Does the WHO 2010 classification of pancreatic neuroendocrine neoplasms accurately characterize pancreatic neuroendocrine carcinomas?

BACKGROUND: The WHO classified pancreatic neuroendocrine neoplasms in 2010 as G1, G2, and neuroendocrine carcinoma (NEC), according to the Ki67 labeling index (LI). However, the clinical behavior of NEC is still not fully studied. We aimed to clarify the clinicopathological and molecular characteristics of NECs.
METHODS: We retrospectively evaluated the clinicopathological characteristics, KRAS mutation status, treatment response, and the overall survival of eleven pNEC patients diagnosed between 2001 and 2014 according to the WHO 2010. We subclassified WHO-NECs into well-differentiated NEC (WDNEC) and poorly differentiated NEC (PDNEC). The latter was further subdivided into large-cell and small-cell subtypes.
RESULTS: The median Ki67 LI was 69.1% (range 40-95%). Eleven WHO-NECs were subclassified into 4 WDNECs and 7 PDNECs. The latter was further separated into 3 large-cell and 4 small-cell subtypes. Comparisons of WDNEC vs. PDNEC revealed the following traits: hypervascularity on CT, 50% (2/4) vs. 0% (0/7) (P = 0.109); median Ki67 LI, 46.3% (40-53%) vs. 85% (54-95%) (P = 0.001); Rb immunopositivity, 100% (4/4) vs. 14% (1/7) (P = 0.015); KRAS mutations, 0% (0/4) vs. 86% (6/7) (P = 0.015); response rates to platinum-based chemotherapy, 0% (0/2) vs. 100% (4/4) (P = 0.067), and median survival, 227 vs. 186 days (P = 0.227).
CONCLUSIONS: The WHO-NEC category may be composed of heterogeneous disease entities, namely WDNEC and PDNEC. These subgroups tended to exhibit differing profiles of Ki67 LI, Rb immunopositivity and KRAS mutation, and distinct response to chemotherapy. Further studies for the reevaluation of the current WHO 2010 classification are warranted.

Introduction

Ki67 is a powerful prognostic marker of pancreatic neuroendocrine neoplasms (pNENs) [1] and, accordingly, the remarkable revision was made from the former 2000 World Health Organization (WHO) classification system to the current WHO 2010 terminology system, in which mitotic count and/or Ki67 labeling index (LI) were adopted as the pivotal indicator of stratification [2]. NENs are now to be categorized into neuroendocrine tumor (NET)-G1, NET-G2, and neuroendocrine carcinoma (NEC). Whereas NETs-G1/G2 are invariably composed of tumor cells with well-differentiated morphology, NECs usually have poorly differentiated histology with Ki67 LI > 20 % [2, 3]. Accordingly, all NENs with Ki67 LI > 20 % are defined as NEC. Clinically, these tumors are treated with the same platinum-based chemotherapy regimens as small-cell lung cancers [4-6]. However, some reports have recently indicated that a proportion of well-differentiated NENs might have proliferative rates above the threshold for NET-G2 [7, 8]. In addition, the Nordic NEC study reported that patients with a Ki67 <55 % had low responses to platinum-based chemotherapy [9]. We suppose that the current NEC category, as defined by the WHO 2010 classification (WHO-NEC), includes two groups that differ in clinical behaviors as well as pathological characteristics. Information about the clinicopathological features of WHO-NEC group is scant [7-10]. Therefore, we aimed to further characterize the WHO-NEC group in terms of pathological findings, molecular characteristics, and clinical behaviors.

Patients and methods

Patients

We retrospectively retrieved all of the pNENs diagnosed between January 2001 and March 2014 from our hospital database. All patients were recategorized as NET-G1, NET-G2, or NEC according to the WHO 2010 classification. Specimens for histological examination were obtained from preoperative endoscopic ultrasound-guided fine needle aspiration (EUS-FNA), biopsy, and/or surgical resection. All patients diagnosed with small-cell carcinoma were subsequently assessed by contrast enhanced (CE) chest MDCT to exclude the possibility of metastasis from a primary lung cancer [11]. This study was approved by our institutional review board.

