Two cases of lung neuroendocrine carcinoma with carcinoid morphology

The 2017 World Health Organization (WHO 2017) classification of tumors separates pancreatic neuroendocrine neoplasms (NENs) into two broad categories—NEN with carcinoid-like morphology and poorly differentiated NEN—and has incorporated a new subclassification to the high-grade NEN with carcinoid-like morphology category, grade 3 neuroendocrine tumor (NET G3). NET G3 shows a carcinoid-like morphology with high proliferative activity and the prognosis is intermediate between NET G2 and neuroendocrine carcinoma (NEC) [1]. This new category algorithm aims to improve outcomes and help better therapeutic strategies for patients.

In the WHO 2015 classification of lung tumors, NETs are classified as low-grade typical carcinoid (TC), intermediate-grade atypical carcinoid (AC), high-grade large cell neuroendocrine carcinoma (LCNEC), and high-grade small cell lung carcinoma (SCLC) with no NET G3 category [2, 3]. Here we report two cases of lung NEC with carcinoid morphology having a mitotic count of > 10/2 mm² that better correspond to NET G3.

SCLC is likely to occur in males and has the strongest relationship with smoking [2]. SCLC usually shows a diffuse growth pattern, without an obvious neuroendocrine morphology, such as organoid, rosette, palisading, and trabecular patterns [2]. The WHO 2015 classification of lung tumors describes that a tumor with carcinoid morphology and mitotic counts > 10/2 mm² is best classified as LCNEC [2], so the differential diagnosis of our cases was LCNEC. Differentiation between LCNEC and SCLC is sometimes difficult, reportedly due to morphological overlap between the two [5, 6]. In a routine diagnostic scene, we emphasize cytological findings, particularly nuclear findings, over tumor growth patterns such as a diffuse growth pattern or organoid pattern, when discriminating between SCLC and LCNEC. Our tumor cells had a high nucleus-to-cytoplasm ratio, low cytoplasm, and fine granular nuclear chromatin, all of which are seen in SCLC. Therefore, we diagnosed the two cases as SCLC. However, we consider that our tumors are not typical of SCLC due to the following four reasons: 1. The tumors occurred in female never-smokers. 2. Histology showed carcinoid morphology without extensive necrosis. 3. Proliferative abilities were extremely low compared to SCLC. 4. The tumors seemed to be biologically less aggressive than SCLC.

Quinn et al. reported twelve cases of lung NEC with carcinoid morphology with mitotic counts > 10/2 mm² [7]. In their report, the average mitotic count was 25/2 mm² and all tumors were completely resected. Eleven patients had recurrence and seven patients died from the tumor. For the seven metastatic cases, four patients were treated with platinum-based chemotherapy with no apparent response, whereas three other patients were treated using a combined therapy of capecitabine and temozolomide against well-differentiated gastroenteropancreatic NETs, of whom two showed good response. They reported that the clinicopathological features of these tumors seemed to be more akin to carcinoid than to LCNEC. Huang et al. classified AC into low- and high-grade AC [8]. Low-grade AC shows carcinoid morphology with the mitotic count ≤10/2 mm² and high-grade AC shows carcinoid morphology with non-massive necrosis with the mitotic count > 10/2 mm². They reported five-year overall survival rates of 83% for low-grade AC, 70% for high-grade AC, 60% for LCNEC and 40% for SCLC. According to their criteria, our cases may correspond to high-grade AC, a midgrade tumor.

In the WHO 2010 classification, gastroenteropancreatic NEN was divided into the following 3 grades based on mitotic count and Ki-67 index: NET grade 1 (NET G1) with mitotic count < 2/2 mm² and/or Ki-67 index ≤2%, NET G2 with mitotic count 2 to 20/2 mm² and/or Ki-67 index 3 to 20% and NEC with mitotic count > 20/2 mm² and/or Ki-67 index > 20% [9]. Regarding pancreatic NEC, a new subtype of tumor was found that exhibits carcinoid-like morphology and shows clinicopathological features different from poorly differentiated tumor. Pancreatic NEC with carcinoid-like morphology has a high SSTR positive rate and is less responsive to platinum-based therapy but has better prognosis than poorly-differentiated tumor [10‐12]. Based on these findings, pancreatic NEC was divided into carcinoid-like morphology type (NET G3) and poorly-differentiated type (NEC G3) in the WHO 2017 classification, and the diagnosis and treatment of pancreatic NEN was greatly changed [1]. Although the Ki-67 index of NET G3 is defined as exceeding 20%, it is usually ≤55%, and its proliferative activity is lower than that of NEC G3.

