Efficacy Study of Cosmetic Product on Xerosis Induced by Systemic Anticancer Treatments

Xerosis Clinical Trial

Official title:

Randomized, Comparative Study to Evaluate the Effects of Cosmetic Balm on Xerosis and Associated Signs and Symptoms, Induced by Systemic Anticancer Treatments in Subjects Receiving Targeted Educational Action Compared to a Control Group

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04181177
• Other study ID #: RV4429A2018386
• Status: Completed
• Start date: February 19, 2019
• Est. completion date: March 1, 2022

Study information

• Verified date: September 2022
• Source: Pierre Fabre Dermo Cosmetique
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Xerosis is one of the most common adverse events in patients treated with new cancer therapies and chemotherapies, such as multi-kinase inhibitors and more specifically, immunological checkpoint inhibitors used in the treatment of several cancers.

Xerosis appears as a result of a deterioration of the stratum corneum which results in a reduction of the hydric power of the skin. It reaches the trunk and limbs, with an incidence of 4-35%, and gradually disappears after the end of treatment.

Preventive targeted educational action is essential before initiation of cancer treatment. Once the xerosis is installed, the management is based on the use of emollients to contribute to the hydric correction of the skin. In the case of inflammation or associated infection, the administration of topical corticosteroids and / or local or oral antibiotic therapy is prescribed.

The aim of this study is to evaluate the efficacy of the cosmetic product (balm) on the improvement of xerosis induced by systemic anticancer treatments, in participants receiving targeted educational action compared to a control group.

Clinical, biological and biometrological assessments will be performed to characterized the effects in both induced xerosis and associated signs and symptoms.

Each group will include 40 participants.

Description:

Systemic anticancer treatments, whether they are conventional molecules or more current molecules such as targeted therapies, are responsible for numerous dermatological adverse effects, notably xerosis, the repercussions of which may lead to a decrease in compliance, dose reductions or even a complete cessation of cancer treatment.

To date, the management of these adverse effects is not performed routinely and published efficacy data on secondary side effects are missing.

The purpose of this comparative study is to evaluate the clinical efficacy of the RV4429A balm combined with a targeted educational action, on the improvement of induced xerosis on the one hand and on the improvement of the signs and symptoms associated with this induced xerosis. on the other hand ; based on clinical, biometrological and biological criteria. The objective is to provide data on this product in this symptomatology.

Xerosis and the associated dermatological signs / symptoms will be assessed individually as well as through overall scores, as measured by both the investigator and the patient as clinical expression is often poorly correlated with psychic and functional impact. Quality of life, cosmetic acceptability and targeted educational action and tolerance will also be assessed.

The improvement of the quality of life of the patients, the reduction of the undesirable effects induced could thus guarantee the observance of the patients vis-à-vis the anticancer treatments.

The study area is the whole body. A target area will be chosen and will be located on one of the upper limbs (outside the hands) or on the trunk (outside a hairy area). The target area is defined as the xerosis area representative of the the most severe xerotic state, according to the investigator's opinion.

The dermatologist who will evaluate the participant should be, as far as possible, the same throughout the study.

A second period will be carried out by the participants of the control group who will enter in the targeted educational action phase of in their turn.

The study includes 2 visits for the informed group and 3 visits for the control group:

• V1 (J1) - Inclusion (common to both groups)

• V2 (J21 ± 2J or J28 ± 2J) - End of study (informed group) - Intermediate (control group)

• V3 (J42 ± 2J or J56 ± 2J) - End of study (control group) The dates of the visits 2 and 3 will be adapted to the frequency of the visits of administration of the anticancer treatment.

The maximum duration of participation for a participant may be 23 days or 44 days or it may be 30 days or 58 days from the inclusion visit to the end-of-study visit, depending on the group and depending the timeframe between cancer treatment visits.

All subjects in the control group will enter onto the informed group after three weeks or one month (depending on the timeframe between cancer treatment visits), regardless of their condition (presence or absence of on-going xerosis).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 29
• Est. completion date: March 1, 2022
• Est. primary completion date: January 25, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Criteria related to the population:

• Subject having signed his/her written informed consent for his/her participation in the study

• Subject affiliated to a social security system or health insurance, or is a beneficiary

• Subject with phototype I, II, III, IV according to the Fitzpatrick scale

• For woman of childbearing potential: use of an effective method of contraception, as assessed by the investigator for at least 4 weeks before inclusion in the study and using it during the whole duration of the study

2. Criteria related to diseases and general health:

• Subject having a grade = 2 of dry skin on NCI-CTCAE scale in 3 grades, assessed on the entire body

• Subject having an intensity of dry skin = 3, according a 5-points scale, on the target area

