Pancreatic Cancer Research

Clinical trialPhase 2Completed

Panitumumab, Chemotherapy, and External-Beam Radiation Therapy in Treating Patients With Locally Advanced Pancreatic Cancer That Cannot be Removed by Surgery

Phase II Study of Panitumumab, Chemotherapy, and External Beam Radiation in Patients With Locally Advanced Pancreatic Cancer

Outcome
Outcome unknown
Phase
Phase 2
Status
Completed
Study type
Interventional
Start
June 2009
Expected end
May 2013
Enrollment
52 participants
Sites
281
Primary outcomes
One Year Survival Rate
Sponsor
Other
Results posted
2017-04-05
Last update
5 April 2017

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Brief summary public domain (ClinicalTrials.gov)

RATIONALE: Monoclonal antibodies, such as panitumumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Drugs used in chemotherapy, such as fluorouracil, capecitabine, and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. External-beam radiation therapy uses high-energy x-rays to kill tumor cells. Panitumumab may also stop the growth of pancreatic cancer by blocking blood flow to the tumor and make tumor cells more sensitive to radiation therapy. Giving panitumumab together with chemotherapy and radiation therapy may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving panitumumab together with chemotherapy and external-beam radiation therapy works in treating patients with locally advanced pancreatic cancer that cannot be removed by surgery.

Detailed description public domain (ClinicalTrials.gov)

OBJECTIVES: Primary * To evaluate the 1-year survival rate in patients with locally advanced pancreatic cancer treated with panitumumab and continuous infusion fluorouracil administered concurrently with external-beam radiotherapy followed by gemcitabine and panitumumab. Secondary * To determine overall survival, time to disease progression, confirmed response rate, duration of response, and time to treatment failure in patients treated with this regimen. * To determine adverse events in patients treated with this regimen. OUTLINE: * Panitumumab and chemoradiotherapy : Patients undergo external-beam radiotherapy once daily on days 1-5, 8-12, 15-19, 22-26, 29-33, and 36-38. Patients also receive panitumumab IV over 1 hour on days 1, 15, and 29 and fluorouracil IV continuously over 24 hours daily OR oral capecitabine twice daily beginning on day 1 and continuing through the last day of radiotherapy. * Panitumumab and chemotherapy: Beginning 4-6 weeks after completion of panitumumab and chemoradiotherapy, patients receive panitumumab IV over 1 hour on days 1 and 15 and gemcitabine IV over 30 minutes on days 1, 8, and 15. Treatment repeats every 28 days for 3 courses. Patients then proceed to maintenance therapy. * Maintenance therapy: Patients receive panitumumab IV over 1 hour on days 1 and 15. Treatment repeats every 28 days for 6 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed every 3 months for 2 years and then every 6 months for 1 year.

Posted results (ClinicalTrials.gov registry) · primary outcome public domain (ClinicalTrials.gov)

One Year Survival Rate [Baseline to 12 months]. Number, proportion of patients (95% Confidence Interval). Panitumumab (n=51): 0.502 (0.354 to 0.632).

Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)

Overall Survival [baseline to 2 years]. Median, months (95% Confidence Interval). Panitumumab (n=51): 12.1 (6.8 to 15.1).

Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)

Progression Free Survival (PFS) [baseline to 2 years]. Median, months (95% Confidence Interval). Panitumumab (n=51): 7.4 (3.7 to 8.6).

Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)

Confirmed Response Rate [baseline to 2 years]. Number, rate of confirmed response (95% Confidence Interval). Panitumumab (n=51): 0.059 (0.012 to 0.162).

Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)

Duration of Response [baseline to 2 years].

Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)

Time to Treatment Failure [baseline to 2 years]. Median, months (95% Confidence Interval). Panitumumab (n=51): 2.71 (1.54 to 4.24).