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Divestment for Artery-involved Pancreatic Cancer

Primary Purpose

Pancreatic Cancer, Locally Advanced Pancreatic Cancer, Neoadjuvant Therapy

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Artery Divestment Technique
Nab-paclitaxel
Sponsored by
The First Affiliated Hospital with Nanjing Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Cancer focused on measuring Artery Divestment Technique, Locally Advanced Pancreatic Cancer, Neoadjuvant Therapy, Borderline Resectable Pancreatic Cancer

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosed with pancreatic cancer staged at cT4NxM0(AJCC Cancer Staging Manual, 8th Edition) based on contrast enhanced CT&MRI scan and tumor markers;
  2. Age > 18 year and <80 year;
  3. Agree to participate in the study with signed informed consent.

Exclusion Criteria:

  1. Evidence of metastasis based on physical examination, enhanced CT or enhanced MRI;
  2. Poor performance status and/or co-morbidity precluding pancreatectomy and chemotherapy;
  3. Focal vessel narrowing or contour irregularity revealed by radiology examinations;
  4. Economic situations cannot afford designed treatment.

Sites / Locations

  • The First Affiliated Hospital of Nanjing Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Surgery Group

NeoChemo Group

Arm Description

In Surgery Group, an artery divestment combined pancreatectomy will be performed if no pre-operative contra-indication or intra-operative metastasis were revealed. Post-operative adjuvant chemotherapies were prescribed according to performance status.

In NeoChemo (Neoadjuvant Chemotherapy) Group, neoadjuvant chemotherapy will be utilized. After 2 circles of neoadjuvant chemotherapies, patients will be reevaluated and curative operation would be attempted if without disease progression.

Outcomes

Primary Outcome Measures

Overall mortality at one year after randomization;

Secondary Outcome Measures

Overall survival rate after 2 years from randomization;
Overall survival rate after 3 years from randomization;
Median survival
Disease-free survival
Margin status of subjects receiving curative surgery
The margin status will be reported as R0, R1 and R2 according to AJCC Cancer Staging Manual 8th ed.
Intra-operative blood transfusion
For both Surgery Group and participants who received operations in NeoChemo Group, category and volume of intra-operative blood transfusion will be reported.
Intra-operative blood loss
For both Surgery Group and participants who received operations in NeoChemo Group, intra-operative blood loss will be measured and reported by milliliter.
Overall surgical complication rate
Overall surgical complication rate for both Surgery Group and participants who received operations in NeoChemo Group will be reported. Post-operative pancreatic fistula, delayed gastric emptying, post-operative hemorrhage, Surgical site infection and other surgical complications will be recorded. Percentage that candidates suffered from surgical complications of surgical cases for both group will be reported.
Incidence of post-operative pancreatic fistula
Post-operative pancreatic fistula (POPF) will be accessed byInternational Study Group of Pancreatic Surgery (ISGPS) standards; Incidence of post-operative pancreatic fistula of surgical cases in both group will be reported.
Incidence of delayed gastric emptying
Delayed gastric emptying (DGE) will be accessed byInternational Study Group of Pancreatic Surgery (ISGPS) standards; Incidence of DGE of surgical cases in both group will be reported.
Incidence of post-operative hemorrhage
Post-operative hemorrhage (POH) will be accessed byInternational Study Group of Pancreatic Surgery (ISGPS) standards; Incidence of POH of surgical cases in both group will be reported.
Incidence of surgical site infection
Surgical site infection was assessed as US CDC guidelines.Incidence of surgical site infection of surgical cases in both group will be reported.
Incidence of other surgical complications
Any other undesirable situations that considered complicated with surgery will be recorded. Incidence of other surgical complications of surgical cases in both group will be reported.
Severe adverse events rate
Feasibility of chemotherapy will be evaluated according to Common Terminology Criteria for Adverse Events, US NCI. Participants receiving neo-adjuvant, adjuvant or palliative chemotherapy will be accessed. Grade 3-5 adverse events, dose reduction or dose delay will be reported.
Quality of life at 0.5 year after randomization
EORTC QLQ-C30 (V3.0) will be enrolled to evaluate quality of life.
Quality of life at 1 year after randomization
EORTC QLQ-C30 (V3.0) will be enrolled to evaluate quality of life.
Quality of life at 2 years after randomization
EORTC QLQ-C30 (V3.0) will be enrolled to evaluate quality of life.
Quality of life at 3 years after randomization
EORTC QLQ-C30 (V3.0) will be enrolled to evaluate quality of life.
Performance status at 0.5 year after randomization
Karnofsky Performance Status Scale will be enrolled to evaluate Performance status.
Performance status at 1 year after randomization
Karnofsky Performance Status Scale will be enrolled to evaluate Performance status.
Performance status at 2 years after randomization
Karnofsky Performance Status Scale will be enrolled to evaluate Performance status.
Performance status at 3 years after randomization
Karnofsky Performance Status Scale will be enrolled to evaluate Performance status.

