Pancreatic cancer with liver metastasis maintaining complete response with gemcitabine monotherapy: A case report

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is associated with a poor prognosis, and it has a recurrence rate of >70%, even in resectable cases. The treatment strategy for recurrent PDAC involves systemic chemotherapy, with gemcitabine (GEM) monotherapy historically serving as the standard of care. The present study describes the case of a patient with PDAC and postoperative liver metastases that maintained clinical complete remission (cCR) for >7 years following GEM monotherapy. A 63-year-old woman with upper abdominal pain was diagnosed with resectable PDAC and underwent pancreaticoduodenectomy. The patient was treated with GEM + S-1 as adjuvant chemotherapy for 6 months. Multiple liver metastases were detected 15 months post-operation and the patient was administered GEM alone. After 12 cycles, computed tomography showed cCR and GEM monotherapy was discontinued after 15 cycles. The patient has had no signs or symptoms of recurrence >7 years after the first recurrence. In addition, the present study analyzed PDAC resection specimens from four patients, including this case, to determine the expression levels of hENT1 protein in the tumor tissues. hENT1 is a transmembrane protein that acts as a nucleoside transporter and is a major mediator of GEM uptake into human cells. In the present case, hENT1 staining exhibited low frequency and weak positivity in the central region, whereas a strong positive reaction was observed in nearly all cell membranes at the invasive front of the cancer. The location, intensity, and frequency of hENT1 staining varied among cases. In conclusion, the efficacy of GEM may be predicted prior to treatment by evaluating hENT1 expression.

Introduction

The prognosis of patients with pancreatic ductal adenocarcinoma (PDAC) is generally poor even in resectable cases. The postoperative recurrence rate exceeds 70% (1) Systemic chemotherapy is the treatment strategy for postoperative recurrence; however, the average survival period after recurrence is 6.8 to 11.1 months (2,3). Since 1997, Gemcitabine (GEM) monotherapy has historically been the standard primary treatment for unresectable or recurrent PDAC (4); however, recently, GEM plus nab-paclitaxel or FOLFIRINOX was shown to be superior to GEM monotherapy in phase III trials (2,3).

GEM is a key drug for pancreatic cancer. This nucleoside analog drug exerts its antiproliferative action after tumoral conversion into active triphosphorylated nucleotides by interfering with deoxyribonucleic acid (DNA) synthesis and targeting ribonucleotide reductase. GEM is a hydrophilic molecule that cannot cross the plasma membrane by passive diffusion; therefore, specialized plasma membrane nucleoside transporters are required for the uptake of GEM into tumor cells (5). hENT1 is a transmembrane protein that acts as a nucleoside transporter and has been reported to be the main mediator of GEM uptake into human cells (5). High expression of hENT1 is considered as a potential predictive biomarker for the response to GEM in several kinds of cancers including pancreatic, biliary, and urinary bladder cancer (6).

We encountered a case of PDAC with postoperative multiple liver metastases that underwent GEM monotherapy and achieved clinical complete remission (cCR) without disease regression for over 7 years. This case prompted our investigation into the factors influencing the therapeutic efficacy of GEM-based chemotherapy focusing on hENT1 protein expression in PDAC post-treated with GEM monotherapy.

Case report

Clinical course of treatment

A 63-year-old woman with epigastric pain was diagnosed with resectable PDAC in January 2011 at National Defense Medical College (Saitama, Japan). Serum carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA19-9) was 1.2 ng/ml (normal value: <5.3) and 10.0 U/ml (normal value: <37), respectively (Table I). A scheduled pancreaticoduodenectomy was performed in March 2011. Postoperative course was uneventful, and the patient was discharged on post operative day 17. Pathological findings were compatible with the diagnosis of PDAC (Fig. 1). The tumor size was 3.2 cm, and lymph node metastasis was positive in one of 24 dissected nodes. Pathologic stage according to 8th UICC (7) was IIB (pT2 pN1 pM0).

Table I.

Preoperative blood tests.

