Long‐term survival after surgery of pancreatic primary squamous cell carcinoma: A case report and literature review

Abstract

Pancreatic primary squamous cell carcinoma is rarer and no optimal treatment has been validated according to the tumor stage. The surgical resection was the only curative option. The radiotherapy or chemotherapy was performed for the other cases.

Pancreatic primary squamous cell carcinoma is rarer and no optimal treatment has been validated according to the tumor stage. The surgical resection was the only curative option. The radiotherapy or chemotherapy was performed for the other cases.

1. INTRODUCTION

Pancreatic cancer is one of the leading causes of cancer‐related death in most Western countries. Adenocarcinoma is the most common subtype. Primary squamous cell carcinoma (SCC) is much rarer, with an incidence rate of 0.2%‐4%.1, 2 Squamous cells do not naturally exist in the pancreas. Squamous metaplasia of ductal columnar cells has been observed in chronic pancreatitis 3 and in 9%‐64% of cases examined at autopsy.4 Despite this high frequency, transformation to SCC is rare. Diagnosis of primary pancreatic SCC is made only after excluding other neoplastic lesions of the pancreas that contain squamous epithelial components, adenosquamous carcinoma, or metastatic disease.3 No optimal treatment has been validated. This study analyzed the management of pancreatic SCC in the literature. Additionally, we present a case of primary SCC in an elderly female with abnormal liver function tests and acute onset of painless jaundice.

1.1. Systematic literature review

We conducted a comprehensive, systematic search of the literature using the Medline and Cochrane Database, combined with a manual search from the years 1945 to 2017. The key words used were “Primary squamous cell carcinoma” OR “SCC” OR “Epidermoid carcinoma”, and “Pancreas.” The primary criteria were age, sex, symptoms, tumor location, tumor size, site of metastasis, tumor markers, imagery, treatment, and overall survival (OS). The advanced T stage of pancreatic cancer was defined according to the involvement of the vessels (superior mesenteric artery, portal vein, and celiac axis).

1.2. Statistical analysis

Statistical analysis was performed using GraphPad Prism, version 6.01. Descriptive statistics were calculated. The Kaplan‐Meier method was used to calculate separate OS curves based on tumor resectability. A P value < .05 was considered statistically significant.

2. CASE REPORT

A 72‐year‐old woman with a medical history of arthrosis was admitted to our institution with jaundice. Laboratory testing indicated elevated transaminase levels (Alanine aminotransferase (ALT): 83 UI/L; aspartate aminotransferase (AST): 206 UI/L) and an elevated total bilirubin level (206 µmol/L). The carcinoembryonic antigen level was normal, and the cancer antigen 19‐9 level was slightly elevated (51 U/mL). The patient received an abdominal ultrasound and chest plus abdominal computed tomography (CT), which revealed a mass in the head of the pancreas measuring 2.2 × 1.7 cm with biliary and pancreatic ductal dilatation (Figure 1A). Positron emission tomography (PET)‐CT was used to investigate the origin of this mass, which revealed a unique pancreatic mass with a standardized uptake value of 12.5 (Figure 1B). Endoscopic ultrasound‐guided fine needle aspiration (FNA) was performed. The histopathology of the biopsy was consistent with SCC. The workup for identifying an alternative primary tumor was negative, including the gynecological, dermatological, “ear, nose, throat” examinations, and endoscopic evaluation of the upper and lower gastrointestinal tracts. A diagnosis of primary SCC of the pancreas was made. Based on the patient's age, performance status, and the nonmetastatic tumor stage, curative therapy was rapidly implemented. The pancreas tumor was treated by “en bloc” resection because it was adherent to transverse colon. We performed a cephalic duodenopancreatectomy (Whipple procedure) and transverse colectomy with manual anastomosis by laparotomy. The definitive histology confirmed the diagnosis of primary pancreatic SCC with perineural neoplastic invasion (Figure 1C–D). Based on the tumor‐node‐metastasis‐resection classification, the tumor was diagnosed as T2N0M0R0. Subsequent to surgery, the patient received chemotherapy using gemcitabine (six cycles). The patient is currently in complete remission after a follow‐up interval of 26 months. The nature and objectives of the study were explained to the patient, and informed consent was formally obtained. No reference to the patient's identity was made at any stage during data analysis or in the report.

