- Open Access
Histological comparison between preoperative and surgical specimens of non-small cell lung cancer for distinguishing between "squamous" and "non-squamous" cell carcinoma
- Tomoko Yamagishi†1,
- Katsuhiko Shimizu†2Email author,
- Nobuaki Ochi†1,
- Hiromichi Yamane†1,
- Isao Irei†3,
- Yoshito Sadahira†3,
- Nagio Takigawa†1,
- Mikio Oka†4 and
- Masao Nakata†2
© Yamagishi et al.; licensee BioMed Central Ltd. 2014
- Received: 5 February 2014
- Accepted: 15 May 2014
- Published: 29 May 2014
Non-small cell lung cancers (NSCLCs) are frequently heterogeneous and in approximately 70% of cases, NSCLCs are diagnosed and staged by small biopsies or cytology rather than by examination of surgically resected specimens. Thus, in most patients, the diagnosis is established based on examination of preoperative specimens alone. Recently, classification of NSCLC into pathologic subtypes has been shown to be important for selecting the appropriate systemic therapy, from both the point of view of treatment efficacy and prevention of toxicity.
We retrospectively reviewed the data of 225 patients to compare the preoperative classification of the NSCLC subtype on biopsy specimens with the postoperative classification based on examination of the resected specimens, in order to compare the accuracy of the two for the diagnosis of various histological subtypes of NSCLC.
In 169 of the 225 (75.1%) patients, the preoperative diagnosis was definite malignancy. Histologically, the final pathologic diagnosis made from the surgical specimens was adenocarcinoma (ADC) in 169 patients, and in 75.5% of these cases, the diagnosis was concordant with the preoperative diagnosis. Among the patients who had squamous cell carcinoma (SQC) in the preoperative specimens, the diagnosis was concordant with the preoperative diagnosis in 65.7% of cases. Misclassified preoperative biopsies included an even number of SQCs and ADCs, with all the misclassified biopsies being ADCs morphologically mimicking SQC due to solid growth. Significantly higher specificity, negative predictive value and accuracy were observed for the diagnosis of SQC.
Our study suggested that the concordance rates for diagnosis of the NSCLC subtypes, especially the "squamous" or "non-squamous" histologies, between preoperative and surgical specimens were satisfactory, as compared with previous reports. Therefore, pretreatment diagnosis of lung cancer using small samples is reasonable for selecting the optimal treatment. However, in order not to lose the opportunity for selecting an effective treatment, we should be aware that the diagnosis in preoperative small samples might be different from that based on examination of the surgical specimens.
The virtual slide(s) for this article can be found here:http://www.diagnosticpathology.diagnomx.eu/vs/2032698427120488
- Epidermal Growth Factor Receptor
- Epidermal Growth Factor Receptor Mutation
- Concordance Rate
Lung cancer is the leading cause of cancer and mortality from cancer worldwide, with 5-year survival rates of <15% across all stages of the disease. Historically, lung cancer is divided into two morphologic types: small cell lung cancer and non-small-cell lung cancer (NSCLC), with NSCLC accounting for approximately 80% to 85% of all histological types of NSCLC.
The International Association for the Study of Lung Cancer, the American Thoracic Society, and the European Respiratory Society recently proposed the classification of NSCLC based on examination of small biopsy and/or cytology specimens into six main subtypes: adenocarcinoma (ADC), squamous cell carcinoma (SQC), NSCLC not otherwise specified (NSCLC-NOS), NSCLC with neuroendocrine morphology, NSCLC with squamous and adenocarcinoma patterns, and poorly differentiated NSCLC with spindle and/or giant cell carcinoma. NSCLCs are frequently heterogeneous and approximately 70% of NSCLCs are diagnosed and staged by examination of small biopsy or cytology specimens rather than by examination of surgically resected specimens; thus, in most patients, the diagnosis is based on examination of preoperative specimens alone. Until now, histological subtyping of NSCLC was not considered to be clinically or therapeutically important, because of the lack of existence of differential treatment options for the various subtypes of NSCLC. However, there is now clear evidence to suggest that the classification of NSCLC into pathologic subtypes is important for the selection of appropriate systemic therapy, from both the point of view of treatment efficacy and prevention of toxicity[6, 7]. For example, large phase III clinical trials have demonstrated that ADC is a strong predictive factor for improved outcome following treatment with the combination of pemetrexed with cisplatin compared with SQC. In addition, the presence of common activating mutations in the tyrosine kinase domain of the epidermal growth factor receptor (EGFR) gene (exon 19 deletion and exon 21 L858R mutation) confers strong sensitivity to gefitinib and erlotinib, which are selective tyrosine kinase inhibitors of EGFR[9, 10]. These EGFR mutations are more commonly encountered in ADCs. Furthermore, the use of vascular endothelial growth factor (VEGF) inhibitors (eg, bevacizumab) has been demonstrated to be associated with an increased risk of fatal pulmonary hemorrhage in patients with SQC. The ALK tyrosine inhibitor crizotinib was demonstrated to show marked antitumor activity in NSCLC patients with EML4-ALK translocation, observed in approximately 3 to 4% of patients with ADC. Thus, a molecular testing guideline has been proposed.
