Randomized, Prospective, Open-label Phase III Trial Comparing Mebo Ointment with Biafine Cream for the Management of Acute Dermatitis during Radiotherapy for Breast Cancer

dc.contributor.authorGeara, Fady B.
dc.contributor.authorEid, Toufic A.
dc.contributor.authorZouain, Nicolas
dc.contributor.authorThebian, Ranim
dc.contributor.authorAndraos, Therese Youssef
dc.contributor.authorChehab, Chirine Y.
dc.contributor.authorRamia, Paul S.
dc.contributor.authorYoussef, Bassem Y.
dc.contributor.authorZeidan, Youssef H.
dc.contributor.departmentRadiation Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:12:22Z
dc.date.available2025-01-24T12:12:22Z
dc.date.issued2018
dc.description.abstractPurpose: Acute radiation dermatitis is a common side-effect of radiotherapy in breast cancer and has a profound impact on patients' quality of life, due to pain and discomfort. The aim of this study is to compare the effect of β-sitosterol (Mebo) ointment to trolamine (Biafine) cream for the prevention and treatment of radiation dermatitis in breast cancer patients receiving adjuvant radiation therapy. Materials and Methods: This is a prospective open-label randomized phase III study developed to assess the efficacy of 2 topical agents used for management of acute radiation dermatitis. Female breast cancer patients who needed a course of radiation therapy in our institution were enrolled and randomized into 2 groups 1 with Mebo ointment and 1 with Biafine cream. Both medications were applied twice per day during the whole period of treatment and skin reactions and related symptoms were assessed weekly during the entire course. Grading of skin reactions was done according to the Radiation Therapy Oncology Group grading system. Results: Between September 2015 and May 2017, a total of 161 patients were recruited for this trial. Mean age was similar for both groups (50.19 12.57 vs. 51.7311.23, respectively, P=0.41). All other patients and treatment characteristics were similar in both groups, except for the use of boost (82.7% in the Biafine group vs. 36.7% in Mebo group, P =0.012). Analysis was done for reactions recorded before the beginning of the boost and for the entire course including the boost. Using univariate and multivariate analysis, there was no significant difference in grades 2 and 3 dermatitis between the 2 groups. However, the incidence of severe pruritus and severe local skin pain were both significantly reduced in the Mebo group (14.1% in Biafine vs. 2.9% in Mebo, P=0.016 for pruritus and 11.5% vs. 1.4%, respectively, P=0.02 for severe pain). Conclusions: This study showed no difference between Mebo and Biafine in the incidence and severity of breast skin dermatitis during radiation therapy. However, the use of Mebo ointment was associated with decreased severe pruritus and pain which could positively affect patient comfort and quality of life. © 2018 Wolters Kluwer Health, Inc. All rights reserved.
dc.identifier.doihttps://doi.org/10.1097/COC.0000000000000460
dc.identifier.eid2-s2.0-85048260810
dc.identifier.pmid29889137
dc.identifier.urihttp://hdl.handle.net/10938/32733
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofAmerican Journal of Clinical Oncology: Cancer Clinical Trials
dc.sourceScopus
dc.subjectBreast cancer
dc.subjectDermatitis
dc.subjectRadiation therapy
dc.subjectAdministration, topical
dc.subjectBreast neoplasms
dc.subjectCarcinoma, ductal, breast
dc.subjectCarcinoma, intraductal, noninfiltrating
dc.subjectCarcinoma, lobular
dc.subjectDermatologic agents
dc.subjectDisease management
dc.subjectEmulsions
dc.subjectFemale
dc.subjectFollow-up studies
dc.subjectHumans
dc.subjectLipids
dc.subjectMiddle aged
dc.subjectPrognosis
dc.subjectProspective studies
dc.subjectRadiodermatitis
dc.subjectRadiotherapy
dc.subjectSitosterols
dc.subjectBiafine
dc.subjectDermatological agent
dc.subjectUnclassified drug
dc.subjectLipid
dc.subjectMoist exposed burn ointment
dc.subjectSitosterol derivative
dc.subjectAcute disease
dc.subjectAdjuvant radiotherapy
dc.subjectAdult
dc.subjectArticle
dc.subjectCancer patient
dc.subjectCancer radiotherapy
dc.subjectControlled study
dc.subjectCream
dc.subjectHuman
dc.subjectMajor clinical study
dc.subjectOintment
dc.subjectOpen study
dc.subjectPatient comfort
dc.subjectPhase 3 clinical trial
dc.subjectProspective study
dc.subjectPruritus
dc.subjectRadiation dermatitis
dc.subjectRandomized controlled trial
dc.subjectSkin manifestation
dc.subjectSkin pain
dc.subjectStudy design
dc.subjectAdministration and dosage
dc.subjectBreast tumor
dc.subjectClinical trial
dc.subjectComparative study
dc.subjectEmulsion
dc.subjectFollow up
dc.subjectIntraductal carcinoma
dc.subjectLobular carcinoma
dc.subjectPaget nipple disease
dc.subjectPathology
dc.subjectTopical drug administration
dc.titleRandomized, Prospective, Open-label Phase III Trial Comparing Mebo Ointment with Biafine Cream for the Management of Acute Dermatitis during Radiotherapy for Breast Cancer
dc.typeArticle

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