Ibrahim E M, Al-Mulhim F A, Al-Muhanna F A, Al-Amri A
Department of Internal Medicine, College of Medicine and Medical Sciences, King Faisal University, Saudi Arabia.
J Family Community Med. 1998 Jan;5(1):37-43.
The study was designed to assess prospectively the efficacy of granulocyte-macrophage colony-stimulating factor (GM-CSF) in the management of chemotherapy-induced oral mucositis in non-neutropenic cancer patients.
In a prospective open study, adult cancer patients with chemotherapy-induced, neutropenia-independent oral mucositis were treated with GM-CSF (Schering Plough Corporation, Kenilworth, NJ) prepared as mouthwash solution (5 to 10 μgm /ml). GM-CSF was administered within 24 hours of occurrence of oral mucositis at a frequency of 4 to 6 times daily. Systemic GM-CSF was not permissible. Oral mucositis was graded according to the modified Radiation Therapy Oncology Group criteria.
Forty-nine patients were recruited but nine were subsequently excluded as they experienced neutropenia during GM-CSF therapy. The remaining 40 patients were all evaluable. Most patients had either Grade 3 or 4 gross (71%) or functional (70%) mucositis. The mean ± SEM gross oral mucositis scores for all 40 patients combined decreased from 3.3 ± 0.11 at baseline to 2.1 ± 0.12 (p<0.0001) after 2 days, 0.95 ± 0.11 (p<0.0001) after 5 days and 0.23 ± 0.07 (p <0.0001) after 10 days of therapy. Likewise, the mean ± SEM functional oral mucositis scores decreased from 3.03 ± 0.13 at baseline to 1.58 ± 0.13 (p<0.0001) after 2 days, 0.68 ± 0.11 (p<0.0001) after 5 days, and 0.15 ± 0.06 (p<0.0001) after 10 days of therapy. The duration of severe oral mucositis was also shortened as Grade 0 or 1 (gross mucositis grading score) was evident in 12 (30%), 29 (73%), and 40 (100%) patients by the 2(nd), 5(th) and 10(th) day of therapy, respectively. Similarly, Grade 0 or 1 (functional mucositis grading score) reported in 19 (48%), 31 (78%), and 40 (100%) patients by the 2(nd), 5(th) and 10(th) day of therapy, respectively. The use of GM-CSF mouthwash was not associated with any apparent ill effect.
GM-CSF mouthwash as used in this study has a significant recuperative efficacy on the severity, morbidity, and duration of chemotherapy-induced oral mucositis. A large randomized, placebo-controlled study is warranted to ascertain that benefit and determine the optimal dosage and schedule.
本研究旨在前瞻性评估粒细胞-巨噬细胞集落刺激因子(GM-CSF)对非中性粒细胞减少的癌症患者化疗所致口腔黏膜炎的治疗效果。
在一项前瞻性开放研究中,对化疗引起的、与中性粒细胞减少无关的口腔黏膜炎的成年癌症患者,使用辉瑞公司(新泽西州肯尼沃思)生产的GM-CSF制成漱口水溶液(5至10μg/ml)进行治疗。在口腔黏膜炎出现后的24小时内开始使用GM-CSF,每天使用4至6次。不允许使用全身性GM-CSF。根据改良的放射治疗肿瘤学组标准对口腔黏膜炎进行分级。
招募了49名患者,但有9名患者在GM-CSF治疗期间出现中性粒细胞减少,随后被排除。其余40名患者均可评估。大多数患者有3级或4级严重(71%)或功能性(70%)黏膜炎。所有40名患者的口腔黏膜炎严重程度评分均值±标准误从基线时的3.3±0.11降至治疗2天后的2.1±0.12(p<0.0001)、5天后的0.95±0.11(p<0.0001)和10天后的0.23±0.07(p<0.0001)。同样,功能性口腔黏膜炎评分均值±标准误从基线时的3.03±0.13降至治疗2天后的1.58±0.13(p<0.0001)、5天后的0.68±0.11(p<0.0001)和10天后的0.15±0.06(p<0.0001)。严重口腔黏膜炎的持续时间也缩短了,在治疗的第2天、第5天和第10天,分别有12名(30%)、29名(73%)和40名(100%)患者的严重口腔黏膜炎分级为0级或1级(严重口腔黏膜炎分级评分)。同样,在治疗的第2天、第5天和第10天,分别有19名(48%)、31名(78%)和40名(100%)患者的功能性口腔黏膜炎分级为0级或1级(功能性口腔黏膜炎分级评分)。使用GM-CSF漱口水未发现明显不良反应。
本研究中使用的GM-CSF漱口水对化疗所致口腔黏膜炎的严重程度、发病率和持续时间具有显著的恢复疗效。有必要进行一项大型随机、安慰剂对照研究以确定其益处并确定最佳剂量和疗程。