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A clinical role of staging laparoscopy in patients with radiographically defined locally advanced pancreatic ductal adenocarcinoma
World Journal of Surgical Oncology volume 14, Article number: 14 (2015)
The aim of current study is to verify usefulness of staging laparoscopy (stag-lap) for patient’s selection and to find prognostic factors in patients with radiographically defined locally advanced (RD-LA) pancreatic ductal adenocarcinoma (PDAC).
The LA disease was defined as an unresectable disease without distant organ metastasis based on resectability status of NCCN guideline in this study. Stag-lap was performed in 67 patients with RD-LA (2007–2012) which were divided into 4 groups according to metastatic site: group CY (peritoneal fluid or washing cytology positive and without any distant organ metastasis); group P (peritoneal dissemination); group L (liver metastasis); group LA (peritoneal fluid or washing cytology negative and without any distant organ metastasis). Clinical backgrounds, survival curves, and prognostic factors were investigated.
There were 16 patients in CY group (24 %), 13 patients in P group (19 %), 10 patients in L group (15 %), and 28 patients in LA group (42 %). Median survival time was 13 months in CY group and 11 months in LA group, which was significantly better than 7 months in P group, respectively (p < 0.05). The rate of emergence of ascites in LA was significantly better than in CY or P groups (p < 0.05). Multivariate analysis showed that the presence of partial response and administration of second-line chemotherapy were significantly independent prognostic factors.
The majority of PDAC patients with RD-LA had occult distant organ metastasis. Clinical features and survival curves were different depending on the site of occult distant organ metastasis. Administration of second-line chemotherapy and responsiveness to chemotherapy were associated with favorable prognosis. Staging laparoscopy should be routinely performed in patients with RD-LA PDAC (UMIN000019936).
Pancreatic ductal adenocarcinoma (PDAC) is a lethal disease with poor prognosis, even in patients who have undergone resection with curative intent . At the time of diagnosis, the majority of patients have unresectable disease with or without distant organ metastasis on imaging modality [1, 2]. Despite the advances and resolution improvement of imaging technologies, less-invasive staging modalities are still limited in their ability to identify accurately metastatic disease of small volume, resulting in inappropriate patient selection for therapy .
Staging laparoscopy is a minimally invasive procedure that can identify occult distant metastases, resulting in appropriate patient selection for chemotherapy or chemoradiation therapy . Stefanidis et al.  stated in their review that staging laparoscopy has an important role in the staging algorithm of PDAC patients and will likely continue to be a valuable tool. Diagnostic laparoscopy guidelines  have proposed that staging laparoscopy should be considered after high-quality imaging studies have excluded metastatic disease in appropriately selected patients with locally advanced pancreatic adenocarcinoma.
We had some clinical questions on the diagnoses and clinical courses in radiographically defined locally advanced (RD-LA) patients, such as the frequency of occult distant organ metastasis, the survival difference according to the occult distant organ metastatic site, and the prognostic factors in this patient population. Therefore, since 2007, we have introduced staging laparoscopy in PDAC patients with RD-LA for further exploration of minute distant organ metastases which were not detected by conventional staging modalities . In the current study, we retrospectively assessed the rate of minute distant organ metastasis in PDAC patients with RD-LA, compared the clinical background and survival rate according to metastatic site, and analyzed the prognostic factors.
A retrospective study was conducted using a prospective database. A total of 70 out of 395 patients with PDAC (267 unresectable and 128 resected) presented with RD-LA between January 2007 and December 2012 at Kansai Medical University Hospital, Osaka, Japan. Three patients refused to undergo staging laparoscopy and therefore, ultimately, staging laparoscopy was performed in 67 patients with RD-LA. The LA disease was defined as an unresectable disease without distant organ metastasis based on resectability status of NCCN guideline  in this study as follows; greater than 180° superior mesenteric artery encasement and any celiac abutment for pancreatic head PDAC; superior mesenteric artery or celiac encasement greater than 180° for pancreatic body and tail PDAC; unreconstructible superior mesenteric/portal vein occlusion and aortic invasion or encasement for both PDAC. These 67 patients were divided into 4 groups according to metastatic site; group CY (cytology positive and without any distant organ metastasis); group P (peritoneal dissemination); group L (liver metastasis); group LA (pure locally advanced disease, without positive cytology and any distant organ metastasis). Clinical backgrounds and survival curves according to metastatic site were compared among groups and investigated as a prognostic factor for this population. All patients were followed up for at least 1 year.
