A multicenter randomized phase II trial of topical betamethasone ointment for preventing severe chemoradiotherapy-induced oral mucositis in head and neck cancer.
Abstract
12015 Background: Severe oral mucositis (OM) is a major unmet clinical problem during cisplatin-based chemoradiotherapy (CRT) for head and neck cancer, with no established preventive strategy. Although topical dexamethasone has shown benefit during radiotherapy alone, its efficacy during CRT is limited. This study represents the first randomized trial evaluating a potent topical corticosteroid, betamethasone ointment, for preventing severe OM during cisplatin-based CRT. Methods: Patients with head and neck cancer receiving CRT with the oral cavity included in the radiation field were enrolled at six institutions in Japan. Upon development of grade 1 OM (CTCAE v5.0), patients were randomized to standard oral care alone (control) or standard oral care plus topical betamethasone ointment applied three times daily (intervention). Treatment continued until completion of radiotherapy or onset of grade 3 OM. The primary endpoint was time to grade 3 OM, analyzed using multivariable Cox proportional hazards models. Secondary endpoints included time to grade 2/3 OM and incidence of oral candidiasis. Results: A total of 68 patients were analyzed (intervention n=35; control n=33). The cumulative incidence of grade 3 OM was significantly lower in the intervention group (14.3%) than in the control group (48.5%). Topical betamethasone significantly reduced the risk of grade 3 OM (HR 0.246, 95% CI 0.081–0.749). Betamethasone also delayed the onset of grade 2/3 OM. Non-use of a spacer was independently associated with grade 2 OM. Betamethasone did not increase oral candidiasis, whereas denture use was a significant risk factor. Conclusions: Topical betamethasone ointment substantially reduced the incidence of severe OM during cisplatin-based CRT without increasing oral candidiasis. This simple, low-cost, and widely accessible intervention could be rapidly implemented in routine clinical practice to mitigate CRT-induced toxicity. To our knowledge, this is the first randomized trial demonstrating the efficacy of a potent topical corticosteroid for preventing severe OM during cisplatin-based CRT. Clinical trial information: jRCTs071200013.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (15)
Sakiko Soutome
Takumi Hasegawa
Graduate School of Advanced Science and Engineering
Mika Nishii
Department of Medical Technology, Division of Dentistry and Rehabilitation, Kob University Hospital, Kobe-Shi, Japan
Yasumasa Kakei
Daisuke Takeda
Department of Oral and Maxillofacial Surgery, Kobe University Graduate School of Medicine, Kobe-Shi, Japan
Shunsuke Sawada
Department of Oral and Maxillofacial Surgery, Kansai Medical University, Hirakata, Japan
Yuka Kojima
Madoka Funahara
Hiroshi Kurita
Department of Oral and Maxillofacial Surgery, Shinshu University School of Medicine, Matsumoto, Japan
Kenichiro Ishibashi
Hirokazu Nakahara
Masaya Akashi
Department of Oral and Maxillofacial Surgery, Kobe University Graduate School of Medicine, Kobe, Japan
Koichiro Irie
Tomohiro Yamada
1Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital, Hematology, Nagoya, Japan
Masahiro Umeda