Diagnostic and prognostic characterization

The following features were recorded for all patients: age, gender, symptoms, hormonal syndromes, primary and metastatic locations, European Neuroendocrine Tumor Society (ENETS) TNM stage [12], and CE-MDCT features such as anatomical location, tumor size, and contrast enhancement. We recorded the details of all treatments administered to the patients, particularly platinum-based chemotherapy [4, 5, 13].

Endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) and sample preparation

EUS-FNA procedures were performed using a convex linear-array echoendoscope (GF-UGT240 or GF-UCT260; Olympus Optical Co Ltd, Tokyo, Japan) paired with an ultrasound machine (SSD5500 or Prosound α10; Aloka, Tokyo, Japan). We used 22-gauge needles (NA-11J-KBor NA-200H-8022; Olympus Medical System Corp. Ltd., Tokyo, Japan or EchoTip-Ultra Needle; Cook Endoscopy Inc., Winston Salem, N.C., USA or Expect; Boston Scientific Japan, Tokyo, Japan).

Aspirated materials were divided for cytopathological evaluation, cell-block preparation, and KRAS mutation analysis. In all patients, specimen adequacy was evaluated on-site by Diff Quick staining (Diff-Quik; Kokusai Shiyaku, Kobe, Japan) by a cytopathologist or cytotechnologist. Cell-blocks were prepared after the fresh specimens were immediately fixed in 10 % formalin and embedded in paraffin. Sliced sections then were stained by hematoxylin and eosin, as well as by immunohistochemical staining (IHC) [14].

Histological evaluation

We defined tumors as NEC that showed diffuse expression of neuroendocrine markers and Ki67 LI of more than 20 %. In accordance with the 2010 WHO classification, tumors characterized by high-grade cytological atypia, apparent pleomorphism, extensive necrosis, and prominent mitotic activity were categorized into poorly differentiated NEC (PDNEC). Of PDNECs, tumors characterized by diffuse growth of highly atypical cells with small-sized to medium-sized nuclei, finely granular chromatin, and inconspicuous nucleoli, were categorized as small-cell NEC (SCNEC). Carcinomas with large nuclei, coarse chromatin and well-visible nucleoli with nested proliferation were categorized as large-cell NEC (LCNEC). Furthermore, we attempted to extract those tumors whose cytological features were blander than that of PDNEC and rather similar to NET-G2; that is, tumors composed predominantly of cells with low nucleocytoplasmic ratio and small-sized to medium-sized, ovoid nuclei, growing with minimal pleomorphism, and lacking extensive necrosis. We designated these tumors as ‘well differentiated NEC (WDNEC)’, and separated them from SCNECs and LCNECs. All slides were reviewed and reclassified by the same pathologist (WH).

Immunohistochemistry and Ki67 labeling index

IHC was performed using monoclonal antibodies for chromogranin A (clone SP12, rabbit, 1:200, Neo Markers), synaptophysin (clone SP11, rabbit, 1:100, Neo Markers, Fremont, CA, USA), Ki67 (clone SP6, rabbit, 1:200; Neo Markers), and Rb (clone 3H9, mouse, 1:300; MBL).

The measurement of Ki67 LI was performed under the assistance of digital pathology technology. Briefly, slides were digitally scanned using a Scan Scope XT (Aperio Technologies, Vista, CA, USA). All sections were reviewed to exclude portions with extensive desmoplasia, necrosis and regions with bleeding. The ultimate Ki67 LI was determined as the highest value found in each specimen using the IHC Nuclear Image Analysis tool (Aperio Technologies, Vista, CA, USA) and was similarly measured and determined in cell-block sections of EUS-FNA specimens as described previously [15].

The prominent concern about EUS-FNA is whether WHO classification (grading) is possible with the biopsy specimens. We previously reported a study [15] about a comparison of grades of pNENs between resected and EUS-FNA specimens by Ki67 immunostaining. The concordance rate rose to 90 % when EUS-FNA samples contained more than 2000 neoplastic cells. In accordance with our previous study, we defined the cases whose neoplastic cells were insufficient for grading (less than 2000 cells) as tumors of ‘uncertain’ grade.

Analysis of KRAS mutation

Genetic analysis was performed on either the fresh specimens or formalin-fixed paraffin-embedded sections. After nucleic acids were extracted and amplified by polymerase chain reaction, gene mutations were analyzed by ABI PRISM 310 Genetic Analyzer (Applied Biosystems) or the Cycleave PCR assay (Takara Co., Ltd); the detail of which was described previously [16, 17].

