- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT05350943
HAIC Combined With Toripalimab and Donafenib for Advanced BTC
Phase II Study to Evaluate the Efficacy and Safety of HAIC Combined With Toripalimab and Donafenib in Patients With Advanced Biliary Tract Cancer
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Forventet)
Fase
- Fase 2
Kontakter og plasseringer
Studiesteder
-
-
-
Shanghai, Kina, 200062
- Fudan University Shanghai Cancer Center
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- 18 to 80 years of age, of any sex;
- Histologically/Cytologically confirmed diagnosis of unresectable advanced adenocarcinoma of the gallbladder, intrahepatic bile duct and extrahepatic bile duct.
- At least one measurable lesion umder CT/MRI as defined by RECIST1.1 criteria
- Patients must have adequate organ and marrow function as defined below:
Blood test:
Hemoglobin (HB) ≥90 g/L Absolute neutrophil count (ANC) ≥1.5×10^9/L; Platelet (PLT) ≥80×10^9/L;
Biochemical test:
total bilirubin≤2×ULN (institutional upper limit of norm) AST(SGOT)/ALT(SGPT)≤2.5 ×ULN creatinine clearance≥ 50 ml/min as calculated by the Cockroft-Gault formula
- Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) score of 0-1;
- Indocyanine Green Retention Rates at 15 min (ICGR15<22%;
- Life expectancy of > 3 months;
Exclusion Criteria
- Patients with other malignant tumors should be excluded
- Female patients who are pregnant or breast-feeding. Female patients who are pregnant during the study should also exit.
- Patient has enter any other clinical trails within 4 weeks prior to study entry.
- Patient known with a severe and/or uncontrolled medical disease.
- Chronic non-healing wound/bone fracture
- History of organ transplant
- Patients with abnormal coagulation function (PT>16s, APTT>43s, TT>21s, Fbg<2g/L), those have bleeding tendency (14 days prior to randomization must meet: INR is within the normal range without any use of anticoagulants); patients treated with anticoagulants or vitamin K antagonists such as warfarin, heparin or analogous therapy; use for preventive purposes is permitted provided that the international normalized ratio of prothrombin time (INR) ≤ 1.5, take low-dose warfarin (1 mg PO, QD) or low-dose aspirin (do not exceed 100 mg per day);
- Previous history of aterial/venous thrombosis such as cerebrovascular accidents, pulmonary embolism or deep venous thrombosis within one year prior to patients recruitment.
- Hitstory of psychiatric drug abuse and hasn't come clean, or with psychiatric illness/social situations that would limit compliance with study requirements
- History of immunodeficiency, or other acquired/congenital immunodeficiency diseases
- Concomitant diseases that severely endanger the safety of the subject or affect the study completion according to the judgment of the investigator
- Willingness to sign a written informed consent document, with good compliance.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: HAIC+Toripalimab+Donafenib
HAIC(GEMOX)+Toripalimab+Donafenib
|
Etter vellykket perkutan leverarteriekanylering, ble arteriogram superior mesenterium og arteriogram levert, og etter å ha bekreftet at forsøkspersonene var kvalifisert for registrering i henhold til resultatene, ble leverarterien kanylert til den forhåndsbestemte posisjonen.
Kateteret ble koblet til en sprøytepumpe på avdelingen for kontinuerlig pumping av legemidler.
1000 mg/m^2 in 100ml saline solution IV, d1, Q3W
85 mg/m^2 in 500ml 5% glucose solution over 2 hours IV, d1, Q3W
3mg/kg (body weight < 60kg) or 240 mg(body weight>= 60kg)in 250 saline soluation, IV, Q3W
0.2mg. P.O, BID, continuously
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Objective response rate (ORR)
Tidsramme: through study completion, an average of 2 year
|
the sum of complete response rate and partial response rate
|
through study completion, an average of 2 year
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Disease Control rate (DCR)
Tidsramme: through study completion, an average of 2 year
|
the sum of complete response rate, partial response rate and stable disease rate
|
through study completion, an average of 2 year
|
|
Progression-free survival (PFS)
Tidsramme: through study completion, an average of 2 year
|
Time from randomization to disease progression
|
through study completion, an average of 2 year
|
|
Overall survival (OS)
Tidsramme: through study completion, an average of 2 year
|
Time from randomization to death for any cause
|
through study completion, an average of 2 year
|
|
Number of participants with treatment-related adverse events as assessed by NCI CTCAE v4.0.
Tidsramme: through study completion, an average of 2 year
|
Unforeseen medical events occurred when the subjects received drug treatment or research, but there is not necessarily a causal relationship with the drugs used. Severe adverse events |
through study completion, an average of 2 year
|
|
Quality of life questionnaire
Tidsramme: through study completion, an average of 2 year
|
The concept of comprehensively evaluating the quality of life
|
through study completion, an average of 2 year
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Neoplasmer etter histologisk type
- Neoplasmer
- Karsinom
- Neoplasmer, kjertel og epitel
- Adenokarsinom
- Fysiologiske effekter av legemidler
- Molekylære mekanismer for farmakologisk virkning
- Anti-infeksjonsmidler
- Antivirale midler
- Enzymhemmere
- Antimetabolitter, antineoplastisk
- Antimetabolitter
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Gemcitabin
- Oksaliplatin
Andre studie-ID-numre
- 2021-GZWK-04
Legemiddel- og utstyrsinformasjon, studiedokumenter
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