Martin Huertas Roberto, Fuentes-Mateos Raquel, Serrano Domingo Juan Jose, Corral de la Fuente Elena, Rodríguez-Garrote Mercedes
Medical Oncology Department, Hospital Universitario Ramon y Cajal, Madrid 28034, Spain.
World J Clin Oncol. 2020 Oct 24;11(10):844-853. doi: 10.5306/wjco.v11.i10.844.
Cholangiocarcinomas are rare and very aggressive tumors. Most patients have advanced-stage or unresectable disease at presentation, and the systemic therapies have limited efficacy. Albumin-bound paclitaxel (nab-paclitaxel) is a solvent-free taxane that has been approved for the treatment of some cancers such as breast, non-small cell lung and pancreatic cancer, however it has not been applied to treat cholangiocarcinoma. We have both preclinical and clinical evidence of the efficacy of nab-paclitaxel in cholangiocarcinoma, yet no phase 3 trials have been made.
A 63-year-old man was diagnosed in December 2016 with stage III B intrahepatic cholangiocarcinoma. Surgery was performed, followed by adjuvant chemotherapy treatment with capecitabine and gemcitabine; although, the gemcitabine was suspended due to allergic reaction after two cycles. In April 2019, metastatic cholangiocarcinoma relapse was diagnosed, and a first-line treatment with FOLFOX scheme was started. Eight cycles were administered, producing an initial clinical improvement and decrease in blood tumor marker levels. Radiological and serological progression was noted in September 2019. As a second-line treatment, FOLFIRI was not recommended due to risk of worsening the patient's tumor-related diarrhea. A combination therapy with gemcitabine was not feasible, as the patient had previously suffered from an allergic reaction to this treatment. We decided to use nab-paclitaxel as a second-line treatment, and four cycles were administered. Both clinical and serological responses were observed, and a radiological mixed response was also noted.
Advanced cholangiocarcinoma could be treated with nab-paclitaxel monotherapy, which should be studied in combination with other types of treatment (chemotherapy, fibroblast growth factor receptor inhibitors).
胆管癌是一种罕见且侵袭性很强的肿瘤。大多数患者在初诊时已处于晚期或无法切除的阶段,全身治疗的疗效有限。白蛋白结合型紫杉醇(纳米紫杉醇)是一种无溶剂的紫杉烷类药物,已被批准用于治疗某些癌症,如乳腺癌、非小细胞肺癌和胰腺癌,但尚未应用于胆管癌的治疗。我们有纳米紫杉醇治疗胆管癌疗效的临床前和临床证据,但尚未进行3期试验。
一名63岁男性于2016年12月被诊断为III B期肝内胆管癌。进行了手术,随后用卡培他滨和吉西他滨进行辅助化疗;然而,由于两个周期后出现过敏反应,吉西他滨被停用。2019年4月,诊断为转移性胆管癌复发,并开始使用FOLFOX方案进行一线治疗。共进行了8个周期,最初临床症状有所改善,血液肿瘤标志物水平下降。2019年9月出现影像学和血清学进展。作为二线治疗,由于担心加重患者与肿瘤相关的腹泻,不推荐使用FOLFIRI。由于患者此前对该治疗有过敏反应,联合使用吉西他滨不可行。我们决定使用纳米紫杉醇作为二线治疗,共进行了4个周期。观察到临床和血清学反应,影像学检查也显示为混合反应。
晚期胆管癌可用纳米紫杉醇单药治疗,应研究其与其他类型治疗(化疗、成纤维细胞生长因子受体抑制剂)联合使用的情况。