Full Information

First Posted
December 17, 2017
Last Updated
February 18, 2018
Sponsor
The First Affiliated Hospital with Nanjing Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03443921
Brief Title
Divestment for Artery-involved Pancreatic Cancer
Official Title
Artery Divestment Technique in Artery-Involved Pancreatic Cancer: A Single-Institution, Open-Labeled Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 2018 (Anticipated)
Primary Completion Date
March 2019 (Anticipated)
Study Completion Date
March 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The First Affiliated Hospital with Nanjing Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Pancreatic cancer is the most lethal malignancy of human being. Surgery is the only potential cure of pancreatic cancer. The invasion of major abdominal arteries is one of the most important factor restricting surgical intervention. For artery-involved pancreatic cancer (ai-PC) patients, pre-operative adjuvant therapies, especially the neoadjuvant chemotherapy, has brought exciting postoperative survival. Yet due to the potential screening effect of this treatment strategy, nearly half of ai-PC patients failed to benefit from surgery because of disease progression, adverse reactions of adjuvant treatment and other reasons. Artery divestment for the treatment of ai-PC firstly reported by our center, can significantly increase resection rate and produce overall survival benefit in some patients. This study is to explore whether up-front surgery with artery divestment combined curative pancreatectomy or the chemotherapy-first strategy would be more beneficial for ai-PC patients' survival. Subjects will be randomized to treatment group either receiving up-front artery divestment combined pancreatectomy (Surgery Group) or adjuvant chemotherapies (Chemo Group). In Surgery Group, an artery divestment combined pancreatectomy will be performed if no pre-operative contra-indication or intra-operative metastasis were revealed. Post-operative adjuvant chemotherapies were prescribed according to performance status. In Chemo Group, adjuvant chemotherapy of gemcitabine or gemcitabine + cisplatin will be utilized according to performance status. After 2 circles of adjuvant chemotherapies, patients will be reevaluated and curative operation would be attempted if without disease progression. Overall mortality at one year after randomization will be the primary endpoint. Other parameters as overall survival after 2 and 3 years, median survival, disease-free survival, margin status of subjects receiving curative surgery, etc. will also be observed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer, Locally Advanced Pancreatic Cancer, Neoadjuvant Therapy, Borderline Resectable Pancreatic Cancer
Keywords
Artery Divestment Technique, Locally Advanced Pancreatic Cancer, Neoadjuvant Therapy, Borderline Resectable Pancreatic Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
122 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Surgery Group
Arm Type
Experimental
Arm Description
In Surgery Group, an artery divestment combined pancreatectomy will be performed if no pre-operative contra-indication or intra-operative metastasis were revealed. Post-operative adjuvant chemotherapies were prescribed according to performance status.
Arm Title
NeoChemo Group
Arm Type
Active Comparator
Arm Description
In NeoChemo (Neoadjuvant Chemotherapy) Group, neoadjuvant chemotherapy will be utilized. After 2 circles of neoadjuvant chemotherapies, patients will be reevaluated and curative operation would be attempted if without disease progression.
Intervention Type
Procedure
Intervention Name(s)
Artery Divestment Technique
Other Intervention Name(s)
Sub-adventitial Resection
Intervention Description
Tunica adventitia was pick up by forceps and opened by electrocoagulation at 1 cm distal from tumor-artery contact. Space between tunica adventitia and external elastic lamina (EEL) were blunt lifting tumor-invaded adventitia by angled clamp. Adventitia was then sectioned to show EEL. Loose dissect space could be achieve along long the plane between EEL and adventitia as long as tumor invasion outside EEL. Tumor and invaded adventitia were further cut open by electrocoagulation proximally. Circumferentially, separation could be done by blunt dissection around EEL. Nourishing blood vessels of the artery would be secured by electrocoagulation or ultrasonic scalpel while major branch would be ligated or transfixed.
Intervention Type
Drug
Intervention Name(s)
Nab-paclitaxel
Intervention Description
After eligibility testing as blood tests, contrast-enhanced CT and MRI scan, 3 cycles were administered (1,000 mg/m2 of gemcitabine and 125 mg/m2 of nab-paclitaxel on days 1, 8, and 15 every 28 days).Patients will be reevaluated and curative operation would be attempted if without disease progression.
Primary Outcome Measure Information:
Title
Overall mortality at one year after randomization;
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Overall survival rate after 2 years from randomization;
Time Frame
2 years
Title
Overall survival rate after 3 years from randomization;
