Palifermin in Preventing Oral Mucositis Caused by Chemotherapy and/or Radiation Therapy in Young Patients Undergoing Stem Cell Transplant

NCT ID: NCT00728585

Last Updated: 2018-08-07

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-03-13

Brief Summary

This randomized phase II trial is studying palifermin to see how well it works compared with a placebo in preventing oral mucositis caused by chemotherapy and/or radiation therapy in young patients undergoing stem cell transplant. Palifermin may help relieve or prevent oral mucositis caused by chemotherapy and radiation therapy in young patients undergoing stem cell transplant.

Detailed Description

PRIMARY OBJECTIVES:

I. To compare whether palifermin versus placebo administered to pediatric patients three days prior to conditioning and three days after autologous or allogeneic hematopoietic stem cell transplantation (HSCT) is associated with a reduction in the incidence of WHO grade 3 or 4 oral mucositis.

SECONDARY OBJECTIVES:

I. To evaluate the safety and tolerability of palifermin. II. To evaluate the long-term effects of palifermin on disease outcome and survival.

III. To compare the incidence, total dose, and duration of parenteral opioid analgesic use (morphine equivalents), and incidence and duration of total parenteral nutrition (TPN) administration in patients treated with these regimens.

IV. To compare the incidence of febrile neutropenia and invasive bacterial infections in patients treated with these regimens.

TERTIARY OBJECTIVES:

I. To determine whether palifermin versus placebo reduces the incidence of WHO grade 3 or 4 oral mucositis among allogeneic HSCT pediatric patients receiving methotrexate as graft-versus-host disease (GVHD) prophylaxis.

II. To determine whether palifermin versus placebo reduces acute and chronic GVHD after allogeneic HSCT.

III. To describe health care utilization (hospitalization duration, and administration of antibiotics, TPN, nasogastric-, nasojejunal- or gastrostomy-administered enteral nutrition, and blood products) in pediatric patients treated with these regimens.

OUTLINE: This is a multicenter study. Patients are stratified according to age in years (1 to 2 vs 3 to 11 vs 12 to 16), type of hematopoietic stem cell transplantation (HSCT) (autologous vs allogeneic), conditioning regimen (either total-body irradiation [TBI] or melphalan vs neither TBI nor melphalan). Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive palifermin IV once daily for 3 days prior to chemotherapy and/or radiotherapy in the absence of unacceptable toxicity. Patients then receive palifermin IV on days 0, 1, and 2 after autologous or allogeneic HSCT.

ARM II: Patients receive placebo IV once daily for 3 days prior to chemotherapy and/or radiotherapy in the absence of unacceptable toxicity. Patients then receive placebo IV on days 0, 1, and 2 after autologous or allogeneic HSCT.

Blood samples are collected at baseline, 32 days, and 100 days after HSCT to evaluate the immunogenicity of palifermin. Oral mucositis is assessed at baseline, daily for 8 days prior to and 32 days after HSCT, or until oral mucositis has resolved by the WHO Mucositis Scale, Oral Mucositis Assessment Scale (OMAS), modified Walsh mucositis scale, Oral Mucositis Daily Questionnaire (OMDQ), and the pain categorical rating scale.

After completion of HSCT, patients are followed periodically for up to 10 years.

Conditions

Gastrointestinal Mucositis; Malignant Neoplasm

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: DOUBLE

Study Groups

Arm I (palifermin)

Patients receive palifermin IV once daily for 3 days prior to chemotherapy and/or radiotherapy in the absence of unacceptable toxicity. Patients then receive palifermin IV on days 0, 1, and 2 after autologous or allogeneic hematopoietic stem cell transplantation.

Group Type: EXPERIMENTAL

Palifermin

Intervention Type: DRUG

Given IV

Arm II (placebo)

Patients receive placebo IV once daily for 3 days prior to chemotherapy and/or radiotherapy in the absence of unacceptable toxicity. Patients then receive placebo IV on days 0, 1, and 2 after autologous or allogeneic hematopoietic stem cell transplantation.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Given IV

Interventions

Palifermin

Given IV

Intervention Type: DRUG

Placebo

Given IV

Intervention Type: OTHER

Other Intervention Names

Growth Factor, Recombinant Human Keratinocyte; Kepivance; Keratinocyte Growth Factor, Recombinant Human; Recombinant Human Keratinocyte Growth Factor; rhKGF; rhu Keratinocyte Growth Factor; placebo therapy; PLCB; sham therapy

Eligibility Criteria

Inclusion Criteria

Criteria:

• Patients undergoing myeloablative autologous or allogeneic hematopoietic stem cell transplantation (HSCT) for any indication
• Any type of myeloablative HSCT conditioning regimen allowed
• Patients undergoing allogeneic HSCT may undergo 1 of the following types of donor stem cells:

1. HLA-matched sibling or parent

2. Partially matched family donor (mismatched for a single HLA locus [class I])

3. Fully matched unrelated marrow or peripheral blood stem cell donor

4. HLA-matched or partially mismatched (at least 4 of 6 match) cord blood (class I or II)

• Fertile patients must use effective contraception
• No HIV positivity
• No known sensitivity to any E. coli-derived products

1. Known grade 1 to 2 allergic reactions to asparaginase allowed

2. No prior grade 3-4 allergies to asparaginase or pegaspargase

• More than 30 days since prior and no concurrent treatment with any of the following therapies:

1. Oral cryotherapy

2. Glutamine as an oral supplement

3. Traumeel

4. Gelclair

5. Oral vancomycin paste

6. Low-level laser therapy

7. An investigational product or device in another clinical trial

• No prior palifermin or other keratinocyte growth factors
• No other concurrent cytotoxic drugs for conditioning or graft-vs-host disease prophylaxis (intrathecal methotrexate or cytarabine for CNS involvement allowed)
• Not pregnant or nursing

• Minimum Eligible Age: 1 Year
• Maximum Eligible Age: 16 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Children's Oncology Group

NETWORK

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Lillian Sung

Role: PRINCIPAL_INVESTIGATOR

Children's Oncology Group

Other Identifiers

NCI-2009-00329

Identifier Type: REGISTRY

Identifier Source: secondary_id

CDR0000588622

Identifier Type: -

Identifier Source: secondary_id

ACCL0521

Identifier Type: OTHER

Identifier Source: secondary_id

ACCL0521

Identifier Type: OTHER

Identifier Source: secondary_id

U10CA095861

Identifier Type: NIH

Identifier Source: secondary_id

View Link

ACCL0521

Identifier Type: -

Identifier Source: org_study_id