Metronomic Capecitabine, Oxaliplatin and UGT1A1 Genotype-directed Irinotecan in Metastatic Pancreatic Cancer Patients

Official title

A Phase II Study of Metronomic Capecitabine, Oxaliplatin and UGT1A1 Genotype-directed Irinotecan in Metastatic Pancreatic Cancer Patients.

Overview

This is a single-centre, non-randomized, open label phase II trial to be conducted at the National Cancer Centre, Singapore (NCCS). Patients diagnosed with metastatic PDAC will be eligible to enrol. The investigators hypothesize the anticancer activity of low dose OXIRI (LD-OXIRI) regimen comprising of metronomic oxaliplatin (O) and metronomic capecitabine (xeloda; X) in combination with UGT1A1-directed dosing of irinotecan (IRI) to be a tolerable regimen in patients with advanced PDAC and will lead to a favourable response rate. Patients will be prospectively enrolled in two stages - In stage 1, patients will be recruited and evaluated for response and toxicity. In stage 2, more patients will be recruited for further evaluation of response and toxicity.

Detailed description

Eligible patients will be recruited from the National Cancer Centre, Singapore (NCCS). Patients will be referred for assessment by the primary physician to a study investigator for screening. Informed written consent for entry into the trial will be obtained from the patient by a delegated investigator.

All patients eligible for study entry will receive the LD-OXIRI regimen at the National Cancer Centre, Singapore. All concomitant medication taken during the study must be recorded. If a drug is administered prophylactically, this must be noted. The patients will not receive any other investigational drugs while on this study.

There will be a screening period of 28 days, a treatment period till disease progression or unacceptable toxicity, and a post-treatment follow up period of up to 24 months.

Interventions

• Drug Low Dose OXIRI (LD-OXIRI)
  The LD-OXIRI regimen will be administered in the following sequence: * metronomic capecitabine (Xeloda; X) 650mg/m2 will administered twice a day on a daily a continuous basis; * intravenous metronomic oxaliplatin (O) 50 mg/m2 will be infused over 120 minutes on days 1 and 8 of a 21 day-cycle; followed by * intravenous irinotecan (I) will be infused over 90 minutes on days 1 and 8 of a 21 day-cycle. The dose of irinotecan will be based on the particular patient's UGT1A1\*6 and UGT1A1\*28 genoty

Primary outcome measures

• Overall Response Rate (ORR). [Time frame: Up to 3 years.]
• Clinical Benefit Rate (CBR). [Time frame: Up to 3 years.]
• The Grade 3-5 Toxicity Rate. [Time frame: Up to 3 years.]

Secondary outcome measures (7)

• Maximum plasma concentration [(Cmax)] of low dose Capecitabine and its intermediary metabolites (5'-deoxy-5-fluorocytidine [DFCR] and 5'- deoxy-5-fluorouridine [DFUR]) and 5FU. [Time frame: At predose, 1 hr, end of irinotecan infusion on Cycle 1 Day 1 (each cycle is 21 days)]
• Trough concentration of low dose capecitabine and its intermediary metabolites and 5FU. [Time frame: At predose of Cycle 2 Day 1 and Cycle 3 Day 1 (each cycle is 21 days)]
• Immunophenotyping from extracted peripheral blood mononuclear cells (PBMCs) - measurement of cytokine and chemokine concentrations in picograms per milliliters using multiplex flow cytometry. [Time frame: Up to 3 years.]
• Genomic analysis of circulating tumour DNA (ctDNA). [Time frame: Up to 3 years.]
• Identification of exosomal proteins secreted by extracellular vesicles from plasma. [Time frame: Up to 3 years.]
• Progression-free survival (PFS). [Time frame: Up to 3 years.]
• Overall survival (OS). [Time frame: Up to 3 years.]

Eligibility criteria

Inclusion criteria

The patient must meet all of the inclusion criteria to participate in the study.

• Aged above 21
• Histopathological diagnosis of pancreatic cancer
• Advanced disease not amenable to curative resection (locally advanced or metastatic disease)
• Measureable disease by RECIST 1.1 criteria
• Life expectancy of at least 12 weeks
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2
• Adequate hematologic function (granulocyte count ≥ 1.5 × 10\*\*9/L, platelet count ≥ 100 × 10\*\*9/L),
• Adequate hepatic function (total bilirubin ≤ 1.5 x the upper limits of normal \[ULN\], AST and ALT, ALP ≤ 3 x ULN or < 5 x ULN in case of hepatic involvement),
• Adequate renal function (creatinine clearance > 50 mL/min) will be eligible for inclusion into the study.
• Able to provide written and informed consent

Exclusion criteria

Any patient meeting any of the exclusion criteria at baseline will be excluded from participation.

• History of another malignancy within 5 years prior to registration. Patients with a past history of adequately treated carcinoma-in-situ, basal cell carcinoma of the skin, squamous cell carcinoma of the skin, and superficial transitional cell carcinoma of the bladder are eligible. Patients with a history of other malignancies are eligible if they have been continuously disease free after definitive primary treatment for at least 5 years.
• Untreated CNS metastases or leptomeningeal disease. Patients with brain metastases that have been treated, and are asymptomatic, and have been stable for 3 or more months after treatment are allowed. A baseline CT or MRI brain is only required if there is clinical suspicion of CNS involvement.
• Concurrent illness, including severe infection, that may jeopardise the ability of the patient to undergo the procedures outlined in this protocol with reasonable safety
• Serious medical or psychiatric conditions that might limit the ability of the patient to comply with the protocol
• Treatment with palliative chemotherapy or radiotherapy within 4 weeks prior to enrolment into the study
• Major surgery within two weeks prior to enrolment into the study
• Patients on chronic immunosuppressive therapy
• Pregnancy, lactation or inadequate contraception. Women of childbearing potential must have a negative pregnancy test within 3 days of enrolment and agree to use a reliable means of contraception. Men must have been surgically sterilised or agree to use a barrier method of contraception
• Patients on anticoagulant therapy with vitamin K antagonists.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

Singapore · 1 center

• National Cancer Centre, Singapore — Singapore

Identifiers

NCT: NCT05929885 · LDOXIRI-PDAC-01

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