Time Frame
3 years
Title
Median survival
Time Frame
3 years
Title
Disease-free survival
Time Frame
3 years
Title
Margin status of subjects receiving curative surgery
Description
The margin status will be reported as R0, R1 and R2 according to AJCC Cancer Staging Manual 8th ed.
Time Frame
1 years
Title
Intra-operative blood transfusion
Description
For both Surgery Group and participants who received operations in NeoChemo Group, category and volume of intra-operative blood transfusion will be reported.
Time Frame
1 years
Title
Intra-operative blood loss
Description
For both Surgery Group and participants who received operations in NeoChemo Group, intra-operative blood loss will be measured and reported by milliliter.
Time Frame
1 years
Title
Overall surgical complication rate
Description
Overall surgical complication rate for both Surgery Group and participants who received operations in NeoChemo Group will be reported. Post-operative pancreatic fistula, delayed gastric emptying, post-operative hemorrhage, Surgical site infection and other surgical complications will be recorded. Percentage that candidates suffered from surgical complications of surgical cases for both group will be reported.
Time Frame
1 years
Title
Incidence of post-operative pancreatic fistula
Description
Post-operative pancreatic fistula (POPF) will be accessed byInternational Study Group of Pancreatic Surgery (ISGPS) standards; Incidence of post-operative pancreatic fistula of surgical cases in both group will be reported.
Time Frame
1 years
Title
Incidence of delayed gastric emptying
Description
Delayed gastric emptying (DGE) will be accessed byInternational Study Group of Pancreatic Surgery (ISGPS) standards; Incidence of DGE of surgical cases in both group will be reported.
Time Frame
1 years
Title
Incidence of post-operative hemorrhage
Description
Post-operative hemorrhage (POH) will be accessed byInternational Study Group of Pancreatic Surgery (ISGPS) standards; Incidence of POH of surgical cases in both group will be reported.
Time Frame
1 years
Title
Incidence of surgical site infection
Description
Surgical site infection was assessed as US CDC guidelines.Incidence of surgical site infection of surgical cases in both group will be reported.
Time Frame
1 years
Title
Incidence of other surgical complications
Description
Any other undesirable situations that considered complicated with surgery will be recorded. Incidence of other surgical complications of surgical cases in both group will be reported.
Time Frame
1 years
Title
Severe adverse events rate
Description
Feasibility of chemotherapy will be evaluated according to Common Terminology Criteria for Adverse Events, US NCI. Participants receiving neo-adjuvant, adjuvant or palliative chemotherapy will be accessed. Grade 3-5 adverse events, dose reduction or dose delay will be reported.
Time Frame
3 years
Title
Quality of life at 0.5 year after randomization
Description
EORTC QLQ-C30 (V3.0) will be enrolled to evaluate quality of life.
Time Frame
0.5 year
Title
Quality of life at 1 year after randomization
Description
EORTC QLQ-C30 (V3.0) will be enrolled to evaluate quality of life.
Time Frame
1 year
Title
Quality of life at 2 years after randomization
Description
EORTC QLQ-C30 (V3.0) will be enrolled to evaluate quality of life.
Time Frame
2 years
Title
Quality of life at 3 years after randomization
Description
EORTC QLQ-C30 (V3.0) will be enrolled to evaluate quality of life.
Time Frame
3 years
Title
Performance status at 0.5 year after randomization
Description
Karnofsky Performance Status Scale will be enrolled to evaluate Performance status.
Time Frame
0.5 year
Title
Performance status at 1 year after randomization
Description
Karnofsky Performance Status Scale will be enrolled to evaluate Performance status.
Time Frame
1 year
Title
Performance status at 2 years after randomization
Description
Karnofsky Performance Status Scale will be enrolled to evaluate Performance status.
Time Frame
2 years
Title
Performance status at 3 years after randomization
Description
Karnofsky Performance Status Scale will be enrolled to evaluate Performance status.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with pancreatic cancer staged at cT4NxM0(AJCC Cancer Staging Manual, 8th Edition) based on contrast enhanced CT&MRI scan and tumor markers; Age > 18 year and <80 year; Agree to participate in the study with signed informed consent. Exclusion Criteria: Evidence of metastasis based on physical examination, enhanced CT or enhanced MRI; Poor performance status and/or co-morbidity precluding pancreatectomy and chemotherapy; Focal vessel narrowing or contour irregularity revealed by radiology examinations; Economic situations cannot afford designed treatment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yi Miao, MD, PhD
Phone
+86-25-68136508
Email
miaoyi@njmu.edu.cn
Facility Information:
Facility Name
The First Affiliated Hospital of Nanjing Medical University
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210029
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yi Miao, MD, PhD
Phone
+86-25-68136508
Email
miaoyi@njmu.edu.cn