A, Blood count
Variable	Result	Normal values
WBC, ×103/µl	4.3	3.3–8.6
RBC, ×106/µl	4.53	3.85–4.92
Hb, g/dl	13.6	11.6–14.8
Hct, %	41.7	35.1–44.4
Plt, ×104/µl	27.3	15-40
B, Biochemistry
T-bil, mg/dl	0.5	0.2–1.2
AST, IU/l	18	8-30
ALT, IU/l	15	5-35
ALP, IU/l	169	100-340
TP, g/dl	6.3	6.5–8.2
Alb, g/dl	3.7	3.8–5.2
Amy, IU/l	74	29-132
HbA1c, %	5.6	4.3–5.8
BUN, mg/dl	14	8-20
Cr, mg/dl	0.85	0.44–0.78
CRP, mg/dl	0.3	≤0.3
C, Tumor markers
CA19-9, U/ml	9	≤37
CEA, ng/ml	1.1	≤5.3
DUPAN-2, U/ml	25	≤150
Span-1, U/ml	7	≤30

WBC, white blood cells; RBC, red blood cells; Hb, hemoglobin; Hct, hematocrit; Plt, platelet; T-bil, total bilirubin; AST, aspartate aminotransferase; ALT, alanine aminotransferase; ALP, alkaline phosphatase; TP, total protein; Alb, albumin; Amy, amylase; HbA1c, hemoglobin A1c; BUN, blood urea nitrogen; Cr, creatinine; CRP, C-reactive protein; CA19-9, carbohydrate antigen 19-9; CEA, carcinoembryonic antigen.

Figure 1.

Pancreaticoduodenectomy was performed on this patient. The tumor was 3.2 cm in diameter, and pathological findings were consistent with the diagnosis of PDAC.

We administered GEM plus S-1 as postoperative adjuvant chemotherapy for 6 months. We checked serum CEA and CA19-9 values every 3 months. CT was performed every 6 months after surgery. We detected multiple liver metastases 15 months after surgery (Fig. 2). The carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA19-9) in the serum at this time were 4.2 ng/ml and 7.6 U/ml, respectively (Table II). There were no signs suggesting the diagnosis of liver abscess such as pyrexia.

Figure 2.

Postoperative CT at 15 months after surgery demonstrating multiple liver nodules (red arrow).

Table II.

Blood tests at relapse.

A, Blood count
Variable	Result	Normal values
WBC, ×103/µl	4.7	3.3–8.6
RBC, ×106/µl	4.52	3.85–4.92
Hb, g/dl	13.4	11.6–14.8
Hct, %	41.3	35.1–44.4
Plt, ×104/µl	28.9	15-40
B, Biochemistry
T-bil, mg/dl	0.5	0.2–1.2
AST, IU/l	26	8-30
ALT, IU/l	20	5-35
ALP, IU/l	309	100-340
TP, g/dl	6.4	6.5–8.2
Alb, g/dl	3.9	3.8–5.2
BUN, mg/dl	13	8-20
Cr, mg/dl	0.84	0.44–0.78
CRP, mg/dl	0.3	≤0.3
C, Tumor markers
CA19-9, U/ml	7.6	≤37
CEA, ng/ml	4.2	≤5.3

WBC, white blood cells; RBC, red blood cells; Hb, hemoglobin; Hct, hematocrit; Plt, platelet; T-bil, total bilirubin; AST, aspartate aminotransferase; ALT, alanine aminotransferase; ALP, alkaline phosphatase; TP, total protein; Alb, albumin; Amy, amylase; BUN, blood urea nitrogen; Cr, creatinine; CRP, C-reactive protein; CA19-9, carbohydrate antigen 19-9; CEA, carcinoembryonic antigen.

The patient did not wish to receive intensive chemotherapy; therefore, GEM monotherapy was initiated (1,000 mg/m² a week) on days 1, 8, and 15, and the course was repeated every 28 days. The patient was followed up weekly. CT at 6 months after the start of chemotherapy revealed remarkable reduction in the size of all metastatic lesions. CT after 12 cycles showed cCR (Fig. 3). We stopped GEM monotherapy after 15 cycles. The last follow-up was in February 2021, the patient has been followed up with no signs or symptoms of recurrence for more than 7 years after the initial recurrence (Fig. 4).

