Phase II Study of Chemoembolization With Drug-Eluting Beads in Patients With Hepatic Neuroendocrine Metastases: High Incidence of Biliary Injury

被引:72
作者
Bhagat, Nikhil [1 ]
Reyes, Diane K. [1 ]
Lin, Mingde [2 ]
Kamel, Ihab [1 ]
Pawlik, Timothy M. [3 ]
Frangakis, Constantine [4 ]
Geschwind, J. F. [1 ]
机构
[1] Johns Hopkins Univ, Med Ctr, Dept Radiol, Div Vasc & Intervent Radiol,Johns Hopkins Hosp, Baltimore, MD 21287 USA
[2] Philips Res North Amer, CIITS, Briarcliff Manor, NY 10510 USA
[3] Johns Hopkins Univ, Med Ctr, Dept Surg, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD 21287 USA
基金
美国国家卫生研究院;
关键词
Biliary injury; Chemoembolization; Drug-eluting beads; Neuroendocrine metastases; TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION; UNRESECTABLE HEPATOCELLULAR-CARCINOMA; BILE-DUCT INJURY; TRANSARTERIAL CHEMOEMBOLIZATION; LIVER METASTASES; CANCER STATISTICS; ENDOCRINE TUMORS; UNITED-STATES; MANAGEMENT; SURVIVAL;
D O I
10.1007/s00270-012-0424-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To evaluate safety in an interim analysis of transarterial chemoembolization (TACE) with doxorubicin-eluting beads (DEB) in 13 patients with hepatic metastases from neuroendocrine tumors (NETs) as part of a phase II trial. Institutional Review Board approval and informed consent were obtained. Thirteen patients completed preliminary safety analysis. Their mean age was 65 years, Eastern Cooperative Oncology Group status was 0/1, tumor burden range was 4-75 %, and mean targeted tumor size was 5.9 cm. Up to four DEB-TACE sessions (100-300 mu m beads loaded with a parts per thousand currency sign100 mg doxorubicin) within 6 months were allowed. Tumor response was assessed by magnetic resonance imaging 1 month after treatment using contrast-enhancement [European Association for the Study of the Liver (EASL) and size Response Evaluation Criteria in Solid Tumors (RECIST)] criteria. Safety was assessed by National Cancer Institute Common Terminology Criteria. DEB-TACE was successfully performed in all 13 patients. At 1 month follow-up, there was a mean 12 % decrease in tumor size (p < 0.0003) and a 56 % decrease in tumor enhancement (p < 0.0001). By EASL criteria, the targeted lesion objective response rate was 78 %. Grade 3 to 4 toxicities were fatigue (23 %), increased alanine amino transferase (15 %), hyperglycemia (15 %), and abdominal pain (8 %). Seven patients developed bilomas (54 %); all of these patients had multiple small (< 4 cm) lesions. Subsequently, four underwent percutaneous drainage, three for abscess formation and one for symptoms related to mass effect. Although biloma and liver abscess are known risks after TACE, the high incidence in our study population was unexpected and forced interruption of the trial. Although this occurred in a small group of patients, we have changed our technique and patient selection as a result of these findings, thus allowing resumption of the trial.
引用
收藏
页码:449 / 459
页数:11
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