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Preventive Effect of EGF Cream for Cutaneous Adverse Event of EGFR Inhibitors

Primary Purpose

Drug-Related Side Effects and Adverse Reactions, Epidermal Growth Factor

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Repair Control EGF®
Cream without rhEGF
Sponsored by
The Catholic University of Korea
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Drug-Related Side Effects and Adverse Reactions focused on measuring Epidermal Growth Factor

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Over 20 years old
  • Patients scheduled to receive EGFR inhibitors (gefitinib, erlotinib, afatinib, cetuximab, etc.) as malignant tumors
  • Patients who can understand and follow the protocol
  • Patients who spontaneously agreed to the study

Exclusion Criteria:

  • Patients with a history of antibiotic treatment, local and systemic steroid therapy within 4 weeks of other skin disorders
  • Patients with existing acne history
  • Breastfeeding or pregnant women
  • Patients who are deemed unsuitable for the examination by the researcher's judgment

Sites / Locations

  • St. Vincent's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Repair Control EGF®

Cream without rhEGF

Arm Description

EGF cream was applied. One half side of face and one hand were treated with emollient containing EGF.

Placebo cream without EGF was applied. The other half side of face and the other hand were treated with only emollient which was not containing EGF.

Outcomes

Primary Outcome Measures

The change of acneiform eruption caused by use of EGFR inhibitor
To evaluate the development and severity of acneiform eruption, the investigators take a photograph of full face and hands on every visit. If the acneiform eruption develop, the severity will be assessed based on the Korean Acne Grading System(KAGS).

Secondary Outcome Measures

the change paronychia caused by use of EGFR inhibitor
The paronychia lesion will be assessed by CTCAE.
the change of skin hydration
It measured with Corneometer® (CM820/825, C-K Electronics, Cologne, Germany). It shows in arbitrary units(AU) and the unit is from 0 to 220.
the change of sebum production
It measured with Sebumeter® (SM815; C-K Electronics, Cologne, Germany). It is measured at forehead, cheek and chin, presented as /㎍ ㎠. It shows in arbitrary units(AU) and the unit is from 0 to 220.
Investigator's global assessment score
Investigator's global assessment (IGA) Score will be assessed with 5-point scale (-1 = worsen to 3 =marked improvement).
Patient's global assessment score
Patient's global assessment (PGA) score will be assessed with a 5-point scale (-1 = worsen, to 3 = marked improvement).
The side effects of product
It will be assessed by patient-report. - Any event developed during the trials can be reported.

Full Information

First Posted
December 2, 2016
Last Updated
February 9, 2017
Sponsor
The Catholic University of Korea
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1. Study Identification

Unique Protocol Identification Number
NCT03051880
Brief Title
Preventive Effect of EGF Cream for Cutaneous Adverse Event of EGFR Inhibitors
Official Title
The Preventive Effect of Topical EGF Cream for Dermatologic Adverse Events Related to EGFR Inhibitors
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 2016 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Catholic University of Korea

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the preventive efficacy of topical EGF cream for dermatologic adverse events related to EGFR inhibitors.
Detailed Description
Epidermal growth factor receptor(EGFR) is involved in cell proliferation and is overexpressed or abnormally activated in malignant tumors originating from the colon, breast, ovary, pancreas, and lung. EGFR tyrosine kinase inhibitor(TKI), gefitinib, erlotinib, and afatinib have been for the treatment of cancer associated with EGFR gene mutation. In addition, monoclonal antibodies to EGFR, such as cetuximab and panitumumab, have been used as a chemotherapy for rectal cancer without ras gene mutation and advanced head and neck cancer. The incidence of cutaneous toxicity of EGFR inhibitors is reported to be 75-80%. Clinical features include acneform folliculitis, xerosis, paronychia, and itching. Of these, about 10% of patients with Grade 3 or greater have a detrimental effect on quality of life and adherence to treatment, resulting in impaired therapeutic results. There have been many attempts to prevent or treat such skin toxicity. However, there has been no scientifically proven treatment until now. There is a growing interest in the role of EGF emulsifiers in the treatment of skin adverse effects of EGFR inhibitors, as a result of studies that improve acne significantly compared to placebo. The purpose of this study is to evaluate the preventive efficacy of EGF cream in the treatment of skin adverse effects in patients with malignant tumors treated with EGFR inhibitor (TKI or monoclonal antibody).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Drug-Related Side Effects and Adverse Reactions, Epidermal Growth Factor
Keywords
Epidermal Growth Factor