If pathological findings are missed, especially when differentiating between "squamous" and "non-squamous" histology, determination of the appropriate treatment is difficult. The aim of this study was to compare the preoperative classification of NSCLC based on biopsy specimens with the postoperative classification made on the basis of examination of resected specimens, and to examine how often accuracy about each histological subtypes of NSCLC.
Between April 2004 and June 2011, 442 patients underwent surgical resection for lung cancer at Kawasaki Medical School Hospital, Kurashiki, Japan. We retrospectively reviewed the data of a consecutive series of 225 (50.9%) patients in whom preoperative diagnosis was made by transbronchial biopsy (TBB) or computed tomography-guided fine needle biopsy (CTNB). For each patient, the clinical information at diagnosis was collected from the medical records. This study was conducted with the approval of the institutional Ethics Committee of Kawasaki Medical School (No.887).
Transbronchial biopsy and computed tomography-guided fine needle biopsy procedures
While TBB is commonly performed in the diagnostic workup of pulmonary peripheral nodules, CTNB is usually performed either when the tumor is not detected bronchoscopically or when it is thought unlikely to be accessible by bronchoscopy. Flexible bronchoscopy is conducted by experienced bronchoscopists, while CTNB is performed by interventional radiologists, with standard techniques for both. All aspirated materials and biopsy specimens were fixed in formalin and embedded in paraffin, and sections are routinely stained with hematoxylin and eosin (H&E). Cytological examinations of sputum, aspirated material and bronchial brushings, and washing were not included in the diagnostic workup in this study, because the aim of the study was histological comparison between preoperative biopsy specimens and surgically resected specimens.
The results of the examination of the small diagnostic specimens were classified as no malignancy, suspected malignancy or definite malignancy. Furthermore, definite malignancy of NSCLC was classified into ADC, SQC, NSCLC or other histological subtypes (others). If there is no clear ADC or SQC morphology, the tumor can be further classified based on immunohistochemocal stains (IHC) and mucin (periodic acid Schiff) stains. If the stains all favor ADC: positive ADC markers (i.e., TTF-1 and/or mucin positive) with negative SQC markers, then the tumor is classified as ADC. If SQC markers (i.e., p63) are positive with negative ADC markers, the tumor is classified as SQC. If the ADC and SQC markers are both strongly positive and negative, the tumor is classified as NSCLC-NOS and others.
Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy were calculated according to the standard definitions for the diagnosis of lung cancer and malignancy. Continuous variables were analyzed by the Student's t- test, and the results were expressed as mean ± standard deviation (SD). Dichotomous variables were analyzed by the Fisher's exact test or the χ2 test, as appropriate. Discontinuous variables were coded as dummy variables. Two-sided p-values of less than 0.05 were considered to be statistically significant. All analyses were performed using the SPSS software (Version 17.0; SPSS Incorporation, Chicago, IL).
Patient characteristics (n = 225)
Age, mean ± SD
69.0 ± 10.2
Sensitivity of preoperative diagnosis for the detection of NSCLC
Comparison between preoperative specimens and surgical diagnosis
Suspicious of NSCLC
Histologically, the final pathological examination of the surgical specimens revealed ADC in 139 patients, of whom in 105 (75.5%) patients, the diagnosis was concordant with the preoperative diagnosis. Of the remaining 34 patients, 2 patients had NSCLC, 5 patients had suspected NSCLC, and 27 patients had no malignancy. In all, 67 patients had SQC of the lung on the preoperative specimens, and in 44 (65.7%) of these patients, the diagnosis was concordant with the preoperative diagnosis. Among the 23 of the remaining 67 (34.3%) with a discordant diagnosis, 3 patients had ADC, 1 patient had NSCLC, 7 patients had suspected NSCLC and 12 patients had no evidence of malignancy. Misclassified preoperative biopsies included an even number of SQCs and ADCs (n = 3), whereas all of the misclassified biopsies were ADC, morphologically mimicking SQC due to the solid growth.
