精准肿瘤学旨在通过识别患者肿瘤内可成药的基因组异常,提供个人化治疗以改善临床结局。对于化疗难治性晚期肿瘤患者而言,提供替代治疗选择尤其重要。
适应症:Hepatocellular Carcinoma、Colorectal Cancer
入组条件
纳入标准
- patients with metastatic, inoperable or advanced solid tumors who are refractory to at least one standard chemo- or targeted drugs.
- The disease is accessible for a biopsy (radiologic or endoscopic) or resection of a metastatic site.
- These patients are seen at a multidisciplinary tumor board meeting prior to referrals.
- aged \>18 years, able to provide written consents to trial participation,
- with an Eastern cooperative oncology group performance status of 0 or 1,
- with measurable disease in accordance with response evaluation criteria in solid tumors (RECIST) version 1.1.
- deem suitable for standard chemo-therapy; i.e. with a normal neutrophil count, hemoglobin \> 9g/dl, serum creatinine, \<1.5 x upper limit of normal, bilirubin \< 1.5 x normal, Aspartate and alanine aminotransferases (\<3 x ULN or \<5x
- those with liver metastasis) and with an ejection Fraction \>50% of normal on echocardiography.
排除标准
- unable to provide informed consent
入组条件维持 ClinicalTrials.gov 原始英文登记资料,实际入组资格以研究团队的正式评估与受试者知情同意书为准。资料来源:ClinicalTrials.gov,每两周自动更新,最后同步:2026年10月8日。