Statistical analysis

Statistical analysis was performed using SPSS 17.0 (SPSS Inc., Chicago, IL, USA) software and P values <0.05 were considered statistically significant. Categorical variables are expressed as absolute (n) and relative (%) frequencies and were compared using the Chi squared test or Fisher’s exact test. Survival was analyzed using the Kaplan–Meier method with the log-rank test.

Results

Ninety-five patients were diagnosed with pNEN at our hospital during the study period. As to grading of pNENs, the WHO classification 2010 suggests two parameters (mitotic count and Ki67 LI) to evaluate the proliferative activity of tumors. We performed grading of pNENs by measuring Ki67 LI and did not employ the mitotic count method, because our study consisted mostly of tumors diagnosed by FNA specimens, which were too small an amount to secure 50 microscopic fields necessary for the calculation of mitotic count. The pNENs were reclassified into uncertain for Ki67 LI (n = 8), NET-G1 (n = 55), NET-G2 (n = 21), and WHO-NEC (n = 11) in accordance with the WHO 2010 classification. The 11 cases of WHO-NEC were the subject of analysis in this study (Fig. 1).

Fig. 1

Algorithm for patient selection from pNEN. NEN neuroendocrine neoplasm, NET neuroendocrine tumor, LCNEC large cell NEC, SCNEC small cell NEC, WDNEC well-differentiated neuroendocrine carcinoma, PDNEC poorly-differentiated neuroendocrine carcinoma

Basic demographic and clinical features of patients with WHO-NEC (Tables 1, 2)

Ten (91 %) of 11 patients were symptomatic, mainly with abdominal pain. The median tumor size was 35 mm (range 20–55 mm). Tumors were located in the head, body, and tail of the pancreas in 2, 5, and 4 patients, respectively. Eight (72 %) patients had liver metastasis at the time of diagnosis, two were treated with surgery (ENETS stageIIb and IIIb) and six who received platinum-based chemotherapy (3 cases were cisplatin + irinotecan and 3 cases were cisplatin + etoposide) had a response rate of 67 %. In the remaining 2 patients, one patient received Gemcitabine (case 3) and another patient received Everolimus because we defined it as WDNEC (case 9). The overall median survival was 314 days (range 60–1202 days).

Imaging features of WHO-NEC on CE-MDCT (Fig. 2; Supplementary Table)

Assessment by CE-MDCT revealed that 9 (82 %) of 11 WHO-NEC in the pancreas were hypovascular. Eight of these tumors had metastasized to the liver, where 7 (88 %) of them were also hypovascular, like the primary tumor (Fig. 2). Before biopsy confirmation, NEN were suspected in only two patients, and the imaging features in the remaining 9 (82 %), suggested pancreatic ductal adenocarcinoma (PDAC). The main pancreatic duct was dilated in 4 (57 %) of 7 patients with tumors located in the head and body of the pancreas.

Fig. 2

Computed tomography findings of respective pNECs. a, b Hypovascular lesions both primary pancreas head site and multiple liver lesions (SCNEC case). c, d Hypervascular lesions both primary pancreas head site and multiple liver lesions (WDNEC case)

Pathological and molecular characteristics of WHO-NEC (Fig. 3, Supplementary Figure; Tables 2, 3)

A total of 11 WHO-NEC cases were submitted to the pathological and molecular analysis. No ductal carcinoma components were noted. All cases showed diffuse and strong immunoreactivity for neuroendocrine markers except 1 case, in which only synaptophysin was positive. In total, chromogranin A was expressed in 91 % and synaptophysin was expressed in 100 % of cases. The median Ki67 LI was 69.1 % (range 40–95 %). Nuclear expression of Rb protein was retained in 5 (45 %) tumors. KRAS mutations were detected in 6 (55 %) tumors. Seven (64 %) and 4 (36 %) of 11 tumors were categorized as PDNEC (4 SCNECs and 3 LCNECs) and WDNEC, respectively, according to their morphologic characteristics that we mentioned in the “Patients and methods” (Fig. 3, Supplementary Figure).

