Reduction of Oral Mucositis Severity using a Topical Vasoconstrictor in Bone Marrow Transplant Patients

Authors

  • Ningfeng Fiona Li Erasmus University Rotterdam, The Netherlands and London University, UK.
  • William E. Fahl McArdle Laboratory for Cancer Research at the University of Wisconsin-Madison, USA.

DOI:

https://doi.org/10.9734/bpi/nfmmr/v10/4000F

Keywords:

Cyclophosphamide, total body irradiation, adrenergic, orotopical

Abstract

Grade 3 oral mucositis (OM) is historically observed in >90% of bone marrow transplant patients who received the cyclophosphamide + total body irradiation (CY+TBI) conditioning regimen. It was previously shown that orotopically applied adrenergic vasoconstrictor prevented up to 100% of radiation-induced oral mucositis in two preclinical animal models. Adrenergic vasoconstrictor (i.e., phenylephrine in an aqueous-alcohol NG11-1 formulation) was orotopically applied to three patients (ages 24-29) who received the CY+TBI conditioning regimen; they were compared to five matched controls who received no orotopical vasoconstrictor. All patients received the CY+TBI conditioning regimen for acute lymphoblastic leukemia within the University of Wisconsin Adult Bone Marrow Transplant Program. Over the seven-day CY+TBI conditioning regimen, 20 min before each treatment, either radiation or chemotherapy, vasoconstrictor was applied topically to the oral cavity, and patients then received either 1.5 Gy whole-body radiation or IV cyclophosphamide. OM severity was scored over a three-week period using: i) physical assessments, ii) daily photos of the oral cavity, iii) oral pain and oral function score sheets, and iv) recorded narcotic consumption.  Both “Grade 3 OM” duration and “any OM” duration in vasoconstrictor-treated patients were substantially lower than for the five control patients. Though nasogastric tube or total parenteral nutrition were used in 3 out of 5 control patients, there was no use of these supportive care measures in the three vasoconstrictor-treated patients.  Orotopically applied NG11-1 vasoconstrictor formulation substantially reduced the incidence and severity of “Grade 3” and “any” oral mucositis when compared to matched control patients, all of whom received the same CY+TBI conditioning regimen. The liquid orotopical formulation was easily tolerated by patients both in its ease of use and lack of side effects. 

Published

2021-08-25

How to Cite

Ningfeng Fiona Li, & William E. Fahl. (2021). Reduction of Oral Mucositis Severity using a Topical Vasoconstrictor in Bone Marrow Transplant Patients. New Frontiers in Medicine and Medical Research Vol. 10, 47–55. https://doi.org/10.9734/bpi/nfmmr/v10/4000F