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The Effect of Urea Cream on Sorafenib-associated Hand-Foot Skin Reaction

Primary Purpose

Hepatocellular Carcinoma

Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Urea Cream 20%
Placebos
Sponsored by
Korea University Guro Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring Urea Cream, Sorafenib

Eligibility Criteria

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

Inclusion Criteria:

  • Patient who was diagnosed with hepatocellular carcinoma, and was accompanied by impossible for radical treatment in disease period or do not reaction for local treatment, and the first time for sorafenib injection.
  • Standard of hepatocellular carcinoma diagnosis (2014, The Korean Liver Cancer Association)

    1. Suitable on hepatocellular carcinoma pathologically
    2. Hepatic nodule size over 1 cm on high-risk patients(hepatitis B virus positive, hepatitis C virus positive and liver cirrhosis) that identified by ultrasonography : In the case of suitable on hepatocellular carcinoma on over in one or two more dynamic contrast enhanced CT, dynamic contrast enhanced MRI, or MRI with Gadolinium Ethoxybenzyl Diethylenetriamine Pentaacetic Acid(Gd-EOB-DTPA)
    3. Hepatic nodule size under 1 cm on high-risk patients that identified by ultrasonography : serum Alpha-fetoprotein(AFP) elevated over normal range constantly when hepatitis activity was restrained, and the case of suitable on hepatocellular carcinoma on over in two more the above image diagnoses

Exclusion Criteria:

  • Unsuitable on inclusion criteria
  • Patient who has had systemic anticancer therapy before (including sorafenib)
  • Patient who is receiving another treatment to hepatocellular carcinoma recent 3 weeks (allow to local treatment of metastasis lesion only)
  • Pregnant or Breastfeeding
  • Urea cream contraindication patient (Acute eczema, Inflammatory dermatopathy and Hypersensitivity on Urea and Methylparaben)

Sites / Locations

  • Korea University Guro Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Urea cream 20%

Placebo

Arm Description

144 patients spread urea cream (urea 20%)

144 patients spread placebo cream (urea 0%)

Outcomes

Primary Outcome Measures

Cumulative incidence of Hand-Foot Skin Reaction(HFSR) on each group
Comparison of cumulative incidence of HFSR between placebo group and urea cream group

Secondary Outcome Measures

Cumulative incidence of severe HFSR on each group
Comparison of cumulative incidence of severe HFSR (grade 2 or grade 3) between placebo group and urea cream group
Incidence of dose reduction or discontinuation of sorafenib due to HFSR on each group
Comparison of incidence of dose reduction or discontinuation of sorafenib due to HFSR on each group
Assessment of Quality Of Life (QOL)
Assessment of QOL related to HFSR using The Hand-Foot Skin Reaction and Quality of Life Questionnaire (HF-QoL) scoring system. HF-QOL instrument comprises a 20-item symptom scale and an 18-item daily activity scale. Each item was scored from 0 (not at all) to 4 (always or extremely). Therefore, the range of score for HF-QoL was from 0 to 152 points. (Ref. Anderson et al. The Oncoligist 2015;20:831-838)
Overall survival
Overall survival of patients
Tumor response
Tumor response using mRECIST criteria
Other side effect
The occurrence rate of other side effect excluding HFSR
Incidence of HFSR on 2, 4, 8, and 12 weeks on each group
Comparison of incidence of HFSR on 2, 4, 8, and 12 weeks between placebo group and urea cream group

Full Information

First Posted
July 2, 2017
Last Updated
August 21, 2019
Sponsor
Korea University Guro Hospital
Collaborators
Hanmi Pharmaceutical Company Limited
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1. Study Identification

Unique Protocol Identification Number
NCT03212625
Brief Title
The Effect of Urea Cream on Sorafenib-associated Hand-Foot Skin Reaction
Official Title
The Effect of Urea Cream on Sorafenib-associated Hand-Foot Skin Reaction in Patients With Korean Hepatocellular Carcinoma Patients: Multicenter, Prospective Randomized Double-Blind Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
January 28, 2016 (Actual)
Primary Completion Date
September 20, 2018 (Actual)
Study Completion Date
September 20, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Korea University Guro Hospital
Collaborators
Hanmi Pharmaceutical Company Limited