Fig. 3

Histologic features of NECs of the pancreas [H&E stain (a–c), and Ki67 (d–f), respectively]. The left column (a, d) is a case of WDNEC, the middle column (b, e) is of LCNEC, and the right column (c, f) is of SCNEC. Morphology of WDNECs shows a close similarity to that of NET-G1/G2, characterized by monomorphic growth of tumor cells with highly preserved endocrine cell features. Although LCNECs have features of endocrine cells as well, they are distinguished from WDNECs by increased nuclear atypia, cellular pleomorphism, and the frequent presence of tumor necrosis. SCNECs are composed of small cells with dense chromatin, scarce cytoplasm, and remarkable mitotic activity. These are reminiscent of small cell carcinomas of the lung

Clinicopathological comparison of well-differentiated and poorly differentiated NEC (Table 4)

The clinicopathological comparison between the WDNEC and PDNEC groups revealed that they were clinically and molecularly different in several aspects as follows: hypervascularity in MDCT images, 50 % (2/4) vs. 0 % (0/7), P = 0.109; median Ki67 LI, 46 % (range 40–53 %) vs. 85 % (range 54–95 %), P = 0.001; nuclear expression of Rb, 100 % (4/4) vs. 14 % (1/7), P = 0.015; KRAS mutations, 0 % (0/4) vs. 86 % (6/7), P = 0.015; response rates to platinum-based chemotherapy, 0 % (0/2) vs. 100 % (4/4) P = 0.067; and median survival, 227 vs. 186 days, P = 0.227.

Discussion

When the WHO 2010 classification was applied to our patients with NENs of the pancreas, we found that 36 % of the high-grade category included tumors with well differentiated morphology. This critical finding has an impact on the treatment strategies, particularly the platinum-based chemotherapy which should be originally administered for only PDNEC.

Our findings suggested that WDNECs differ from PDNECs and are rather more closely related to NETs-G2 in terms of clinicopathological and molecular characteristics. Firstly, MDCT consistently showed hypervascularity in WDNEC, but not in PDNEC. Some reports indicated that tumor vascularity correlated with the proliferation index and/or WHO classification [18, 19]. Our findings indicated that only 18 % of WHO-NEC cases were suspected of pNEN according to imaging findings before EUS-FNA, with most being considered PDAC or pancreatic adeno-squamous carcinoma. That is, a significant proportion (82 %) of NECs could not be correctly diagnosed by imaging, especially the PDNEC type.

Histologically, WDNECs shared more morphological traits with NETs-G2 than PDNECs, allowing us to presume that WDNECs correspond to well-differentiated NETs with high proliferative activity. The Ki67 LI tended to be lower in WDNEC than in PDNEC. Notably, KRAS and Rb genes are promising molecular markers with which to distinguish these types of tumors. The result that KRAS mutations were not found in WDNECs supports the notion that this category lies in close proximity to NET-G2, as no pancreatic NETs-G1/G2 have been reported to possess KRAS mutations, whereas PDNECs have been shown to harbor KRAS mutations [10, 16, 20]. Loss of expression of Rb was found in 86 % of PDNEC cases, whereas all of the WDNEC cases retained its expression. Aberration of the Rb/p16 pathway has been reported to be frequently involved in PDNECs of the pancreas, gallbladder, and ampulla, but not in pancreatic well-differentiated NETs [10, 20–22]. Concerning pancreatic NEN, Yachida et al. [10] conducted immunohistochemical and genetic analyses of several oncogenes and tumor suppressor genes including KRAS and Rb, and revealed that the aberrations of both genes were common in PDNECs but none in NETs-G1/G2. Their conclusion that PDNECs were molecularly distinct from well-differentiated NETs is in keeping with our findings. Taken together, the difference between WDNEC and PDNEC appears to be clinically, histologically, and molecularly significant, and we consider that WDNECs are more likely to be in the category of well-differentiated NET rather than NEC, thus, favoring the designation, namely “NET-G3”.