• Subject having a general state of clinical and/or physical health adequate(s) to carry out the study according to the investigator's opinion, and presenting a total score = 1 according to the "performance status" scale of WHO (World Health Organization) in 5-points

3. Criteria related to treatments:

• On-going systemic anticancer treatment, whatever the dosage and whatever the duration of treatment

Exclusion Criteria:

1. Criteria related to the population:

• For woman of childbearing potential: pregnant or breastfeeding or planning to be pregnant during the study

• Subject unable to understand the information given including study procedures (for linguistic or psychiatric reasons) and to give his/her consent in writing

• Subject who, in the judgement of the investigator, is not likely to be compliant during the study

• Subject who has forfeited his/her freedom by administrative or legal award or is under guardianship

• Subject is in a position likely to represent a conflict of interest and/or is a family member of any people involved in the conduct of the study (secretary, nurse, technician,…), of the investigational site

• Subject who is currently participating, who plans to participate or who has participated within the previous weeks in another clinical study liable to interfere with the study assessments according to the investigator's assessment

• Subject unable to write required information in a subject diary

2. Criteria related to diseases and general health

• Subject having a grade= 3 of pruritus on NCI-CTCAE scale in 3 grades, assessed on the entire body

• Subject presenting infectious (viral, bacterial, fungal) or inflammatory complications, on the entire body

• Subject with a history of atopic or contact dermatitis

• Subject presenting any other dermatological condition the day of the visit (atopic or contact dermatitis, chronic xerosis, ..), liable to interfere with the study assessments, according to the investigator's opinion

• Subject with history of allergy or intolerance to any of the study products ingredients

3. Criteria related to treatments and cosmetic products

• Radiotherapy in progress or planned during the study

• Application of dermocorticoïdes during 5 consecutive days within the 10 days previous the visit

• Any other topical or systemic treatment previously used or on-going (other than systemic anticancer treatment and antihistaminic) liable to interfere with the study assessments or incompatible with the study procedures, according to the investigator's opinion

• Application of any other topical treatment or topical cosmetic product (except hygiene product), liable to interfere with the study assessments, according to the investigator's opinion, on the entire body, the day of the visit

Related Conditions & MeSH terms

• Xerosis

Intervention

Other:
• Cosmetic product
Cosmetic balm: application twice daily on the whole body in sufficient quantity to cover all the xerosis areas. It contains an I-modulia(r) complex which decreases the sensation of itching, CER-OMEGA which are lipids similar to those of the skin, help repair and nourish the skin, finally Avène Thermal Spring Water which have soothing and softening properties. Targeted education action consist in advices and preventive measures (including hygiene) regarding xerosis and associated dermatological signs / symptoms. Emollient and application tips and other supportive care tips will be provided. The targeted educational action will be monitored by the medical and paramedical teams (specialized nurses).

Locations

Country	Name	City	State
France	Centre Hospitalier de Cahors	Cahors
France	Centre Hospitalier de Carcassonne	Carcassonne
France	Centre Hospitalier de Tarbes	Tarbes
France	Institut Universitaire du Cancer Toulouse- Oncopole	Toulouse

Sponsors (1)

