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Irinotecan, Oxaliplatin, and Capecitabine as First-Line Therapy in Treating Patients With Metastatic or Unresectable Locally Advanced Small Bowel Cancer

NCT00433550

CompletedPhase 2

Sponsor: Alliance for Clinical Trials in Oncology

Conditions: Small Intestine Adenocarcinoma, Recurrent Small Intestine Cancer

Interventions: capecitabine, irinotecan hydrochloride, oxaliplatin

Countries: United States

This phase II trial studies how well giving irinotecan hydrochloride together with oxaliplatin and capecitabine works as first-line therapy in treating patients with metastatic or unresectable locally advanced small bowel cancer. Drugs used in chemotherapy, such as irinotecan hydrochloride, oxaliplatin, and capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells.

Eligibility overview

Sex: ALL

Age: 18 Years to —

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria

* Confirmation UDP glucuronosyltransferase 1 family, polypeptide A complex locus (UGT1A1) TA indel genotype of 6/6, 6/7, or 7/7 after pre-registration but prior to registration
* Patient willingness to provide a serum sample for analysis for celiac disease (tissue transglutaminase antibodies)
* Small bowel adenocarcinoma, either metastatic or locally advanced and not surgically resectable; NOTE: periampullary carcinoma and appendiceal cancer are not eligible
* Histologic or cytologic confirmation of adenocarcinoma consistent with small bowel origin; biopsy can be of primary tumor or can be from a metastatic site if there is a primary small bowel tumor currently or previously present
* Measurable disease; for patients with lesions \>= 1 cm but \< 2 cm, spiral computed tomography (CT) scan imaging must be used for tumor assessments
* Life expectancy \>= 12 weeks
* Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1, or 2
* \>= 4 weeks since prior major surgery to time of registration
* \>= 2 weeks from completion of any radiation treatment
* Absolute neutrophil count (ANC) \>= 1,500/mm\^3
* Platelets \>= 100,000/mm\^3
* Serum glutamic oxaloacetic transaminase (SGOT) =\< 5 x upper normal limit (UNL); =\< 2.5 x UNL if no liver metastases
* Total bilirubin:

  * For 6/6 patients: =\< upper limit of normal (ULN)
  * For 6/7 or 7/7 patients: =\< 2.0 x ULN
* Hemoglobin \>= 9.0 g/dL
* Creatinine =\< 1.5 x UNL (if \> 1.5 x UNL, calculated creatinine clearance should be checked.; if it is \> 60 mL/min, then the patient is eligible for the study)
* Negative pregnancy test done =\< 7 days prior to registration, for women of childbearing potential only

Exclusion Criteria

* Prior chemotherapy regimen for advanced small bowel cancer (prior adjuvant chemotherapy with fluorouracil (5FU)/leucovorin is permitted if last dose was administered \>= 3 months prior to registration); prior oxaliplatin or irinotecan use as adjuvant therapy is not permitted
* Prior radiotherapy to \> 25% of bone marrow
* Active or uncontrolled infection
* Evidence of serious intercurrent illness (e.g., unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiac arrhythmia)
* Pregnant women; women of child-bearing potential and men must agree to use adequate contraception (diaphragm, birth control pills, injections, foams, intrauterine device \[IUD\], or abstinence, etc.) for the duration of study participation; if a woman becomes pregnant or suspects that she is pregnant while participating in this study, she should inform her treating physician immediately and all study treatment discontinued
* Nursing women; breast-feeding should be discontinued when the mother is treated with these agents
* Men or women of childbearing potential who are unwilling to employ adequate contraception
* Current evidence of other malignancy besides small bowel adenocarcinoma, with exception of non-melanoma skin cancer
* Known central nervous system metastases or carcinomatous meningitis
* Preexisting sensory neuropathy \>= grade 2 from any cause interfering with function
* Concurrent therapy with sorivudine, brivudine, lamivudine, or stavudine

Locations (115)

Hartford, Connecticut, United States
Boise, Idaho, United States
Cedar Rapids, Iowa, United States
Cedar Rapids, Iowa, United States
Des Moines, Iowa, United States
Des Moines, Iowa, United States
Des Moines, Iowa, United States
Des Moines, Iowa, United States
Des Moines, Iowa, United States
Des Moines, Iowa, United States
Sioux City, Iowa, United States
Sioux City, Iowa, United States
Sioux City, Iowa, United States
Chanute, Kansas, United States
Dodge City, Kansas, United States
El Dorado, Kansas, United States
Fort Scott, Kansas, United States
Independence, Kansas, United States
Kingman, Kansas, United States
Lawrence, Kansas, United States
Liberal, Kansas, United States
Newton, Kansas, United States
Parsons, Kansas, United States
Pratt, Kansas, United States
Salina, Kansas, United States
Wellington, Kansas, United States
Wichita, Kansas, United States
Wichita, Kansas, United States
Wichita, Kansas, United States
Wichita, Kansas, United States
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