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Completed

NCT Number: NCT00283621

Aranesp and Neulasta in Patients With Sarcoma Receiving Adriamycin and Ifosfamide

To determine the percentage of patients and number of cycles in which a packed red blood cell transfusion was administered due to anemia and in which antibiotics were administered due to neutropenic fever.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UT MDAnderson Cancer Center

Houston, Texas, 77030, United States

About this study

The use of hematopoietic growth factors have been shown to reduce neutropenic complications and red cell transfusion requirements associated with chemotherapy. This trial will study the combination of pegfilgrastim and darbepoetin alfa administered once per cycle of chemotherapy. Prior experience with growth factors in this setting provides historical data for comparison of safety and activity of these newer longer acting growth factors in reducing the incidence of febrile neutropenia requiring antibiotics and anemia requiring transfusions. The once dosing per cycle would simplify the patient management and would improve patient convenience and compliance.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with sarcoma which is locally advanced, at high risk for relapsed or metastatic for whom treatment with AI is indicated
  • Must be between 18-65 years of age
  • Women of childbearing potential should use effective contraceptive measures
  • Adequate hematologic, renal, and hepatic functions
  • Karnofsky performance status above or equal to 80

Exclusion criteria

  • Pregnant or lactating women.
  • Patients with comorbid condition which renders patients at high risk of treatment complication
  • Patients with metastatic disease to CNS
  • Patients with significant cardiac abnormalities
  • History of seizure disorder in the past 5 years
  • Patient has received any packed red blood cell transfusion within 2 weeks before study entry
  • Prior surgery or radiation therapy within 2 weeks of study entry
  • History of prior chemotherapy for sarcomas
  • Iron deficiency
  • Hypersensitivity to E.coli derived products

Treatment and study plan

Aranesp (darbepoetin alfa)

Drug

Neulasta (pegfilgrastim)

Drug

Adriamycin

Drug

Other names: Doxorubicin Hydrocholoride, Adriamycin PFS, Adriamycin RDF

ifosfamide

Drug

Other names: Ifex

Primary outcomes

  1. CBC diff/platelet counts

    Time frame: Monitored at least twice a week and daily during severe myelosuppression.

  2. Iron Stores

    Time frame: Blood drawn at baseline during cycle 3 and at the end of study.

  3. Peripheral blood and bone marrows

    Time frame: Performed at baseline and post treatment.

Secondary outcomes

  1. Neurocognitive functions and Symptom burden assessment

    Time frame: Assessed at baseline, after 3 cycles of treatment and at the end of the study.

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Collaborators

  • Amgen

Registry information

Official study title

A Pilot Study of Aranesp (Darbepoetin Alfa) and Pegfilgrastim (Neulasta) in Patients With Sarcoma Receiving Adriamycin and Ifosfamide

Important dates

Study start
2003
Primary completion
2006
Study completion
2006
First posted
Jan 30, 2006
Registry last updated
Nov 7, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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