Analysis of lung biopsies using the 2015 WHO criteria and detection of sensitizing mutations——a single-institution experience of 5032 cases

According to the newly released report of cancer epidemiology in China, lung cancer is the most common malignant tumor and the leading cause of cancer death [1], which is a conclusion that can be drawn from cases worldwide [2, 3]. Unfortunately, two-thirds of the patients with lung cancer are already in the advanced stage when they are first diagnosed and thus do not qualify for surgery [4]. Their treatment options are mainly dictated by histological diagnosis based on small biopsy specimens. Furthermore, with the introduction of lung cancer screening program and advances in radiologic imaging techniques and availability, the early detection rates and the overall number of lung cancer cases identified have increased. The rapid advancement of precision lung cancer medicine has necessitated the requirement to provide complete diagnostic evaluations of small biopsy specimens. Accordingly, the 2015 WHO classification of lung tumors established the first chapter addressing the handling of small lung biopsies, and proposed corresponding criteria and terminology for the diagnosis of small biopsy specimens [5]. In this context, 5032 small lung biopsies were received by the First Affiliated Hospital of Nanjing Medical University during 2015–2018.

The purpose of this study is to explore and summarize the experience of applying the newly proposed classifications and criteria to clinical practice by clarifying the distribution of age, gender, pathologic categories and mutational status of this subset of small lung biopsies and demonstrating the relationship between these factors.

Lung cancer is a malignancy with the highest incidence and mortality not only in China, but also in the United States, Europe and every other place around the world [1, 3]. For the reason that most patients of lung cancer have lost surgery opportunity at the time of diagnosis, small biopsy has become the best choice for these patients to determine the tumor histological type and molecular genetic characteristics, and to guide their follow-up treatment. CT-guided percutaneous needle biopsy was for the first time introduced to the clinicians in 1960s, and now it has gradually developed into a mature minimally invasive diagnostic technique [6]. In the meantime, with the development of endoscopic techniques, bronchoscopy has long been an important means for the diagnosis of lung cancer and one of the main methods for early detection of lung cancer [7]. In addition, in recent years, the application of diverse pathological techniques, especially immunohistochemical staining, has become increasingly mature and extensive, and the specificity and sensitivity of antibodies have been constantly improved. On the basis of this background, the postoperative diagnosis has been partially replaced by preoperative diagnosis, providing guidance for more accurate treatment. In this context, small lung biopsy is playing an increasingly important role in the diagnosis of lung cancer. This study demonstrated the distribution of a subset of 5032 small lung biopsies and revealed the clinicopathological and genetic characteristics of lung cancer from a large Chinese institution, in order to provide better assistance for clinical treatment.

We applied the criteria and terminology from the 2015 WHO classification for small lung biopsies in our study. In the previous clinical practice, a diagnosis of NSCLC was enough for the clinicians to make treatment decisions, and the diagnosis of small biopsies mostly referred to the diagnostic criteria and terminology of surgical specimens. However, the deepening of lung cancer research and the rapid development of targeted therapy have heightened the requirement for more detailed histological classification. Moreover, the diagnosis of small biopsies referring to the diagnostic criteria of surgical specimens is always not accurate and precise enough due to the heterogeneity of tumor tissues and the randomness of biopsy technique. As a result, the 2015 WHO classification of lung tumors for the first time provided a specialized classification for small biopsies (bronchoscopic, needle, or core biopsies).

The latest WHO classification emphasized the importance of saving specimens in the diagnostic process of small lung biopsies. In addition to making H&E sections and immunohistochemical sections, we should set aside adequate specimens for molecular pathologic detection to guide targeted therapy. For patients with clearly defined adenocarcinoma differentiation, patients with poor morphological differentiation and immunophenotypic tendency toward adenocarcinoma, patients with large cell carcinoma as well as patients with NSCC, NOS, the testing of EGFR, ALK, ROS1 and other tumor driver genes should be performed to help find probable therapeutic targets. The specialized terms for small biopsies are roughly in correspondence with those of surgical specimens, while the former feels more conciliatory. Those cases which are obviously inconsistent with small cell carcinoma in morphology and do not have the typical morphological features of adenocarcinoma or squamous cell carcinoma should be firstly classified as non-small cell carcinoma (NSCC). Then, a diagnostic tendency should be defined on basis of morphological features and immunophenotypic characteristics, such as “favor adenocarcinoma”, “favor squamous cell carcinoma”, “with spindle cell and/or giant cell carcinoma”, and so forth. Some cases lack typical morphological features of squamous cell carcinoma, adenocarcinoma or neuroendocrine tumor while their immunophenotype is atypical or even completely naked. This part of cases should be divided into non-small cell carcinoma, not otherwise specified (NSCC, NOS). If these cases still do not have typical morphology and specific immunostaining after radical resection and adequate sampling, they will be diagnosed as large-cell carcinoma. Pathologists should pay attention that, due to the limited amount of tissue, it could be very hard to determine the origin of a malignancy merely with small biopsy specimens. Therefore, the substitution of non-small cell carcinoma (NSCC) for non-small cell lung cancer (NSCLC) can make the diagnosis more accurate and cautious. The diagnostic terms of small lung biopsies provided by the latest version of the WHO classification are more moderate and cautious, and simultaneously correspond one-to-one to those from the diagnostic classification of surgical specimens. In this way, pathologists can render diagnoses based on both small biopsies and surgical specimens more flexibly. In the meantime, clinicians and patients can have a better understanding of the randomness and limitations of small biopsies.

