MATERIALS AND METHODS

This study was approved by the Ethical Committee of Universiti Kebangsaan Malaysia Ref No. UKM 1.5.3.5/244/JEP-2016-089 and was exempted from informed consent by the institutional review board (IRB). All cases diagnosed as primary lung squamous cell carcinoma and adenocarcinoma between January 2008 and December 2016 were reviewed. Cases that fulfilled the inclusion and exclusion criteria with sufficient tissue samples were selected for this study. Hematoxylin and eosin stained slides were reviewed by two pathologists to confirm the diagnosis. Tumours were graded on the basis of WHO classification. The tissues were obtained from routine formalin-fixed paraffin-embedded blocks of small biopsies and resected specimens of 35 lung squamous cell carcinoma and 35 lung adenocarcinoma cases. Information on patient details was retrieved from the Computerized Medical Record System. Patient identity remained anonymous and each subject was coded accordingly.

Primary antibodies

Two antibodies were used in this study, mouse monoclonal p63 antibody (Clone DAK-p63, Ready-To-Use, Code IR662, Dako, Glostrup, Denmark) and mouse monoclonal p40 antibody (1:100, clone BC28, Code Ab172731, Abcam, Cambridge, UK). Normal skin and laryngeal squamous cell carcinoma tissues were used as the positive controls for p63 and p40, respectively.

Immunohistochemical staining method

Immunohistochemical staining was performed on tissue sections using the protocol from EnVision FLEX+, Mouse, High pH (Code No. K8012, Dako). Primary antibody was diluted to optimal concentration using Antibody Diluent, Dako REAL (Code No. S2022, Dako).

The tissue blocks were sectioned to approximately 3 μm thickness. The tissue slides were incubated on hot plates at 60ºC for 1 hour and initial deparaffinization and pre-treatment was performed in the Decloaking Chamber NxGen (Ref. No: DC2012-220V, Biocare Medical, Pacheco, CA, USA) using En-Vision FLEX Target Retrieval Solution, High pH (Code No. DM828, Dako) at 110°C for 30 minutes. Slides were incubated with the primary antibodies for 20 minutes at room temperature, followed by incubation with EnVision FLEX/HRP (Code No. DM822, Dako) for 20 minutes. Sections were then incubated with 1× DAB-containing Substrate Working Solution for 10 minutes. Slides were then counterstained with Hematoxylin 2 (REF 7231, Thermo Scientific, Rockford, IL, USA).

Immunohistochemical staining analysis

The staining intensity of both p40 and p63 markers were scored as 0, 1+, 2+, or 3+ (Fig. 1) and the percentage of immunoreactive cells were recorded [9]. Cases were considered positive if 5% or more of the tumour cells showed brown nuclear staining. Cases with less than 5% staining or no areas of positive staining were regarded as negative.

Statistical analysis

Data analysis was performed using the SPSS software program ver. 20.0 (IBM Corp., Armonk, NY, USA). Pearson chisquare test was used to assess the association between positivity of each marker and tumour diagnosis. Here, p-values less than .05 were considered statistically significant.

RESULTS

Epidemiologic and clinico pathologic data

A total of 70 cases of NSCLC were investigated. More than half of the cases presented with distant metastasis at diagnosis (64.2%). For squamous cell carcinoma, 32 (91.4%) cases were males and three cases (8.6%) were females. The mean age at squamous cell carcinoma diagnosis was 68 years, ranging from 36 to 98 years. Adenocarcinoma had a more similar sex distribution, with 19 cases (54.3%) in males and 16 cases (45.7%) in females. The mean age for adenocarcinoma was 59 years, ranging from 25 to 90 years. Squamous cell carcinomas comprised seven well, 11 moderately, and 15 poorly differentiated tumours. Among the adenocarcinomas, there were nine well, 14 moderately, and 12 poorly differentiated carcinomas. The clinical information is summarised in Table 1.

