University of Kansas Medical Center

Conditions

• Ampulla of Vater Carcinoma
• Appendix Carcinoma
• Carcinoma of Unknown Primary With Gastrointestinal Profile
• Colon Carcinoma
• Esophageal Carcinoma
• Gastric Carcinoma
• Gastroesophageal Junction Carcinoma
• Malignant Digestive System Neoplasm
• Rectal Carcinoma
• Small Intestinal Carcinoma

Eligibility

Eligible Ages

Over 18 Years

Eligible Sex

All

Accepts Healthy Volunteers

Yes

Criteria

Inclusion Criteria:

- * REGISTRATION ELIGIBILITY CRITERIA (STEP 1)

- Histologic confirmation of invasive cancer that is confirmed or suspected to
arise from the gastrointestinal (GI) tract

- Any stage for which FOLFOX-based chemotherapy is a clinically-indicated,
standard-of-care treatment (adjuvant, neoadjuvant, or first-line chemotherapy)

- Eligible primary tumor sites include the esophagus, gastroesophageal junction,
stomach, small intestine, ampulla of Vater, appendix, colon, rectum, and
cancers of unknown primary with suspected GI origin

- Prior systemic therapy for GI cancer (other than cycle 1 of FOLFOX-based
chemotherapy) is not allowed. Prior radiation-sensitizing chemotherapy is
permitted

- The planned duration of FOLFOX-based chemotherapy must be at least four cycles
(1 cycle = 14 days)

- Cycle 1, day 1 of FOLFOX-based chemotherapy must be completed 1 to 8 days prior
to registration

- Cycle 1, day 1 of FOLFOX-based chemotherapy must include minimum ordered doses
of oxaliplatin (≥ 65 mg/m^2) and infusional 5-FU (2400 mg/m^2/46 hours). Use of
the 5-FU bolus is at the discretion of the treating physician

- Patients who require primary prophylactic white blood cell growth factor with
cycle 1 of FOLFOX chemotherapy due to high risk for fever and neutropenia are
not eligible

- History of hypersensitivity reaction to oxaliplatin or other platinum-based
drugs, to fluorouracil, or to leucovorin, and the excipients in their
formulations are not eligible

- Age ≥ 18 years

- ECOG performance status ≤ 2

- Absolute neutrophil count (ANC) ≥ 1,000/mm^3

- Platelet count ≥ 100,000/mm^3

- Total bilirubin ≤ 3 x upper limit of normal (ULN)

- AST (SGOT)/ALT (SGPT) ≤ 5 x upper limit of normal (ULN)

- Calc. creatinine clearance ≥ 30 mL/min

- Not pregnant and not nursing, because this study involves agents that have
known genotoxic, mutagenic and teratogenic effects. Therefore, for women of
childbearing potential only, a negative pregnancy test done ≤ 30 days prior to
registration is required

- Patients with treated brain metastases are eligible if follow-up brain imaging
after CNS-directed therapy shows no evidence of progression

- Patients with known HIV infection are eligible if receiving effective
anti-retroviral therapy with undetectable viral load within 6 months prior to
registration

- Patients with known chronic hepatitis B virus (HBV) infection are eligible if
HBV DNA is undetectable when measured within 6 months prior to registration

- Patients with a known history of hepatitis C virus (HCV) infection are eligible
if HCV RNA is undetectable when measured at least 12 weeks after completion of
antiviral therapy

- Patients with known history or current symptoms of cardiac disease are eligible
if the New York Heart Association Functional Classification is class I or II

- Patients with a known history of congenital long QT syndrome are ineligible

- Patients with known DPD deficiency are ineligible

- * NON-PATIENT (ONCOLOGY PHYSICIAN OR ONCOLOGY ADVANCED PRACTICE PROVIDER
ELIGIBILITY:

- The non-patient provider participant is a medical oncologist or oncology
advanced practice provider with responsibility for signing and making necessary
modifications to chemotherapy orders for a subject assigned to the intervention
arm (Arm B). Non-patient participants may not be enrolled more than once over
the course of the study

- The non-patient participant must be proficient in the English language

- The non-patient participant must be age 21 years or older

Recruiting Locations

Study Contact

Detailed Description

The primary and secondary objectives of the study: PRIMARY OBJECTIVE: I. To compare the proportion of chemotherapy cycles with unplanned delays in patients receiving FOLFOX chemotherapy under standardized usual care (control) versus (vs) according to the PAGODA dose modification algorithm (intervention). SECONDARY OBJECTIVES: I. To compare the mean number of health care contact days (time toxicity) for patients receiving FOLFOX chemotherapy according to assignment to the control vs intervention arms. II. To compare the incidence moderate-to-severe neutropenia (absolute neutrophil count less than 1000/mm3 in patients receiving FOLFOX chemotherapy according to assignment to the control vs intervention arms. III. To compare the relative dose-intensity of bolus 5-FU, oxaliplatin, and infusional 5-FU in patients receiving FOLFOX chemotherapy according to assignment to the control vs intervention arms, both overall and among the subgroup of participants treated with curative intent. OUTLINE: This is an interventional study. Patients are randomized to 1 of 2 arms. ARM A: Patients receive chemotherapy delays and dose modifications at the discretion of the treating clinician during cycles 2-7 of SOC FOLFOX chemotherapy on study. ARM B: Patients receive chemotherapy delays and dose modifications based on PAGODA algorithm followed by treating clinician decision during cycles 2-7 of SOC FOLFOX chemotherapy on study.