Figure 3.

Liver metastases disappeared 12 months after chemotherapy (red circle).

Figure 4.

Changes in CEA and CA19-9 levels following the clinical course are summarized. Liver metastasis was found 15 months after surgery. CT shows the complete disappearance of hepatic tumors after GEM monotherapy at 27 months after surgery. Red arrow indicates areas of liver metastasis. Yellow arrow indicates complete disappearance of liver tumor. CEA, carcinoembryonic antigen; CA199, carbohydrate antigen; GEM, gemcitabine; PR, partial response; CR, complete response.

Intratumoral expression levels of hENT1

We analyzed surgically resected PDAC specimens from four patients, including the present case, to determine the intratumor protein expression level of hENT1, and compared two responders (including the present case) and two non-responders. All patients received GEM-based chemotherapy following postoperative recurrence. We defined responders as patients who maintained partial or complete response for more than 1 year after receiving GEM-based chemotherapy, and non-responders as patients who did not achieve a response (Table III). Tissue sections and slides were stained with an automated immunostainer (DISCOVERY XT; Ventana Medical Systems, Tucson, AZ, USA) using heat-induced epitope retrieval and a standard diaminobenzidine detection kit. The primary antibody used was anti-hENT1 (1:50; ab182023, Abcam, Cambridge, UK) and the secondary antibody was the universal secondary antibody (#760-4205, Ventana Medical Systems). Incubation times for anti-hENT1D and the secondary antibody were 12 and 1 h, respectively. All tissue sections were counterstained with hematoxylin.

Table III.

hENT1 expression in samples from gemcitabine responders and non-responders.

Case	Preoperative chemotherapy	Surgical procedure	Evans classification	Adjuvant chemotherapy	Recurrence after surgery	Treatments	Date of operation
Present case	No	SSPPD	-	GEM + S-1	15 months	cCR	March 2011
Responder	GEM (6 months) + GEM + nab-PTX (6 months)	SSPPD	Grade III	S-1	24 months	Tumor shrunk with chemotherapy; after chemotherapy, conversion surgery was performed	December 2018
Non-responder case 1	GEM + S-1 (2 cycle)	SSPPD	Grade Ib	S-1	6 months	GEM + S-1, and GEM + nab-PTX performed after recurrence but no response	February 2020
Non-responder case 2	GEM + S-1 (2 cycle)	SSPPD	Grade Ia	GEM	5 months	Cancer recurred during adjuvant chemotherapy	March 2021

GEM, gemcitabine. nab-PTX, nab-paclitaxel; SSPPD, subtotal stomach-preserving pancreaticoduodenectomy. Evans classification, tumor cell destruction Grade I <10%, Grade IIa 10–50%, Grade IIb 50–90%, Grade III >90%, Grade IV no viable cells.

In the present case, hENT1 staining exhibited low frequency and weak positivity in the central region, whereas a strong positive reaction was observed in nearly all cell membranes at the invasive front of the cancer (Fig. 5A-D). In the responders, hENT1 expression was highly and strongly detected in both the central and invasive front cancer areas (Fig. 6A and B). In the nonresponders, hENT1 expression had a low-frequency and was weakly positive in both the central and advanced cancer areas (Fig. 6C and D) and mixed findings of strong and weak positives were found in the invasive front areas of the cancer (Fig. 6E and F).

Figure 5.

Results of hENT1 immunostaining. (A) hENT1 staining showedlow-frequency and weak positivity in the central area, (B) whereas it exhibited strong staining in the invasive front of the cancer. (C) Staining of almost all cellmembranes was found in the invasive front of the cancer. (D) In the other invasive front cancer cells, strong staining of the cell membrane was found.

Figure 6.

Results of hENT1 immunostaining in gemcitabine response and non-response cases. hENT1 expression is frequently detected in both the (A) central area and (B) invasive front cancer area in response cases. The frequency of hENT1 expression is low and weakly positive in both the (C) central area and (D) advanced cancer area in non-response case 1. Mixed findings of (E) strongly and positive (F) weakly hENT1 expression are found in the invasive front areas of the cancer in non-response case 2.