Our study showed that both WDNEC and PDNEC patients harbored unfavorable outcome (median overall survival of 227 days and 186 days, respectively), which is in stark contrast to NET-G2 patients whose median overall survival is reportedly 162 months [1]. Although WDNEC and PDNEC shared aggressiveness clinically and pathologically, the efficacy of the treatment between them tended to be different; all WDNEC cases did not exhibit response to the platinum-based chemotherapy while all of the PDNEC cases did. The Nordic NEC study [9] found that WHO-NEC with Ki67 LI > 55 % responded to platinum-based chemotherapy, whereas those with Ki67 LI < 55 % did not. Although the Nordic NEC study mainly focused on the treatment and prognostic aspects, there was no detailed description of the pathologic characteristics of the cases. We suppose that some of their WHO-NEC included WDNEC as defined herein. Based on the results of the Nordic NEC study, the NCCN guidelines noted in footnotes that “intermediate Ki67 levels in the 20–50 % range may not respond well to platinum/etoposide as patients with small cell histology or extremely high Ki67 and so, a clinical judgment should be used”. When NEN is diagnosed as WHO-NEC, clinically the toxic platinum-based chemotherapy is usually administered as a first-line regimen. However, a recent case report showed a good response of high-grade NET to molecular targeted therapy with agents such as Everolimus [23]. In fact, one patient who was diagnosed with WDNEC and received Everolimus obtained partial response. The current WHO 2010 classification might be flawed in terms of the management of patients with NEC and the classification scheme for NECs should be revised as the clinical, pathological, and molecular characteristics of this high-grade NEN become more fully clarified.

In regard to IHC, chromogranin A was expressed in 91 % of WHO-NEC cases, and synaptophysin was expressed in 100 %. In a similar fashion, previous articles reported that chromogranin A was expressed in 81–94 %, and synaptophysin was expressed in 88–96 % [7-9]. Taken together, stainability of chromogranin A and synaptophysin is high not only in WDNEC but also in PDNEC.

In our institute, we perform EUS-FNA for the diagnosis of pancreatic tumors on a routine basis, and have been reported its usefulness so far [11, 14–16, 24]. The diagnostic accuracy of overall pancreatic tumors was 91.8 % (918/996) [14]. We previously detected KRAS mutations in 87 % (266/307) of EUS-FNA specimens from pancreatic masses in patients with PDAC [24] and none among 25 well-differentiated endocrine tumors [16]. Jiao et al. [20] also reported the absence of KRAS mutations in NET-G1/G2.

To the best of our knowledge, this is the first study which examined the clinicopathological characteristics of pNECs, with an emphasis on the difference between WDNEC and PDNEC. However, some limitations should be addressed. The retrospective design hindered precise analysis of all required data, imposed potential selection bias, and the patient cohort was small due to the natural rarity of pNECs that account for <1 % of all pancreatic carcinomas, and 2–7.5 % of all pNEN [2, 25]. Intratumoral heterogeneity is another important consideration. In our 11 cases of NEC, we did not note any adenocarcinoma component histologically nor immunohistochemically. Also, the result of the high frequency of Rb aberration in our series minimizes the possibility of a hidden presence of concomitant adenocarcinomas, as Rb aberration has been reported to be a rare event in PDACs (5–6 %) [26, 27]. Although the above observations do not fully rule out the possibility that some of the cases might contain an accompanying adenocarcinoma, this may be a relatively uncommon occurrence given the low frequency of an associated ductal adenocarcinoma in PDNECs reported by Basturk et al. [8] (6/44, 14 %). Finally, we address the feasibility of grading for pNENs diagnosed by FNA specimens, which constituted most of our series. Past studies of ours and of others claimed that grading by Ki67 LI can be applicable to FNA specimens by showing high concordance between the grade given by the FNA specimens and that by the corresponding resected specimens (concordance rate 78–90 %) [15, 28–31]. Indeed, downgrading or upgrading between G1 and G2 occurred in a small proportion of cases, but there was no tumor observed among the 5 studies that was graded as G3 by EUS-FNA and was downgraded to G2 by surgical resection. This observation, as well as the poor outcome of the current study, indicates that the admixture of ‘overestimated’ NETs-G2 in our cohort seemed unlikely to happen.

In conclusion, we identified a significant number of “WDNEC” cases among pNECs that were defined by the current WHO classification system. The clinicopathological and molecular analyses suggested that WDNEC is distinct from PDNEC. Though the number of cases we analyzed was limited, we believe that our scheme of subcategorizing pancreatic NEC showed promise. Further larger-scale studies are warranted to validate our stratification of WHO-NECs, which will facilitate a more personalized treatment of the patients with this rare malignant neoplasm.

