other histologic types were current or previous smokers. Other clinicopathologic characteristics of the patients are listed in Table 1.

Table 1.

Expression of Bax and clinicopathologic characteristics

	Low Bax (%)	High Bax (%)	P valuea
Gender
Female	22 (14)	23 (48)	<0.0001
Male	135 (86)	25 (52)
Age
≤63b	84 (54)	28 (58)	0.621
>63	73 (46)	20 (42)
History of smoking
Yes	140 (89)	25 (52)	<0.0001
No	17 (11)	23 (48)
Operation
Lobectomyc	100 (64)	39 (81)	0.023
Pneumonectomy	57 (36)	9 (19)
Histologic types
Squamous	89 (57)	7 (15)	<0.0001
Adeno	54 (34)	36 (75)
Adenosquamous	7 (4)	5 (10)
Othersd	7 (4)	0 (0)
Tumor size (cm)
≤3.9e	76 (48)	29 (60)	0.187
>3.9	81 (52)	19 (40)
Stagef
I	72 (46)	25 (52)	0.658
II	38 (24)	8 (17)
IIIA	35 (22)	10 (21)
IIIB	12 (8)	5 (10)
Resection margin
Negative	140 (89)	45 (94)	0.420
Positive	17 (11)	3 (6)
Adjuvant treatment
No	89 (57)	28 (58)	0.773
Chemotherapy	7 (4)	1 (2)
Chemoradiotherapy	44 (28)	12 (25)
Radiotherapy	17 (11)	7 (15)
Expression of p53
Low	89 (57)	35 (73)	0.063
High	68 (43)	13 (27)
Expression of galectin-3
Low	88 (56)	12 (25)	<0.0001
High	69 (44)	36 (75)

aFisher’s exact test. bMedian age. cIncluding two patients with wedge resection. dIncluding five patients with large cell carcinoma, one with mucoepidermoid carcinoma and one with carcinosarcoma. eMedian longest diameter of primary tumor. fPost-operative pathologic staging.

Association of Expression of Apoptosis-Related Proteins with Clinicopathologic Characteristics

High expressions of Bax, p53 and galectin-3 were observed in 48 (23%), 81 (40%) and 105 (51%) patients, respectively. High expression of p53 was associated with male gender (P = 0.024), history of smoking (P = 0.002), post-pneumonectomy status (P = 0.046) and squamous cell histology (P = 0.033). In addition, high expression of galectin-3 correlated with no smoking history (P = 0.023), post-lobectomy status (P = 0.011), adenocarcinoma (P < 0.0001) and negative resection margin (P = 0.018). Low expression of Bax was significantly associated with male gender (P < 0.0001), history of smoking (P < 0.0001), squamous cell histology (P < 0.0001) and low expression of galectin-3 (P < 0.0001) (Table 1). In terms of subtypes of adenocarcinoma, high expression of Bax showed a trend of correlation with bronchioloalveloar carcinoma (P = 0.094) (Table 2).

Table 2.

Relationship between the expression of apoptosis-related proteins and subtypes of adenocarcinoma

Subtype	Bax			p53			Galectin-3
	Low (%)	High (%)	P valuea	Low (%)	High (%)	P valuea	Low (%)	High (%)	P valuea
Acinar	38 (70)	22 (61)	0.094	42 (67)	18 (67)	0.093	21 (78)	39 (62)	0.622
BAC	6 (11)	10 (28)		12 (19)	4 (15)		3 (11)	13 (21)
Papillary	3 (6)	3 (8)		6 (10)	0 (0)		1 (4)	5 (8)
Solidb	7 (13)	1 (3)		3 (5)	5 (19)		2 (7)	6 (10)

BAC, Bronchioloalveolar carcinoma. aFisher’s exact test. bIncluding one patient with signet-ring adenocarcinoma.

