Patients receiving high-dose chemotherapy/conditioning prior to stem cell transplantation (SCT) are at high risk for developing painful lesions in the oral cavity, known as oral mucositis (OM). In this high risk adult population, the study objectives are to investigate the efficacy and tolerability of Gelclair® (GEL; an FDA cleared medical device indicated for the management of painful oral lesions) and ideal timing of initiation of therapy (at the time of conditioning or after mild OM is diagnosed) for the management of oral mucositis (OM), relative to a commercially available compounded mouth wash (First® Mouthwash BLM "Magic Mouth Wash"; MMW) initiated after mild OM is diagnosed. The study may be adapted based on an interim analysis and recommendations of the interim data review committee.
Adult patients at high risk for developing OM receiving one of the following myeloablative (MA) pre-transplant conditioning regimens prior to allogeneic transplant along with methotrexate (MTX) as part of graft vs. host disease (GVHD) prophylaxis meeting all other eligibility criteria will be enrolled: * FluBu based regimens: either fludarabine: 30 mg/m\^2 x 4 days and busulfan 0.8 mg/kg IV q6h x 4 days; both given daily starting at day -4 OR fludarabine: 40 mg/m\^2 and busulfan: 3.2 mg/kg both given daily on days -6 through -3. * Bu/Cy: busulfan, 0.8 mg/kg IV q6h x 4 days (-7 through -4); cyclophosphamide: 60 mg/kg IV once on days -3 and -2 * Cy/TBI: Cyclophosphamide, 60 mg/kg IV given twice between days -3 and -1 and TBI fractionated (generally over 3 days) for a total of 12Gy GVHD Prophylaxis: • Regimens including methotrexate (MTX; 15 mg/m\^2 planned to be given on days 1, 3, 6 and 11); addition of other agents given along with MTX (e.g., tacrolimus, sirolimus) is acceptable. Duration of treatment: * Arm 1: GEL treatment a minimum of 4x/day initiated from 1st day of conditioning through OM resolution (G0), up to a maximum of 20d. * Arms 2 (GEL) and 3 (MMW): Treatment a minimum of 4x/day initiated when G1 or G2 OM diagnosed during observation period (through Day +14 relative to stem cell infusion) through OM resolution (G0), up to a maximum of 20d.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
28
Polyvinylpyrrolidone (PVP) and Sodium Hyaluronate-Containing Oral Gel
Viscous Lidocaine, Diphenhydramine, and Aluminum-magnesium Hydroxide/Simethicone Antacid Suspension Mouthwash
Massachusetts General Hospital
Boston, Massachusetts, United States
Brigham & Women's Hospital/Dana-Farber Cancer Institute
Boston, Massachusetts, United States
Incidence/occurrence of any grade Oral Mucositis
Incidence/develop of any grade of OM as assessed via WHO OM grading scale (Grades possible: 1-4)
Time frame: Initial study period (initiation of conditioning through day +14 post-transplant)
Area under the curve in mouth and throat soreness (MTS)
Time frame: While OM ongoing during study period (initiation of conditioning through day +28 post-transplant)
Time to onset of any grade OM
WHO Grades 1-4
Time frame: Initial study period (initiation of conditioning through day +14 post-transplant)
Duration of any grade OM
WHO Grades 1-4
Time frame: Study period (initiation of conditioning through day +28 post-transplant)
Severity of OM
WHO Grades 1-4
Time frame: Study period (initiation of conditioning through day +28 post-transplant)
Incidence of severe OM
WHO Grades 3-4
Time frame: Study period (initiation of conditioning through day +28 post-transplant)
Time to onset of severe OM
WHO Grades 3-4
Time frame: Study period (initiation of conditioning through day +28 post-transplant)
Duration of severe OM
WHO Grades 3-4
Time frame: Study period (initiation of conditioning through day +28 post-transplant)
Magnitude of OM-related pain control
Based on subject grading of mouth and throat soreness (VAS 0 (no pain) to 10 (max pain possible)) prior to each randomized/rescue OM treatment.
Time frame: While OM ongoing during study period (initiation of conditioning through day +28 post-transplant)
Duration of pain control
Based on time at a given mouth and throat soreness level and/or need for rescue treatment to control mouth and throat soreness.
Time frame: While OM ongoing during study period (initiation of conditioning through day +28 post-transplant)
Opiate and other background pain medication use
Time frame: While OM ongoing during study period (initiation of conditioning through day +28 post-transplant)
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