p40 immunostaining

Twenty-seven cases of primary lung squamous cell carcinoma (77.1%) were positive for p40 (Table 2). The reactivity of p40 nuclear staining in lung squamous cell carcinoma was strong and diffuse; 71.4% of cases had intensity score of 3+ in more than 50% of tumour cells (Table 3, Fig. 2). Remarkably, eight cases that were previously diagnosed as primary lung squamous cell carcinoma showed negative staining. Of these, six cases (17.1%) had intensity score of 0 and two cases (5.7%) showed minimal reactivity (less than 5% of tumour cells) with intensity score of 1+. The original slides were reviewed and all of these cases are poorly differentiated tumours with focal squamouslike morphology including solid growth pattern, abundant eosinophilic cytoplasm (resembling cytoplasmic keratinization), sharp cell borders, and intercellular bridges (Fig. 2). Six cases had prior immunohistochemistry and the diagnosis of squamous cell carcinoma was made on the basis of negative TTF1 and p63 positivity (n = 3). The other two cases were diagnosed as squamous cell carcinoma based on morphology alone. In contrast, all (100%) lung adenocarcinomas were negative for p40.

Two cases of lung adenocarcinoma showed weak p40 expression (1+). However, the immunoreactive cells were minimal (in less than 5% of tumour cells) and scattered with no specific pattern. Immunopositivity of p40 and p63 according to tumour differentiation is shown in Table 4.

Table 5 summarizes immunohistochemical profile of p40-negative squamous cell carcinoma and histologic grading.

p63 immunostaining

Thirty cases (85.7%) of lung squamous cell carcinoma were positive for p63 (Table 2). The expression of p63 in lung squamous cell carcinoma was also strong and diffuse, equivalent to that of p40, and 74.3% of cases had intensity score of 3+ in more than 50% of tumour cells. Among lung adenocarcinomas, 13 cases (37.1%) showed p63 positivity. These cases demonstrated a vast range of immunoreactivity, with minimal reactivity (less than 5% of tumour cells) in nine cases, focal reactivity (5 to 50% of tumour cells) in 11 cases, and diffuse reactivity (more than 50% of tumour cells) in two cases (Table 3, Fig. 2).

All p63 negative cases were also negative for p40. Conversely, three p40 negative cases were p63 positive (Table 5). In their benign counterparts, both p40 and p63 showed nuclear staining in basal bronchial cells.

As shown in Table 6, the specificity of p40 for lung squamous cell carcinoma was 100% compared to 62.9% for p63. The sensitivity of p40 and p63 was 77.1% and 85.7%, respectively. p40 has a higher positive predictive value for lung squamous cell carcinoma than p63 (100% vs 69.8%). Both markers had similar negative predictive values.

DISCUSSION

NSCLC, constituting tumours other than small cell carcinoma, accounts for 85% of all lung cancers; lung adenocarcinoma and squamous cell carcinoma are the most frequent histologic subtypes [4,13]. Morphologically, adenocarcinoma is identified by glandular differentiation and mucin production. Squamous differentiation is recognized by keratinization, keratin pearls, and intercellular bridges [4]. However, distinguishing between the two can be challenging, particularly in poorly differentiated tumours. In such cases, immunohistochemical markers are recommended for precise histologic subtyping [4]. To date, the WHO recommends that cases should be classified as NSCLC, favouring adenocarcinoma when they are positive for an adenocarcinoma marker (TTF1 or mucin) with a negative squamous marker (p63 or p40). Conversely, cases with at least moderate diffuse staining for a squamous marker and negative adenocarcinoma marker should be classified as NSCLC, favouring squamous cell carcinoma.

Although most lung tumours can be accurately subtyped by co-expression of TTF1 and p63, a small percentage of cases showed overlapping (TTF1+/p63+) or indeterminate staining patterns (TTF1/weak p63+), leading to misinterpretation and incorrect diagnosis [7,11]. p63 is a sensitive marker for squamous differentiation, but its specificity is only 60%–82% [9,10]. Frequent p63 reactivity, particularly in adenocarcinoma and lymphoma, is a significant pitfall in diagnosis of lung cancer [9].

Accurate histologic diagnosis and subtyping has major therapeutic implications [14]. Current clinical practice guidelines recommend patients with lung adenocarcinoma or NSCLC favouring adenocarcinoma should undergo molecular testing [15]. Incorrect diagnosis of squamous cell carcinoma may exclude patients from receiving targeted therapy, or worse, it may endanger patients to complications of the treatment [3,4].