Association of Expression of Apoptosis-Related Proteins with Patient Outcome

The median follow-up duration of surviving patients was 79 months (range: 35–149 months), and one patient with recurrence was lost during follow-up because the patient immigrated to another country. At the time of analysis, 132 of 205 patients (64%) had died, while 14 patients with either recurrence (11 patients) or second primary cancer (three patients) were alive. Seven patients who died of post-operative complication were excluded from further survival analysis. Five-year DFS and OS of total patients were 37 and 46%, respectively (Fig. 2). High expressions of p53 and galectin-3 were not associated with poor DFS or OS (Table 3). Moreover, there was no significant correlation between low expression of Bax and outcome of patients (Fig. 3 and Table 3). However, in patients with non-squamous histology (108 patients), low expression of Bax was a significant independent predictor of poor DFS (P = 0.017) and OS (P = 0.037) in multivariate analysis (Fig. 4 and Table 4). In addition, in patients with Stage II or III, low expression of Bax significantly correlated with poor DFS (P = 0.004) (Table 5). It was also the most significant independent prognostic factor second only to a large primary tumor size in Stage II or III patients with non-squamous histology (P = 0.001 for DFS, P = 0.013 for OS) in multivariate analysis as well as in univariate analysis (Fig. 5 and Table 6).

Figure 2.

Disease-free and overall survival of resected non-small cell lung cancer patients.

Table 3.

Disease-free and overall survival of the patients according to various characteristicsa

Characteristics	Number of patients	5-year disease-free survival (%)	P valueb	5-year overall survival (%)	P valueb
Gender
Female	45	42	0.623	55	0.327
Male	153	36		44
Age
≤63c	111	38	0.875	47	0.648
>63	87	36		46
History of smoking
Yes	158	34	0.230	43	0.080
No	40	50		59
Operation
Lobectomyd	138	37	0.419	49	0.063
Pneumonectomy	60	37		42
Histologic type
Squamous	90	40	0.687	46	0.746
Non-squamous	108	35		46
Tumor size (cm)
≤3.9e	103	44	0.019	52	0.026
>3.9	95	29		41
Stagef
I	95	51	<0.0001	59	<0.0001
II	45	33		44
IIIA	44	20		29
IIIB	14	7		21
Resection margin
Negative	181	38	0.155	49	0.037
Positive	17	24		24
Expression of Bax
Low	151	35	0.381g	45	0.247h
High	47	45		53
Expression of p53
Low	121	38	0.579	48	0.566
High	77	36		44
Expression of galectin-3
Low	96	34	0.237	42	0.157
High	102	40		50

aExcluding seven patients who died of post-operative complication. bLog-rank test. cMedian age. dIncluding wedge resection. eMedian longest diameter of primary tumor. fPost-operative pathologic staging. gP = 0.103 according to the Wilcoxon test. hP = 0.057 according to the Wilcoxon test.

Figure 3.

Disease-free survival (A) and overall survival (B) of resected non-small cell lung cancer patients according to the expression of Bax (P value was obtained using the Wilcoxon test).

Figure 4.

Disease-free survival (A) and overall survival (B) of non-small cell lung cancer patients with non-squamous histology according to the expression of Bax (P value was obtained using the Wilcoxon test).

Table 4.

Multivariate analysis of disease-free survival and overall survival in non-squamous histology (n = 108)a

Prognostic factors	Disease-free survival			Overall survival
	HR	95% CI	P valueb	HR	95% CI	P valueb
Operation
Lobectomyc	1.00			1.00
Pneumonectomy	1.41	0.77–2.62	0.269	2.63	1.45–4.79	0.002
Tumor size (cm)
≤3.9d	1.00			1.00
>3.9	2.14	1.33–3.45	0.002	1.53	0.90–2.61	0.118
Stagee
I	1.00			1.00
II	2.65	1.42–4.96	0.002	1.93	0.97–3.85	0.062
IIIA	3.76	2.09–6.77	<0.0001	2.58	1.40–4.76	0.002
IIIB	5.23	2.08–13.11	<0.0001	3.52	1.44–8.62	0.006
Expression of Bax
High	1.00			1.00
Low	1.87	1.12–3.14	0.017	1.79	1.04–3.08	0.037

HR, hazard ratio; CI, confidence interval. aExcluding one patient who died of post-operative complication. bCox proportional-hazards regression model. cIncluding wedge resection. dMedian longest diameter of primary tumor. ePost-operative pathologic staging.

