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Standard Versus Extended Lymphadenectomy in Pancreatoduodenectomy for Patients With Pancreatic Head Adenocarcinoma

Standard Versus Extended Lymphadenectomy in Pancreatoduodenectomy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02928081
Enrollment
320
Registered
2016-10-07
Start date
2016-01-31
Completion date
2021-04-30
Last updated
2016-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carcinoma, Pancreatic Ductal

Brief summary

The aim of this study is to determine whether the performance of extended lymphadenectomy in association with pancreatoduodenectomy improves the long-term survival in patients with pancreatic head ductal adenocarcinoma.Half of participants will receive pancreatoduodenectomy with extended lymphadenectomy,while the other half will receive pancreatoduodenectomy with standard lymphadenectomy.

Detailed description

Pancreatic cancer is a common malignant disease of the digestive system, and its incidence has been steadily increasing recently. Currently, the only potential curative treatment for pancreatic cancer is radical surgery. However, due to the peculiarity of the anatomical location of pancreas (in the retroperitoneum, surrounded by peripheral nerves and blood vessels) and its biological characteristics (neurotropic, highly malignant, and with probable skip metastasis), it is difficult to achieve R0 resection in patients with pancreatic cancer. High postoperative recurrence and distant metastasis rate are key factors in reducing long-term survival of patients with pancreatic cancer. The radical surgery modalities for pancreatoduodenectomy to achieve R0 resection involve extended lymphadenectomy, multivisceral resections, with or without simultaneous vein removals. Currently, the lymphadenectomy extent and approaches used to achieve R0 status are diverse. In 2014, the International Study Group for Pancreatic Surgery (ISGPS) reached a consensus to strive to resect lymph nodes (LNs) 5, 6, 8a, 12b1, 12b2, 12c, 13a, 13b, 14a, 14b, 17a, and 17b in standard lymphadenectomy for pancreatoduodenectomy. However, no consensus was reached on dissection of LN 16 due to variation in the literature and different expert opinions. On the current evidence, benefit of extended lymph node dissection seems to be outweighed by the risks. But deficiencies exist in the design of previous RCTs, such as insufficient sample size, lack of certain critical data for statistical analysis, inclusion of other pathological types of pancreatic neoplasms and variable retroperitoneal lymph node resection and nerve plexus dissection . Therefore, the power of evidence was low. Most studies report a high frequency of lymph node metastasis to LNs 13, 14, 17, 12 and 16 in pancreatic cancer, and tendency to metastasis from LNs 13, 14 to LN 16. In a lot of case reports, only nodal station 16a2 and 16b1 were positive in LN 16. This study is performed to confirm whether pancreatoduodenectomy with extended lymphadenectomy could improve survival. Subjects undergoing surgery will be randomized to pancreatoduodenectomy with extended lymphadenectomy including nerve tissues around CHA and the SMA and nodes around the celiac trunk and SMA (No.16a2, 16b1) versus standard pancreatoduodenectomy. Subjects will be followed every three months for survivorship or death. The primary endpoint of 5-year overall or disease-free survival survival will be determined at five year post surgery.

Interventions

Extended lymphadenectomy with nerve tissues around CHA and the SMA and nodes around the celiac trunk and SMA (No.16a2, 16b1)

Lymph node dissection includes(LN5, LN6),(LN8a, 8b),(LN12b1, 12b2, 12c),(LN13a, 13b),(LN14a, 14b),(LN17a, 17b)

Sponsors

Royal Liverpool University Hospital
CollaboratorOTHER_GOV
West China Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Subject was diagnosed with pancreatic ductal adenocarcinoma supported by pathological and radiological examination preoperatively * Subject with absence of vascular invasion and metastasis * Subject with absence of prior history of cancer

Exclusion criteria

* Subject was diagnosed that other pancreatic tumour types (neuroendocrine tumors, intraductal papillary mucinous neoplasm, serous cystadenoma, mucinous cystadenocarcinoma, solid pseudopapillary neoplasm and pancreatitis) * Subject was found with liver, omental, mesenteric or peritoneal metastasis intraoperatively * Subject with presence of other significant diseases (e.g., coronary heart disease)

Design outcomes

Primary

MeasureTime frameDescription
5-year overall survival rate5 yearsThe percentage of patients that are alive at a 5 year

Secondary

MeasureTime frameDescription
Bile leakageWithin 30 days or before dischargeISGLS definition
Delayed gastric emptyingWithin 30 days or before dischargeISGPS definition
Post-pancreatectomy haemorrhageWithin 30 days or before dischargeISGPS definition
Intra-abdominal infectionWithin 30 days or before dischargePresence of fever, signs of peritonitis, high leukocytes count or positive peritoneal drainage fluid culture
Postoperative pancreatic fistulaWithin 30 days or before dischargeISGPS definition
Postoperative mortalityWithin 30 days or 60 daysDeath due to any cause before or at postoperative day 30 and 60
Quality of life1 or 3 or 5 yearEORTC QLQ-C30, according to the scoring manual published by the EORTC Quality of Life group
5-year disease-free survival rate5 yearsThe percentage of patients alive without recurrence at a 5 year
Wound infectionWithin 30 days or before dischargeRequiring invasive treatment, for example: positive wound exudate culture and requiring continuous re-open drainage or invasive treatment

Countries

China

Contacts

Primary ContactXubao Liu, MD
liuxb2011@126.com86-28-85422474
Backup ContactJunjie Xiong, MD
junjiex2011@126.com86-28-85422474

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026