All patients had a pathological evidence of PDAC before or during staging laparoscopy. Resectability was assessed with cine-imaging MDCT, using the Aquilion® CT system (Toshiba Medical Systems, Tochigi, Japan). Arterial- and portal-phase images were collected using a 1.0 × 64 mm detector configuration. After reconstruction of the raw scans, data from serial 1.0-mm-thick slices with a 0.5-mm interval were transferred to a workstation (AquariusNet Viewer, TeraRecon Inc., San Mateo, CA, USA). After creating two- and three-dimensional coronal and sagittal anatomical reconstructions, the cine images were evaluated by an experienced hepatopancreatobiliary surgeon and a consultant radiologist. The clinical response rate was based on the Response Evaluation Criteria in Solid Tumors (RECIST) , and partial response was defined as at least a 30 % decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters.
Patients with resectable, borderline resectable, and metastatic PDAC based on cine-imaging MDCT were excluded from the study. Patients with cancer of the pancreatic body and tail, with celiac trunk invasion, but with no invasion of the superior mesenteric and pancreaticoduodenal arteries, were also classified as potential candidates for resection with curative intent in this institution and thus excluded from participation. Positron emission tomography (PET) scanning was performed in patients with suspicion of metastatic disease in the lung, cervical, or para-aortic lymph nodes on cine-imaging MDCT. All patients with a suspicion of distant organ metastasis diagnosed by PET scanning were excluded after confirmation of adenocarcinoma in the biopsy specimens from locations such as the liver, lung, cervical lymph nodes, and bone. Although the patients with omental cake or multiple peritoneal nodules greater than 10-mm diameter were also excluded from the study, patients with suspicion of peritoneal metastasis less than 10-mm diameter on MDCT or ascites limited to the Pouch of Douglas were recruited.
The location of the metastatic site diagnosed by the staging laparoscopy was recorded. Patients with occult distant organ metastasis were treated with gemcitabine or S-1-based chemotherapy or combination chemotherapy of gemcitabine and S-1. Radiation therapy was added as the first-line treatment concomitant with chemotherapy in 15/28 patients with locally advanced tumor or 5/16 patients with positive cytology. Second-line chemotherapy (gemcitabine, S-1, or gemcitabine and S-1) was administered to patients with their consent and if they also had a good performance status. The time of development of ascites according to the site of distant organ metastasis was also recorded.
Informed consent was obtained from each patient included in the study, in accordance with the provisions of the Declaration of Helsinki. Patient data were obtained from the prospective database of pancreatic disease at Kansai Medical University Hospital.
Briefly, after establishing the pneumoperitoneum through a 12-mm trocar inserted at the umbilical area, a flexible laparoscope was inserted and two additional 5-mm ports were placed. First, an inspection focusing on the presence or absence of nodules on the parietal peritoneum and the liver surface was carefully performed. Second, a cytological examination was performed in cases where ascites was present. When there was no ascitic fluid, the peritoneal cavity was washed with 100 ml of physiologic saline solution. After placing the patient in Trendelenburg’s position, the presence or absence of nodules in the Pouch of Douglas was checked by inserting the laparoscope through filled water into the Pouch of Douglas. Subsequently, cytologic washings from the Pouch of Douglas were obtained for pathological examination. Third, the entire mesentery was examined by grasping the small intestine from the first jejunal loop to the ileocecal junction to locate the minute peritoneal nodules. Biopsies were taken from any regions suspected of containing metastatic nodules. Neither the lesser nor the greater sac was opened in this study. This clinical study was registered as UMIN000019936.
