Sustained Clinical Response to Ivosidenib in Previously Treated Patients with Advanced Intrahepatic Cholangiocarcinoma Harboring an IDH1 R132 Mutation: Two Case Reports.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2024-07-15 eCollection Date: 2024-01-01 DOI:10.1159/000539665
Christian Müller, Sabine Franke, Timo Reisländer, Verena Keitel, Marino Venerito
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Abstract

Introduction: Patients with progressing intrahepatic cholangiocarcinoma (iCCA) harboring an isocitrate dehydrogenase 1 (IDH1) mutation who received ivosidenib showed a median progression-free survival (PFS) benefit of 1.3 months compared to placebo in the phase 3 ClarIDHy trial.

Case presentations: We describe 2 consecutive patients with previously treated unresectable and metastatic iCCA harboring an IDH1 R132 mutation who achieved durable clinical responses with ivosidenib 500 mg once daily for >12 months until disease progression. In one case with a mixed response, a single progressive liver metastasis was additionally treated locally with interstitial brachytherapy, while ivosidenib was continued until further progression. Ivosidenib therapy resulted in long-term disease control with PFS of 20 and 13 months and duration of treatment of 26 and 13 months, respectively, with no relevant side effects.

Conclusion: Patients with unresectable or metastatic IDH1-mutated iCCA can achieve sustained clinical responses for >12 months with ivosidenib. No new safety signals were observed during long-term treatment with ivosidenib.

曾接受过治疗的携带 IDH1 R132 突变的晚期肝内胆管癌患者对伊沃西地尼的持续临床反应:两个病例报告。
简介在 ClarIDHy 3 期试验中,携带异柠檬酸脱氢酶 1(IDH1)突变的肝内胆管癌(iCCA)进展期患者接受伊沃西地尼治疗后,与安慰剂相比,中位无进展生存期(PFS)获益 1.3 个月:我们连续描述了2例既往接受过治疗的携带IDH1 R132突变的不可切除性和转移性iCCA患者,他们在接受伊沃西地尼500毫克、每天一次的治疗后获得了持久的临床应答,持续时间超过12个月,直至疾病进展。在一个混合反应的病例中,单个进展性肝转移灶在局部接受了间质近距离放射治疗,同时继续使用伊伐替尼治疗,直至病情进一步进展。伊伐替尼治疗使疾病得到长期控制,PFS分别为20个月和13个月,疗程分别为26个月和13个月,且无相关副作用:结论:不可切除或转移性IDH1突变iCCA患者使用伊沃西地尼可获得超过12个月的持续临床应答。结论:IDH1突变的iCCA未切除或转移患者使用伊沃西地尼可获得超过12个月的持续临床应答,在伊沃西地尼长期治疗期间未观察到新的安全性信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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