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

NCT ID: NCT00701857

Last Updated: 2016-04-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-02-29
• Study Completion Date: 2015-09-30

Brief 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.

Detailed 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.

Conditions

Esophageal Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Pemetrexed, Cisplatin, Radiation Therapy

Concomitant Pemetrexed and CDDP Plus Radiation Therapy

Group Type: EXPERIMENTAL

cisplatin

Intervention Type: DRUG

Standard weekly dose

Pemetrexed

Intervention Type: DRUG

Biweekly pemetrexed dose escalation

radiation therapy

Intervention Type: RADIATION

Weekly standard dose radiation therapy

Interventions

cisplatin

Standard weekly dose

Intervention Type: DRUG

Pemetrexed

Biweekly pemetrexed dose escalation

Intervention Type: DRUG

radiation therapy

Weekly standard dose radiation therapy

Intervention Type: RADIATION

Other Intervention Names

CDDP; Pemetrexed disodium; RT

Eligibility Criteria

Inclusion Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 120 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

University of Arizona

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Emad Elquza, MD

Role: PRINCIPAL_INVESTIGATOR

University of Arizona

Locations

University of Arizona Cancer Center

Tucson, Arizona, United States

Countries

United States

References

Elquza E, Babiker HM, Howell KJ, Kovoor AI, Brown TD, Patel H, Malangone SA, Borad MJ, Dragovich T. Phase I Study of Concomitant Pemetrexed and Cisplatin Plus External Beam Radiation Therapy in Patients with Locally Advanced or Metastatic Esophageal or Gastroesophageal Junction Carcinomas. Cancer Invest. 2016;34(2):57-63. doi: 10.3109/07357907.2015.1108426. Epub 2016 Jan 25.

Reference Type: DERIVED

PMID: 26810581 (View on PubMed)

Other Identifiers

P30CA023074

Identifier Type: NIH

Identifier Source: secondary_id

View Link

UARIZ-07-0612-04

Identifier Type: OTHER

Identifier Source: secondary_id

UARIZ-BIO07067

Identifier Type: OTHER

Identifier Source: secondary_id

UARIZ-SRC18084

Identifier Type: OTHER

Identifier Source: secondary_id

LILLY-UARIZ-07-0612-04

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

07-0612-04

Identifier Type: -

Identifier Source: org_study_id