A Real-world Study of the Safety and Efficacy of Surufatinib in the Treatment of Biliary Tract Carcinoma
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|ClinicalTrials.gov Identifier: NCT05064852|
Recruitment Status : Not yet recruiting
First Posted : October 1, 2021
Last Update Posted : October 1, 2021
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|Condition or disease||Intervention/treatment|
|Biliary Tract Carcinoma||Drug: Surufatinib|
|Study Type :||Observational|
|Estimated Enrollment :||200 participants|
|Official Title:||A Real-world Study of the Safety and Efficacy of Surufatinib in the Treatment of Biliary Tract Carcinoma|
|Estimated Study Start Date :||September 20, 2021|
|Estimated Primary Completion Date :||December 20, 2022|
|Estimated Study Completion Date :||December 20, 2023|
Patients with BTC visited the site from 2021 to 2023 and received Surufatinib therapy.
The study is a real-world study. According to the actual medical history of patients, the usage of Surufatinib was collected.
- Progression-free survival (PFS) [ Time Frame: 6 months after the last patient enrolled ]PFS was defined as the length of time from the administration of the first-dose until disease progression or death from any cause before disease progression.
- Safty [ Time Frame: up to 4 weeks after the last dose ]The rate of AE and SAE in patients with BTC receiving surufatinib,AEs/SAEs were evaluated using NCI-CTCAE v5.0
- Disease Control Rate(DCR) [ Time Frame: 6 months after the last patient enrolled ]DCR was defined as the percentage of patients with complete response (CR), partial response (PR) and stable disease (SD) according to Response Evaluation Criteria in Solid Tumours (RECIST).
- Overall survival (OS) [ Time Frame: 6 months after the last patient enrolled ]
OS was defined as the length of time from the administration of the first-dose until death from any cause.
or lost of follow-up
- Objective Response Rate (ORR) [ Time Frame: 6 months after the last patient enrolled ]ORR was defined as the percentage of patients with complete response (CR) and partial response (PR) according to Response Evaluation Criteria in Solid Tumours (RECIST).
- QoL [ Time Frame: 6 months after the last patient enrolled ]Using quality of life questionnaire (EORTC QLQ-C30) to collect the score. Scale range is 30~126, higher values are considered to be a better outcome.
- Biomarkers [ Time Frame: before the first dose ]Explore the correlation between curative effect and different biomarkers, such as EGFR mutation, FGFR etc.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
|Ages Eligible for Study:||18 Years and older (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||Yes|
|Sampling Method:||Non-Probability Sample|
- Age ≥18, male or female;
- Patients with histologically or cytologically confirmed unresectable or metastatic BTC, including intrahepatic cholangiocarcinoma (IHCC), extrahepatic cholangiocarcinoma (EHCC), and gallbladder cancer (GBC); Surgical resection with positive margins are allowed;
- ECOG score 0-2;
- Expected survival of ≥12 weeks;
- Confirmed measurable (or evaluable) lesions that meet the requirements of RECIST 1.1;
It is not less than 7 days since the end of the last systematic treatment, and the palliative treatment of the limited area is allowed
Treatment has been over 4 weeks;
- The function of major organs and bone marrow was basically normal;
- Fully understand this study, voluntarily participate in it, and sign the informed consent.
- Fertile male or female patients shall volunteer to use effective contraceptive methods, such as double barrier contraception, condoms, oral or injected contraceptives, and intrauterine devices, during the study period and within 90 days after the last dosing of the investigational drug. All-female patients will be considered fertile unless they have had natural menopause, or artificial menopause, or sterilization (such as hysterectomy, bilateral adnexectomy, or ovarian radiation)
- Fine basal skin that has been diagnosed with other malignant tumors within the past 5 years and has been effectively treated (Except for cell carcinoma, squamous cell carcinoma of the skin, or in situ cervical cancer and breast cancer after effective resection outside);
- Receiving other investigational drugs or approved or under development antitumor therapies;
- Patients with contraindications to Surufatinib (e.g., active bleeding, ulcers, intestinal perforation, bowel)Obstruction, medically uncontrolled hypertension, grade III-IV cardiac dysfunction, major surgery within 30 days, severe liver and kidney insufficiency, etc.);
- The patient has any current disease or condition that affects the absorption of the drug, or the patient cannot take it orally Surufatinib;
- Demonstrated allergy to any component of the test drug and/or its excipients;
- Pregnant (positive pregnancy test before dosing) or breast-feeding women;
- Patients with large pleural effusion or ascites requiring drainage;
- Taken a drug containing hyperforin perforatum within 3 weeks prior to the first study, or before taken other CYP3A4 strong inducer or inhibitor within 2 weeks;
- The investigator determined that liver metastases accounted for 50% or more of the total volume of the liver;
- Clinically intervened biliary obstruction was not in remission or required anti-infective therapy as determined by the investigator 14 days prior to the first study drug treatment;
- Previous liver transplantation;
- Clinically significant electrolyte abnormalities as determined by the investigator;
- Any other diseases with clinically significant metabolic abnormalities, abnormal physical observations, or abnormal laboratory findings, which are judged by the investigator as evidence that the patient has a disease or condition that is unsuitable for the study drug (e.g., epileptic seizures requiring treatment), or that would interfere with the interpretation of the study results, or that may put the patient at high risk.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05064852
|Contact: Yunfei Xu, M.D.||firstname.lastname@example.org|
|Responsible Party:||Qilu Hospital of Shandong University|
|Other Study ID Numbers:||
|First Posted:||October 1, 2021 Key Record Dates|
|Last Update Posted:||October 1, 2021|
|Last Verified:||September 2021|
|Studies a U.S. FDA-regulated Drug Product:||No|
|Studies a U.S. FDA-regulated Device Product:||No|
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type