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Neoadjuvant PDT in the Treatment of Cholangiocarcinoma

Primary Purpose

Cholangiocarcinoma Resectable

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Neoadjuvant PDT + radical surgery
Radical surgery
Sponsored by
First Affiliated Hospital Xi'an Jiaotong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cholangiocarcinoma Resectable focused on measuring Cholangiocarcinoma,Neoadjuvant therapy,Photodynamic therapy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with age between 18 to 75 years;
  • Patients'gender was not limited;
  • Patients with locally advanced cholangiocarcinoma who have a clear diagnosis of the primary disease and require surgical resection or potential surgical resection;
  • No history of radiotherapy and chemotherapy;
  • Willing to accept this clinical trial, sign informed consent and be able to cooperate with follow-up.

Exclusion Criteria:

  • Women during pregnancy or breastfeeding, and those with mental illness;
  • Patients allergic to porphyrin drugs, porphyria;
  • Long-term use of glucocorticoids or autoimmune suppression;
  • Surgical contraindication, including:

Child-Pugh C with hepatic encephalopathy Anyone with heart, lung, kidney dysfunction or other organ dysfunction, and cannot tolerate surgery.Hepatic ducts stone disease, who was diagnosed as Acute Cholangitis of Severe Type, especially complicated with bacteremia or septic shock. End stage disease, complicated with biliary cirrhosis or portal hypertension.Patients with long- term obstructive jaundice, dehydration, electrolyte disturbance or coagulation defects; Patients have the tendency or history of bleeding.

Sites / Locations

  • Yi Lv

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

neoadjuvant PDT + radical surgery

radical surgery

Arm Description

Photodynamic therapy for neoadjuvant treatment of cholangiocarcinoma

Patients with cholangiocarcinoma undergo radical surgical resection

Outcomes

Primary Outcome Measures

R0 resection rate
Compare the incidence of positive margins of bile duct after surgical resection of cholangiocarcinoma between the two groups
Local recurrence rate
Compare the local recurrence rate of cholangiocarcinoma between the two groups
Survival time
Compare the 5-year survival time of the two groups

Secondary Outcome Measures

Bilirubin level
Compare the Bilirubin level of the two groups
Complication rate
Compare the incidence of bile leakage, cholangitis, phototoxicity and other complications between the two groups
Tumor-free margin length
Compare the length of the tumor-free margin of the two groups of cholangiocarcinoma tissues

Full Information

First Posted
March 24, 2021
Last Updated
March 30, 2021
Sponsor
First Affiliated Hospital Xi'an Jiaotong University
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1. Study Identification

