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. 2013 Feb 1;27(9):1071–1080. doi: 10.1111/jdv.12082

Table 1.

List of key references recommending the use of cosmetic agents in combination with chemotherapy

Author Study design Title Comments
Lacouture9 Review Mechanisms of cutaneous toxicity
Segaert S et al.7 Review article Clinical signs, pathophysiology and management skin toxicity Adequate sun protection
Avoid skin drying cosmetic products
An emollient on hands and limbs to prevent fissures
Segaert S et al.6 Review article Skin toxicities of targeted therapy Maximize skin hydration
Sun protection
Rash: Avoid retinoids
Xerosis: oil-in-water creams, 5-10% urea
Paronychia: Topical antiseptic
Robert C et al.5 Review article Cutaneous side-effects of kinase inhibitors and blocking antibodies Camouflage cosmetics for folliculitis
Xerosis: prescribe 5–10% urea
Ouwerkerk, J et al.30 Review article Anti EGFR for metastatic colorectal cancer Sunscreen >15+
Avoid cleaning detergents
Mild body cleansers
Moisturizers
Avoid alcohol-based products
Cosmetics to conceal rash
Gentle non-alcohol-based cleansers
Perez-Soler et al.14 Guideline HER1/EGFRI assoc rash: future directions for mgt and outcomes from the HER1/EGFRI rash management forum Cover rash with make-up
Use a skin-friendly make-up remover
Use emollients to prevent skin dryness
Use a good sunscreen
Avoid over-the-counter acne medication
Burtness et al.1 Guideline Task force report. Management of dermatological and other toxicities associated with EGFRI in patients with cancer. Initiate treatment early
Avoid using antiacne medication
Thick emollients
Mild soap
Bernier et al.36 Guideline Consensus guidelines for the mgt of radiation dermatitis and acne-like rash in patients receiving radiotherapy+ EGFRI for the treatment of head and neck squamous cell carcinoma Use gentle cleansers
Topical cosmetics for symptomatic relief
Avoid sun exposure (mineral sunblocks or clothing)
Avoid perfumes and alcohol-based lotions.
Lynch TJ et al.6 Guideline EGFRI dermatologic toxicity overview of outcomes. Expert opinion
Initiation of treatment, moisturize dry areas twice daily
Thick alcohol-free emollient
Broad-spectrum sunscreen 15+ or higher
Add Medical treatment if severity increases.
Infections
 Grenader T et al23 Case report Staph aureus on culture following erlotinib treatment
Author Study Design Population Intervention Sample size Outcome measurement Results
Fluhr 21 3-week, controlled, monocentric, study Experiencing dry, sensitive skin during chemotherapy Application of acidic pH 5.5 washing emulsion and body lotion 30 Skin-surface pH Improved skin physiology
TEWL Sig increase in stratum corneum hydration P < 0.001
Corneometer Reduced TEWL P > 0.007
Sebumeter Significant reduction of skin symptoms P < 0.001
Clinical evaluation
Roé E et al29 Prospective, uncontrolled study of toxicity Cetuximab or erlotinib Severity graded 30 Application of an emollient for treatment of xerosis Good control of symptoms. No description of which cosmetic products used when.
Antiseptic soaps
Pre-emptive skin-care management reduces incidence and severity of skin rash
Wohlrab34 Monocentre POC Breast cancer chemotherapy Application of an emollient 13 DLQI – quality-of-life questionnaire Maintains quality of life and reduces frequency of adverse events Poster
Ocvirk J et al 22 Prospective, monocentre, uncontrolled study cetuximab Review of local practice for management of skin toxicity Application of an emollient after the first documented cutaneous toxicity 31 Skin toxicity Classification using NCI CTCAE v3.0 29.03% grade 1 – advised emollients Recommend prompt application of topical emollients. Add topical of systemic medication for increasing severity.
Xerosis Grade 1 were treated with emollients 51.61% grade 2 – advised emollients + topical antibiotic
fissures Grade 2 emollients+ antibiotics 19.36% grade 3 – interruption of treatment then emollients + topical antibiotics
Grade 3 emollients+ systemic antibiotics Xerosis – advised emollients 2–5% urea
Fissures – creams + dexpanthenol
Use of beauty care and cosmetics improves quality of life and management of side-effects
Boone SL et al13 Qualitative Survey Oncology providers 51 item, open-ended questionnaire pertaining to incidence of rash among patients on EGFRI, treatment practices, patient perceptions, outcome treating rash 110 71–90% of patients experience rash.
8% of providers surveyed obtained a dermatology consult.
Grade 3 and 4 rash interfered with EGFRI therapy (3%).
Taggart L et al39 Pilot study Cancer patients Participation at a look-good–feel-better workshop 20 Self-image NSC Improved self-image (P < 0.005)
Anxiety STAI Reduced anxiety (P < 0.01)
Haley et al18 Monocentre, uncontrolled study Cancer patients receiving either cytotoxic chemotherapy, targeted, or hormonal and/or radiotherapy Applied three test products after first toxicity visit skin and face moisturizer and face wash 99 Q of L: Skindex questionnaire Significant decrease (P = 0.0003) from baseline in mean overall skindex score
Merial-Kieny C et al52 Multicentre qualitative survey Visible cutaneous side-effects following chemotherapy Participated in a make-up training seminar 90 Self-completed questionnaire on tolerance, quality of life and the make-up techniques 95,4% very or satisfied with tolerance
Applied a hypoallergenic make-up 81,2% improved their quality of life.
Amiel P et al40 Multicentre, qualitative survey Cancer patients Survey of patient experience receiving various beauty-care services 60 Observation and semistructured interviews 18/40 appreciated information on treating skin problems
23/40 appreciated information on make-up techniques
Titeca G et al41 Prospective, randomized, controlled multicentre study Breast cancer Antitumor chemotherapy 2H cosmetic care interview 27 VQ dermatological questionnaire less discouraged (P = 0.032)
more self-confident (P = 0.032)
Williams S et al46 Outpatient chemotherapy clinics First chemotherapy Breast cancer patients Informational audiotapes for self care 70 STAI Treatment group increased use of management techniques
Symptoms decreased

TEWL, Trans Epidermal Water Loss; NCI-CTC, National Cancer Institute cutaneous toxicity Criteria.