Data are expressed as median values and ranges. Clinical background and clinical course were compared according to metastatic site in Table 1. Continuous or categorical variables were compared by Mann–Whitney U test, chi-square test, or Fisher’s exact test as appropriate. Overall survival curve, defined as the time from initial treatments to death or the last follow-up date, were compared using the log-rank test according to metastatic site. In addition, profound factors identified by the univariate analysis were further examined by multivariate Cox proportional-hazard models to determine independent significant factors for survival. The hazard ratio and 95 % confidence intervals were calculated for all estimates. A two-tailed p value less than 0.05 was considered to be statistically significant. Statistical analyses were performed using SPSS version 18.0 for Windows (Chicago, IL, USA).
Outcome measures of staging laparoscopy
Median operative time was 67 min (34–168) and median extent of blood loss was 0 ml (0–168). Past history of previous surgery was found in 12 out of 67 patients (18 %). Three patients needed open mini-laparotomy converted from staging laparoscopy because of severe adhesion due to previous surgeries. Biopsy specimens were obtained from 43 patients (64 %) for evaluating if occult distant organ metastasis was present. One patient incidentally had intestinal perforation during staging laparoscopy, and primary closure was immediately done. Her postoperative course was uneventful and underwent chemotherapy without delay.
Exploration using staging laparoscopy clearly demonstrated the presence of occult distant organ metastasis in 39 out of 67 patients (58 %). There was positive cytology in 16 patients (CY, 24 %), peritoneal dissemination in 13 patients (P, 19 %), liver metastasis only or concomitant with peritoneal metastasis in 10 patients (L including 3 patients with concomitant peritoneal metastasis, 15 %), and locally advanced disease in 28 patients (LA, 42 %), respectively.
Comparison of clinical backgrounds and clinical course according to metastatic site
With regard to the clinical backgrounds and the clinical course, as shown in Table 1, the L or P groups had a higher frequency of pancreatic body and tail cancer, compared with the LA or CY groups. Addition of radiation therapy during chemotherapy was frequently performed in the LA and CY groups according to the departmental policy. The clinical response rate, as based on the RECIST , was higher in the LA or CY groups than in either the P or L groups. When the rate of emergence of ascites according to the site of occult distant organ metastasis was compared, it was significantly lower in the LA group than in CY or P group (Fig. 1, p < 0.05). Development of ascites within 1 year after initial treatment was found most frequently in patients in the P group (11 out of 13 patients, 85 %), which was higher than in the other 3 groups. Second-line chemotherapy was administered less frequently in P group (1 out of 13 patients, 8 %), relative to the other three groups (Table 1). Moreover, duration of chemotherapy in P group was shorter than in the other groups.
Median survival time was 13 months in the CY group (including 2 patients who underwent surgical resection), 11 months in the LA group (including 1 patient who underwent surgical resection), and 7 months in the P and L groups, respectively. Actual 1-year survival rates in the 4 groups were as follows: 46 % (LA), 63 % (CY), 23 % (P), and 20 % (L). No patient in the P and L groups was alive beyond the 2-year follow-up. Thus, as shown in Fig. 2a, the overall survival curve in P group was significantly worse than in either the LA or CY groups (p = 0.04 and p = 0.007, respectively). No significant differences in the survival curves were seen between CY and LA, P and L, or LA and L groups. As shown in Fig. 2b, the survival curve in the LA + CY groups was significantly better than in the P + L groups (p = 0.011). In the LA or CY groups, additional radiation therapy was administered to approximately 30–50 % of patients, PR according to RECIST  was observed in approximately 35 % of patients, and second-line chemotherapy was administered to around 60 % of patients. In this study, out of 44 patients in LA and CY groups, conversion surgery was performed in two patients in the CY group (one alive after 60 months; the other died at 18 months, respectively) and one patient in the LA group (alive after 17 months). The multivariate analysis showed that the presence of partial response and administration of second-line chemotherapy were significantly independent favorable factors for prognosis (Table 2).
