Sunitinib in Treating Patients With Metastatic Pancreatic Cancer That Progressed After First-Line Therapy With Gemcitabine

National Cancer Institute (NCI)

Status and phase: Completed; Phase 2

Conditions: Stage IV Pancreatic Cancer; Duct Cell Adenocarcinoma of the Pancreas; Recurrent Pancreatic Cancer; Acinar Cell Adenocarcinoma of the Pancreas

Treatments: Drug: sunitinib malate

Study type: Interventional

Funder types: NIH

Identifiers

NCT00397787

NCI-2012-02823

CALGB-80603

U10CA031946 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This phase II trial is studying how well sunitinib works in treating patients with metastatic pancreatic cancer that progressed after first-line therapy with gemcitabine. Sunitinib may stop the growth of pancreatic cancer by blocking blood flow to the tumor and by blocking some of the enzymes needed for cell growth.

Full description

PRIMARY OBJECTIVES:

I. To determine the response rate to sunitinib malate in patients with previously treated metastatic pancreatic adenocarcinoma.

SECONDARY OBJECTIVES:

I. To determine the duration of response, progression-free survival and overall survival of sunitinib malate in patients with previously treated metastatic pancreatic adenocarcinoma.

II. To determine the safety of sunitinib malate in patients with previously treated metastatic pancreatic adenocarcinoma.

OUTLINE: This is a multicenter, nonrandomized study.

Patients receive oral sunitinib malate daily on days 1-28. Treatment repeats every 6 weeks in the absence of disease progression or unacceptable toxicity.

After completion of study, patients are followed every 3 months until 2 years from study entry or until disease progression.

Enrollment: 64 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Histologic or cytologic documentation of pancreatic adenocarcinoma with evidence of disease progression following first-line therapy is required

• No brain metastases

• Patients with measurable disease

  • Lesions that can be accurately measured in at least one dimension (longest diameter to be recorded as >= 20 mm with conventional techniques or as>= 10 mm with spiral computed tomography (CT) scan; of particular note, the primary pancreatic tumor does not constitute measurable disease; therefore, patients with locally advanced pancreatic cancer as the sole site of disease are not eligible

• Patients must have received one of the following prior therapies containing gemcitabine:

  • One and only one prior therapy for metastatic disease with gemcitabine, or a gemcitabine-containing cytotoxic combination, or
  • One prior chemoradiation therapy containing gemcitabine for inoperable locally advanced pancreatic cancer, as long as the patient has subsequently progressed and has measurable disease outside a radiation port, or
  • One prior adjuvant chemotherapy regimen or chemoradiation therapy containing gemcitabine if the patient subsequently progressed within 3 months of completion of adjuvant therapy; patients who have received chemoradiation in the adjuvant setting must have measurable disease outside the radiation port

• No prior therapy with any other antiangiogenic agent (e.g., bevacizumab, sorafenib, pazopanib, AZD2171, PTK787, VEGF Trap, etc.)

• At least 4 weeks must have elapsed prior to initiation of treatment since the completion of chemotherapy and/or radiation therapy

• At least 4 weeks must have elapsed prior to registration since any major surgery

• Prior erlotinib is permitted; the last dose must have been administered 14 or more days prior to initiation of treatment; all erlotinib related side effects must have resolved to < grade 1 prior to registration

• No significant cardiac disease including:

  • QTc prolongation (defined as a QTc interval equal to or greater than 500 msec) or other significant EKG abnormalities
  • History of myocardial infarction, cardiac arrhythmia, stable/unstable angina, symptomatic congestive heart failure, or coronary/peripheral artery bypass graft or stenting within 12 months prior to registration
  • History of class III or IV heart failure within 12 months prior to registration as defined by the NYHA functional classification system

• In addition, patients with history of hypertension must be well controlled (< 140/90) on a regimen of anti-hypertensive therapy

• Patients with a history of hypothyroidism are eligible, provided they are currently euthyroid

• The use of inhibitors and inducers of CYP3A4 is not permitted:

  • The following inhibitors of CYP3A4 is prohibited within 7 days before beginning and during treatment with sunitinib:

    • Azole antifungals (ketoconazole, itraconazole)
    • Diltiazem
    • Clarithromycin
    • Erythromycin
    • Verapamil
    • Delavirdine
    • HIV protease inhibitors (indinavir, saquinavir, ritonavir, atazanavir, nelfinavir)

  • The following inducers of CYP3A4 are prohibited within 12 days before beginning and during treatment with sunitinib:

    • Rifampin
    • Rifabutin
    • Carbamazepine
    • Phenobarbital
    • Phenytoin
    • St. John's wort
    • Efavirenz
    • Tipranavir

  • Other inhibitors or inducers of CYP3A4 may be used if necessary, but their use is discouraged

• The use of agents with proarrhythmic potential (e.g., quinidine, procainamide, disopyramide, sotalol, probucol, bepridil, haloperidol, risperidone, indapamide, flecainide) is not permitted during the study

• ECOG performance status 0-2

• No history of cerebrovascular accident (CVA) or transient ischemic attack within 12 months prior to registration

• No history of pulmonary embolism within the past 6 months

• Patients who require use of therapeutic doses of coumadin-derivative anticoagulants such as warfarin are excluded, although doses of up to 2 mg daily are permitted for prophylaxis of thrombosis; Note: Low molecular weight heparin is permitted provided the patient's PT INR is < 1.5

• No serious or non-healing wound, ulcer, or bone fracture

• No history (within 6 months) of significant bleeding events (e.g., upper or lower GI bleeding, hemoptysis, or hematuria), abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 28 days of treatment

• No evidence of duodenal invasion by the tumor on CT scan

• No "currently active" second malignancy other than non-melanoma skin cancers; patients are not considered to have a "currently active" malignancy if they have completed therapy and are considered by their physician to be at less than 30% risk of relapse

• Non-pregnant and not breast feeding; pregnant women are excluded from this study because sunitinib is an antiangiogenic agent with the potential for teratogenic or abortifacient effects; because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with sunitinib, breastfeeding should be discontinued if the mother is treated with sunitinib malate

• ANC >= 1,500/μl

• Platelet count >= 100,000/μl

• Bilirubin < 1.5 mg/dL

• PT and PTT =< 1.5 X ULN

• Creatinine =< 1.5 mg/dL

• AST (SGOT) =< 2.5 X ULN if no liver metastases (=< 5 X ULN if liver metastases)

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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64 participants in 1 patient group

Treatment (sunitinib malate)

Experimental group

Description:

Patients receive oral sunitinib malate daily on days 1-28. Treatment repeats every 6 weeks in the absence of disease progression or unacceptable toxicity.

Treatment:

Drug: sunitinib malate