Figure 1.

A, Abdominal CT scan showed a head pancreatic mass with greatest dimensions of 2.2 × 17 cm. B, PET scan showed hypermetabolic mass. C, Image of carcinoma with central necrosis and focal squamous differentiation (hematoxylin and eosin stain (H&E) ×200). D, H&E stained cell block shows a group of malignant squamous cells (×400)

3. DISCUSSION AND LITERATURE REVIEW

The literature search identified 44 eligible articles, written in English, French, German, or Spanish. A total of 52 cases of primary pancreatic SCC were included in the analysis (Table 1).1, 4, 9, 10, 11, 21, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53 The median age at diagnosis was 63.5 (range: 33‐81) years, and the majority (58.8%) of patients were male. A comparison of the clinicopathologic characteristics (n = 40) indicated that 31(75%) patients experienced abdominal pain, 19 (47.5%) anorexia or weight loss, and 11 (27.5%) jaundice. Of the reported cases with sufficient information (n = 45), tumor location was variable: head (48.9%), body (17.8%), tail (20%), and corporeo‐caudal (17.8%). In approximately half of the cases, a large pancreatic tumor (median size: 6.2 [range: 3‐10] cm) was diagnosed at the metastatic stage. The most common metastatic sites were the liver and lymph nodes. Of 36 patients with available information, abdominal CT, abdominal ultrasound, and PET were performed in 94.7%, 38.9%, and 16.7% of patients, respectively. The histological diagnosis was confirmed for 42 (82.4%) patients.

Table 1.