Table 5.

Multivariate analysis of disease-free survival and overall survival in Stages II and III (n = 103)a

Prognostic factors	Disease-free survival			Overall survival
HR	95% CI	P valueb	HR	95% CI	P valueb
Age
≤62c	1.00			1.00
>62	1.40	0.84–2.34	0.202	2.06	1.21–3.53	0.008
Histologic type
Squamous	1.00			1.00
Non-squamous	2.84	1.65–4.89	<0.0001	1.75	0.99–3.07	0.052
Tumor size (cm)
≤3.9d	1.00			1.00
>3.9	2.00	1.26–3.20	0.004	1.94	1.18–3.19	0.009
Stagee
II	1.00			1.00
IIIA	1.51	0.91–2.49	0.110	1.66	0.96–2.86	0.069
IIIB	1.83	0.93–3.57	0.079	2.29	1.15–4.56	0.019
Resection margin
Negative	1.00			1.00
Positive	2.07	1.04–4.13	0.039	2.21	1.10–4.44	0.026
Chemotherapy
Yes	1.00			1.00
No	1.55	0.98–2.45	0.061	1.47	0.89–2.45	0.136
Expression of Bax
High	1.00			1.00
Low	2.51	1.35–4.66	0.004	1.77	0.92–3.40	0.086

aExcluding five patients who died of post-operative complication. bCox proportional-hazards regression model. cMedian age. dMedian longest diameter of primary tumor. ePost-operative pathologic staging.

Figure 5.

Disease-free survival (A) and overall survival (B) of non-small cell lung cancer patients in Stage II or III with non-squamous histology according to the expression of Bax (P value was obtained using the Wilcoxon test).

Table 6.

Multivariate analysis of disease-free survival and overall survival in Stages II and III with non-squamous histology (n = 48)a

Prognostic factors	Disease-free survival			Overall survival
	HR	95% CI	P valueb	HR	95% CI	P valueb
Operation
Lobectomy	1.00			1.00
Pneumonectomy	1.45	0.67–3.13	0.347	2.36	1.11–4.99	0.025
Tumor sizec (cm)
≤3.9	1.00			1.00
>3.9	4.12	2.01–8.43	<0.0001	2.69	1.25–5.83	0.012
Staged
II	1.00			1.00
III	1.41	0.74–2.68	0.291	1.42	0.62–3.27	0.407
Expression of Bax
High	1.00			1.00
Low	3.05	1.56–5.97	0.001	2.34	1.20–4.56	0.013

aExcluding one patient who died of post-operative complication. bCox proportional-hazards regression model. cMedian longest diameter of primary tumor. dPost-operative pathologic staging.

DISCUSSION

We evaluated the expression of p53, Bax and galectin-3 under the assumption that abnormalities in these apoptosis-related proteins may be associated with poor outcome in patients with NSCLC treated with surgical resection either with or without adjuvant treatment.

The most frequently investigated apoptosis-related protein in NSCLC is p53 (11,12,17–22). Although a meta-analysis demonstrated the association of abnormal p53 status with poor prognosis of resected NSCLC, the prognostic significance of p53 still remains controversial (11,12,17–22). Among the reports regarding the role of galectin-3 in NSCLC, one study with only Stage II patients showed the association of high expression of galectin-3 with poor outcome (23–25). The results of the present study showed that high expression of galectin-3 was frequently found in adenocarcinoma, which is consistent with results reported in a previous study (25). In addition, high expressions of p53 and galectin-3 were not associated with poor outcome in patients with resected NSCLC.