The WHO 2018 expert consensus proposed a new classification of NEN for other organs system including lung based on the same concept as the pancreatic NENs: 1. Well-differentiated tumors are classified as NET and poorly-differentiated tumors are classified as NEC based on the degree of differentiation. 2. According to proliferative ability, NETs are subclassified into G1, G2, and G3 [13]. In this proposed classification, TC and AC, well-differentiated tumors, correspond to NET G1 and NET G2, respectively, while SCLC and LCNEC, poorly-differentiated tumors, correspond to NEC [13].

Recently, regarding lung NETs, the WHO classification recommends the detection of immunohistochemical markers to confirm the neuroendocrine nature of tumor cells [2]. Commonly used markers include neuroendocrine markers (chromogranin A, synaptophysin, CD56). Most lung carcinoids and 80–90% of SCLCs are positive for neuroendocrine markers [2]. The tumors we studied were strongly positive for chromogranin A, synaptophysin, and CD56. Tumor expression of TTF-1 may also be utilized to aid in the diagnosis of lung NETs. TTF-1 is usually absent in lung carcinoids but positive in approximately 90% of SCLCs [2]. These immunohistochemical markers can be used when the histologic features are considered equivocal or the pathologist is looking for additional information. However, these markers cannot distinguish between subtypes of lung NETs. SSTR-2 exhibits mainly membranous immunostaining, and its expression is important for the diagnosis and management of patients with NEN [14]. SSTR-2 immunostaining was scored by Volante et al. as follows [4]: score 0: absence of immunoreactivity; score 1: pure cytoplasmic immunoreactivity, either focal or diffuse; score 2: membranous reactivity in less than 50% of tumor cells, irrespective of the presence of cytoplasmic staining; score 3: circumferential membranous reactivity in more than 50% of tumor cells, irrespective of the presence of cytoplasmic staining. According to this report, scores of 0 or 1 were considered negative, while scores > 1 were considered positive for SSTR-2 expression. It is reported that positive rate of SSRT-2 staining in pancreatic NET G3 is significantly higher than that in NEC G3, and its expression is considered to be indicative of good prognosis [10, 15, 16]. Tsuta et al. reported that in lung TC, AC, LCNEC and SCLC, immunoexpression of SSTR-2 was observed in 96.6, 77.8, 60 and 69% of cases, respectively. They suggested that SSTR-2 showed a tendency toward decreased expression in well- to poorly-differentiated tumors [17]. Case 1 was positive for SSTR-2 with score “2”, whereas case 2 was negative with score “0”. The expression of SSTR-2 in lung NEC with carcinoid morphology remains unclear. Ki-67, which may help separate lung carcinoid from LCNEC and SCLC, is only recommended as a complementary tool in the differential diagnosis of lung NETs. Although a grading system based on the Ki-67 index has previously been proposed [18, 19], it has not yet been included in the current WHO classification of the lung. Ki-67 index < 20% is in favor of carcinoid, while NECs show much higher proliferative activity than carcinoids, that is, Ki-67 index of SCLC is 50 to 100% (averaging ≥80%) and that of LCNEC is 40 to 80% [2]. The Ki-67 index of the tumors we studied were extremely low compared to SCLC.

SCLC has a poor prognosis with a median overall survival time of 12.9 months for limited disease [20]. This poor prognosis reflects the rapid growth of SCLC, its propensity for spreading to lymph nodes and distant organs, and the higher proportion of advanced disease presenting at diagnosis. Only 4% of patients present with a solitary nodule, and the rate of surgical resection is 1–6% [21, 22]. The cases we presented here were diagnosed at a resectable stage, and without adjuvant chemotherapy following surgery, the patients did not have a recurrence for almost two years, suggesting that these tumors may have less aggressive behavior than SCLC.

It is reported that lung NETs with carcinoid morphology having a mitotic count of > 10/2 mm² corresponding to NET G3 are rare, not well characterized and need further study [7, 13]. The clinical and pathological features of our tumors seemed to be different from those of SCLC and they may fall into the category of NET G3. We consider identification of this subset to be relevant for therapeutic management.

We presented two cases of lung neuroendocrine carcinoma with carcinoid morphology. There is no NET G3 category in the current WHO 2015 classification of lung tumors. However, we consider that our tumors may match the category of NET G3 and may be called “lung NET G3”. It is important to identify this subset for further therapeutic management.