Grimaudo Maria Susanna, Laffi Alice, Gennaro Nicolò, Fazio Roberta, D'Orazio Federico, Samà Laura, Siracusano Licia Vanessa, Sicoli Federico, Renne Salvatore Lorenzo, Santoro Armando, Bertuzzi Alexia Francesca
Department of Oncology and Hematology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
Front Oncol. 2023 May 31;13:1190123. doi: 10.3389/fonc.2023.1190123. eCollection 2023.
Regorafenib is a tyrosine kinase inhibitor (TKI) approved in metastatic gastrointestinal stromal tumor (GIST), colorectal cancer, and hepatocarcinoma. Anyway, the toxicity profile of Regorafenib standard schedule is associated with poor compliance and a high rate of discontinuation. For this reason, there is a growing need for a Regorafenib personalized schedule emerging from the scientific community.
The aim of this case series was to describe the experience of our sarcoma referral center with the continuous administration of Regorafenib as an alternative regimen to treat metastatic GIST patients.
We retrospectively collected clinical, pathological, and radiological data of patients with metastatic GIST treated with daily personalized Regorafenib at a single tertiary referral center from May 2021 to December 2022.
We identified three patients fulfilling the inclusion criteria. The average follow-up since the start of Regorafenib was 19.1 months (12-25 months). All three patients had started a standard third-line Regorafenib schedule according to guidelines. The reasons for switching to a continuous schedule were as follows: exacerbation of symptoms during week-off treatment in the first patient, a serious adverse event (AE) in the second patient, and a combination of both conditions in the third. After switching, none of the patients reported severe AEs, and they improved control of tumor-related symptoms. Two of the patients experienced disease progression after 16 months (9 months of which is continuous schedule) and 12 months (8.1 months of which is continuous schedule) of Regorafenib, respectively; the third patient is still receiving continuous Regorafenib at the time of writing, with a progression-free survival of 25 months (14 months after the modified schedule start).
With a similar efficacy and lower toxicities, a daily, personalized Regorafenib schedule seems to be a promising alternative to the standard regimen for metastatic GIST patients, including the frail ones. Further prospective analyses are needed to confirm the safety and efficacy of such regimen.
瑞戈非尼是一种酪氨酸激酶抑制剂(TKI),已被批准用于治疗转移性胃肠道间质瘤(GIST)、结直肠癌和肝癌。然而,瑞戈非尼标准给药方案的毒性特征与依从性差和停药率高有关。因此,科学界对瑞戈非尼个性化给药方案的需求日益增长。
本病例系列的目的是描述我们肉瘤转诊中心连续使用瑞戈非尼作为治疗转移性GIST患者的替代方案的经验。
我们回顾性收集了2021年5月至2022年12月在一家三级转诊中心接受每日个性化瑞戈非尼治疗的转移性GIST患者的临床、病理和放射学数据。
我们确定了三名符合纳入标准的患者。自开始使用瑞戈非尼以来的平均随访时间为19.1个月(12 - 25个月)。所有三名患者均已根据指南开始标准的三线瑞戈非尼给药方案。改为连续给药方案的原因如下:第一名患者在停药期症状加重,第二名患者发生严重不良事件(AE),第三名患者则是两种情况兼具。改为连续给药方案后,所有患者均未报告严重AE,并且他们对肿瘤相关症状的控制得到改善。两名患者分别在接受瑞戈非尼治疗16个月(其中9个月为连续给药方案)和12个月(其中8.1个月为连续给药方案)后出现疾病进展;第三名患者在撰写本文时仍在接受连续瑞戈非尼治疗,无进展生存期为25个月(修改给药方案开始后14个月)。
每日个性化瑞戈非尼给药方案具有相似的疗效和更低的毒性,似乎是转移性GIST患者(包括体弱患者)标准方案的一个有前景的替代方案。需要进一步的前瞻性分析来证实该方案的安全性和有效性。