Müller Christian, Franke Sabine, Reisländer Timo, Keitel Verena, Venerito Marino
Department of Gastroenterology, Hepatology and Infectious Diseases, University Hospital of Magdeburg, Magdeburg, Germany.
Institute of Pathology, University Hospital of Magdeburg, Magdeburg, Germany.
Case Rep Oncol. 2024 Jul 15;17(1):753-762. doi: 10.1159/000539665. eCollection 2024 Jan-Dec.
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.
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.
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.
在3期ClarIDHy试验中,携带异柠檬酸脱氢酶1(IDH1)突变的进展期肝内胆管癌(iCCA)患者接受艾伏尼布治疗,与安慰剂相比,中位无进展生存期(PFS)获益为1.3个月。
我们描述了2例连续的先前接受过治疗的不可切除和转移性iCCA患者,他们携带IDH1 R132突变,接受每日一次500 mg艾伏尼布治疗,直至疾病进展,均获得了持久的临床缓解,缓解时间超过12个月。在1例疗效混合的病例中,对单个进展性肝转移灶额外进行了间质近距离放射治疗,同时继续使用艾伏尼布直至疾病进一步进展。艾伏尼布治疗实现了长期疾病控制,PFS分别为20个月和13个月,治疗持续时间分别为26个月和13个月,且无相关副作用。
不可切除或转移性IDH1突变型iCCA患者使用艾伏尼布可实现超过12个月的持续临床缓解。在艾伏尼布长期治疗期间未观察到新的安全信号。