The majority of patients with PDAC have unresectable disease at initial presentation, and their prognosis is extremely poor. The median survival time of these patients ranges from 6 to 12 months in spite of developed, advanced, and newly provided regimens of chemotherapy [8–11]. Accurate staging is necessary for selecting patients who should be curatively resected, for introducing new regimens of chemotherapy or chemo(radio)therapy, or for conducting a clinical trial. Several articles have reported that the use of staging laparoscopy to further explore locally advanced PDAC, initially diagnosed by CT scan, has identified the presence of occult distant organ metastasis [4, 5, 12–17]. However, less information is available on clinical background and clinical course according to occult distant metastatic site diagnosed by staging laparoscopy in patients with RD-LA PDAC. Understanding the clinical features according to the site of occult distant organ metastasis is important for the development of new strategies and improving prognosis in patients with locally advanced PDAC.
We have focused on RD-LA PDAC defined by the NCCN guidelines , excluding resectable, borderline resectable, and metastatic diseases. The results of staging laparoscopy in this study showed occult distant organ metastasis in 58 % of patients including positive cytology in 24 %, peritoneal dissemination in 19 %, and liver metastasis in 15 %, respectively. Finally, pure locally advanced disease without minute distant organ metastasis was found in 42 % of patients only. Clark et al.  reported that diagnostic laparoscopy for borderline resectable and unresectable locally advanced diseases showed occult distant organ metastasis in 58 of 202 patients (29 %) including positive peritoneal lavage cytology in 20 % (n = 41), liver metastasis in 13 % (n = 26), and peritoneal metastases in 3 % (n = 5) (Table 3). Relative to Clark et al. , our study consisted of a more limited population of unresectable, locally advanced PDAC. As shown in Table 3, compared with other studies, our study consisted of high frequency of pancreatic body and tail cancer, which was associated with unresectability and the presence of occult distant organ metastasis [4, 5]. In our experience, we had an aggressive attitude towards surgical resection, even in patients with portal or superior mesenteric vein invasion, common hepatic artery invasion, and celiac axis invasion for pancreatic body cancer. The definition of local unresectability for our patients was strictly limited. Moreover, we also recruited patients with suspicion of peritoneal metastasis less than 10-mm diameter on MDCT or ascites limited to the Pouch of Douglas. Therefore, this could explain why a high incidence of occult distant organ metastasis (58 %) and peritoneal metastasis (19 %) was found in our study.
We have introduced palliative chemotherapy in patients with distant organ metastasis including peritoneal metastasis, and chemo(radio)therapy for tumor remission in patients with LA or CY. The clinical findings by staging laparoscopy can provide to change the paradigm of the treatment in patients with RD-LA PDAC. Actually, peritoneal and/or liver metastasis was observed in 34 % of patients, who were treated with palliative chemotherapy. Thus, the results of staging laparoscopy changed the treatment according to distant organ metastatic sites. Considering the high frequency of patients with occult distant organ metastasis, staging laparoscopy should be routinely performed in patients with RD-LA PDAC.
With regard to the comparison of survival curves according to the site of occult distant organ metastasis, P or L groups had a worse prognosis than either the CY or LA groups in our study. Actual 1-year survival rate was 46 % in LA, 63 % in CY, 23 % in P, and 20 % in L groups. In the LA or CY groups, high frequency of additional radiation, PR according to RECIST, second-line chemotherapy and conversion surgery might result in better prognosis. Appearance of partial or complete response after chemo(radio)therapy can sometimes lead to subsequent surgical resection. It has been reported that the overall survival rate in patients with initially unresectable PDAC who underwent surgical resection after favorable response to anti-cancer treatments over a period of time was similar to that in patients with resectable PDAC [18, 19]. Even in patients with initially unresectable disease, long-term survival can be expected if an unresectable tumor was surgically resected after tumor shrinkage. Advanced chemotherapy or chemoradiation therapy may have a role in downsizing an unresectable tumor sufficiently to render it resectable. Thus, a new strategy to shrink the tumor in LA or CY group should be introduced where possible to allow for subsequent surgical resection, which is associated with long-term survival.