Clinical and radiological features of patients

Reference	Year	Sex	Symptoms	Tumor location	Size (cm)	Extra pancreatic sites	Tumor markers	Imagery	Diagnosis method	Therapy	Survival (Mo)
1	57	F	Epigastric pain	Body and tail	5 × 6	LN	CA 19‐9 (ND)	CT scan	Biopsy	Neoadjuvant radio‐chemo and surgery	10
4	72	M	Painless jaundice	Head	6	Invasion of the mesenteric vessels	NR	AUS ERCP CT Scan EUS	FNA	Palliative Roux en Y hepato‐jejunostomy and gastro‐enterostomy.	4
42	77	M	NR	Head	6.5	Lymph node	NR	NR	Surgery	Surgery	26 (A)
5	61	M	Fatigue, weight loss, jaundice, pain, dark urine, and light‐colored stool	Head	6.5 × 5.9	Liver	ACE (ND)CA 19‐9 (ND)	CT Scan	NR	Palliative care	2
6	68	F	Abdominal pain	Head	3 × 4	Invasion of the superior mesenteric	CA 19‐9 (ND)	CT scan EUS	FNA	Palliative Radio	3
7	62	M	Tarry stool, fever, and general fatigue	Body, Tail	8	Expanding to the spleen and the left transverse colon with suspected invasion in the stomach	CA 19‐9 (ND) ACE (ND)	EG CT scan	Surgery	1) Pancreatectomy, total gastrectomy, splenectomy, and partial colectomy	16 (A)
8	70	M	Weight loss, pruritus, and icterus	Head	5.5	LN	NR	AUS CT scan ERCP	Surgery	1) Pancreaticoduodenectomy 2) Recurrence at 2 mo: Cisplatine 3) Docetaxel	17
9	76	M	Weight loss, painless jaundice, and abdominal pain	Head	5.8	Lymph node	NR	CT scan PET scan ERCP	FNA	Radio + 5 FU	18
10	56	M	Pain	Tail	13	None	NR	NR	Surgery	1) Surgery 2) Recurrence at 3 mo: chemo	3 (A)
11	79	M	Asymptomatic	Tail	5	LN, Liver	NR	CT scan MRI PET‐CT	Biopsy	1) Tegafur/Gimeracil/Oteracil (S‐1) 2) Gemcitabine	7
12	61	M	Anorexia, epigastric pain	Head	NR	Liver	CEA (ND) CA 19‐9 (ND)	CT Scan EUS PET‐CT	NR	1) Gemcitabine + cisplatin +5FU 2) Leucoverin	9.9
14	66	F	Epigastric pain	Body	4 × 3	Superior mesenteric and celiac arteries	CA 19‐9 (ND) ACE (ND)	ASU CT scan	FNA	1) Gemcitabine + Oxaliplatine 2) Gemcitabine only	9
14	79	F	Upper abdominal pain and vomiting	Uncinate process	5 × 8	Invasion of the retroperitoneum	NC	CT scan	Autopsy	None	1.5
15	70	M	NR	NR	NR	Liver	NR	NR	NR	5 FU + Cisplatine	15
16	55	M	NR	Head	5	NR	NR	NR	Surgery	Pancreaticoduodenectomy	10
17	63	F	Anorexia	Body	3 × 2	Invasion of the celiac axis, the supraclavicular node, liver, cervical vertabra	CA 19‐9:209 UI/ml	CT scan	Node Biopsy FNA	1) 5 FU + Cisplatine 2) Gemcitabine + Vinotelbine (2nd lign) + Radio	12
18	48	F	Anorexia, pain, jaundice	Head and uncinate process	4.4 × 4.2	Liver, spleen	NR	ASU CT scan	Liver Biopsy	Gastrojejunostomy, choledochojejunostomy, open cholecystectomy and then, Gemcitabine + Carboplatine	4
19	67	F	Anorexia, back pain	Tail	6 × 6 × 7	LN	ACE (ND) CA 19‐9 (ND)	CT scan	Surgery	1) Total gastrectomy, distal pancreatectomy and splenectomy 2) Recurrence at 4 mo: Radio	11
20	69	F	Abdominal pain, jaundice	Head	5 × 5 × 6	LN Locoregional invasion	NR	CT scan MRI ERCP	Surgery	Pancreaticoduodenectomy	3
20	49	M	NR	Tail	7.5	Peritoneal, lombo‐aortique, mediastinal adenopathy, Liver	NR	NR	Liver Biopsy	1) Radio + 5 FU + Cisplatine 2) Gemcitabine	8
20	68	M	Abdominal pain, weight loss	Body	NR	None	NR	CT scan	FNA	Surgery	3
20	63	M	Abdominal pain, weight loss	NR	NR	Lung	NR	CT scan	FNA	Cisplatine + 5 FU and Radio	1
20	80	M	Abdominal pain, weight loss	NR	NR	Lung Liver Bone	NR	CT scan	FNA	Cisplatine + 5 FU and Radio	1.5
20	79	M	Abdominal pain, weight loss	NR	NR	None	NR	CT scan	FNA	Radio	3.5
21	63	M	Abdominal pain, weight loss	NR	NR	Lung Liver Bone	NR	CT scan	FNA	Cisplatine + Vinblastine	7
21	38	M	Abdominal pain, weight loss	NR	NR	Lung Liver	NR	CT scan	FNA	Radio	1
22	69	F	Epigastric pain	Body	5	Superior mesenteric artery	NR	CT scan ERCP	Biopsy	Radio	7 (A)
22	48	M	Epigastric pain	Head	4 × 6	Superior mesenteric artery	CA19‐9:980 U/mL	AUS CT scan	CT‐ guided biopsy	1) 5‐FU + Cisplatine 2) Palliative radio	9
23, 38	42	M	Vomiting, periumbilical pain.	Body and tail	4 × 3.7 × 3.1	Splenic vessels	CA 19‐9 (–)	AUS CT scan	Surgery	Spleno‐corporeo‐caudal pancreatectomy and FUFOL	26 (A)
24	73	M	Abdominal pain, anorexia	Tail	6 × 5.7 × 5.5	NR	CA 19‐9:464 µ/mL	CT scan PET scan	FNA biopsy	Palliative care	2
25	58	F	NR	Body and tail	8	Infiltration of the gastric wall and mucosal ulceration, invasion of the spleen, the left renal capsule, the left adrenal gland.	NR	CT scan	Surgical biopsy	Surgery and Cisplatine + 5 FU	3 (A)
26	68	F	Abdominal pain, weight loss	Body	7	None	NR	CT scan	Surgery	Surgery	8 (A)
27	57	M	Hypercalcemia	Body and tail	NR	Periaortic, Peripancreatic, mediastinal LN, Liver, kidneys, adrenal gland metastasis	NR	NR	Autopsy	None	3
28	63	M	NR	Head	3.5	Liver	NR	NR	NR	Gemcitabine + 5 FU + Leucoverine	6
29	52	M	Melena, icteric, a large painful liver	NR	NR	Stomach, Liver	NR	AUS	Autopsy	None	0.4
30	69	F	NR	Head	4	NR	NR	NR	Intraoperative needle aspiration	Palliative care	4
31	26	F	Rapidly worsening, jaundice	Head	3.5	LN, muscle, bone	NR	CT scan	Surgery	Surgery and Gemcitabine + Oxaliplatine	8 (A)
32	57	F	NR	Tail	10.5	None	NR	NR	Surgery	Surgery	6
33	76	M	NR	Body and tail	9	LN, metastasis	NR	NR	NR	None	1
34	70	F	NR	Head	6	Porta hepatis	NR	NR	NR	Radio	3
35	50	M	NR	Tail + Head	8	Liver	NR	NR	NR	Gemcitabine, FU and Goserelin	5
36	33	F	NR	Head	13	Lymph node	NR	NR	NR	Unconventional Immunotherapeutic regimen	9 (A)
37	76	M	Painless jaundice.	Head	5	None	NR	CT scan	EUS biopsy	Chemo (5FU) + radio then surgery	10 (A)

