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NCT Number: NCT02890602

Erythropoietin for Management of Anemia Caused by Chemotherapy

This is a phase Ⅱ study of erythropoietin for management of anemia caused by chemotherapy in patients with Diffuse Large B-cell Lymphoma. The investigators want to investigate hematopoietic response of darbepoietin alfa and the quality of life assessment of increasement of hemoglobin.

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Key information

About this study

Darbepoietin alfa may cause the body to make more red blood cells. They are used to treat anemia caused by chemotherapy in patients with malignant lymphoma. Darbepoietin will be applied to R-CHOP(Rituximab, Cyclophosphamide, Adriamycin, Vincristine, Prednisolone) chemotherapy every 21days ± 2days with fixed 360㎍. It will be applied to chemotherapy until increment of hemoglobin 12.0g/dL. If the hemoglobin level exceeds 12.0g/dL, administration of darbepoietin will be temporarily stopped.

And, the questionnaire of the quality of life will be conducted at the baseline, after 2th darbepoietin alfa administration, at study completion.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histologically confirmed diffuse large B cell lymphoma treated with R-CHOP(Rituximab, Cyclophosphamide, Adriamycin, Vincristine, Prednisolone) chemotherapy
  • hemoglobin < 10.0 g/dL are shown at least 3 cycles after starting R-CHOP(Rituximab, Cyclophosphamide, Adriamycin, Vincristine, Prednisolone)
  • Currently receiving or planning to receive at least 4 times of darbepoetin
  • Age > 18 years
  • ECOG(Eastern Cooperative Oncology Group) performance status 0-2
  • Bilirubin < 2 times upper limit of normal
  • ALT(alanine aminotransferase) or AST(aspartate aminotransferase) < 5 times upper limit of normal
  • Creatinine < 2 times upper limit of normal
  • HIV negative
  • Ferritin > 20 mcg/L (i.e., not obviously iron deficient)
  • Can read Quality of life as measured by Functional Assessment of Cancer Therapy Scales for Anemia
  • Agree with informed consent

Exclusion criteria

  • Received radiation therapy at least 4 weeks before starting chemotherapy
  • serious pre-existing medical condition (e.g., cardiac failure [New York Heart Association Class III or IV, or left ventricular ejection fraction <50%], active peptic ulceration, uncontrolled diabetes mellitus, or acute diffuse infiltrative pulmonary disease)
  • uncontrolled hypertension, defined as systolic blood pressure (BP) ≥ 180 mm Hg and/or diastolic BP ≥ 100 mm Hg, despite medical therapy
  • arrhythmia NCI CTCAE grade ≥ 2
  • History of previously treated seizures allowed provided the patient has been seizure-free for a minimum of 3 months
  • active systemic infection requiring treatment, a known diagnosis of human HIV, or active hepatitis B (hepatitis B carriers were permitted)Malignancy was treated surgically or with local radiation therapy with curative intent and the patient has been disease free for > 3 years
  • known hypersensitivity to darbepoetin alfa
  • pregnant or nursing and Negative pregnancy test
  • previous diagnosis of another malignancy with radiographic or biochemical evidence of residual disease (except completely resected basal cell carcinoma, squamous cell carcinoma of the skin, or an in-situ malignancy)
  • combined iron deficiency anemia
  • received erythropoietin at least one months before starting darbepoetin
  • considered autologous stem cell transplantation before finish 6 cycles of chemotherapy
  • untreated primary or metastatic CNS(central nervous system) malignancy

Treatment and study plan

darbepoetin alfa

Drug

Darbepoietin alfa will be administered subcutaneously at a fixed dose of 360㎍. If it is impossible, administration by intravenous infusion is okay.

Other names: Nesp

R-CHOP

Drug

R-CHOP regimen is a practical procedure in patients with Diffuse Large B-cell Lymphoma. Darbepoietin alfa will be administered to these patients.

Other names: Rituximab, Cyclophosphamide, Adriamycin, Vincristine, Prednisolone

Primary outcomes

  1. Hematopoietic response

    Time frame: hemoglobin level of day 21 after Darbepoietin alfa administration

    Hemoglobin level after Darbepoietin alfa administration

Secondary outcomes

  1. Quality of life as measured by Functional Assessment of Cancer Therapy Scales for anemia

    Time frame: at baseline, Day 21 after 2th darbepoietin alfa administration, Day 21 after last darbepoietin alfa administration

  2. Adverse events as measured by CTCAE v3.0

    Time frame: From the date of first drug administration to the date of the 30th days of last drug administration.

  3. Proportion of patients requiring red blood cell transfusions

    Time frame: From the date of first darbepoietin alfa administration to day 21 after last darbepoietin alfa administration

  4. Mean time to response of hemoglobin

    Time frame: From the date of first darbepoietin alfa administration to day 21 after last darbepoietin alfa administration

Sponsors and collaborators

Lead sponsor

Kosin University Gospel Hospital

Other

Registry information

Official study title

A Phase Ⅱ Study of Erythropoietin for Management of Anemia Caused by Chemotherapy in Patients With Diffuse Large B-cell Lymphoma

Important dates

Study start
2012
Primary completion
2017
Study completion
2017
First posted
Sep 7, 2016
Registry last updated
Feb 20, 2020

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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