A Phase I Study of S-1 Plus Irinotecan and Oxaliplatin in Advanced Gastrointestinal Malignancy (TIROX)

National Cancer Center (NCC)

Status and phase

Unknown

Phase 1

Conditions

Colorectal Neoplasm

Gastric Neoplasm

Secondary

Treatments

Drug: S-1, Irinotecan, Oxaliplatin

Study type

Interventional

Funder types

Other

Identifiers

NCT00506207

NCCCTS-06-166

Details and patient eligibility

About

This study is an open-label, single center, and a dose-escalating phase I study to determine the maximal tolerated dose and the recommended dose of S-1 combined with irinotecan/oxaliplatin in patients with unresectable or metastatic colorectal or gastric carcinoma.

Full description

Dose level and escalating schedule are followings;

S-1 (level 1/2, 3/4, 5/6: 60, 70, 80 mg/m2/day) every 12-h p.o. on days 1(evening)-15 (morning)
Irinotecan (level 1,2/3, 4/5, 6: 120, 130, 140, 150 mg/m2) mixed in d5w or normal saline 500 ml iv over 90 min on day 1
Oxaliplatin 85 mg/m2 fixed dose mixed in d5w 250 ml iv infusion over 2-h on day 1

Treatment will be administered every 3 weeks. Start at dose level 1. Thereafter, dose level 2, 3, 4, 5, and 6. If dose-limiting toxicity (DLT) occurs at dose level 1, dose level at -1 will follow

Dose escalation will be continued until more than one-third of the patients in a given cohort show dose-limiting toxicity (DLT) during treatment cycle 1. At least three patients will be enrolled in each cohort. Before escalating to the next dose level, all three patients should have received at least one treatment cycle. If none of the first three treated patients develops DLT in the first cycle at a specific dose level, dose escalation will be continued. If one of the first three treated patients develops DLT at any dose level, then three additional patients are to be entered on the same dose level. If only one in six patients at a given level experiences a DLT, escalation will proceed. The MTD is defined as the dose level at which at least one-third of patients experienced a DLT. The RD for the subsequent phase II study is defined as the preceding dose level before the MTD is attained. Intra-patient dose escalation will not be permitted. Treatment will be continued in the absence of disease progression or unacceptable toxicity with maximum 12 cycles. For purpose of determining the MTD, only DLT occurring during the first cycle of therapy will be considered.

DLTs are defined as any of following;

Grade 4 neutropenia lasting at least 7 days or grade 3 or 4 neutropenia associated with fever  38.3C as single axillary temperature or 38 C for 1-h
Grade 4 thrombocytopenia
Grade 3 or 4 non-hematological toxicity except alopecia, and nausea/vomiting
Grade 3 or 4 nausea/vomiting not reduced to grade 1 with aggressive antiemetic support
Inability of the patient to take 75% of the planned chemotherapy dose during the treatment period

Enrollment

23 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Histologically or cytologically confirmed unresectable or metastatic colorectal or gastric carcinoma
Eastern Cooperative Oncology Group (ECOG) performance status 0-2
Measurable disease, according to the RECIST criteria or non-measurable disease Measurable lesions
Previous adjuvant, palliative chemotherapy including 5-FU, oxaliplatin and irinotecan, molecular targeted therapy and/or radiotherapy is allowed
Adequate major organ functions
Patients should sign a written informed consent before study entry

Exclusion criteria

Prior history of peripheral neuropathy
Inadequate cardiovascular
Serious concurrent infection or nonmalignant illness
Other malignancy within the past 3 years except non-melanomatous skin cancer or carcinoma in situ of the cervix
Psychiatric disorder that would preclude compliance
Pregnant, nursing women or patients with reproductive potential without contraception
Patients receiving a concomitant treatment with drugs interacting with S-1 such as flucytosine, phenytoin, or warfarin et al.