Unique Protocol Identification Number
NCT04824742
Brief Title
Neoadjuvant PDT in the Treatment of Cholangiocarcinoma
Official Title
A Prospective Randomized Controlled Study of Neoadjuvant PDT in the Treatment of Cholangiocarcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 1, 2021 (Anticipated)
Primary Completion Date
April 1, 2023 (Anticipated)
Study Completion Date
April 1, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
First Affiliated Hospital Xi'an Jiaotong 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
For patients with locally advanced cholangiocarcinoma with resectable margins, patients who meet the selection criteria are randomly divided into two groups A and B. Group A: neoadjuvant PDT therapy combined with radical surgery; Group B: radical surgery. This study aims to explore the clinical effectiveness and safety of neoadjuvant photodynamic therapy for cholangiocarcinoma, as well as its role in destroying local tumors and enhancing systemic inflammation.
Detailed Description
The average 5-year survival rate of patients with cholangiocarcinoma is about 5-10%. Only 30%-40% of patients have the opportunity to obtain radical surgery. Surgical resection is limited by the extent of tumor spread along the bile duct branches and segments, and the degree of involvement of the portal vein and (or) hepatic artery branches. Complete resection with negative margins (R0) is the only possible radical treatment. Only 60%-78% of radical surgery for cholangiocarcinoma are considered to achieve true R0 resection, and the tumor-free margin is often very short. Even after R0 resection, the recurrence rate is as high as 50%-76%. Photodynamic therapy is a tumor specific ablation method with small side effects and repeated treatments will not produce drug resistance. It provides a new prospect for the treatment of cholangiocarcinoma. For the current patients with locally advanced cholangiocarcinoma, neoadjuvant photodynamic therapy is used to make them resectable. Demotion and subsequent resection may potentially improve their results. Similarly, patients with resectable margins can benefit from tumor downgrading by increasing their chances of undergoing R0 resection. In order to increase the negative rate of resection margins, and to ensure sufficient tumor-free margins of the bile duct stumps, the research is still blank. For patients with locally advanced cholangiocarcinoma with resectable margins, patients who meet the selection criteria are randomly divided into two groups A and B. Group A: neoadjuvant PDT therapy combined with radical surgery; Group B: radical surgery. This study aims to explore the clinical effectiveness and safety of neoadjuvant photodynamic therapy, as well as its role in destroying local tumors and enhancing systemic inflammation.This study plans to enroll 50 patients. It is planned to complete the enrollment operation within 2 years, and the follow-up observation will be continued for 5 years after the operation. All patients are expected to complete neoadjuvant PDT treatment and radical surgery within 2 years, survival period (5 years survival rate), R0 resection rate and local recurrence rate are the main observation indicators, and the bilirubin level, the number of intraoperative freezing, the length of the tumor-free margin of the tumor tissue, and the incidence of complications (biliary leakage, cholangitis, phototoxicity) are the secondary observation indicators.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholangiocarcinoma Resectable
Keywords
Cholangiocarcinoma,Neoadjuvant therapy,Photodynamic therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
neoadjuvant PDT + radical surgery
Arm Type
Experimental
Arm Description
Photodynamic therapy for neoadjuvant treatment of cholangiocarcinoma
Arm Title
radical surgery
Arm Type
Active Comparator
Arm Description
Patients with cholangiocarcinoma undergo radical surgical resection
Intervention Type
Procedure
Intervention Name(s)
Neoadjuvant PDT + radical surgery
Intervention Description
Patients with cholangiocarcinoma will undergo radical surgery after photodynamic therapy
Intervention Type
Procedure
Intervention Name(s)
Radical surgery
Intervention Description
Patients with cholangiocarcinoma will only receive radical surgery
Primary Outcome Measure Information:
Title
R0 resection rate
Description
Compare the incidence of positive margins of bile duct after surgical resection of cholangiocarcinoma between the two groups
Time Frame
During operation
Title
Local recurrence rate
Description
Compare the local recurrence rate of cholangiocarcinoma between the two groups
Time Frame
1-year post operation
Title
Survival time
Description
Compare the 5-year survival time of the two groups
Time Frame
5-year post operation
Secondary Outcome Measure Information:
Title
Bilirubin level
Description
Compare the Bilirubin level of the two groups
Time Frame
1,3,6,12-month post operation
Title
Complication rate
Description
Compare the incidence of bile leakage, cholangitis, phototoxicity and other complications between the two groups
Time Frame
1, 2,3,4,5,6,7,8-week Post operation
Title
Tumor-free margin length
Description
Compare the length of the tumor-free margin of the two groups of cholangiocarcinoma tissues
Time Frame
During operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with age between 18 to 75 years; Patients'gender was not limited; Patients with locally advanced cholangiocarcinoma who have a clear diagnosis of the primary disease and require surgical resection or potential surgical resection; No history of radiotherapy and chemotherapy; Willing to accept this clinical trial, sign informed consent and be able to cooperate with follow-up. Exclusion Criteria: Women during pregnancy or breastfeeding, and those with mental illness; Patients allergic to porphyrin drugs, porphyria; Long-term use of glucocorticoids or autoimmune suppression; Surgical contraindication, including: Child-Pugh C with hepatic encephalopathy Anyone with heart, lung, kidney dysfunction or other organ dysfunction, and cannot tolerate surgery.Hepatic ducts stone disease, who was diagnosed as Acute Cholangitis of Severe Type, especially complicated with bacteremia or septic shock. End stage disease, complicated with biliary cirrhosis or portal hypertension.Patients with long- term obstructive jaundice, dehydration, electrolyte disturbance or coagulation defects; Patients have the tendency or history of bleeding.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yi Lv, MD,PHD
Phone
86-29-85323900
Email
luyi169@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rongfeng Wang, MD
Phone
86-29-85324467
Email
15877553630@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yi Lv, MD,PHD
Organizational Affiliation
China, Shaanxi First Affiliated Hospital of Xian JiaotongUniversity
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yi Lv
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710061
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yi Lv, MD,PHD
Phone
0086-13991200581
Email
luyi169@126.com
First Name & Middle Initial & Last Name & Degree
Xiaogang Zang, MD
Phone
0086-15877553630
Email
15877553630@163.com
First Name & Middle Initial & Last Name & Degree
Yi Lv, MD,PHD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
12767091
Citation
Wiedmann M, Caca K, Berr F, Schiefke I, Tannapfel A, Wittekind C, Mossner J, Hauss J, Witzigmann H. Neoadjuvant photodynamic therapy as a new approach to treating hilar cholangiocarcinoma: a phase II pilot study. Cancer. 2003 Jun 1;97(11):2783-90. doi: 10.1002/cncr.11401.
Results Reference
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PubMed Identifier
26561801
Citation
Wagner A, Wiedmann M, Tannapfel A, Mayr C, Kiesslich T, Wolkersdorfer GW, Berr F, Hauss J, Witzigmann H. Neoadjuvant Down-Sizing of Hilar Cholangiocarcinoma with Photodynamic Therapy--Long-Term Outcome of a Phase II Pilot Study. Int J Mol Sci. 2015 Nov 6;16(11):26619-28. doi: 10.3390/ijms161125978.
Results Reference
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Neoadjuvant PDT in the Treatment of Cholangiocarcinoma

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