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Repair Control EGF®
Arm Type
Experimental
Arm Description
EGF cream was applied. One half side of face and one hand were treated with emollient containing EGF.
Arm Title
Cream without rhEGF
Arm Type
Placebo Comparator
Arm Description
Placebo cream without EGF was applied. The other half side of face and the other hand were treated with only emollient which was not containing EGF.
Intervention Type
Drug
Intervention Name(s)
Repair Control EGF®
Other Intervention Name(s)
EGF cream containing 10 ppm of rhEGF
Intervention Description
A Split face study was done. Patients applied 1 finger tip unit of EGF cream on one side of face, twice a day for 8 weeks. Also, to evaluate the preventive effect of paronychia, patients applied same cream on the finger tips of one side hand, twice a day for 8 weeks. EGF cream(Repair Control EGF®) containing 10 ppm of rhEGF was prepared at D.N. Co., Ltd. (Seoul, South Korea)
Intervention Type
Drug
Intervention Name(s)
Cream without rhEGF
Intervention Description
A Split face study was done. Patients applied 1 finger tip unit of cream on the other side of face, twice a day for 8 weeks. Patients applied same cream on the finger tips of the other side hand, twice a day for 8 weeks. Placebo cream was prepared at at D.N. Co., Ltd. (Seoul, South Korea), consisted of same ingredient with EGF cream except rhEGF
Primary Outcome Measure Information:
Title
The change of acneiform eruption caused by use of EGFR inhibitor
Description
To evaluate the development and severity of acneiform eruption, the investigators take a photograph of full face and hands on every visit. If the acneiform eruption develop, the severity will be assessed based on the Korean Acne Grading System(KAGS).
Time Frame
Baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Secondary Outcome Measure Information:
Title
the change paronychia caused by use of EGFR inhibitor
Description
The paronychia lesion will be assessed by CTCAE.
Time Frame
Baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Title
the change of skin hydration
Description
It measured with Corneometer® (CM820/825, C-K Electronics, Cologne, Germany). It shows in arbitrary units(AU) and the unit is from 0 to 220.
Time Frame
Baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Title
the change of sebum production
Description
It measured with Sebumeter® (SM815; C-K Electronics, Cologne, Germany). It is measured at forehead, cheek and chin, presented as /㎍ ㎠. It shows in arbitrary units(AU) and the unit is from 0 to 220.
Time Frame
Baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Title
Investigator's global assessment score
Description
Investigator's global assessment (IGA) Score will be assessed with 5-point scale (-1 = worsen to 3 =marked improvement).
Time Frame
Baseline, 8 weeks
Title
Patient's global assessment score
Description
Patient's global assessment (PGA) score will be assessed with a 5-point scale (-1 = worsen, to 3 = marked improvement).
Time Frame
Baseline, 8 weeks
Title
The side effects of product
Description
It will be assessed by patient-report. - Any event developed during the trials can be reported.
Time Frame
Baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Over 20 years old Patients scheduled to receive EGFR inhibitors (gefitinib, erlotinib, afatinib, cetuximab, etc.) as malignant tumors Patients who can understand and follow the protocol Patients who spontaneously agreed to the study Exclusion Criteria: Patients with a history of antibiotic treatment, local and systemic steroid therapy within 4 weeks of other skin disorders Patients with existing acne history Breastfeeding or pregnant women Patients who are deemed unsuitable for the examination by the researcher's judgment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jung Min Bae, MD, PhD
Phone
82-31-249-8209
Email
jminbae@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ho jung An, MD, PhD
Phone
82-10-8737-4285
Email
strhojung@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jung Min B, MD, PhD
Organizational Affiliation
The Catholic University of Korea
Official's Role
Study Chair
Facility Information:
Facility Name
St. Vincent's Hospital
City
Suwon
State/Province
Gyeonggi-do
ZIP/Postal Code
16247
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jung Min Bae, MD
Phone
82-31-249-8209
Email
jminbae@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Preventive Effect of EGF Cream for Cutaneous Adverse Event of EGFR Inhibitors

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