The goal of this clinical trial is to learn if traditional pancreaticoduodenectomy (PD) combined with TRIANGLE (extended PD surgery) can increase disease-free survival (DFS) in patients with pancreatic head cancers compared to traditional minimally invasive PD. The main questions it aims to answer are: * Does extended PD surgery increase disease-free survival (DFS)? * Does extended PD surgery could improve postoperative and long-term quality of life for patients? Researchers will compare extended PD surgery to traditional PD surgery to see if extended PD surgery could extend the survival time of patients. Participants will: * Accept traditional minimally invasive PD surgery or minimally invasive PD combined with TRIANGLE surgery. * Visit the clinic once every 3 months for checkups and tests. * Keep a diary of their symptoms.
Pancreaticoduodenectomy (PD) currently stands as the sole option for treating resectable pancreatic head cancer; however, the long-term post-operative survival quality of patients remains unpromising. According to statistics from international multicenter studies, the 5-year survival rate of patients post-surgery does not exceed 20%. The principal causes for the suboptimal survival quality are the high recurrence and metastasis tendencies of pancreatic cancer, along with its low sensitivity and poor response to the existing neoadjuvant therapy. In contrast to traditional PD, PD combined with the TRIANGLE procedure (expanded PD) enables more thorough resection, effectively addressing the early recurrence and metastasis issues of pancreatic cancer and holds significant potential in enhancing patients' long-term survival quality. Nevertheless, there exists no high-level clinical evidence regarding the improvement of short-term complications for this surgical approach. Simultaneously, minimally invasive pancreatic surgeries have been demonstrated in high-throughput pancreatic centers to improve patients' short-term quality of life, yet the effect on long-term prognosis remains ambiguous. Hence, our center innovatively proposes minimally invasive PD in combination with the TRIANGLE procedure for the treatment of resectable pancreatic cancer, with the aim of integrating the advantages of both intervention measures to improve patients' post-operative quality of life and long-term survival quality. This research will carry out a randomized controlled trial on patients with resectable pancreatic cancer who are scheduled to undergo minimally invasive PD in six Chinese centers and two foreign centers, comparing the prognostic disparities between traditional PD and the expanded PD procedure. The primary outcome measure is the postoperative disease-free survival (DFS), defined as "the time from randomization to disease recurrence or death for any reason." The projected enrollment period is 15 months, and the follow-up duration is 3 years.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
270
Traditional minimally invasive pancreaticoduodenectomy combined with the TRIANGLE procedure
Traditional minimally invasive pancreaticoduodenectomy
Disease-free survival after resection
the primary outcome was DFS defined "as the time from randomisation until disease recurrence or death from any cause"
Time frame: 3, 6, 12, 18, 24, 30, 36 months after surgery (or early termination of the trial)
the rate of microscopically complete margin clearance
the rate of \>0.1 cm margin clearance, R0(CRM-)
Time frame: Intraoperative
the rate of microscopic margin clearance ≤ 0.1 cm
rate of R0(CRM+)
Time frame: Intraoperative
the rate of microscopic margin involvement (R1) resections
the rate of R1 resection, defined according to the 8th edition of the UICC TNM classification
Time frame: Intraoperative
the rate of postoperative pancreatic fistula
the POPF was defined by the International Study Group of Pancreatic Surgery (ISGPS)
Time frame: Day of discharge, postoperative days 5, 10-12 and 90
the rate of postpancreatectomy haemorrhage
PPH was defined by the ISGPS
Time frame: Day of discharge, postoperative days 5, 10-12 and 90
the rate of delayed gastric emptying
DGE was defined by the ISGPS
Time frame: Day of discharge, postoperative days 5, 10-12 and 90
the rate of bile leakage
Bile leakage was defined by the International Study Group of Liver Surgery (ISGLS)
Time frame: Day of discharge, postoperative days 5, 10-12 and 90
the rate of lymphatic fistula
Lymphatic fistula was defined by the ISGPS
Time frame: Day of discharge, postoperative days 5, 10-12 and 90
the rate of diarrhoea
Diarrhoea was graded by the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Time frame: Day of discharge, postoperative days 5, 10-12 and 90
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