Farrés M T, de Baere T, Lagrange C, Ramirez L, Rougier P, Munck J N, Roche A
Department of Interventional Radiology, Institut Gustave Roussy, Villejuif, France.
Cardiovasc Intervent Radiol. 1998 Sep-Oct;21(5):399-403. doi: 10.1007/s002709900287.
To determine the effects of percutaneous intratumoral chemotherapy with mitoxantrone (PIM) in the palliative treatment of malignant liver lesions.
We treated 15 progressive lesions in nine patients in whom either previous therapy failed or serious complications developed as a result. Seven lesions were metastatic and eight were due to foci of hepatocellular carcinoma. Under computed tomography (CT) guidance, we percutaneously injected 10-20 mg of mitoxantrone mixed with 0.5 ml of contrast medium into the tumor, performing one to three treatments at intervals of 1 month.
There were no complications. The morphologic responses of the tumors after treatment were: minor response in one case, no change in 11 cases, progressive disease in three cases. Mitoxantrone induced tumor necrosis with no viable cancer tissue in eight of 11 biopsies. Recurrence was observed in nine of the treated lesions 2-9 months after treatment. New lesions were observed in five of nine patients 1-9 months after treatment.
In patients with malignant liver lesions with no other therapeutic possibilities, minimally invasive intratumoral mitoxantrone injection was carried out safely with good tumor delivery of chemotherapy, and tumor necrosis was demonstrated at biopsy. We feel this approach warrants further investigation.
确定米托蒽醌经皮瘤内化疗(PIM)在恶性肝病变姑息治疗中的效果。
我们对9例患者的15个进展性病变进行了治疗,这些患者既往治疗失败或因此出现严重并发症。7个病变为转移性病变,8个病变为肝细胞癌病灶。在计算机断层扫描(CT)引导下,我们将10 - 20毫克米托蒽醌与0.5毫升造影剂混合后经皮注入肿瘤内,每隔1个月进行1至3次治疗。
未出现并发症。治疗后肿瘤的形态学反应为:1例轻度反应,11例无变化,3例疾病进展。在11次活检中的8次,米托蒽醌诱导肿瘤坏死,无存活的癌组织。治疗后2至9个月,在9个治疗病变中的9个观察到复发。治疗后1至9个月,在9例患者中的5例观察到新病变。
在没有其他治疗可能性的恶性肝病变患者中,经皮瘤内注射米托蒽醌的微创治疗安全进行,化疗药物在肿瘤内的递送良好,活检显示有肿瘤坏死。我们认为这种方法值得进一步研究。