The multivariate analysis showed that the presence of partial response and administration of second-line chemotherapy were significantly independent favorable factors for prognosis (Table 2). The curve of emergence of ascites in CY or P group was significantly worse than in LA group (Fig. 1, p < 0.05). The P group in particular had ascites in 85 % of patients within 1 year after initial treatment. Moreover, no patient survived longer than 2 years after initial treatment in P group. A lower frequency of second-line chemotherapy and clinical response and shorter duration of chemotherapy in P group were found in this study, probably due to emergence of ascites and poor performance status. Thus, conventional chemotherapy may not be effective for patients with peritoneal metastasis, and therefore, a new regimen to control or prevent ascites will be required for achieving better prognosis. In this regard, intraperitoneal chemotherapy may be one option for patients with peritoneal metastasis that should be investigated. A Japanese case report described the success of intraperitoneal paclitaxel combined with systemic chemotherapy of S-l and gemcitabine for locally advanced PDAC with peritoneal carcinomatosis . After 20 months, all peritoneal deposits had disappeared and a radical resection of the tumor was performed. Sugarbaker et al.  have conducted a phase II study of hyperthermic intraoperative gemcitabine and long-term intraperitoneal gemcitabine in the adjuvant setting for resectable PDAC patients. Further protocol-based studies should be performed to investigate whether prognosis in patients with occult peritoneal metastasis can be improved or not.
The limitation of the study was the small number of patients recruited retrospectively and the presence of undetectable liver metastasis deep within the liver and/or other organ metastasis.
In conclusion, staging laparoscopy is necessary for selecting patients with occult distant organ metastasis which is the majority population of patients with RD-LA PDAC. Clinical features and survival curves were different depending on the site of occult distant organ metastasis. Administration of second-line chemotherapy and responsiveness to chemotherapy were associated with favorable prognosis. Staging laparoscopy should be routinely performed in PDAC patients with RD-LA.
Li D, Xie K, Wolff R, Abbruzzese JL. Pancreatic cancer. Lancet. 2004;363:1049–57.
White R, Winston C, Gonen M, D’Angelica M, Jarnagin W, Fong Y, et al. Current utility of staging laparoscopy for pancreatic and peripancreatic neoplasms. J Am Coll Surg. 2008;206:445–50.
Satoi S, Yamamoto H, Toyokawa H, Inoue K, Wada K, Yamamoto T, et al. Selective Use of staging laparoscopy based on Carbohydrate Antigen 19–9 level and tumor size in patients with radiographicallydefined potentially or borderline resectable pancreatic cancer. Pancreas. 2011;40:426–32.
Stefanidis D, Grove KD, Schwesinger WH, Thomas Jr CR. The current role of staging laparoscopy for adenocarcinoma of the pancreas: a review. Ann Oncol. 2006;17:189–99.
Hori Y, SAGES Guidelines Committee. Diagnostic laparoscopy guidelines: This guideline was prepared by the SAGES Guidelines Committee and reviewed and approved by the Board of Governors of the Society of American Gastrointestinal and Endoscopic Surgeons (SAGES), November 2007. Surg Endosc. 2008;22:1353-83.
National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in oncology. Version 1. Ft Washington, PA: NCCN; 2012.
Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, et al. New guidelines to evaluate the response to treatment in solid tumors: European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000;92:205–16.
Burris HA 3rd, Moore MJ, Andersen J, Green MR, Rothenberg ML, Modiano MR, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: A randomized trial. J Clin Oncol. 1997;15:2403–13.
Moore MJ, Goldstein D, Hamm J, Figer A, Hecht JR, Gallinger S, et al. Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: a phase III trial of the National Cancer Institute of Canada Clinical Trials Group. J Clin Oncol. 2007;25:1960–6.