Abbreviations: (A), Alive; ASU, abdominal sonography ultrasound; Chemo, chemotherapy; CT, computerized tomography; EG, Esophago‐gastroscopy; ERCP, endoscopic retrograde cholangio‐pancreatography; EUS, endoscopy sonography ultrasound; F, female; FNA, fine needle aspiration; FU, fluorouracil; FUFOL, 5‐fluorouracil; folinic acid; LN, lymph node M, male; MRI, magnetic resonance imaging; ND, not detected; NR, not reported; Radio, radiotherapy; PET, positron emission tomography‐computed tomography.

A total of 15 of 50 (30%) SCC cases were resectable. Of these 15 patients, 2 (13.3%) received neoadjuvant chemoradiotherapy and 3 (20%) received adjuvant chemotherapy (Figure 2). Three (20%) cases of local recurrence or metastasis were observed in this group after curative treatment (Figure 2).

Figure 2.

Flowchart of the management of patients (n = number of patients, (%) percentage)

A total of 11 patients had a locally advanced tumor, and 10 (90%) of these patients received chemo‐ or radiotherapy (Table 2). The 24 (38.5%) patients with metastasis received palliative care (Table 2). The majority of patients with inoperable SCC received gemcitabine and cisplatin, either alone or in combination, as a first‐line treatment (Table 1).1, 4, 9, 10, 11, 21, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53 A total of eight cases in the metastasis group were excluded from the survival analysis because of insufficient information. The median OS was 17 months in the resectable group, compared with 8 months in the locally advanced tumor group and 4 months in the metastasis group (P = .0008; Figure 3).

Table 2.

Management of patients with locally advanced tumor or metastasis

	Palliative surgery	Chemotherapy	Radiotherapy	Chemo‐radiotherapy	Palliative care	Not reported
Locally advanced tumorn = 11	1 (9%)	3 (27.3%)	5 (45.5%)	2 (18.2%)	0 (0%)	0 (0%)
Metastatic SCC n = 26	1 (3.8%)	6 (23.1%)	1 (3.8%)	6 (23.1%)	10 (38.5%)	2 (7.7%)

Abbreviation: n, number of patients.

