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米托蒽醌低氧肝灌注治疗多灶性转移和不可切除的原发性肿瘤:单中心 42 例系列研究。

Hypoxic liver perfusion with mitomycin-C for treating multifocal metastases and unresectable primary tumours: a single-centre series of 42 patients.

机构信息

UO Oncologia Medica, Ospedale San Giuseppe, Via San Vittore 12, 20123, Milano, Italy.

出版信息

Radiol Med. 2011 Dec;116(8):1239-49. doi: 10.1007/s11547-011-0724-3. Epub 2011 Sep 2.

Abstract

PURPOSE

The purpose of our study was to retrospectively evaluate the feasibility, toxicity and impact on overall (OS) and disease-free (DFS) survival of intra-arterial liver perfusion with mitomycin-C (MMC) [hypoxic liver perfusion with MMC (HLPM)] in patients with multifocal liver metastases or with unresectable primary liver tumours.

MATERIALS AND METHODS

Forty-two patients underwent 56 intra-arterial liver infusions with MMC between June 2001 and May 2009. The patients presented specific characteristics, i.e. they were all refractory to locoregional (LR) and/or systemic treatments. HLPM consists of selective catheterisation of the common hepatic artery, permanent occlusion of the gastroduodenal artery at its origin using metal coils, an inflated balloon catheter placement at the origin of the proper hepatic artery to block blood flow and induce hypoxia for around 10 min, MMC infusion and vascular-bed occlusion through injection of an absorbable haemostatic agent. During the procedure, the patients received anaesthesiological monitoring. Biochemical and morphological responses were evaluated, as were haematological, hepatic and systemic toxicity.

RESULTS

Patients were hospitalised for 10 days on average (range 7-15). Side effects were liver toxicity in all cases, acute pancreatitis in one case and liver failure in one case. Computed tomography performed at 30 days documented a partial response (PR) in 29%, stable disease (SD) in 45% and progressive disease (PD) in 26% of patients. The response lasted 4 months on average (range 3-6). Mean overall survival (OS) was 20 months for all patients, reaching 30 months in those with colorectal carcinoma.

CONCLUSIONS

The procedure is feasible, and treatmentrelated toxicity and mortality rates are acceptable. It may be considered a palliative treatment option in patients with advanced liver disease in centres with adequately experienced medical teams.

摘要

目的

本研究旨在回顾性评估丝裂霉素 C (MMC)经肝动脉内灌注(MMC 缺氧性肝灌注[HLPM])治疗多发性肝转移或不可切除原发性肝肿瘤患者的可行性、毒性以及对总生存期(OS)和无疾病生存期(DFS)的影响。

材料和方法

2001 年 6 月至 2009 年 5 月,42 例患者共进行了 56 次肝内 MMC 灌注。这些患者具有特定的特征,即均对局部区域(LR)和/或全身治疗无效。HLPM 包括肝总动脉选择性插管,使用金属线圈永久性闭塞胃十二指肠动脉起始处,在肝固有动脉起始处放置充气球囊导管以阻断血流并诱导缺氧约 10 分钟,然后进行 MMC 灌注和血管床闭塞,方法是注射可吸收止血剂。在手术过程中,患者接受了麻醉学监测。评估了生化和形态学反应以及血液学、肝脏和全身毒性。

结果

患者平均住院 10 天(范围为 7-15 天)。所有病例均出现肝毒性,1 例出现急性胰腺炎,1 例出现肝功能衰竭。30 天 CT 检查显示,29%的患者有部分缓解(PR),45%的患者有稳定疾病(SD),26%的患者有疾病进展(PD)。缓解期平均为 4 个月(范围为 3-6 个月)。所有患者的平均总生存期(OS)为 20 个月,结直肠癌患者达到 30 个月。

结论

该操作是可行的,治疗相关的毒性和死亡率是可以接受的。在经验丰富的医疗团队所在的中心,对于晚期肝病患者,它可以被视为一种姑息治疗选择。

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