Conroy T, Desseigne F, Ychou M, Bouché O, Guimbaud R, Bécouarn Y, et al. FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N Engl J Med. 2011;364:1817–25.
Ueno H, Ioka T, Ikeda M, Ohkawa S, Yanagimoto H, Boku N, et al. Randomized phase III study of gemcitabine plus S-1, S-1 alone, or gemcitabine alone in patients with locally advanced and metastatic pancreatic cancer in Japan and Taiwan: GEST study. J Clin Oncol. 2013;31:1640–8.
Clark CJ, Traverso LW. Positive peritoneal lavage cytology is a predictor of worse survival in locally advanced pancreatic cancer. Am J Surg. 2010;199:657–62.
Morak MJ, Hermans JJ, Smeenk HG, Renders WM, Nuyttens JJ, Kazemier G, et al. Staging for locally advanced pancreatic cancer. Eur J Surg Oncol. 2009;35:963–8.
Contreras CM, Stanelle EJ, Mansour J, Hinshaw JL, Rikkers LF, Rettammel R, et al. Staging laparoscopy enhances the detection of occult metastases in patients with pancreatic adenocarcinoma. J Surg Oncol. 2009;100:663–9.
Shoup M, Winston C, Brennan MF, Bassman D, Conlon KC. Is there a role for staging laparoscopy in patients with locally advanced, unresectable pancreatic adenocarcinoma? J Gastrointest Surg. 2004;8:1068–71.
Liu RC, Traverso LW. Diagnostic laparoscopy improves staging of pancreatic cancer deemed locally unresectable by computed tomography. Surg Endosc. 2005;19:638–42.
Tilleman EH, Busch OR, Bemelman WA, van Gulik TM, Obertop H, Gouma DJ. Diagnostic laparoscopy in staging pancreatic carcinoma: developments during past decades. J Hepatobiliary Pancret Surg. 2004;11:11–6.
Satoi S, Yamaue H, Kato K, Takahashi S, Hirono S, Takeda S, et al. Role of adjuvant surgery for patients with initially unresectable pancreatic cancer with a long-term favorable response to non-surgical anti-cancer treatments: results of a project study for pancreatic surgery by the Japanese Society of Hepato-Biliary-Pancreatic Surgery. J Hepatobiliary Pancreat Sci. 2013 May 10. [Epub ahead of print].
Bickenbach KA, Gonen M, Tang LH, O'Reilly E, Goodman K, Brennan MF, et al. Downstaging in pancreatic cancer: a matched analysis of patients resected following systemic treatment of initially locally unresectable disease. Ann Surg Oncol. 2012;19:1663–9.
Kimura H, Fushida S, Mukawa A. A resected case of effective treatment with S-1/gemcitabine and paclitaxel combination chemotherapy for advanced pancreatic cancer with peritoneal and liver metastasis. Gan To Kagaku Ryoho. 2009;36:1191–4.
Sugarbaker PH, Stuart OA, Bijelic L. Intraperitoneal gemcitabine chemotherapy treatment for patients with resected pancreatic cancer: rationale and report of early data. Int J Surg Oncol.161862. doi: 10.1155/2011/161862. Epub 2011 Dec 12.
The authors declare that they have no competing interests.
SS and HY contributed to all aspects of this study and article. TY, HT, SH, SY, and HR contributed to the study conception and design, collection of the data, and critical revision of the article. SSO, KI, TM, YM, and MK contributed to the collection of the data and critical revision of the article. All authors read and approved the final manuscript.
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Satoi, S., Yanagimoto, H., Yamamoto, T. et al. A clinical role of staging laparoscopy in patients with radiographically defined locally advanced pancreatic ductal adenocarcinoma. World J Surg Onc 14, 14 (2015). https://doi.org/10.1186/s12957-016-0767-y
- Staging laparoscopy
- Peritoneal carcinomatosis
- Occult distant organ metastasis
- Second-line chemotherapy
- Locally advanced PDAC