Saif Muhammad Wasif, Wasif Komal, Goodman Martin D, Hegde Sanjay, Sterling Mark, Yacavone Robert, Jaiswal Sunny, Weinstein Barbara, Daly Kevin, Relias Valerie
Northwell Health Cancer Institute & Donald and Barbara Zucker School of Medicine, Hofstra, NY, USA.
Tufts University School of Medicine, Tufts Cancer Center, Boston, MA, USA.
JOP. 2019 Nov;20(5):121-124.
Carcinoma of unknown primary represents a therapeutic challenge in oncological practice. Evidence lacks to support particular chemotherapy selection and empirical therapies are commonly extrapolated from data on patients where primary tumor site is known. Gemcitabine, Oxaliplatin, Leucovorin and 5-Fluorouracil was previously developed to treat pancreatic cancer. These agents have also demonstrated activities in other gastrointestinal malignancies. Considering promising anti-tumor effects of GOLF, we performed a retrospective study to investigate anti-tumor activity and safety of a simplified Gemcitabine, Oxaliplatin, Leucovorin and 5-Fluorouracil in patients with Carcinoma of unknown primary in whom immunohistostaining was suggestive of either upper gastrointestinal cancers or pancreatobiliary cancers.
This retrospective study included 18 patients recorded to have a diagnosis of Carcinoma of unknown primary between Aug 2010-Dec 2015, who received biweekly G 1000 mg/m, O 85 mg/m, L 200 mg/m and F 2400 mg/m over 46-h on day 1 with pegfilgrastim on day 3 every 14 days. IHC staining pattern favored upper GI origin, including stomach, bile duct or pancreas. Tumor assessments were repeated every 8 weeks.
Median age was 67 years (range: 46-76), with ECOG PS<2, and 50% were women. Median number of cycles was 4 (range: 3-14). 7 partial responses were obtained (RR: 39%) and 7 achieved stable disease with overall disease control of 78%. Median time to tumor progression was 4 months (range: 2-9). 8 (44%) patients received liver-directed therapy and 1 underwent HIPEC (5%). Median survival time was 10.5 months (range: 6.7-14.5) and 1-year overall survival rate was 35%. Grade 3-4 toxicities included neutropenia, febrile neutropenia, thrombocytopenia, nausea, diarrhea, mucositis and oxaliplatin-induced neuropathy.
Simplified Gemcitabine, Oxaliplatin, Leucovorin and 5-Fluorouracil regimen appears to be feasible with promising activity for Carcinoma of unknown primary and deserves to be evaluated in future trials.
原发灶不明的癌在肿瘤学实践中是一项治疗挑战。缺乏支持特定化疗选择的证据,经验性治疗通常是从已知原发肿瘤部位患者的数据推断而来。吉西他滨、奥沙利铂、亚叶酸钙和5-氟尿嘧啶先前被开发用于治疗胰腺癌。这些药物在其他胃肠道恶性肿瘤中也显示出活性。鉴于GOLF有令人鼓舞的抗肿瘤效果,我们进行了一项回顾性研究,以调查简化的吉西他滨、奥沙利铂、亚叶酸钙和5-氟尿嘧啶方案在免疫组化染色提示为上消化道癌或胰胆管癌的原发灶不明癌患者中的抗肿瘤活性和安全性。
这项回顾性研究纳入了2010年8月至2015年12月期间记录诊断为原发灶不明癌的18例患者,他们每14天在第1天接受为期46小时的双周化疗,吉西他滨1000mg/m²、奥沙利铂85mg/m²、亚叶酸钙200mg/m²和5-氟尿嘧啶2400mg/m²,第3天给予聚乙二醇化重组人粒细胞刺激因子。免疫组化染色模式倾向于上消化道起源,包括胃、胆管或胰腺。每8周重复进行肿瘤评估。
中位年龄为67岁(范围:46 - 76岁),东部肿瘤协作组体能状态评分(ECOG PS)<2,50%为女性。中位周期数为4个(范围:3 - 14个)。获得7例部分缓解(缓解率:39%),7例病情稳定,总体疾病控制率为78%。中位肿瘤进展时间为4个月(范围:2 - 9个月)。8例(44%)患者接受了肝脏定向治疗,1例接受了腹腔内热灌注化疗(HIPEC)(5%)。中位生存时间为10.5个月(范围:6.7 - 14.5个月),1年总生存率为35%。3 - 4级毒性包括中性粒细胞减少、发热性中性粒细胞减少、血小板减少、恶心、腹泻、黏膜炎和奥沙利铂引起的神经病变。
简化的吉西他滨、奥沙利铂、亚叶酸钙和5-氟尿嘧啶方案似乎可行,对原发灶不明癌有令人鼓舞的活性,值得在未来试验中进行评估。