Postpartum related intrahepatic cholangiocarcinoma with FGFR2 fusion and severe hyperbilirubinemia with response to FGFR inhibitor pemigatinib: case report and review

被引:0
|
作者
Washburn, Leslie [1 ]
Mahipal, Amit [2 ]
Jatoi, Aminah [1 ]
Kottschade, Lisa [1 ]
Tran, Nguyen [1 ]
机构
[1] Mayo Clin, Dept Oncol, 200 1st St SW, Rochester, MN 55905 USA
[2] Case Western Reserve Univ, Univ Hosp Seidman Canc Ctr, Dept Oncol, Cleveland, OH 44106 USA
关键词
Cholangiocarcinoma; hyperbilirubinemia; postpartum; fibroblast growth factor receptor fusion (FGFR fusion); FGFR inhibitor; case report; OPEN-LABEL; PREGNANCY; CHEMOTHERAPY; MULTICENTER; FUTIBATINIB;
D O I
10.21037/jgo-23-693
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Cholangiocarcinoma during postpartum or pregnancy is a rare presentation. There are limited cases reported in the literature. Diagnosis can be delayed as presenting signs and symptoms may be attributed to pregnancy or postpartum state. Case Description: We present the case of a 33-year-old postpartum woman with intrahepatic cholangiocarcinoma with severe hyperbilirubinemia who was found to have fibroblast growth factor receptor 2 (FGFR2)-adenosylhomocysteinase like 1 (AHCYL1) fusion on next-generation sequencing (NGS). She initially was treated with two doses of gemcitabine and cisplatin with increasing hyperbilirubinemia requiring hold of further chemotherapy. NGS showed FGFR2-AHCYL1 fusion, and she was started on the FGFR inhibitor pemigatinib, with dramatically decreasing bilirubin within 10 days. She eventually normalized her bilirubin values and had partial response on follow-up imaging. Conclusions: This is the first report, to our knowledge of response to an FGFR inhibitor in the postpartum setting, as well to show response in the setting of life-threatening hyperbilirubinemia. Our patient did not tolerate standard chemotherapy, likely due to liver dysfunction, but responded to pemigatinib, suggesting that the liver dysfunction was driven by her disease. This case underscores the need to include NGS as part of initial workup to identify important therapeutic targets and increase available lines of therapy, including those patients who are postpartum or pregnant.
引用
收藏
页码:2627 / 2636
页数:10
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