12. IPD Sharing Statement

Citations:
PubMed Identifier
25427123
Citation
Ryan DP, Hong TS, Bardeesy N. Pancreatic adenocarcinoma. N Engl J Med. 2014 Nov 27;371(22):2140-1. doi: 10.1056/NEJMc1412266. No abstract available.
Results Reference
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PubMed Identifier
25936471
Citation
Zhang H, Wroblewski K, Jiang Y, Penney BC, Appelbaum D, Simon CA, Salgia R, Pu Y. A new PET/CT volumetric prognostic index for non-small cell lung cancer. Lung Cancer. 2015 Jul;89(1):43-9. doi: 10.1016/j.lungcan.2015.03.023. Epub 2015 Apr 9.
Results Reference
background
PubMed Identifier
26687001
Citation
Tang K, Lu W, Qin W, Wu Y. Neoadjuvant therapy for patients with borderline resectable pancreatic cancer: A systematic review and meta-analysis of response and resection percentages. Pancreatology. 2016 Jan-Feb;16(1):28-37. doi: 10.1016/j.pan.2015.11.007. Epub 2015 Dec 2.
Results Reference
background
PubMed Identifier
28055103
Citation
Siegel RL, Miller KD, Jemal A. Cancer Statistics, 2017. CA Cancer J Clin. 2017 Jan;67(1):7-30. doi: 10.3322/caac.21387. Epub 2017 Jan 5.
Results Reference
background
PubMed Identifier
22997452
Citation
Seufferlein T, Bachet JB, Van Cutsem E, Rougier P; ESMO Guidelines Working Group. Pancreatic adenocarcinoma: ESMO-ESDO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2012 Oct;23 Suppl 7:vii33-40. doi: 10.1093/annonc/mds224. No abstract available.
Results Reference
background
PubMed Identifier
195543
Citation
Fortner JG, Kim DK, Cubilla A, Turnbull A, Pahnke LD, Shils ME. Regional pancreatectomy: en bloc pancreatic, portal vein and lymph node resection. Ann Surg. 1977 Jul;186(1):42-50. doi: 10.1097/00000658-197707000-00007.
Results Reference
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PubMed Identifier
20379794
Citation
Chua TC, Saxena A. Extended pancreaticoduodenectomy with vascular resection for pancreatic cancer: a systematic review. J Gastrointest Surg. 2010 Sep;14(9):1442-52. doi: 10.1007/s11605-009-1129-7. Epub 2010 Apr 9.
Results Reference
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Divestment for Artery-involved Pancreatic Cancer

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