RALOX as Second Line Treatment for Advanced Malignant Biliary System Tumor (RALOXBTC)
Primary Purpose
Cholangioadenoma
Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Raltitrexed combined with oxaplatin
Sponsored by
About this trial
This is an interventional treatment trial for Cholangioadenoma focused on measuring cholangioadenoma, first line treatment failure, raltitrexed;, oxaliplatin
Eligibility Criteria
Inclusion Criteria
- 18-75 years old.
- Patients with unresectable advanced advanced Gallbladder carcinoma or Cholangiocarcinoma confirmed by histology or cytology.
- First-line chemotherapy failure (toxic side effects can not be tolerated, disease progression during treatment or relapse after treatment) ;Or the disease recurred within 6 months after completion of adjuvant chemotherapy.
- At least one measurable lesion according to RECIST1.1 criteria.
- ECOG: 0 ~ 1.
- Life expectancy ≥ 12 Weeks.
- The major organs were functioning normally, and the laboratory examination results within 1 week met the following conditions before enrollment:①Absolute neutrophil count (ANC)≥1.5×109/L ②Platelet count(PLT)≥80.0 × 109/L ③Hemoglobin concentration(HB) ≥90g/L④ Total bilirubin(TB)≤1.5×ULN ⑤ Serum creatinine (Cr)≤l.5×ULN ,Endogenous creatinine clearance >60ml/min(Cockcroft-Gault Formula )⑥Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), Alkaline phosphatase(AP): ≤3 ×ULN (≤5 ×ULN for metastases to liver).
- Sign the informed consent voluntarily.
Exclusion Criteria
- Allergic to any research drug and its excipients.
- Prior use of raltitrexed or oxaliplatin.
- History of other malignancies, except cured Basal cell or squamous Cell Carcinoma of the skin and carcinoma in situ of the cervix.
- There is a history of brain metastases.
- History of psychotropic drug abuse and cannot quit or has a mental disorder.
- Uncontrolled chronic infectious and non-infectious diseases.
- Active or clinically poorly controlled severe infection
- Other conditions that the researchers think should be ruled out.
Sites / Locations
- the Second Affiliated Hospital of Medical College of Zhejiang UniversityRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
RALOX
Arm Description
Raltitrexed combined with oxaplatin
Outcomes
Primary Outcome Measures
PFS(Progression Free Survival)
PFS is defined as the time interval from initiation of treatment to the first date of documented tumor progression or death from any cause, whichever occurs first.
Secondary Outcome Measures
ORR
Overall Response Rate
OS
Overall Survival
DCR
Disease Control Rate
Qol ( quality of life )
EORTC-QLQ-C30 is a cancer-specific instrument
AE
Adverse Event
Full Information
NCT ID
NCT05148143
First Posted
November 18, 2021
Last Updated
December 6, 2021
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
1. Study Identification
Unique Protocol Identification Number
NCT05148143
Brief Title
RALOX as Second Line Treatment for Advanced Malignant Biliary System Tumor
Acronym
RALOXBTC
Official Title
Raltitrexed Combined With Oxaplatin as Second Line Treatment for Advanced Malignant Biliary System Tumor
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2020 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The purpose of this study was to explore the safety and efficacy of raltitrexed combined with oxaplatin as second line treatment for advanced malignant biliary system tumor.
Detailed Description
The purpose of this study was to explore the safety and efficacy of raltitrexed combined with oxaplatin as second line treatment for advanced malignant biliary system tumor. Single arm,phase II study for patients with cholangiocarcinoma or gallbladder carcinoma after first line treatment failure to explore effection and safety of raltitrexed combined with oxaplatin as second line treatment;Sample size:50.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholangioadenoma
Keywords
cholangioadenoma, first line treatment failure, raltitrexed;, oxaliplatin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
RALOX
Arm Type
Experimental
Arm Description
Raltitrexed combined with oxaplatin
Intervention Type
Drug
Intervention Name(s)
Raltitrexed combined with oxaplatin
Other Intervention Name(s)
Sai Wei Jian
Intervention Description
Raltitrexed combined with oxaplatin as second line treatment of cholangiocarcinoma
Primary Outcome Measure Information:
Title
PFS(Progression Free Survival)
Description
PFS is defined as the time interval from initiation of treatment to the first date of documented tumor progression or death from any cause, whichever occurs first.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
ORR
Description
Overall Response Rate
Time Frame
24 months
Title
OS
Description
Overall Survival
Time Frame
36 months
Title
DCR
Description
Disease Control Rate
Time Frame
24 months
Title
Qol ( quality of life )
Description
EORTC-QLQ-C30 is a cancer-specific instrument
Time Frame
24 months
Title
AE
Description
Adverse Event
Time Frame
12 months
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
18-75 years old.
Patients with unresectable advanced advanced Gallbladder carcinoma or Cholangiocarcinoma confirmed by histology or cytology.
First-line chemotherapy failure (toxic side effects can not be tolerated, disease progression during treatment or relapse after treatment) ;Or the disease recurred within 6 months after completion of adjuvant chemotherapy.
At least one measurable lesion according to RECIST1.1 criteria.
ECOG: 0 ~ 1.
Life expectancy ≥ 12 Weeks.
The major organs were functioning normally, and the laboratory examination results within 1 week met the following conditions before enrollment:①Absolute neutrophil count (ANC)≥1.5×109/L ②Platelet count(PLT)≥80.0 × 109/L ③Hemoglobin concentration(HB) ≥90g/L④ Total bilirubin(TB)≤1.5×ULN ⑤ Serum creatinine (Cr)≤l.5×ULN ,Endogenous creatinine clearance >60ml/min(Cockcroft-Gault Formula )⑥Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), Alkaline phosphatase(AP): ≤3 ×ULN (≤5 ×ULN for metastases to liver).
Sign the informed consent voluntarily.
Exclusion Criteria
Allergic to any research drug and its excipients.
Prior use of raltitrexed or oxaliplatin.
History of other malignancies, except cured Basal cell or squamous Cell Carcinoma of the skin and carcinoma in situ of the cervix.
There is a history of brain metastases.
History of psychotropic drug abuse and cannot quit or has a mental disorder.
Uncontrolled chronic infectious and non-infectious diseases.
Active or clinically poorly controlled severe infection
Other conditions that the researchers think should be ruled out.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ying Yuan, Ph.D&MD
Phone
13858193601
Email
yuanying1999@zju.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ying Yuan, Ph.D&MD
Organizational Affiliation
Second Affiliated Hospital, School of Medicine, Zhejiang University
Official's Role
Principal Investigator
Facility Information:
Facility Name
the Second Affiliated Hospital of Medical College of Zhejiang University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ying Yuan
Phone
13858193601
Email
yuanying1999@zju.edu.cn
First Name & Middle Initial & Last Name & Degree
Ying Yuan, Ph.D & MD
12. IPD Sharing Statement
Learn more about this trial
RALOX as Second Line Treatment for Advanced Malignant Biliary System Tumor
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