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Many investigators have studied for prevention and care of Hand-Foot Skin Reaction(HFSR), and urea cream is typical representative. Recent study was performed prevention effect of urea cream for Hand-Foot Skin Reaction(HFSR) on 871 Chinese. But the study did not designed as placebo-control group and it had big defect in double-blinded. Therefore, it needs complementary study as double-blinded placebo-controlled trial and effect of urea cream on Korean patient group.
Detailed Description
Sorafenib is multiple tyrosine kinase inhibitor. It blocks path that such as Raf-1, Vascular Endothelial Growth Factor Receptor (VEGFR), Platelet-Drived Growth Factor Receptor-β (PDGFR-β), c-Jit, Flt-3. Sorafenib was known to increase life rate about processed hepatocellular carcinoma. So it is advised as standard treatment for liver cancer patient who has processed Barcelona Clinic Liver Cancer (BCLC) disease period C. Sorafenib related side effect has reported such as fatigue, diarrhea, vomit, nausea, pruritus, depilation, Hand-Foot Skin Reaction(HFSR). Among the symptoms, Hand-Foot Skin Reaction(HFSR) is the most occurrence after using sorafenib and major reason of drug dose de-escalation, it function as decrease anti-cancer effect of sorafenib. It is known for the reason of Hand-Foot Skin Reaction(HFSR) occurrence is caused by tyrosine kinase inhibitive action, and its characteristic symptom is known as keratocyte necrosis, dermal edema, parakeratosis, hyperkeratosis. The level is categorized grade 1,2,3 according to the severity. The result of meta-analysis of 24 clinical trials that contained 6000 patients, Hand-Foot Skin Reaction(HFSR) occured 39% of sorafenib used patients and 9% of total patients had grade 3 Hand-Foot Skin Reaction(HFSR). But prevalence rate on hepatocellular carcinoma patients who used sorafenib is about 51% on Japanese, 45% on Asia-pacific patient (inclusive Korean) and 73.6% on Chinese. Prevalence rate of Hand-Foot Skin Reaction(HFSR) is different from result of each study, but about 50% of sorafenib used patients has had Hand-Foot Skin Reaction(HFSR) generally and Asian has more higher degree of prevalence rate. Therefore, prevent and care of Hand-Foot Skin Reaction(HFSR) on Korean hepatocellular carcinoma patients who used sorafenib is required. Urea cream is typical representative for prevention and care of Hand-Foot Skin Reaction(HFSR). As stability-guaranteed drug, it is relatively cheap, locally affect and has used for psoriasis treatment. Also it is known for curative effacement on Hand-Foot Skin Reaction(HFSR) after use tyrosine kinase inhibitor such as sorafenib, sunitinib. Therefore, it needs complementary study as double-blinded placebo-controlled trial and effect of urea cream on Korean patient group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma
Keywords
Urea Cream, Sorafenib

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
288 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Urea cream 20%
Arm Type
Experimental
Arm Description
144 patients spread urea cream (urea 20%)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
144 patients spread placebo cream (urea 0%)
Intervention Type
Drug
Intervention Name(s)
Urea Cream 20%
Other Intervention Name(s)
Urea group
Intervention Description
Sorafenib 400mg (twice daily), Spread urea cream (urea 20%)
Intervention Type
Drug
Intervention Name(s)
Placebos
Other Intervention Name(s)
Placebo group
Intervention Description
Sorafenib 400mg (twice daily), Spread placebo cream (urea 0%)
Primary Outcome Measure Information:
Title
Cumulative incidence of Hand-Foot Skin Reaction(HFSR) on each group
Description
Comparison of cumulative incidence of HFSR between placebo group and urea cream group
Time Frame
12 weeks treatment
Secondary Outcome Measure Information:
Title
Cumulative incidence of severe HFSR on each group
Description
Comparison of cumulative incidence of severe HFSR (grade 2 or grade 3) between placebo group and urea cream group
Time Frame
12 weeks treatment
Title
Incidence of dose reduction or discontinuation of sorafenib due to HFSR on each group
Description
Comparison of incidence of dose reduction or discontinuation of sorafenib due to HFSR on each group
Time Frame
12 weeks treatment
Title
Assessment of Quality Of Life (QOL)
Description
Assessment of QOL related to HFSR using The Hand-Foot Skin Reaction and Quality of Life Questionnaire (HF-QoL) scoring system. HF-QOL instrument comprises a 20-item symptom scale and an 18-item daily activity scale. Each item was scored from 0 (not at all) to 4 (always or extremely). Therefore, the range of score for HF-QoL was from 0 to 152 points. (Ref. Anderson et al. The Oncoligist 2015;20:831-838)
Time Frame
12 weeks treatment
Title
Overall survival
Description
Overall survival of patients
Time Frame
12 weeks treatment
Title
Tumor response
Description
Tumor response using mRECIST criteria
Time Frame
12 weeks treatment
Title
Other side effect
Description
The occurrence rate of other side effect excluding HFSR
Time Frame
12 weeks treatment
Title
Incidence of HFSR on 2, 4, 8, and 12 weeks on each group
Description
Comparison of incidence of HFSR on 2, 4, 8, and 12 weeks between placebo group and urea cream group
Time Frame
2, 4, 8, and 12 weeks

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient who was diagnosed with hepatocellular carcinoma, and was accompanied by impossible for radical treatment in disease period or do not reaction for local treatment, and the first time for sorafenib injection. Standard of hepatocellular carcinoma diagnosis (2014, The Korean Liver Cancer Association) Suitable on hepatocellular carcinoma pathologically Hepatic nodule size over 1 cm on high-risk patients(hepatitis B virus positive, hepatitis C virus positive and liver cirrhosis) that identified by ultrasonography : In the case of suitable on hepatocellular carcinoma on over in one or two more dynamic contrast enhanced CT, dynamic contrast enhanced MRI, or MRI with Gadolinium Ethoxybenzyl Diethylenetriamine Pentaacetic Acid(Gd-EOB-DTPA) Hepatic nodule size under 1 cm on high-risk patients that identified by ultrasonography : serum Alpha-fetoprotein(AFP) elevated over normal range constantly when hepatitis activity was restrained, and the case of suitable on hepatocellular carcinoma on over in two more the above image diagnoses Exclusion Criteria: Unsuitable on inclusion criteria Patient who has had systemic anticancer therapy before (including sorafenib) Patient who is receiving another treatment to hepatocellular carcinoma recent 3 weeks (allow to local treatment of metastasis lesion only) Pregnant or Breastfeeding Urea cream contraindication patient (Acute eczema, Inflammatory dermatopathy and Hypersensitivity on Urea and Methylparaben)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ji Hoon Kim, MD
Organizational Affiliation
Associate Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Korea University Guro Hospital
City
Seoul
ZIP/Postal Code
08308
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
No
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The Effect of Urea Cream on Sorafenib-associated Hand-Foot Skin Reaction

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