Diagnostic value of preoperative diagnosis between adenocarcinoma and squamous cell carcinoma
p-value (ADC vs. SQC)
Comparison of H&E stain vs. IHC for subtyping NSCLC
Comparison of H&E stain vs IHC for subtyping NSCLC
IHC predicted phenotype
Comparison of TBB vs. CTNB for the sensitivity or concordance of lung cancer diagnosis
Comparison of TBB vs. CTNB for sensitivity/concordance rate
Suspicious of malignancy
Comparison of the sensitivity or concordance rate of the histological type between preoperative and surgical specimens in relation to the tumor size
Comparison between tumor size and sensitivity/concordance rate
Suspicious of malignancy
We assessed the accuracy of diagnosis of the histological type of lung cancer between preoperative and surgical specimens. The reported accuracy for bronchoscopic biopsy as compared to histopathology of resected or autopsy specimens for differentiating among histological subtypes of lung cancer is in the range of 62% to 97.5%[15–19]. In our study, the concordance rates for diagnosis of the NSCLC subtypes between preoperative biopsies and histopathology of surgical specimens was 66.8% (127/190), which seemed to be slightly low as compared to previous reports; however, many studies excluded tumors that were confirmed as not being malignant: in our study, 50 (26.3%) of 190 patients were diagnosed as not having malignant lesions before excision. After patients without malignancies as determined in preoperative specimens were excluded, the concordance rate was 90.7% (127/140). We found a better accuracy for the diagnosis of SQC than for that of ADC (89.3% vs. 80.4%, p = 0.012), which was also in agreement with previous studies[13, 20]. On the other hand, the sensitivity for ADC was slightly better than that for SQC (75.7% vs. 65.6%, p = 0.138), indicating that ADC seems to have little oversight by preoperative specimens.
IHC studies are usually required if obvious morphological features of squamous or glandular differentiation are not identified. Similar to the findings of this study, prior studies found that ~75% of bronchial NSCLC samples may be subtyped using morphology alone, and 93% of all NSCLC cases may be subtyped when combined immunostaining. Other studies also demonstrated that only a low population (6%) of cases remained without a probable subtype after morphologic examination and IHC. The low not-typed rate in these studies suggests that we should perform IHC as a routine utilization for subtyping of difficult cases.
Several factors affect the diagnostic accuracy. The frequency of diagnostic errors induced by some of these factors, including the biopsy size and degree of differentiation has been described. In our study, the tumor size was correlated with the sensitivity and concordance rate: the larger the diameter, the greater the sensitivity and cell type agreement.
Until date, therapeutic decisions are heavily dependent on the histological subtype of lung cancer (SQC vs. non-SQC) and its molecular characteristics (e.g., EGFR mutation and ALK rearrangement states). Furthermore, many previous studies showed the expression and functions of proteins and genes in lung cancer, and it may be significantly related to tumor progression and metastasis[23–26].
Both EGFR mutation and ALK rearrangements are almost exclusively seen in ADC. According to multiple large phase III crinical trials[11, 27–29], the new classification recommends that all patients with advanced lung ADC be tested for EGFR mutation, as EGFR tyrosine kinase inhibitors can be used as first-line chemotherapy for patients with EGFR mutations. Crizotinib has been approved by the US Food and Drug Administration (FDA) for advanced ADC with ALK rearrangements. Therefore, testing for EGFR mutations and ALK rearrangements in patients with advanced ADC is no longer only a research tool, and should be performed in clinical practice. On the other hand, several molecular targets such as FGFR1 amplification and DDR2 mutation have been discovered in SQC[31, 32]. Target therapies that might be beneficial in this selected subpopulation have never been reported. These results indicate that misdiagnosis of ADC as SQC in preoperative specimens should be avoided so as to prevent the loss of opportunity to select beneficial molecular-targeted therapy for these patients in clinical practice. Although such a result was not seen, there were three (1.3%) misclassifications between ADC and SQC in the preoperative specimens, and in all, SQC was diagnosed as ADC. Fortunately, there was only a lone patient who might have lost the opportunity to receive EGFR-TKI therapy by missed diagnosis (0.44%, shown as case report).
Our retrospective study had some limitations. First, only half of the patients who underwent surgery received preoperative diagnosis by TBB or CTNB. Second, there may be variability between intra- and inter- pathologist in lung cancer diagnosis. Because a smaller amount of tissue is obtained, the diagnostic assessment might be more difficult and more inconsistencie in the diagnosis of pathologists might occur. In such cases, multidisciplinary approach and expert consultation are recommended.
In conclusion, our study suggested that the concordance rate for the diagnosis of NSCLC subtypes, especially "squamous" or "non-squamous" histology, between preoperative and surgical specimens was satisfactory as compared with other reports. Pretreatment diagnosis of lung cancer using small samples is reasonable for selection of the optimal treatment. However, our case report presented above serves to emphasize the need to be aware that diagnosis based on preoperative small samples might be different from that made from surgical specimens, so as to not lose the opportunity for effective treatment.
Written informed consent was obtained from the patient for the publication of this report and any accompanying images.
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