Supplementary material 1 (TIFF 11224 kb) Supplementary Figure. Immunostaining for synaptophysin (A, B) and Rb (C, D) in WDNEC and PDNEC. (A) and (C) are the WDNEC case identical to that shown in Fig. 3a. (B) and (D) are the LCNEC case identical to that shown in Fig. 3b. The intermingled lymphocytes show positive nuclear staining of Rb, serving as a positive internal control (D, arrow)

Supplementary material 2 (DOCX 14 kb)

Table 1

Patient characteristics (n = 11)

Gender
Male/female	6/5
Age
Median (range)	59 years (28–74)
Symptom
Yes (%)	91 % (abdominal pain)
Site of pancreas tumor
Head/body/tail	2/5/4
Tumor size
Median (range)	35 mm (20–55)
Metastasis
Yes (%)	72 % (liver metastasis)
Treatment
Operation/chemotherapy/BSC	2/8/1

Table 2

Clinical, pathological features, treatment and response for chemotherapy of WHO-NEC patients

Case	Age/sex	Location	Size (mm)	ENETS stage	Tissue sampling	Histology	Ki67 LI (%)	CGA	Synaptophysin	Rb	KRAS	Treatment	Response for platinum-based regimen
1	30, M	Body	45	IIb	Biopsy and surgical resection	WDNEC	40	Positive	Positive	Positive	WT	Operation	ND
2	59, F	Body	30	IIIb	Biopsy and surgical resection	PDNEC (small cell)	80	Positive	Positive	Positive	MT	Operation	ND
3	49, F	Body	35	IV	Biopsy	PDNEC (large cell)	85	Positive	Positive	Negative	MT	CT (Gemcitabine)	ND
4	68, F	Tail	36	IV	Biopsy	WDNEC	48	Positive	Positive	Positive	WT	CT (IP)	PD
5	63, F	Body	33	IV	Biopsy	PDNEC (large cell)	54	Positive	Positive	Negative	MT	CT (IP)	PR
6	61, M	Body	45	IV	Biopsy	PDNEC (large cell)	90	Positive	Positive	Negative	MT	CT (EP)	PR
7	74, M	Head	20	IV	Biopsy	PDNEC (small cell)	90	Positive	Positive	Negative	WT	BSC	ND
8	37, M	Head	20	IV	Biopsy	PDNEC (small cell)	80	Positive	Positive	Negative	MT	CT (EP)	PR
9	50, F	Tail	35	IV	Biopsy	WDNEC	45	Negative	Positive	Positive	WT	CT (Everolimus)	ND
10	55, M	Tail	30	IV	Biopsy	WDNEC	53	Positive	Positive	Positive	WT	CT (EP)	PD
11	66, M	Tail	70	IV	Biopsy	PDNEC (small cell)	95	Positive	Positive	Negative	MT	CT (IP)	PR

CGA chromogranin A, WT wild type, MT mutant, CT chemotherapy, IP cisplatin + irinotecan, EP cisplatin + etoposide, BSC best supportive care, ND not done, PD progressive disease, PR partial response

Table 3

Pathological and molecular characteristics of WHO-NEC

Ki67 labeling index
Median (range)	69.1 % (40–95 %)
Morphology
WDNEC/PDNEC	4/7
Subtypes of PDNEC
Large-cell type/small-cell type	3/4
Rb immunopositivity	45 % (5/11)
KRAS mutation	54 % (6/11)

WDNEC well-differentiated NEC, PDNEC poorly differentiated NEC

Table 4

Clinicopathological comparison of WDNEC and PDNEC

	WDNEC (n = 4)	PDNEC (n = 7)
Vascularity in pancreas tumor
Yes (%)	50 % (2/4)	0 % (0/7)
Ki67 labeling index
Median (range)	46.3 % (40–53 %)	85 % (54–95 %)
Rb immunopositivity	100 % (4/4)	14 % (1/7)
KRAS mutation	0 % (0/4)	86 % (6/7)
Response rate of platinum-based regimen	0 % (0/2)	100 % (4/4)
Prognosis
Median	227 days	186 days

WDNEC well-differentiated NEC, PDNEC poorly differentiated NEC