The lung is the only organ that receives blood and lymph circulation from the whole body. The dense capillary network in the lung is the first barrier for tumor cells to enter the venous system from the lymphatics [8]. Therefore, metastatic tumors are more common in lung than in other organs, and tumors originating from almost any part of the body can metastasize to the lung. In this study, there were 165 cases of metastatic tumors, the most common metastasis to lung was from breast carcinoma (55 cases, 33.3%), followed by 34 cases (20.6%) of colorectal carcinoma and 12 cases (7.3%) of renal cell carcinoma. According to the data from International Registry Lung Metastases and another similar study of Indian population, the top three lung metastatic tumors were colorectal carcinoma (33–37%), breast carcinoma (17–19%), and renal cell carcinoma (12–17%) [9‐12]. Actually, the global incidence of colorectal cancer is lower than that of breast cancer [3]. Therefore, it can be speculated that colorectal cancer is more likely to metastasize to the lung than breast cancer, and breast cancer is more likely to metastasize to the lung in the Chinese population than in others.

It is difficult to determine the origin of tumor only by small lung biopsies. Usually, pathologists can provide clinicians with some clues based on H&E morphology and immunostaining. Distinguishing pulmonary enteric adenocarcinoma (PEAC) from metastatic colorectal adenocarcinoma (MCAC) is of particular concern. Both of PEAC and MCAC can be present with a morphology of colorectal carcinoma, and CK20, CDX2 and MUC2 can be immunohistochemically positive in both of them. Usually, MCAC does not have other morphological subtypes except enteric morphology, and CK7, TTF-1 and Napsin A are generally negative in MCAC [13]. In rare cases, the MCAC can express TTF-1, where it may not be completely distinguished from PEAC [14]. Therefore, for the patients with a history of colorectal cancer and a lung lesion of microscopical enteric morphology, a diagnosis of MCAC is a priority. Currently, only after MCAC is clinically excluded by colonoscopy can a pathologist render a diagnosis of primary PEAC. Recent studies have shown that PEAC demonstrates similar mutational characteristics to non-small cell lung cancer, rather than to primary or metastatic colorectal adenocarcinoma [14].

The proportion of adenocarcinoma, squamous cell carcinoma and small cell carcinoma was slightly higher than that of Asian population from SEER database, which were 61.4% vs 58.1, 23.3% vs 15.5, 10.1% vs 7.8% respectively. We can find that adenocarcinoma account for the majority of primary lung cancer in our study, which has been a growing trend in recent decades.

In this study, 444 patients underwent surgery after small biopsy, among which 368 patients received a consistent diagnosis. These cases made up a concordance rate of 82.9%, without treatment option changes. Among the 17 cases that received different histopathological diagnostics based on the surgery after small biopsy, the most common situation was that adenosquamous carcinoma was misdiagnosed as adenocarcinoma (4 cases) or squamous cell carcinoma (1 case) in the previous diagnosis. These cases fully demonstrated the heterogeneity of lung cancer and the randomness and limitations of small biopsy. Therefore, as pathologists, we should be aware that we can never be too scrupulous when dealing with small lung biopsies.

The frequency of EGFR mutation in this study was 56.1%, which was close to that of the Chinese population, 50.2%, reported by PIONEER study [15]. According to previous studies and this one, we can find that the frequency of EGFR mutation in China and other countries/regions in East Asia (approximately 30–64%) [15‐17] is significantly higher than that in India (22.2%) and among white people (approximately 20%) [18]. We found that the amount of EGFR mutations was significantly higher in female adenocarcinoma patients than in male, which was also supported by the data from PIONEER study. It was demonstrated in our study that frequency of EGFR mutation in well-differentiated adenocarcinoma was significantly higher than that in poorly-differentiated adenocarcinoma, while PIONEER study showed that the mutational rate of EGFR was significantly higher in invasive adenocarcinoma than in bronchioloalveolar carcinoma, which is currently called pulmonary adenocarcinoma in situ. Therefore, it can be speculated that the amount of EGFR mutation is higher in invasive adenocarcinoma with distinct morphological differentiation, which needs to be confirmed through further research.

The previously reported prevalence of ALK mutation was 3–7% [19‐22]. In this study, ALK mutation was found positive in 5.7% cases through ARMS-PCR and in 4.2% cases through IHC(D5F3), which was slightly lower than the mutational rate of 6.1% detected by Wang through IHC(D5F3) [23]. The overall frequency of ALK mutation was 4.5% in this study, which was almost consistent with previous reports. The frequency of ROS1 mutation was 0.9% in this study, which was slightly lower than that in previous reports (1.2–2.2%) [24‐29], probably because of the small amount of our ROS1-tested cohort.

This single-institution study demonstrated the distribution of a large number of small lung biopsies and revealed the clinicopathological and genetic characteristics of lung cancer from a large Chinese institution. On the basis of that, we found EGFR mutations were more common in females, younger age groups, and well-differentiated adenocarcinoma. Simultaneously, ALK mutation tended to be more common in older age groups, poorly-differentiated adenocarcinoma, and had no gender difference. The criteria and terminology provided by the 2015 WHO classification for small lung biopsies can help predict the mutational status of primary lung carcinomas, and they should be applied to pathologists’ daily work.