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Completed

NCT Number: NCT00845819

Study of Epidermal Growth Factor on Oral Mucositis Induced by Intensive Chemotherapy for Hematologic Malignancies

The purpose of this study is to determine efficacy and toxicity of recombinant human epidermal growth factor (rhEGF) as a preventive drug of oral mucositis during intensive chemotherapy with stem cell transplantation in patients with hematologic malignancies.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Seoul National University Hospital

Seoul, 110-744, South Korea

About this study

Oral mucositis is one of the most common adverse events during chemotherapy and affects quality of life of patients receiving chemotherapy in relation to the dose of drugs. However, there is only one drug (palifermin) approved by the US FDA for the prevention of oral mucositis and the other methods to prevent or treat oral mucositis are just empirical and lack evidences. The results of recent study demonstrated promising efficacy and minimal toxicity of recombinant human epidermal growth factor (rhEGF) as a preventive drug of oral mucositis in head and neck cancer patients undergoing radiotherapy (Wu HG, et al. Cancer 2009;115(16):3699-3708). This clinical trial is a double-blind randomized prospective single-institutional phase II study to evaluate efficacy and toxicity of recombinant human epidermal growth factor (rhEGF) as a preventive drug of oral mucositis during intensive chemotherapy with stem cell transplantation in patients with hematologic malignancies.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with confirmed diagnosis of hematologic malignancies including acute & chronic leukemia, lymphoma, plasma cell dyscrasia, myelodysplastic syndrome, aplastic anemia, etc.
  • Patients who are planned to receive high-dose chemotherapy with SCT
  • ECOG performance status 0-2
  • Informed consent

Exclusion criteria

  • Patients having previous history of hypersensitivity to this drug or similar drugs
  • Patients having oral ulcer or herpes or severe dental disease at the time of inclusion
  • Patients received chemotherapy, radiotherapy, or surgery within 3 weeks
  • Patients who had finished clinical trials which could affect the results of this trial within 4 weeks or are attending one at the time of inclusion
  • Patients having another diseases which have worse prognosis than patients' hematologic malignancy
  • Patients with major psychotic disorder or drug/alcohol abuser
  • Women who are pregnant or breastfeeding
  • Refusal at patients' will
  • Inappropriate patients according to the investigators' opinion

Treatment and study plan

rhEGF + povidone iodine, chlorhexidine, & nystatin

Drug

Topical application of 50 µg/mL rhEGF solution twice daily + oral gargling with povidone iodine (1%), chlorhexidine (0.5%) & nystatin (5,000IU/mL) three times a day.

Application of drugs begins with start of intensive chemotherapy and ends at the time of recovery from neutropenia (ANC>1000/µL for 3 days) or disappearance of oral mucositis.

For each application of rhEGF, spray total 6 times at palate, oropharynx, both buccal mucosa, tongue, and gingiva.

Other names: Nepidermin, Easyef(R)

Placebo + povidone iodine, chlorhexidine, & nystatin

Drug

Topical application of placebo drug twice daily + oral gargling with povidone iodine (1%), chlorhexidine (0.5%), and nystatin (5,000IU/mL) three times a day.

Application of drugs begins with start of intensive chemotherapy and ends at the time of recovery from neutropenia (ANC>1000/µL for 3 days) or disappearance of oral mucositis.

For each application of placebo drug, spray total 6 times at palate, oropharynx, both buccal mucosa, tongue, and gingiva.

Other names: Placebo

Primary outcomes

  1. Incidence of oral mucositis of grade 2 or higher (NCI CTCAE 3.0)

    Time frame: Assessed daily during application of study drugs

Secondary outcomes

  1. Adverse events

    Time frame: Assessed daily during application of study drugs

  2. Day of onset and duration of oral mucositis of grade 2 or higher (NCI CTCAE 3.0)

    Time frame: Assessed daily during application of study drugs

  3. Incidence, day of onset, and duration of oral mucositis of grade 3 or higher (NCI CTCAE 3.0)

    Time frame: Assessed daily during application of study drugs

  4. Incidence, day of onset, and duration of oral mucositis of grade 2 or higher (WHO)

    Time frame: Assessed daily during application of study drugs

  5. Incidence, day of onset, and duration of oral mucositis of grade 3 or higher (WHO)

    Time frame: Assessed daily during application of study drugs

  6. Incidence, day of onset, and duration of oral mucositis of grade 4 or higher (WHO)

    Time frame: Assessed daily during application of study drugs

  7. OMDQ (oral mucositis daily questionnaire) score during treatment

    Time frame: Assessed daily during application of study drugs

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Collaborators

  • Daewoong Pharmaceutical Co. LTD.

Registry information

Official study title

Randomized Phase II Study of Recombinant Human Epidermal Growth Factor (rhEGF) on Oral Mucositis Induced by Intensive Chemotherapy for Hematologic Malignancies

Acronym: EGFOM

Important dates

Study start
2009
Primary completion
2014
Study completion
2014
First posted
Feb 18, 2009
Registry last updated
Jan 21, 2015

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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