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新EPOC研究中的疾病进展模式、进展性疾病的治疗及进展后生存期

Patterns of progression, treatment of progressive disease and post-progression survival in the New EPOC study.

作者信息

Pugh Siân A, Bowers Megan, Ball Alexandre, Falk Stephen, Finch-Jones Meg, Valle Juan W, O'Reilly Derek A, Siriwardena Ajith K, Hornbuckle Joanne, Rees Myrddin, Rees Charlotte, Iveson Tim, Hickish Tamas, Maishman Tom, Stanton Louise, Dixon Elizabeth, Corkhill Andrea, Radford Mike, Garden O James, Cunningham David, Maughan Tim S, Bridgewater John A, Primrose John N

机构信息

University Surgery and Cancer Sciences Division, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, UK.

Southampton Clinical Trials Unit, Southampton, UK.

出版信息

Br J Cancer. 2016 Aug 9;115(4):420-4. doi: 10.1038/bjc.2016.208. Epub 2016 Jul 19.

Abstract

BACKGROUND

The addition of cetuximab (CTX) to perioperative chemotherapy (CT) for operable colorectal liver metastases resulted in a shorter progression-free survival. Details of disease progression are described to further inform the primary study outcome.

METHODS

A total of 257 KRAS wild-type patients were randomised to CT alone or CT with CTX. Data regarding sites and treatment of progressive disease were obtained for the 109 (CT n=48, CT and CTX n=61) patients with progressive disease at the cut-off date for analysis of November 2012.

RESULTS

The liver was the most frequent site of progression (CT 67% (32/48); CT and CTX 66% (40/61)). A higher proportion of patients in the CT and group had multiple sites of progressive disease (CT 8%, 4/48; CT and CTX 23%, 14/61 P=0.04). Further treatment for progressive disease is known for 84 patients of whom 69 received further CT, most frequently irinotecan based. Twenty-two patients, 11 in each arm, received CTX as a further line agent.

CONCLUSIONS

Both the distribution of progressive disease and further treatment are as expected for such a cohort. The pattern of disease progression seen is consistent with failure of systemic micrometastatic disease control rather than failure of local disease control following liver surgery.

摘要

背景

对于可手术切除的结直肠癌肝转移患者,在围手术期化疗(CT)中加入西妥昔单抗(CTX)会导致无进展生存期缩短。现将疾病进展的详细情况进行描述,以进一步说明主要研究结果。

方法

总共257例KRAS野生型患者被随机分为单纯CT组或CT联合CTX组。在2012年11月分析截止日期时,对109例(CT组48例,CT联合CTX组61例)出现疾病进展的患者,获取了有关疾病进展部位和治疗的数据。

结果

肝脏是最常见的疾病进展部位(CT组67%(32/48);CT联合CTX组66%(40/61))。CT联合CTX组中,有更高比例的患者出现多个疾病进展部位(CT组8%,4/48;CT联合CTX组23%,14/61;P = 0.04)。已知84例疾病进展患者接受了进一步治疗,其中69例接受了进一步的CT治疗,最常用的是以伊立替康为基础的治疗。22例患者(每组11例)接受CTX作为进一步治疗药物。

结论

对于这样一组患者,疾病进展的分布和进一步治疗情况均符合预期。所观察到的疾病进展模式与全身微转移疾病控制失败一致,而非肝切除术后局部疾病控制失败。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05b7/4985352/906b99072b51/bjc2016208f1.jpg

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