Lapatinib, Cisplatin, Gemcitabine as First-Line Therapy in Treating Patients With Locally Advanced or Metastatic Urothelial Cancer
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Purpose
RATIONALE: Lapatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cisplatin, and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving lapatinib together with combination chemotherapy may kill more tumor cells.
PURPOSE: This phase I trial is studying the side effects and best dose of lapatinib when given together with cisplatin and gemcitabine as first-line therapy in treating patients with locally advanced or metastatic urothelial cancer.
| Condition | Intervention | Phase |
|---|---|---|
|
Bladder Cancer Transitional Cell Cancer of the Renal Pelvis and Ureter |
Drug: cisplatin Drug: gemcitabine hydrochloride Drug: lapatinib ditosylate Other: pharmacological study |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase I Study of Cisplatin, Gemcitabine and Lapatinib as First Line Treatment in Advanced/Metastatic Urothelial Cancer |
- Maximum tolerated dose of lapatinib ditosylate in combination with cisplatin/gemcitabine hydrochloride and cisplatin/gemcitabine hydrochloride based on the documentation of the acute dose-limiting toxicity in course 1 [ Designated as safety issue: Yes ]
- Pharmacokinetic profile of lapatinib ditosylate in combination with cisplatin/gemcitabine hydrochloride and cisplatin/gemcitabine hydrochloride [ Designated as safety issue: No ]
- Antitumor activity according to RECIST [ Designated as safety issue: No ]
| Estimated Enrollment: | 25 |
| Study Start Date: | November 2007 |
| Estimated Study Completion Date: | August 2012 |
| Estimated Primary Completion Date: | June 2012 (Final data collection date for primary outcome measure) |
OBJECTIVES:
Primary
- Determine the maximum tolerated dose and recommended doses of lapatinib ditosylate when administered with gemcitabine hydrochloride and cisplatin, and determine on the basis of acute dose-limiting toxicity in course 1 in patients with locally advanced or metastatic transitional cell carcinoma of the urothelial tract.
Secondary
- To determine any relationship between drug exposure and adverse events in these patients.
- To assess the antitumor activity in these patients.
OUTLINE: This is a multicenter, dose-escalation study of lapatinib ditosylate.
- Lapatinib ditosylate, cisplatin, and gemcitabine hydrochloride: Patients receive oral lapatinib ditosylate once daily on days 1-28, cisplatin IV on day 2, and gemcitabine hydrochloride IV over 30 minutes on days 1, 8, and 15. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity until the recommended dose of lapatinib ditosylate is determined.
- Lapatinib ditosylate, cisplatin, gemcitabine hydrochloride: Subsequently enrolled patients receive oral lapatinib ditosylate (beginning at one dose level below the recommended dose determined in the previous combination) once daily on days 1-21, cisplatin IV on day 1, gemcitabine hydrochloride IV over 30 minutes. Courses repeat every 3 weeks in the absence of disease progression or unacceptable toxicity.
All patients undergo blood sample collection periodically for pharmacokinetic analysis.
After completion of study treatment, patients are followed weekly.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
Histologically proven transitional cell carcinoma of the urothelial tract
- Metastatic or locally advanced disease
Measurable disease according to RECIST
- Involvement of at least one target not in previously irradiated fields
- Overexpressing HER1 and/or HER2 receptors (HER2 3+ by IHC OR HER2 FISH or CISH positive)
- No clinical signs of CNS involvement
PATIENT CHARACTERISTICS:
- WHO performance status 0-1
- ANC ≥ 1,500/mm³
- Thrombocytes > 100,000/mm³
- Bilirubin ≤ 1.5 times upper limit of normal (ULN)
- AST/ALT ≤ 3 times ULN
- Creatinine clearance ≥ 60 mL/min
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective double-barrier contraception during and for 3 months after completion of study treatment
- Cardiac ejection fraction normal
- Normal 12 lead ECG
No serious cardiac illness or medical condition within the past 6 months including, but not limited to, any of the following:
- Documented congestive heart failure
- High-risk uncontrolled arrhythmias
- Angina pectoris requiring antianginal medication
- Clinically significant valvular heart disease
- Evidence of transmural infarction on ECG
- Poorly controlled hypertension (e.g., systolic blood pressure [BP] > 180 mm Hg or diastolic BP > 100 mm Hg)
- No peripheral neuropathy > grade 1
- Able to swallow and retain oral medication
- No other malignancy within the past 3 years except basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix
- No active or uncontrolled infections, serious illnesses, malabsorption syndrome or medical conditions, hepatitis, HIV, and/or cirrhosis
- No psychological, familial, sociological, or geographical condition potentially hampering study protocol compliance or follow-up schedule
- No current active hepatic or biliary disease (with the exception of Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver metastases or stable chronic liver disease)
PRIOR CONCURRENT THERAPY:
- Recovered from any effects of surgery
- Intravesicle therapy for superficial disease allowed
Prior neoadjuvant or adjuvant chemotherapy allowed
- Must have a minimum interval of six months between the completion of neoadjuvant or adjuvant chemotherapy and the diagnosis of metastatic disease
- No prior chemotherapy for metastatic disease
- No radiotherapy within the past 4 weeks
- No drugs and herbal inducers or inhibitors of CYP3A4 (e.g., bergamottin or glabridin) within 10 days prior to study treatment and while receiving lapatinib ditosylate therapy
- No other concurrent anticancer therapy or investigational agents
- No other concurrent anticancer agents
- No concurrent treatment with other investigational therapy for other diseases or conditions
- No concurrent prophylactic antibiotics
- No concurrent prophylactic filgrastim (G-CSF)
- At least 14 days since prior and no concurrent herbal or dietary supplements
- No concurrent consumption of grapefruit juice
Contacts and Locations| Denmark | |
| Rigshospitalet - Copenhagen University Hospital | |
| Copenhagen, Denmark, 2100 | |
| Study Chair: | Gedske Daugaard, MD, DMSc | Rigshospitalet, Denmark |
More Information
Additional Information:
No publications provided
| Responsible Party: | European Organisation for Research and Treatment of Cancer - EORTC |
| ClinicalTrials.gov Identifier: | NCT00623064 History of Changes |
| Other Study ID Numbers: | EORTC-30061, EORTC-30061, EUDRACT-2006-002976-16, GSK-EORTC-30061 |
| Study First Received: | February 22, 2008 |
| Last Updated: | April 23, 2012 |
| Health Authority: | European Union: European Medicines Agency |
Keywords provided by European Organisation for Research and Treatment of Cancer - EORTC:
|
transitional cell carcinoma of the bladder stage IV bladder cancer stage III bladder cancer metastatic transitional cell cancer of the renal pelvis and ureter regional transitional cell cancer of the renal pelvis and ureter |
Additional relevant MeSH terms:
|
Urinary Bladder Neoplasms Carcinoma, Transitional Cell Kidney Neoplasms Ureteral Neoplasms Urologic Neoplasms Urogenital Neoplasms Neoplasms by Site Neoplasms Urinary Bladder Diseases Urologic Diseases Carcinoma Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Kidney Diseases Ureteral Diseases |
Gemcitabine Lapatinib Cisplatin Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Radiation-Sensitizing Agents Physiological Effects of Drugs Antimetabolites, Antineoplastic Antimetabolites Molecular Mechanisms of Pharmacological Action Antiviral Agents Anti-Infective Agents Enzyme Inhibitors Immunosuppressive Agents |
ClinicalTrials.gov processed this record on May 19, 2013