In studies conducted on mainly resected specimens, p40 demonstrated 98%–100% specificity with comparable sensitivity to that of p63, indicating its reliability for diagnosing squamous cell carcinoma [9,10,12]. Our study was conducted to investigate the expression of p40 and p63 in predominantly small biopsies and few resected specimens of lung squamous cell carcinoma and adenocarcinoma. The present study was in line with previous reports in concluding that p40 is more specific than the standard p63 antibody for diagnosing lung squamous cell carcinoma. However, our study demonstrated a lower sensitivity for p40 compared to prior studies.

Based on a literature review, a case with negative p40 is less likely to be squamous cell carcinoma. A study by Tacha et al. [12] described six cases of poorly differentiated lung squamous cell carcinoma (5.6%) that were negative for p40; subsequent staining with other squamous markers were also negative. Kadota et al. [5] reclassified 31 cases (6.5%) of lung tumours that were originally diagnosed as squamous cell carcinoma into other histologic subtypes based on negative p40 staining. Rekhtman et al. [16] reclassified three tumours with an initial diagnosis of squamous cell carcinoma and lack of p40 expression as solid adenocarcinoma. In the present study, eight cases originally diagnosed as squamous cell carcinoma were negative for p40. Based on the review of histology sections of these cases as well as the p40 findings, these cases were reclassified as poorly differentiated or solid type adenocarcinoma. Thus, p40 is highly recommended in cases of poorly differentiated carcinomas to confirm or exclude the line of squamous differentiation.

Three discrepant cases with p63 positivity, p40 negativity, and TTF1 negativity were initially diagnosed as squamous cell carcinoma. These cases were poorly-differentiated tumours with focal areas displaying squamoid morphology such as intercellular bridging and abundant eosinophilic cytoplasm (Fig. 3). TTF1 is not exhibited in 25% of lung adenocarcinomas, and the three discrepant cases in this study could be categorized as adenocarcinoma. Since there are few discrepant cases, future studies involving larger sample sizes of poorly differentiated cases are recommended to determine the sensitivity and specificity of p63 and p40 markers in defining subtypes of NSCLC. A three-panel approach of using p63, p40, and TTF1 in cases of carcinoma with complex tumour differentiation would assist in reaching a specific diagnosis.

The majority of cases (92.9%) in the current study were small biopsy tissues (n = 65) with only five resected specimens (7.1%). As addressed by Travis et al. [3], small biopsy specimens may not be representative of the total tumour due to histologic heterogeneity of lung cancers. Also, the distinguishable morphologic features of squamous or adenocarcinoma differentiation are only identifiable if the solid tumour component was sampled [17].

Two p40 antibodies are available for current laboratory use, rabbit polyclonal p40 (RPp40) and mouse monoclonal p40 (MMp40, BC28). RPp40 was used in the above-mentioned studies [5,9,10]. Nonaka [10] reported variable background staining that did not hinder the staining interpretation. RPp40 has been demonstrated to stain macrophages in lung tissue and non-specific cytoplasmic staining in neoplastic cells while MMp40 has clear nuclear staining without non-specific background staining [12]. Mouse monoclonal antibody was used in the present study, and distinctive nuclear staining with a clean background was observed.

In summary, we demonstrated strong and diffuse p40 expression in the majority of lung squamous cell carcinomas and absence of p40 expression in all lung adenocarcinomas. Expression of p63 is similar to that of p40 in lung squamous cell carcinoma, but there was variable p63 immunoreactivity in lung adenocarcinoma. In poorly differentiated cases, a three-panel approach of p63, p40, and TTF-1 may help to distinguish adenocarcinoma from squamous cell carcinoma. Thus, p40 is an excellent marker for distinguishing lung squamous cell carcinoma from adenocarcinoma, and that its expression is equivalent to that of p63 in lung squamous cell carcinoma.

Acknowledgments

Fig. 1.

Intensity score for positive p40 and p63 nuclear staining in tumour cells. (A) Score 1+ for weak positivity. (B) Score 2+ for moderate positivity. (C) Score 3+ for strong positivity.

Fig. 2.

Analysis of p40 and p63 expression in lung squamous cell carcinoma and adenocarcinoma. (A) Intensity score. (B) Tumour cell immunoreactivity.

Fig. 3.

Poorly differentiated tumour with squamous-like morphology. Tumour cells with abundant eosinophilic cytoplasm and distinct cell borders (A), intercellular bridges (B), and keratinization features (C).

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Figure & Data

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