Figure 3.

Kaplan‐Meier survival estimates regarding overall survival (OS), by resectability status

Squamous cell carcinoma of the pancreas is exceedingly rare, with an incidence rate of 0.5%‐5%.39 Because of this rarity, it is often presumed to be a result of metastasis from another primary site.40 The pathogenesis is not well understood, and a number of mechanisms underlying its development have been proposed: malignant transformation of squamous metaplasia of ductal cells, squamous metaplasia in adenocarcinoma, and squamous differentiation with malignant transformation of pluripotent primitive cells.41 The first case of SCC was described by Lowry in 1949.42 Since then, only case reports from the literature have been available to guide workup and treatment. This review is the first study to examine the management of SCC and to describe the neoadjuvant, adjuvant, and palliative chemoradiotherapy used to treat it. Identification of the initial stage is necessary for the management of pancreatic cancer. Patients who may be eligible for potentially curative surgery must be identified accurately. Patients with locally advanced disease or metastasis must also be identified and treated with chemotherapy or radiotherapy.

3.1. Clinical symptoms

The literature review confirmed that the clinical presentation of SCC was similar to that of adenocarcinoma,5 with anorexia and epigastric pain as the main symptoms. The presenting symptom was often obstructive jaundice with involvement of the pancreatic head. The tumor location was the pancreatic head in 53% of cases and the body or tail in 20% of cases. A recent epidemiologic study, which identified 214 cases during 2000‐2012 using the Surveillance, Epidemiology, and End Results database, reported tumor locations of the pancreatic head in 47.7% of cases and the body or tail in 27.1% of cases.2

3.2. Examinations

In many of the cases included in this review, diagnosis of primary SCC of the pancreas was confirmed after eliminating other possibilities, in addition to immunohistological confirmation prior to treatment. In our case, the patient received an otorhinolaryngological assessment, endoscopic examination of the gastrointestinal tract, and gynecological examination, which were all normal. Additional biopsies may be needed to confirm that the malignant cells are not of adenosquamous origin.6 Minimally invasive methods, such as FNA, are replacing traditional surgical approaches to obtaining pancreatic tissue.7 FNA was the method used in this case report. Abdominal CT is often the first imaging test performed when a patient's symptoms suggest a pancreatic tumor.43 Other procedures and imaging tests used to aid diagnosis and identify metastasis include PET and pancreatic MRI.

3.3. Histological analysis

Histological examination of the pancreatic lesion confirmed the diagnosis of SCC.

3.4. Management of resectable tumors

It is necessary to identify the pancreatic tumor stage (resectable, locally advanced, or metastatic tumor) prior to initiating treatment. Surgery is the only effective therapy for pancreatic SCC. The quality of surgery is considered a key factor in the long‐term survival of patients with pancreatic cancer. In our case, the patient had a small, localized pancreatic tumor and received a cephalic duodenopancreatectomy with transverse colectomy followed by adjuvant chemotherapy. The resectability rate of SCC in this review was 29.4%, similar to the rates reported by Makarova‐Rusher et al: 10.4% for patients with SCC and 14.2% for patients with pancreatic adenocarcinoma.2 Although significant progress has been made in the field of pancreatic resection recently, only 15%‐25% of patients present with resectable disease at the time of the primary diagnosis.44 This finding emphasizes the need for early diagnosis of, and therapeutic approaches to, pancreatic cancer.

