Lapatinib Ditosylate and Capecitabine in Treating Patients With Metastatic Pancreatic Cancer

Pancreatic Cancer Clinical Trial

Official title:

A Phase II Study of Lapatinib and Capecitabine in the Treatment of Metastatic Pancreatic Cancer.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00962312
• Other study ID #: 08-39 ICORG
• Secondary ID: ICORG-08-39EUDRA
• Status: Completed
• Phase: Phase 2
• First received: August 19, 2009
• Last updated: December 30, 2014
• Start date: January 2009

Study information

• Verified date: October 2012
• Source: ICORG- All Ireland Cooperative Oncology Research Group
• Contact: n/a
• Is FDA regulated: No
• Health authority: Ireland: Irish Medicines Board
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Lapatinib ditosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving lapatinib ditosylate together with capecitabine may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving lapatinib ditosylate together with capecitabine works in treating patients with metastatic pancreatic cancer.

Description:

OBJECTIVES:

Primary

• To evaluate the efficacy of lapatinib ditosylate and capecitabine as first-line therapy, in terms of overall survival, in patients with metastatic pancreatic cancer.

Secondary

• To evaluate the progression-free survival of patients treated with this regimen.

• To evaluate the overall response rate (complete and partial responses) in patients treated with this regimen.

• To evaluate the clinical benefit (complete response, partial response, or stable disease for ≥ 6 months) of this regimen in these patients.

• To evaluate the qualitative and quantitative toxicity associated with this regimen in these patients.

• To determine the intra-tumoral expression of ErbB1 (EGFR) and ErbB2 (HER2/neu) in these patients.

• To seek pilot information on the intra-tumoral expression of markers of tumor resistance and sensitivity to treatment, including resistance drug pump expression and growth factor receptor expression.

• To collect pre- and post-treatment serum samples from these patients for proteomic analyses to elucidate if any serum cancer marker profiles can be detected.

OUTLINE: This is a multicenter study.

Patients receive oral lapatinib ditosylate once daily on days 1-21 and oral capecitabine twice daily on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up every 6-12 weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 9
• Est. primary completion date: December 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed metastatic adenocarcinoma of the pancreas

• Measurable or non-measurable disease

• Measurable disease is defined as = 1 lesion that can be accurately measured in = 1 dimension (longest diameter to be recorded) as = 20 mm with conventional techniques or as = 10 mm with spiral CT scan

• No known brain metastases or leptomeningeal disease

PATIENT CHARACTERISTICS:

• ECOG performance status 0-1

• Life expectancy > 12 weeks

• ANC = 1,500/mm^3

• Platelet count = 100,000/mm^3

• Hemoglobin = 9 g/dL

• Albumin = 2.5 g/dL

• Serum bilirubin = 1.5 times upper limit of normal (ULN) (2.5 times ULN if Gilbert's syndrome is present)

• AST and ALT = 3 times ULN (5 times ULN if documented liver metastases are present)

• Creatinine < 1.5 times ULN

• Cardiac ejection fraction normal by ECHO or MUGA scan

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• Able to swallow and retain oral medication

• No gastrointestinal (GI) tract disease resulting in an inability to take oral medication, malabsorption syndrome, requirement for IV alimentation, or uncontrolled inflammatory GI disease (e.g., Crohn's disease or ulcerative colitis)

• No active hepatic or biliary disease, except for Gilbert's syndrome, asymptomatic gallstones, liver metastases, or stable chronic liver disease per investigator assessment

• No active cardiac disease within the past 6 months, including any of the following:

• Uncontrolled angina

• Clinically significant arrhythmia, except for asymptomatic atrial fibrillation requiring anticoagulation

• Myocardial infarction

• Uncontrolled or symptomatic congestive heart failure

• Any other cardiac condition that, in the opinion of the treating physician, would make this study unreasonably hazardous for the patient

• No concurrent uncontrolled illness including, but not limited to, ongoing or active infection or psychiatric illness/social situation that would limit compliance with study requirements

• No known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to lapatinib ditosylate or any of its excipients, capecitabine, or fluorouracil

• No known dihydropyrimidine dehydrogenase (DPD) deficiency

• No other malignancy within the past 5 years except for completely resected nonmelanoma skin cancer or successfully treated in situ carcinoma

PRIOR CONCURRENT THERAPY:

• Recovered from prior radiotherapy or surgery

• No prior surgical procedures affecting absorption

• No prior EGFR- or ErbB2-targeting therapies

• No prior capecitabine

• No prior chemotherapy for locally advanced or metastatic pancreatic cancer

• At least 3 months since prior adjuvant chemotherapy

• Prior fluorouracil allowed as a radiosensitizer only

• More than 30 days (or 5 half-lives) since prior investigational drugs

• No concurrent radiotherapy or surgery for metastatic cancer

• No concurrent combination antiretroviral therapy for HIV-positive patients

• No concurrent CYP3A4 inducers or inhibitors

• No other concurrent investigational agents or anticancer therapy (e.g., cytotoxic or biologic therapy)

• No concurrent herbal (alternative) medicines

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Pancreatic Cancer
• Pancreatic Neoplasms

Intervention

Drug:
• capecitabine

• lapatinib ditosylate

Locations

Country	Name	City	State
Ireland	Cork University Hospital	Cork
Ireland	Mercy University Hospital	Cork
Ireland	Adelaide and Meath Hospital, Dublin Incorporating the National Children's Hospital	Dublin
Ireland	Beaumont Hospital	Dublin
Ireland	Mater Misericordiae University Hospital	Dublin
Ireland	Mater Private Hospital	Dublin
Ireland	St. James's Hospital	Dublin
Ireland	St. Vincent's University Hospital	Dublin
Ireland	University College Hospital	Galway

Sponsors (1)

Lead Sponsor	Collaborator
ICORG- All Ireland Cooperative Oncology Research Group

Country where clinical trial is conducted

Ireland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	6-month survival rate		6 months	No
Secondary	Progression-free survival	Progression-free survival (PFS) will be measured as the number of days between patient's enrolment and his or her date of progression of disease. Patients who are still living six months after the last patient has been enrolled will be censored for the analyses, using the number of days between enrolment and the date of last follow-up. Disease progression will be determined according to definitions established in the modified response evaluation criteria in solid tumours (RECIST) (refer to Appendix G). For patients with non-measureable tumours disease progression will be determined by the treating physician in consultation with the Chief investigator for the study.	6 months	No
Secondary	Overall response rate	The overall response rate will be an aggregation of the complete responses and partial responses. For patients to be given the status of complete response or partial response a confirmatory disease assessment should be performed no less than four weeks after the criteria for response are first met.	up to 6 months	No
Secondary	Clinical benefit	A patient will be regarded as` having experienced clinical benefit if they have shown a complete response, a partial response, or stable disease for at least six months.	6 months	No
Secondary	Safety and tolerability		Throughout course of study	Yes
Secondary	Tumour biomarker analysis	Characterising the patient population by determination of intra-tumoural expression of ErbB1 (EGFR) and ErbB2 (Her2/neu).Seeking pilot information as to the intra-tumoural expression of markers of tumour resistance and sensitivity to treatment. Proteomic analysis of serum samples for potential markers.	Currently ongoing	No