Pemetrexed, Cisplatin, and Radiation Therapy in Treating Patients With Esophageal or Gastroesophageal Junction Cancer

Esophageal Cancer Clinical Trial

Official title:

Phase I Study of Concomitant Pemetrexed and CDDP Plus Radiation Therapy in Patients With Locally Advanced or Metastatic Esophageal or Gastroesophageal (GEJ) Carcinomas

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00701857
• Other study ID #: 07-0612-04
• Secondary ID: P30CA023074UARIZ
• Status: Completed
• Phase: Phase 1
• First received: June 18, 2008
• Last updated: April 19, 2016
• Start date: February 2008
• Est. completion date: September 2015

Study information

• Verified date: April 2016
• Source: University of Arizona
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Pemetrexed may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Cisplatin may make tumor cells more sensitive to radiation therapy. Giving pemetrexed together with cisplatin and radiation therapy may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of pemetrexed when given together with cisplatin and radiation therapy in treating patients with stage III or stage IV esophageal cancer or gastroesophageal junction cancer.

Description:

OBJECTIVES:

Primary

• To establish the maximum tolerated dose of pemetrexed disodium in combination with cisplatin and standard-dose radiotherapy in patients with stage III or IV esophageal or gastroesophageal junction carcinoma.

Secondary

• To specifically characterize the toxicity profile of this regimen.

• To investigate, preliminarily, the anti-tumor activity of this regimen, as measured by standard response criteria (RECIST criteria), in patients with measurable disease.

OUTLINE: This is a dose-escalation study of pemetrexed disodium.

Patients receive pemetrexed disodium IV over 10 minutes on days 1, 15, and 29 and cisplatin IV over 10 minutes on days 1, 8, 15, 22, and 29. Patients also undergo external beam radiotherapy once daily, 5 days a week, for up to 6 weeks.

After completion of study therapy, patients are followed for 30 days and then every 3 months for 1 year.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: September 2015
• Est. primary completion date: April 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 120 Years

Eligibility

DISEASE CHARACTERISTICS:

• Diagnosis of esophageal or gastroesophageal junction carcinoma

• Stage III or IV disease

• Treatment with chemoradiotherapy is considered appropriate

• Measurable or evaluable disease

• Clinically significant pleural or pericardial effusions or ascites allowed provided they were drained prior to study entry

• No pleurodesis within the past 2 weeks

• Controlled brain metastasis allowed provided patient is clinically stable with no signs of progression by MRI or CT scan of the brain = 60 days after completion of treatment AND is asymptomatic and does not require steroids

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2

• Life expectancy = 12 weeks

• WBC = 2,500/mm^3

• ANC = 1,500/mm^3

• Hemoglobin = 9 g/dL

• Platelet count = 100,000/mm^3

• Total bilirubin normal

• Alkaline phosphatase AND AST and ALT meeting the following criteria:

• Alkaline phosphatase normal AND AST or ALT = 3 times upper limit of normal (ULN) (= 5 times ULN for patients with liver metastases)

• Alkaline phosphatase = 2.5 times ULN AND AST or ALT = 1.5 times ULN

• Alkaline phosphatase = 5 times ULN AND AST or ALT normal

• Creatinine clearance = 45 mL/min

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception during and for 3 months after completion of study therapy

• Able to take folic acid, vitamin B_12, or corticosteroids

• No known severe hypersensitivity reaction to study drugs

• No uncontrolled serious active infection

• No pre-existing peripheral neuropathy > grade 1

• No significant cardiac disease, including any of the following:

• Uncontrolled high blood pressure

• Unstable angina

• Congestive heart failure within the past 6 months

• Left ventricular ejection fraction below the lower limit of normal

• Myocardial infarction within the past year

• Serious cardiac arrhythmias requiring medication

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• No prior systemic therapy regimens

• No prior radiotherapy to gastric/esophageal fields

• No aspirin or other NSAID before and after pemetrexed disodium administration

• No concurrent colony-stimulating factors (CSF) to maintain WBC and ANC eligibility values

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Esophageal Cancer
• Esophageal Neoplasms

Intervention

Drug:
• cisplatin
Standard weekly dose
• Pemetrexed
Biweekly pemetrexed dose escalation

Radiation:
• radiation therapy
Weekly standard dose radiation therapy

Locations

Country	Name	City	State
United States	University of Arizona Cancer Center	Tucson	Arizona

Sponsors (2)

Lead Sponsor	Collaborator
University of Arizona	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The maximum tolerated dose (MTD) of pemetrexed		6 months	Yes
Secondary	Toxicity profile		12 months	Yes
Secondary	Response (complete response, partial response, progressive disease, and stable disease) as measured by RECIST criteria		12 months	No