The most important finding of the current study was the prognostic significance of the low expression of Bax in patients with resected NSCLC, having non-squamous histology or locally advanced disease (Stages II and III), although it did not predict poor outcome in the entire group of patients. In the present study, the frequency of low expression of Bax was very high (94%) in squamous cell carcinoma. Previous studies also revealed the association of low expression of Bax with squamous cell carcinoma in NSCLC (19,26). Therefore, Bax seems to be of little value as a prognostic indicator in NSCLC patients with squamous cell histology. On the other hand, in adenocarcinoma, the high expression of Bax demonstrated a trend of correlation with the bronchioloalveolar subtype, which has relatively higher prevalence in non-smokers and females (27). The mechanism of extremely high frequency of low expression of Bax in squamous cell carcinoma remains to be determined. Considering that almost all squamous cell carcinoma patients had a history of smoking and there was a strong correlation between smoking history and low expression of Bax even in adenocarcinoma in the present study (P = 0.014, data not shown), there is a possibility that smoking might cause the change in the expression of Bax. However, further study is essential to prove this speculation. Recently, Tanaka et al. (28) reported relevant results, which showed that Bax inhibitor-1 gene expression in adenocarcinoma was higher in patients with a bronchioloalveolar component and low smoking index. Since high expression of Bax in adenocarcinoma demonstrated similar significant association with bronchioloalvelolar subtype and no history of smoking in the present study, further investigation of the relationship between Bax and the Bax inhibitor-1 may provide valuable information for better understanding of the role of Bax in NSCLC.

To our knowledge, this study is the largest research project that has investigated the role of Bax in NSCLC. Unlike for p53 or Bcl-2, there are fewer studies that discuss the prognostic significance of Bax in NSCLC (11,12,19–22,29–31). In addition, only one study that investigated 61 patients in a predominantly advanced stage (Stage IV, 54%) demonstrated the correlation between a low expression of Bax and poor outcome (29).

The poor outcome of patients with low expression of Bax may be attributed to the intrinsic aggressiveness of the tumor (11,32). The prognostic value of low expression of Bax was more significant in patients with non-squamous histology, which had relatively lower proportion of current or previous smokers compared with squamous cell carcinoma in the present study. In addition, there was a very strong association between smoking history and low expression of Bax in patients with non-squamous histology (P < 0.0001, data not shown). These findings suggest the possibility that more extensive genetic damage such as low expression of Bax caused by smoking may result in intrinsic aggressiveness of the tumor, leading to poor outcome. On the other hand, we may suppose that resistance to adjuvant chemotherapy or radiotherapy in tumors with low expression of Bax may be the cause of poor prognosis, based on the results of the present study, which demonstrated that the low expression of Bax predicted poor DFS in Stages II or III when adjuvant treatments were commonly given (80% of patients) (8,11–13).

The present study has several potential limitations. First, this is a retrospective analysis from a single institution with patients’ cohort within a relatively long period of time. Second, adjuvant chemotherapy was individualized according to the discretion of the treating oncologists, which resulted in rather heterogeneous chemotherapy regimens, although cisplatin was included in almost all. Third, the low expression of Bax did not demonstrate prognostic significance in the entire study population.

The association of low expression of Bax with poor DFS in Stages II or III has a clinical relevance, because adjuvant chemotherapy has recently been established as a standard of care for resected Stage II or III NSCLC, and the majority of patients in these stages in the current study received adjuvant chemotherapy either with or without radiotherapy (62%) (2,4–7). In Stage II or III patients with non-squamous histology, the 5-year OS of patients with low expression of Bax was significantly lower compared with that of high expression (22 versus 43%, P = 0.012, Wilcoxon test), while low expression of Bax was one of the significant independent predictors of poor prognosis in multivariate analysis. Therefore, the present study suggests that locally advanced (Stage II or III) non-squamous NSCLC patients with low expression of Bax may require more effective adjuvant treatment or an intensified follow-up.

In conclusion, low expression of Bax was significantly associated with the poor outcome in patients with non-squamous NSCLC. If the prognostic significance of low expression of Bax is validated by further prospective studies with larger numbers of patients, a relatively simple immunohistochemical staining of surgical specimens for the Bax protein may provide valuable information to the oncologist for selecting effective adjuvant treatments or follow-up strategies.

Funding

Ajou University Medical Center, Suwon, Korea. Funding to pay the Open Access publication charges for this article was provided by Ajou University Medical Center.