Bepanthen Versus Cetomacrogol in Epidermal Growth Factor Receptor Inhibitors (EGFRI) (BeCet)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01136005
Recruitment Status : Completed
First Posted : June 3, 2010
Last Update Posted : November 13, 2017
CB Boers ORG.
Memorial Sloan Kettering Cancer Center
Leiden University Medical Center
Information provided by (Responsible Party):
Impaqtt Foundation

June 2, 2010
June 3, 2010
November 13, 2017
September 2010
December 2016   (Final data collection date for primary outcome measure)
  • grade 2 or more papulopustular eruption [ Time Frame: 6 weeks ]
    The incidence of grade ≥ 2 papulopustular eruption during the 6 week skin treatment within Bepanthen and Cetomacrogol, as measured by the CTCAE v4.0 and DERETT-H, an dermatologic specific healthcare provider questionnaire for Dermatological Reactions Targeted Therapy.
  • impact of papulopustular eruptions on HRQoL [ Time Frame: 6 weeks ]
    Assess the impact of papulopustular eruptions on HRQoL as measured by the Functional Assessment of Cancer Therapy Questionnaire - EGFRI (FACT-EGFRI) and newly developed symptom experience diary Dermatological Reactions Targeted Therapy - Patients (DERETT-P).
Same as current
Complete list of historical versions of study NCT01136005 on Archive Site
  • patient tolerability and satisfaction of study cream [ Time Frame: 6 weeks ]
    Determine the patient tolerability and satisfaction of Bepanthen®/ Cetomacrogol cream as measured by DERETT-P.
  • effectiveness of study cream on the adherence [ Time Frame: 6 weeks ]
    Determine the effectiveness of Bepanthen® cream versus Cetomacrogol cream on the adherence to anticancer agents as measured by FACT-EGFRI and DERETT-P.
  • other dermatological side effects [ Time Frame: 6 weeks ]
    Assessments during the 6-week skin treatment period of the incidence and time to onset of other dermatological side effects which can appear together with papulopustular eruptions as measured by DERETT-H.
Same as current
Not Provided
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Bepanthen Versus Cetomacrogol in Epidermal Growth Factor Receptor Inhibitors (EGFRI)
Phase III Randomized Double-Blind Trial of Bepanthen® Cream Versus Cetomacrogol Cream in the Prevention of Papulopustular Eruption in Patients Receiving Epidermal Growth Factor Receptor Inhibitors (EGFRI): BeCet


To assess the preemptive effect of Bepanthen® on decreasing the incidence of specific ≥ grade 2 dermatological side effects of interest in respect of compliance to EGFRI agents, HRQoL and the adherence during the 6-week skin treatment period. The adherence to the study creams will also be studied.


Dermatological side effects, such as papulopustular eruption, xerosis, pruritus, periungual inflammation, mucosal-, and hair abnormalities, and edema occur in up to 90% of patients during treatment with epidermal growth factor receptor inhibitors (EGFRI). Patients are hindered in their daily activities and cannot maintain privacy about their illness because of the prominent side effects. The aesthetic discomfort, which is frequently associated with itching or painful skin or nails can lead to a decreased health related quality of life (HRQoL) and to dose reduction or discontinuation of anticancer treatment.

Patients with dermatological side effects have also an increased risk for cutaneous infections (at least 38%) which can complicate dermatological side effects.

At present, evidence of the effectiveness of the management options for dermatological side effects is lacking, and the effect of the dermatological side effects on HRQoL and adherence remains poorly understood.

Dexpanthenol cream (Bepanthen®, Bayer) has been used extensively to ameliorate acute radiation induced skin toxicity, diaper dermatitis, irritant hand dermatitis, graft-donor site wound healing and burn patients. The hypothesis is that its skin healing possibilities decreases this kind of side effects.

Study design:

Multicenter, two-arm randomized, double blind, prospective parallel group design, phase III study

Study population:

Each patient starting for the first time with EGFRI anticancer therapy which can cause papulopustular eruption (cetuximab, panitumumab, erlotinib, gefitinib, lapatinib, or other), will be included.


80 patients will receive for the first 6 weeks of treatment Bepanthen cream, 80 patients Cetomacrogol cream to apply twice daily. Using FACT-EGFRI, a dermatology-specific questionnaire, this study examines the effect of these side effects on three domains of HRQoL - symptoms, emotions, and functioning. Severity of dermatological side effects will be assessed using the NCI-CTCAE v4.0. Correlation of dermatology HRQoL scores with NCI-CTCAE grade, sex, age, type of EGFRI, and cancer type will be conducted.

Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
  • Cancer
  • Skin Rash
  • Other: dexpanthenol 5% cream
    Apply at least two times a day on face, chest and upper arms during the 6 week treatment period
    Other Names:
    • Bepanthen
    • Provitamin
  • Other: Cetomacrogol cream
    Apply at least two times a day on face, chest and upper arms during the 6 week treatment period
  • Experimental: dexpanthenol 5% cream
    dexpanthenol 5% cream
    Intervention: Other: dexpanthenol 5% cream
  • Active Comparator: cetomacrogol cream
    a vehicle
    Intervention: Other: Cetomacrogol cream

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Same as current
March 2017
December 2016   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male and female subjects
  • ≥18 years of age.
  • Patients must have signed an approved informed consent form prior to registration on study.
  • Histological proof of cancer.
  • A planned course of EGFRI treatment for any type of cancer. Patients must be entered on study ≤ 7 days before EGFRI treatment begins.
  • Have an Eastern Co-operative Oncology Group (ECOG) performance status ≤ 2.
  • Ability to complete questionnaire(s) by themselves or with assistance.
  • Patients need to be free of infection and not using any topical treatments on the skin.

Exclusion Criteria:

  • Use of other concurrent topical creams or lotions at baseline.
  • Concomitant use of medications that may affect trial results (e.a. concurrent use of topical antibiotics, topical steroids, and other topical treatments on face and chest within 14 days of Day 0 (baseline); treatment with any systemic antibiotics within 7 days prior to Day 0.
  • Active dermatological conditions other than papulopustular eruption that may affect trial results. A skin examination reveals the presence of another skin disease in face or chest that may obscure rash to EGFRI and/or condition (excessive facial hair, excessive scarring, sunburn, or other disfigurement) located on the skin that, in the study physician's opinion, would confound the evaluation of the papulopustular eruption.
  • Known allergy or hypersensitivity to ingredients in Bepanthen® or Cetomacrogol.
  • Known sensitivity, papulopustular eruption or other abnormal skin reaction to topical or systemic medications or cleansing products at baseline.
  • Prior treatment with targeted therapy of any kind.
  • Current use of agents that are known to be strong inducers or inhibitors of CYP3A4 that can not be stopped
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
Contact information is only displayed when the study is recruiting subjects
M010-025 ( Other Identifier: Medical research ethics committee: METC Noord Holland )
Not Provided
Not Provided
Impaqtt Foundation
Impaqtt Foundation
  • CB Boers ORG.
  • Memorial Sloan Kettering Cancer Center
  • Leiden University Medical Center
  • Bayer
Study Chair: Christine Boers-Doets, MSc Waterland Hospital, Purmerend, the Netherlands
Principal Investigator: Mario Lacouture, MD Memorial Sloan-Kettering Cancer Center, USA
Principal Investigator: Johan Nortier, PhD Leiden University Medical Centre, the Netherlands
Impaqtt Foundation
November 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP