Irinotecan Liposomes +5-FU/LV Versus Capecitabine in Patients of Recurrence After Resection of Resectable BTC

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorSir Run Run Shaw Hospital

About this trial

Irinotecan liposome combined with 5-FU/LV has shown good efficacy and has certain advantages in reducing the adverse reactions of conventional chemotherapy drugs. Adjuvant treatment of high-risk factors after surgery for biliary tract tumors can be further explored and attempted. Therefore, this study intends to conduct an exploratory study comparing oral capecitabine with irinotecan liposome +5-FU/LV for adjuvant therapy in high-risk patients after resection of resectable biliary malignancies, and evaluate the effectiveness and safety of irinotecan liposome +5-FU/LV as adjuvant therapy for high-risk patients after resection of resectable biliary malignancies. So it can provide more treatment options for patients with postoperative adjuvant therapy of biliary tract malignant tumor.

The DFS rate one year after surgery for biliary malignancy was assumed to be 51.4% with a maximum response rate of poor efficacy and 71.4% with a minimum response rate of good efficacy. A two-stage design was adopted with α=0.05 and certainty (1-β) =0.8, and Minimax was adopted. If a response occurs in 7 out of 14 patients or less, treatment options are rejected; In the second phase, if 24 or fewer responses occur in 38 patients, the protocol is rejected. A total of 38 samples were designed in two stages. The 1-year DFS rate was at least 65.8% in the total population of the test and control groups.

Eligibility criteria

Qualifiers

Age 18-75 years old.

Patients with histologically confirmed, resectable biliary malignancies with R0 resection.

Postoperative pathology indicated the following risk factors: positive lymph nodes, vascular invasion, nerve invasion and so on.

Has not received systemic chemotherapy before.

Disqualifiers

Patients allergic to the investigational drug and its excipients.

Known or suspected central nervous system or lymphatic metastasis.

Cannot discontinue use or has not discontinued use of CYP3A, CYP2C8, and UGT1A1 potent depressants or inducers (e.g., anticonvulsants [phenytoin, phenobarbital, or carbamazepine] within 2 weeks prior to enrollment), rifampicin, rifambutin, St.John's Wort, Grapefruit juice, clarithromycin, Itraconazole, Lopinavir, Nefazodone, Nelfinavir, Ritonavir, Saquinavir, Terrapivir, voriconazole, Azanavir, Gefilozil, Indinavir, etc.).

There are signs and symptoms of intestinal obstruction.

Trial design

Treatments tested in this trial

  • Irinotecan Liposome
  • Capecitabine

Treatment groups

76 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Sir Run Run Shaw Hospital

Lead sponsor

Zhejiang Cancer Hospital

Collaborator

RenJi Hospital

Collaborator

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Collaborator

Fujian Provincial Hospital

Collaborator

Ningbo No. 1 Hospital

Collaborator

Shaoxing People's Hospital

Collaborator

Southern Medical University, China

Collaborator

First Affiliated Hospital, Sun Yat-Sen University

Collaborator