Medical Oncology Unit, ASST del Garda, Desenzano del Garda Hospital, Località Montecroce 1, 25015, Desenzano del Garda, BS, Italy.
Medical Oncology Department, ASST Monza San Gerardo Hospital, Monza, Italy.
BMC Cancer. 2022 Aug 24;22(1):915. doi: 10.1186/s12885-022-10018-3.
The non-inferiority of dexamethasone (DEX) on day 1, with or without low-dose DEX on days 2 and 3, combined with oral NEPA (netupitant/palonosetron), compared with the guideline-consistent use of DEX was demonstrated in cisplatin. Here, we complete the analysis by assessing the impact of emesis on daily lives of patients receiving DEX-sparing regimens using the Functional Living Index-Emesis (FLIE).
Chemotherapy-naïve patients undergoing cisplatin (≥70 mg/m), were given NEPA and DEX (12 mg) on day 1 and randomized to receive either 1) no further DEX (DEX1), 2) oral DEX (4 mg daily) on days 2-3 (DEX3), or 3) DEX (4 mg twice daily) on days 2-4 (DEX4; control). Patients completed the FLIE questionnaire on day 6 of cycle 1. Endpoints included the FLIE nausea domain, vomiting domain, and overall combined domain scores, as well as the proportion of patients with no impact on daily life (NIDL; overall score > 108). This was a protocol-planned analysis.
In the DEX1 group, no significant differences were observed in the FLIE nausea score (48.9 [±1.8; SE] vs. 53.7 [±1.5]), vomiting score (56.6 [±1.4] vs. 58.7 [±0.8]) and overall score (105.6 [±2.8] vs.112.4 [±1.9]) versus DEX4 control; similar results were observed in the DEX3 group for nausea score (49.6 [±1.7]), vomiting score (58.2 [±1]) and overall score (107.8 [±2.4]) versus control. There were no significant between-group differences in the proportion of patients reporting NIDL.
Reducing DEX, when administered with NEPA, does not seem to adversely impact the daily functioning in patients undergoing cisplatin.
ClinicalTrials.gov NCT04201769 . Registration date: 17/12/2019 - Retrospectively registered.
与指南一致地使用地塞米松(DEX),在第 1 天,联合或不联合第 2 和第 3 天低剂量 DEX,与接受 NEPA(奈妥匹坦/帕洛诺司琼)的安慰剂相比,在顺铂中显示出非劣效性。在此,我们通过使用功能性生活指数-呕吐(FLIE)评估接受 DEX 节约方案的患者呕吐对日常生活的影响,来完成分析。
接受顺铂(≥70mg/m)的化疗初治患者给予 NEPA 和 DEX(12mg)在第 1 天,并随机分为 1)不再接受 DEX(DEX1),2)第 2-3 天口服 DEX(4mg 每日)(DEX3),或 3)第 2-4 天 DEX(4mg 每日两次)(DEX4;对照组)。患者在第 1 周期的第 6 天完成 FLIE 问卷。终点包括 FLIE 恶心评分、呕吐评分和总体联合评分,以及日常生活无影响的患者比例(NIDL;总分>108)。这是一项方案计划的分析。
在 DEX1 组中,FLIE 恶心评分(48.9[±1.8;SE] vs. 53.7[±1.5])、呕吐评分(56.6[±1.4] vs. 58.7[±0.8])和总体评分(105.6[±2.8] vs. 112.4[±1.9])与 DEX4 对照组相比,差异无统计学意义;在 DEX3 组中,恶心评分(49.6[±1.7])、呕吐评分(58.2[±1])和总体评分(107.8[±2.4])与对照组相比,差异也无统计学意义。报告 NIDL 的患者比例在组间无显著差异。
在给予 NEPA 时,减少 DEX 似乎不会对接受顺铂治疗的患者的日常功能产生不利影响。
ClinicalTrials.gov NCT04201769。注册日期:2019 年 12 月 17 日-回顾性注册。