Lead Sponsor	Collaborator
Pierre Fabre Dermo Cosmetique

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	dry skin on scale NCI CTCAE 5.0	Grade1: Covering <10% BSA* and no associated erythema or pruritus; Grade2: Covering 10 - 30% BSA* and associated with erythema or pruritus; limiting instrumental ADL*; Grade3: Covering >30% BSA* and associated with pruritus; limiting self care ADL* * BSA : Body Surface Area, ADL : Activities of Daily Living	Change from baseline to 3 weeks or 4 weeks later according to the frequency of participant's oncologic received treatment, for each group, on the entire body
Secondary	dry skin on scale NCI CTCAE 5.0	Grade1: Covering <10% BSA* and no associated erythema or pruritus; Grade2: Covering 10 - 30% BSA* and associated with erythema or pruritus; limiting instrumental ADL*; Grade3: Covering >30% BSA* and associated with pruritus; limiting self care ADL* * BSA : Body Surface Area, ADL : Activities of Daily Living	Day 21 or Day 28 (according to the frequency of participant's oncologic received treatment) and Day 42 or Day 56 (according to the frequency of participant's oncologic received treatment), for group control, on the entire body
Secondary	pruritus on scale NCI CTCAE 5.0	Grade1: Mild or localized; topical intervention indicated; Grade2: Widespread and intermittent; skin changes from scratching (e.g., edema, papulation, excoriations, lichenification, oozing/crusts); oral intervention indicated; limiting instrumental ADL; Grade3: Widespread and constant; limiting self care ADL or sleep; systemic corticosteroid or immunosuppressive therapy indicated	Change from baseline to 3 weeks or 4 weeks later according to the frequency of participant's oncologic received treatment, for each group, on the entire body
Secondary	pruritus on scale NCI CTCAE 5.0	Grade1: Mild or localized; topical intervention indicated; Grade2: Widespread and intermittent; skin changes from scratching (e.g., edema, papulation, excoriations, lichenification, oozing/crusts); oral intervention indicated; limiting instrumental ADL; Grade3: Widespread and constant; limiting self care ADL or sleep; systemic corticosteroid or immunosuppressive therapy indicated	Day 21 or Day 28 (according to the frequency of participant's oncologic received treatment) and Day 42 or Day 56 (according to the frequency of participant's oncologic received treatment), for each group, on the entire body
Secondary	dry skin on 5-points scale	0: absent; 1: very mild; 2: mild; 3: moderate; 4: severe	Change from baseline to 3 weeks or 4 weeks later according to the frequency of participant's oncologic received treatment, for each group, on the target area
Secondary	dry skin on 5-points scale	0: absent; 1: very mild; 2: mild; 3: moderate; 4: severe	Day 21 or Day 28 (according to the frequency of participant's oncologic received treatment) and Day 42 or Day 56 (according to the frequency of participant's oncologic received treatment), for each group, on the target area
Secondary	Investigator Global Assessment (IGA) on 5-points scale	0: aggravation; 1: no change; 2: slight improvement; 3: clear improvement; 4: total improvement	Day 21 or Day 28 (according to the frequency of participant's oncologic received treatment) and Day 42 or Day 56 (according to the frequency of participant's oncologic received treatment), for each group, on the target area
Secondary	Patient Global Assessment (PGA) on 5-points scale	0: aggravation; 1: no change; 2: slight improvement; 3: clear improvement; 4: total improvement	once a week at home (before application if any), during 3 weeks or 4 weeks according to the frequency of participant's oncologic received treatment, for informed group, on the target area
Secondary	Patient Global Assessment (PGA) on 5-points scale	0: aggravation; 1: no change; 2: slight improvement; 3: clear improvement; 4: total improvement	once a week at home (before application if any), during 6 weeks or 8 weeks according to the frequency of participant's oncologic received treatment, for control group, on the target area
Secondary	dryness/tightness; tingling; warming/burning; pruritus/itching; discomfort	Numeric Scale 0-10	once a week at home (before application if any), during 3 weeks or 4 weeks according to the frequency of participant's oncologic received treatment, for informed group, on the target area
Secondary	dryness/tightness; tingling; warming/burning; pruritus/itching; discomfort	Numeric Scale 0-10	once a week at home (before application if any), during 6 weeks or 8 weeks according to the frequency of participant's oncologic received treatment, for control group, on the target area
Secondary	Dermatology Life Quality Index questionnaire (DLQI)	Questionnaire Score 0-30	Change from baseline to 3 weeks or 4 weeks later according to the frequency of participant's oncologic received treatment, for each group
Secondary	Dermatology Life Quality Index questionnaire (DLQI)	Questionnaire Score 0-30	Day 21 or Day 28 (according to the frequency of participant's oncologic received treatment) and Day 42 or Day 56 (according to the frequency of participant's oncologic received treatment), for each group
Secondary	Cosmetic acceptability questionnaire	Questionnaire ad-hoc	3 weeks or 4 weeks according to the frequency of participant's oncologic received treatment, for informed group
Secondary	Cosmetic acceptability questionnaire	Questionnaire ad-hoc	6 weeks or 8 weeks according to the frequency of participant's oncologic received treatment, for control group
Secondary	Targeted educational action questionnaire	Questionnaire ad-hoc	3 weeks or 4 weeks according to the frequency of participant's oncologic received treatment, for informed group
Secondary	Targeted educational action questionnaire	Questionnaire ad-hoc	6 weeks or 8 weeks according to the frequency of participant's oncologic received treatment, for control group
Secondary	Hydration Index (IH)	Measure by corneometer	Change from baseline to 3 weeks or 4 weeks later according to the frequency of participant's oncologic received treatment, for each group, on target area
Secondary	Hydration Index (IH)	Measure by corneometer	Day 21 or Day 28 (according to the frequency of participant's oncologic received treatment) and Day 42 or Day 56 (according to the frequency of participant's oncologic received treatment), for each group, on target area
Secondary	Corneocytes quantification	Sampling performed with DSquame disc and image taking with C-Cube probe.	Change from baseline to 3 weeks or 4 weeks later according to the frequency of participant's oncologic received treatment, for each group, on target area
Secondary	Corneocytes quantification	Sampling performed with DSquame disc and image taking with C-Cube probe.	Day 21 or Day 28 (according to the frequency of participant's oncologic received treatment) and Day 42 or Day 56 (according to the frequency of participant's oncologic received treatment), for each group, on target area