Epoetin Beta in Treating Anemia in Patients With Cervical Cancer

Cervical Cancer Clinical Trial

Official title:

Management Of Anemia Under RadioChemotherapy (MARCH): An Open, Randomized Multicenter Study Of The Effect Of NeoRecormon On Treatment Outcome In Patients With Advanced Cervical Cancer Stage IIB -IVA Treated With Primary Simultaneous Radiochemotherapy (Radiotherapy Plus Cisplatin)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00046969
• Other study ID #: AGOSG-OVAR-MO16375-MARCH
• Secondary ID: CDR0000257189EU-
• Status: Completed
• Phase: Phase 4
• First received: October 3, 2002
• Last updated: May 29, 2013
• Start date: July 2002
• Est. completion date: June 2007

Study information

• Verified date: March 2007
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Epoetin beta may stimulate red blood cell production to prevent or control anemia in patients treated with chemotherapy and radiation therapy.

PURPOSE: Randomized phase IV trial to determine the effectiveness of epoetin beta in treating anemia in patients who are receiving cisplatin and radiation therapy for stage IIB, stage III, or stage IVA cervical cancer.

Description:

OBJECTIVES:

• Compare the effectiveness of epoetin beta vs standard care for anemia management, in terms of increased hemoglobin levels and the correlation with reduced relapse/treatment failure rate, in patients with stage IIB, III, or IVA cervical cancer treated with cisplatin and radiotherapy.

• Compare the safety of these regimens in these patients.

• Compare the relapse-free and overall survival of patients treated with these regimens.

• Compare the frequency and localization of relapses and metastases in patients treated with these regimens.

• Compare the quality of life of patients treated with these regimens.

• Compare the type, frequency, and degree of adverse events in patients treated with these regimens.

• Compare the overall response rate in patients treated with these regimens.

OUTLINE: This is a randomized, open-label, parallel-group, multicenter study. Patients are stratified according to country, disease stage, and brachytherapy technique. Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients undergo radiotherapy 5 days a week for 6 weeks. Patients also undergo high-dose rate, low-dose rate, or boost brachytherapy. Patients receive cisplatin IV beginning on day 1 of radiotherapy and continuing weekly for 6 weeks. Patients also receive epoetin beta subcutaneously 3 times a week beginning 2 weeks before radiotherapy and continuing for 8 weeks.

• Arm II: Patients undergo radiotherapy and brachytherapy and receive cisplatin as in arm I.

Quality of life is assessed at baseline, after the last treatment, and at 3 months.

Patients are followed every 3 months for 2 years and then every 6 months thereafter.

PROJECTED ACCRUAL: A total of 80-450 patients will be accrued for this study within 4-22.5 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 450
• Est. completion date: June 2007
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed stage IIB, III, or IVA cervical cancer

• No chorion carcinoma or neuroendocrine small cell carcinoma

• Previously untreated disease

• Must be scheduled to undergo radiotherapy and receive cisplatin as primary therapy

• Hemoglobin 8.0-13.0 g/dL

• No relevant acute bleeding within the past 3 months, including anemia caused by gross bleeding from tumor

• No distant metastasis

• No positive para-aortic lymph nodes

PATIENT CHARACTERISTICS:

Age

• Over 18

Performance status

• WHO 0-2

Life expectancy

• At least 3 months

Hematopoietic

• See Disease Characteristics

• WBC greater than 3,000/mm3

• Platelet count greater than 100,000/mm3

• No hemolytic anemia

• No transferrin saturation less than 20% that cannot be treated with IV iron

• No hemoglobinopathies (i.e., sickle cell disease or thalassemia of all types)

Hepatic

• Bilirubin no greater than 1.5 times upper limit of normal (ULN)

• Transaminases no greater than 2.5 times ULN

• Alkaline phosphatase no greater than 2.5 times ULN

Renal

• Creatinine clearance greater than 60 mL/min

Cardiovascular

• No chronic heart failure

• No New York Heart Association class II-IV heart disease

• No uncontrolled arterial hypertension (systolic blood pressure at least 170 mmHg, diastolic blood pressure at least 100 mmHg)

• No prior deep vein thrombosis

• No thrombocytosis

Other

• No vitamin B12 deficiency

• No folic acid deficiency

• No newly diagnosed (unstable) epilepsy

• No acute infection

• No other malignancy within the past 5 years except basal cell carcinoma in situ

• No known peripheral neuropathy or moto-sensory neurotoxicity grade 2 or greater

• No impaired hearing grade 2 or greater

• No hypersensitivity to benzyl alcohol, benzoic acid, benzalkonium chloride, or any excipients of cisplatin preparations

• Not pregnant or nursing

PRIOR CONCURRENT THERAPY:

Biologic therapy

• At least 3 months since prior epoetins or related compounds

Chemotherapy

• See Disease Characteristics

Endocrine therapy

• Not specified

Radiotherapy

• See Disease Characteristics

• No prior radiotherapy for cervical cancer

Surgery

• Not specified

Other

• At least 30 days since prior investigational drugs

• No prior systemic antineoplastic therapy for cervical cancer

• No other concurrent investigational drugs

Study Design

Allocation: Randomized, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Anemia
• Cervical Cancer
• Uterine Cervical Neoplasms

Intervention

Biological:
• epoetin beta

Drug:
• cisplatin

Radiation:
• brachytherapy

• radiation therapy

Locations

Country	Name	City	State
Germany	Martin Luther Universitaet	Halle

Sponsors (1)

Lead Sponsor	Collaborator
AGO Study Group

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of treatment failures within 6 months after beginning radiochemotherapy (RCT) (stage I)
Primary	Overall survival after RCT (stage II)
Secondary	Progression/relapse-free survival
Secondary	Overall response rate to RCT
Secondary	Overall survival after RCT (stage I)
Secondary	Frequency and localization of relapses and/or metastases
Secondary	Change in hemoglobin from baseline during therapy
Secondary	Quality of life as assessed by the Functional Assessment of Cancer Therapy-Anemia
Secondary	Type, frequency, and degree of adverse events
Secondary	Safety
Secondary	Vital signs
Secondary	Number of treatment failures within 6 months after beginning RCT (stage II)