Alberts Steven R, Al-Khatib Hani, Mahoney Michelle R, Burgart Lawerence, Cera Peter J, Flynn Patrick J, Finch Tom R, Levitt Ralph, Windschitl Harold E, Knost James A, Tschetter Loren K
Division of Medical Oncology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.
Cancer. 2005 Jan 1;103(1):111-8. doi: 10.1002/cncr.20753.
Gemcitabine has broad activity in a variety of solid tumors including biliary tract carcinomas. The authors evaluated 6-month survival, response, and toxicity associated with a combination of gemcitabine, 5-fluorouracil (5-FU), and leucovorin (LV) in patients with unresectable or metastatic biliary tract or gallbladder adenocarcinoma (ACA).
A 4-week course included 1000 mg/m2 gemcitabine by intravenous infusion over 30 minutes on Days 1, 8, and 15, 25 mg/m2 LV by intravenous push, and 600 mg/m2 5-FU by intravenous push after LV.
Forty-two patients were enrolled in 6 months, 35 of whom had metastatic disease. Patients with biliary tract ACA included 24 with hepatic disease (19 patients had intrahepatic disease and 5 patients had extrahepatic disease) and 4 with disease in the ampulla of Vater. All patients were evaluable and received a median of 4 courses of treatment (range, 1-21 courses). Commonly occurring severe toxicity (NCI CTC Grade 3 or worse) included: dyspnea (four patients), nausea (four patients), fatigue (seven patients), thrombocytopenia (six patients), emesis (four patients), and diarrhea (four patients). Five partial responses (9.5%) occurred, 3 of which were sustained for > or = 8 weeks. No treatment-related deaths occurred. Thirty-two patients had disease progression and 38 died after a median follow-up of 20 months (range, 1.4-24 months). The median time to disease progression was 4.6 months (95% confidence interval [95% CI], 2.4-6.6%). The median survival period was 9.7 months (95% CI, 7-12%).
This combination regimen was manageable in patients with advanced biliary tract and gallbladder ACA. Of 42 patients, 24 (57%) survived > or = 6 months, satisfying the primary end point of the trial. The length of survival suggested that gemcitabine, 5-FU, and LV had benefit equivalent to gemcitabine alone.
吉西他滨在包括胆管癌在内的多种实体瘤中具有广泛活性。作者评估了吉西他滨、5-氟尿嘧啶(5-FU)和亚叶酸钙(LV)联合方案用于不可切除或转移性胆管或胆囊腺癌(ACA)患者的6个月生存率、反应及毒性。
一个4周疗程包括第1、8和15天静脉输注1000mg/m²吉西他滨,持续30分钟,静脉推注25mg/m²LV,LV之后静脉推注600mg/m²5-FU。
6个月内纳入42例患者,其中35例有转移性疾病。胆管ACA患者包括24例有肝脏疾病(19例有肝内疾病,5例有肝外疾病)和4例在Vater壶腹有疾病。所有患者均可评估,接受治疗的中位数为4个疗程(范围1-21个疗程)。常见的严重毒性(NCI CTC 3级或更严重)包括:呼吸困难(4例患者)、恶心(4例患者)、疲劳(7例患者)、血小板减少(6例患者)、呕吐(4例患者)和腹泻(4例患者)。出现5例部分缓解(9.5%),其中3例持续≥8周。未发生与治疗相关的死亡。32例患者疾病进展,38例在中位随访20个月(范围1.4-24个月)后死亡。疾病进展的中位时间为4.6个月(95%置信区间[95%CI],2.4-6.6%)。中位生存期为9.7个月(95%CI,7-12%)。
该联合方案在晚期胆管和胆囊ACA患者中易于管理。42例患者中,24例(57%)存活≥6个月,达到试验的主要终点。生存时间表明吉西他滨、5-FU和LV的疗效与单用吉西他滨相当。