No studies have evaluated the efficacy of neoadjuvant chemotherapy or radiotherapy in pancreas SCC. All patients with resectable pancreatic tumors received curative surgery, subsequent to neoadjuvant radiochemotherapy if the patient's general condition permitted (13.3%). Neoadjuvant or exclusive chemoradiotherapy is critical in the management of rectal, anal, and esophageal SCC.45, 46, 47 The pancreas is a deep organ located near large vessels, and any progression of the tumor can render surgery impossible. Similar to adenocarcinoma of the pancreas, neoadjuvant treatment may be deemed unnecessary by radiochemotherapy or chemotherapy if the pancreatic SCC is resectable.48

Only 20% of patients received chemotherapy after curative surgery. For pancreatic adenocarcinoma, there is now irrefutable evidence that adjuvant chemotherapy improves both overall and disease‐free survival and that gemcitabine is the gold standard adjuvant drug.49 For other squamous cell cancers, such as of the esophagus, adjuvant chemotherapy is not systematically recommended but may be indicated based on poor prognostic factors such as incomplete resection.50

3.5. Management of locally advanced tumors

The majority of patients with locally advanced tumors received radiotherapy or chemoradiotherapy exclusively. This treatment has been validated for other tumor locations, including anal, rectal, and esophageal SCCs.51 In pancreatic adenocarcinoma, neoadjuvant treatment is indicated only for patients initially staged as locally advanced/unresectable, enabling one‐third of patients to receive curative surgery.51 Since the approval of gemcitabine in 1997, more effective cytotoxic substances, such as nab‐paclitaxel, and combination regimens, such as FOLFIRINOX, have become available for locally advanced tumors, possibly leading to more effective adjuvant and neoadjuvant treatment concepts for potentially resectable tumors.8 Gemcitabine and cisplatin were the two principle drugs utilized.

3.6. Metastatic tumors

In this review, the majority (51%) of patients with SCC had stage IV disease on initial presentation, similar to the rate of 56.4% reported by Makarova‐Rusher et al.2 The primary metastatic seeding sites were the liver and lung. The majority of metastatic patients received palliative care, which was also the preferred treatment for patients in generally poor health. The other patients were treated with a combination of cisplatin and 5‐fluorouracil or gemcitabine and, less frequently, with radiochemotherapy. This approach is consistent with the recommendations for patients with pancreatic metastatic adenocarcinoma.

3.7. Survival

Even with therapy, SCC of the pancreas is associated with a high mortality rate and overall poor prognosis.52 Resectable cases had significantly better OS than that of nonresectable cases (17 months vs 7 months [locally advanced tumors] and 3 months [metastatic tumors]). Klain et al reported that prognosis remained poor whether the disease was resectable (median survival of 15 months) or unresectable (median survival of 3 months).53 Makarova‐Rusher et al reported a median OS of 9 months for the patients who underwent surgery compared with 3 months for those who received palliative treatment.2

This review has several limitations. The analysis was based on retrospective registers, and only case reports and case series were retrieved. Misclassification as primary pancreatic carcinoma is possible in the case of metastatic disease from another site. Consequently, there are few estimates of the degree of misdiagnosis. Despite these limitations, this review is the first study to evaluate the management of pancreatic SCC. This review reflects a global perspective, utilizing data from many countries, and can be used by medical personnel for treatment of a new case of pancreatic SCC.

4. CONCLUSION

Squamous cell carcinoma of the pancreas is aggressive and rare. Clinical presentation and diagnostic approaches are similar to those for other pancreatic tumors. Surgical resection is the only curative option but is often limited by local and distant metastases. A multidisciplinary approach is needed to improve long‐term survival in this still‐challenging disease. Prospective international research is required to validate the management of SCC.

CONFLICT OF INTEREST

None declared.

AUTHOR CONTRIBUTIONS

AT: involved in conception of paper, writing, and critical appraisal. JJ: involved in writing and critical appraisal. SDF: involved in writing and critical appraisal. AC: involved in conception of paper, writing. SBM: involved in writing and critical appraisal. NC: involved in critical appraisal. FF: involved in critical appraisal DV: treated the patients MM: involved in critical appraisal, expert opinion, and current oncology evidence.

Taibi A, Jacques J, Durand Fontanier S, et al. Long‐term survival after surgery of pancreatic primary squamous cell carcinoma: A case report and literature review. Clin Case Rep. 2019;7:2092–2101. 10.1002/ccr3.2429