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肿瘤大小的最初变化可预测接受联合化疗的转移性结直肠癌患者的反应和生存。

The initial change in tumor size predicts response and survival in patients with metastatic colorectal cancer treated with combination chemotherapy.

机构信息

Department of Diagnostic Radiology, Institution for Molecular Medicine and Surgery, Karolinska University Hospital Solna and Karolinska Institutet, Stockholm, Sweden.

出版信息

Ann Oncol. 2012 Apr;23(4):948-54. doi: 10.1093/annonc/mdr350. Epub 2011 Aug 10.

Abstract

BACKGROUND

To determine whether the change in tumor diameters at the first follow-up computed tomography (CT) examination after baseline examination (first change) correlates with outcome in patients with metastatic colorectal cancer (mCRC) treated with combination chemotherapy.

PATIENTS AND METHODS

The first change was analyzed in a multicenter randomized phase III trial (Nordic VI, N = 567) comparing first-line irinotecan with either bolus or infused 5-fluorouracil. Cox proportional hazards multiple regression model and Kaplan-Meier survival analyses after correction for guarantee-time bias were carried out to evaluate correlations between first change, objective response according to RECIST 1.0, progression-free survival (PFS), and overall survival (OS).

RESULTS

The hazard ratios for PFS and OS decreased along with first change. A decrease between 10% and <30%, albeit RECIST does not regard this as a partial response, was a positive prognostic factor for PFS and OS. Patients who had new lesions or unequivocal progression of nonmeasurable lesions had a worse prognosis than those with only an increase in size of >20%.

CONCLUSIONS

The change in tumor size at the first follow-up CT is strongly prognostic for PFS and OS in mCRC.

摘要

背景

为了确定基线检查后第一次随访计算机断层扫描(CT)检查时肿瘤直径的变化是否与接受联合化疗的转移性结直肠癌(mCRC)患者的结局相关。

患者和方法

在一项多中心随机 III 期试验(北欧 VI 期,N=567)中分析了第一次变化,该试验比较了一线伊立替康与推注或输注氟尿嘧啶。进行 Cox 比例风险多因素回归模型和 Kaplan-Meier 生存分析,以校正保证时间偏倚,评估第一次变化、根据 RECIST 1.0 评估的客观缓解、无进展生存期(PFS)和总生存期(OS)之间的相关性。

结果

PFS 和 OS 的风险比随第一次变化而降低。虽然 RECIST 不将 10%至<30%的减少视为部分缓解,但这是 PFS 和 OS 的一个阳性预后因素。有新病变或不可明确的非可测量病变进展的患者比只有>20%的肿瘤大小增加的患者预后更差。

结论

mCRC 患者在第一次随访 CT 时肿瘤大小的变化与 PFS 和 OS 具有很强的预后相关性。

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