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结直肠癌肝转移新辅助经导管肝内治疗(DEBIRI(®))用伊立替康洗脱微球的影像学评估不能预测肿瘤坏死或长期疗效。

Radiological assessment of response to neoadjuvant transcatheter hepatic therapy with irinotecan-eluting beads (DEBIRI(®)) for colorectal liver metastases does not predict tumour destruction or long-term outcome.

机构信息

School of Cancer Studies, Institute of Translational Medicine, University of Liverpool, Liverpool, UK; Northwestern Hepatobiliary Unit, Aintree University Hospital, Liverpool, UK.

出版信息

Eur J Surg Oncol. 2013 Oct;39(10):1122-8. doi: 10.1016/j.ejso.2013.07.087. Epub 2013 Aug 6.

Abstract

INTRODUCTION

Transcatheter hepatic therapy with irinotecan-eluting beads (DEBIRI(®)) allows targeted delivery of irinotecan direct to liver tissue and colorectal liver metastases (CRLM). Accurate assessment of tumour response to therapy is vital to guide optimal treatment. Preliminary work has suggested existing criteria for radiological response may not reflect pathological response after neoadjuvant DEBIRI. This study assessed the relationship between existing and novel radiological response criteria and pathological tumour response as well as long-term outcome.

METHODS

Patients with easily resectable CRLM were treated with DEBIRI 4 weeks prior to resection and pathological tumour response graded using a validated system. Radiological response was assessed using RECIST and novel morphological response criteria.

RESULTS

Twenty-two patients with 37 lesions were treated with DEBIRI. Median residual tumour was 20% (range 0-80), median necrosis 45% (10-100) and median fibrosis 10% (10-70). Twenty patients (91%) demonstrated stable disease by RECIST, with 11 (50%) demonstrating partial morphological response. Neither radiological response criteria correlated with pathological response. Overall median disease free survival (DFS) was 13.6 months (95% CI 4.7-22.5). Radiological response was not associated with DFS.

CONCLUSION

Existing criteria reporting short-term radiological response to DEBIRI do not accurately predict pathological tumour response or long-term outcome. Further work is necessary to define the optimum timing and method of assessing response to DEBIRI.

摘要

简介

经导管肝内治疗用伊立替康洗脱微球(DEBIRI(®))可将伊立替康直接靶向递送至肝组织和结直肠癌肝转移(CRLM)。准确评估肿瘤对治疗的反应对于指导最佳治疗至关重要。初步研究表明,现有的放射学反应标准可能无法反映新辅助 DEBIRI 后的病理反应。本研究评估了现有和新的放射学反应标准与肿瘤病理反应以及长期预后之间的关系。

方法

对易于切除的 CRLM 患者在切除前 4 周进行 DEBIRI 治疗,并使用验证过的系统对肿瘤进行病理分级。使用 RECIST 和新的形态学反应标准评估放射学反应。

结果

22 例患者共 37 个病灶接受 DEBIRI 治疗。残留肿瘤中位数为 20%(范围 0-80),坏死中位数为 45%(10-100),纤维化中位数为 10%(10-70)。根据 RECIST,20 例患者(91%)表现为疾病稳定,其中 11 例(50%)表现为部分形态学反应。两种放射学反应标准均与病理反应无关。总无病生存(DFS)中位数为 13.6 个月(95%CI 4.7-22.5)。放射学反应与 DFS 无关。

结论

报告 DEBIRI 短期放射学反应的现有标准不能准确预测肿瘤的病理反应和长期预后。需要进一步研究来确定评估 DEBIRI 反应的最佳时机和方法。

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