Delayed response to maintenance therapy after first-line chemotherapy in metastatic intrahepatic cholangiocarcinoma: A case report

被引:2
|
作者
Marciano R. [1 ]
Servetto A. [1 ]
Bianco C. [2 ]
Bianco R. [1 ]
机构
[1] Department of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, Naples
[2] Department of Experimental and Clinical Medicine, University of Catanzaro Magna Grecia, Catanzaro
关键词
Gemcitabine; Intrahepatic cholangiocarcinoma; Maintenance chemotherapy;
D O I
10.1186/s13256-017-1443-8
中图分类号
学科分类号
摘要
Background: Intrahepatic cholangiocarcinoma is an aggressive tumor originating in the epithelium of the bile duct, often associated with distant dissemination. The prognosis is poor and treatment is challenging due to low response rate to standard chemotherapy and lack of targeted therapies. Case presentation: Here we report the case of a 74-year-old white woman affected by intrahepatic cholangiocarcinoma with metastatic involvement of spleen, lung, peritoneum, and intra-abdominal lymph nodes. As first-line chemotherapy, she was given cisplatin-gemcitabine chemotherapy. The treatment was well tolerated with the exception of grade 1 constipation and a single episode of grade 4 thrombocytopenia occurring after the fourth course. After the first three courses of chemotherapy a computed tomography scan evaluation demonstrated no change; her CA19-9 levels were slightly decreased. However, after the sixth course of chemotherapy a computed tomography scan revealed a dimensional enlargement of the lung metastases; her CA19-9 levels increased. She was then treated with gemcitabine alone. After 2 months of gemcitabine monotherapy a significant regression of lung and spleen metastases, as well a CA19-9 level reduction, occurred. Eight months after the start of gemcitabine monotherapy no signs of progression were reported. Conclusions: Treatment of metastatic intrahepatic cholangiocarcinoma with gemcitabine as maintenance therapy after first-line chemotherapy could be continued until clear evidence of disease progression since delayed responses are possible. © 2017 The Author(s).
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