Discussion

The response rates of various chemotherapy drugs for pancreatic cancer have been reported: FOLFIRINOX=31.6%, GEM + Nab-PTX=23% (2,3), GEM + S-1=29.3%, GEM alone=13.3%, and S-1 alone=21.0% (8). The response rates for single agents were low. To the best of our knowledge, this is the first report of a patient with metastatic pancreatic cancer who achieved cCR for 7 years using GEM monotherapy.

Recently, cCR after chemotherapy in PDAC has been sporadically but increasingly reported. These patients were mostly treated with combination chemotherapy such as FOLFIRINOX, GEM + nab-paclitaxel, GEM + S-1, or GEM + erlotinib (9–11). cCR with GEM monotherapy is extremely rare, and remission was gained after only 3 months of GEM administration in the present case.

hENT1 protein expression has been reported to be a predictor of the therapeutic efficacy of GEM-based chemotherapy (12). Immunohistochemically detected hENT1 expression was significantly associated with prolonged disease-free survival and overall survival in patients receiving surgical resection followed by GEM-based adjuvant chemotherapy for PDAC (13). Previous studies reported the frequency of hENT1 expression and that the cytoplasm and membrane were stained (14); however, there have been no reports on the frequency of staining in the tumor center or limbus. In the present case, hENT1 staining had a low frequency and was weakly positive in the central area of the cancer but was very strongly positive in almost all cell membranes in the invasive front of the cancer. As hENT1 is a transporter located on the cell membrane, immunostaining may show that hENT1 expression is strongly expressed on the cell membrane. Our results suggest that the origin of the liver metastases in the present case was the tumor cells in the invasive front area of the cancer that had strong hENT1 staining, not the cells in the central area that had weak hENT1 staining. However, further studies are needed to confirm this hypothesis because we did not perform hENT1 staining with the tumors of the hepatic metastases. A previous study investigated the predictive role of hENT-1 localization in tumor cells of cholangiocarcinoma patients receiving adjuvant GEM (15). Moreover, Brandi et al reported that membrane hENT-1 positive patients had longer disease-free survival than those who were negative or positive only in the cytoplasm of tumor cells (14). Their findings support our hypothesis, as we found the invasive front was strongly positive for hENT1 membrane staining.

As described above, chemotherapy options are now being expanded. Predicting the efficacy of GEM prior to treatment by investigating the expression of hENT1 may improve prognosis and lead to personalized medicine.

There remains the possibility that the multiple liver metastases found at 15 months postoperatively might be liver abscesses (Fig. 2). Although we have not confirmed the diagnosis pathologically, we clinically consider these lesions as liver metastases. The reasons were that these lesions were not seen on preoperative or postoperative images, and that this patient did not present any signs of cholangitis such as high fever, and that these lesions shrank gradually after the treatment (Fig. 3).

In conclusion, we report a rare case of liver metastasis of pancreatic cancer that achieved cCR with GEM monotherapy and remained in remission for 9 years after discontinuation of treatment. Our findings suggest a relationship between hENT1 expression and GEM efficacy.

Funding Statement

Funding: No funding was received.

Availability of data and materials

The data generated in the present study may be requested from the corresponding author.

Authors' contributions

OM and TT were involved in drafting the manuscript, revising it critically for important intellectual content, and have made substantial contributions to data acquisition. TE and YKi made substantial contributions to the conception and design. KI, FK, KK, NY, YT, MT, AN, YKa and HU contributed to data acquisition, conception, and reviewed and edited the manuscript. Yoshiki Kajiwara and HU confirm the authenticity of all the raw data. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The present study was approved by the Institutional Review Board of the National Defense Medical College (approval no. 4610), and was conducted following the human and ethical principles of the Declaration of Helsinki. We have obtained written informed consent from each patient, including this case, to participate in this study.

Patient consent for publication

Written informed consent was obtained from four patients for the publication of detailed clinical information.

Competing interests

The authors declare that they have no competing interests.