Iddings Douglas, Ahmad Aziz, Elashoff David, Bilchik Anton
Department of Surgical Oncology, John Wayne Cancer Institute at Saint John's Health Center, Santa Monica, CA 90404, USA.
Ann Surg Oncol. 2006 Nov;13(11):1386-92. doi: 10.1245/s10434-006-9120-y. Epub 2006 Sep 29.
The prognostic relevance of lymphatic micrometastases in colorectal carcinoma is unclear. To determine the prognostic significance of micrometastases in colorectal cancer, a meta-analysis was performed on all studies, which reported 3-year disease-free survival (DFS) and overall survival (OS).
Published studies selected for meta-analysis contained sufficient data from which to extrapolate estimates of 3-year DFS and/or OS. From 1991-2003, 25 studies re-examined N0 lymph nodes by serial sectioning and immunohistochemical (IHC) staining or reverse transcriptase-polymerase chain reaction (RT-PCR) assay. Eight studies (566 patients) with IHC detected micrometastases and three (173 patients) with RT-PCR micrometastases were used to determine DFS and OS. Weighted estimates of 3-year survival were combined across studies within each group, and the combined survival estimates were compared across groups using a binomial test.
Micrometastases were identified in all IHC studies; upstaging, including N1, N1mi and N0(i+), was achieved in 32% (179/566 patients). All RT-PCR studies identified micrometastases; upstaging to N0(mol+) was achieved in 37% (64/173 patients). There was a statistically significant difference in 3-year OS between RT-PCR positive N0(mol+) patients (77.8%) and those for whom micrometastases were not detected (96.6%) (P < .001).
The prognostic value of micrometastases detected retrospectively by RT-PCR is significant in AJCC stage II colorectal patients. Studies utilizing RT-PCR performed a more complete nodal analysis when compared to studies using IHC techniques. RT-PCR may also be more specific for the detection of clinically relevant micrometastases compared to IHC detected cytokeratins. Prospective studies are needed to evaluate the potential benefit of systemic chemotherapy in patients with molecular metastases.
结直肠癌中淋巴微转移的预后相关性尚不清楚。为了确定微转移在结直肠癌中的预后意义,对所有报告了3年无病生存期(DFS)和总生存期(OS)的研究进行了一项荟萃分析。
为荟萃分析所选的已发表研究包含足够的数据,可据此推断3年DFS和/或OS的估计值。1991年至2003年期间,25项研究通过连续切片及免疫组化(IHC)染色或逆转录聚合酶链反应(RT-PCR)检测对N0淋巴结进行了重新检查。八项研究(566例患者)采用IHC检测到微转移,三项研究(173例患者)采用RT-PCR检测到微转移,用于确定DFS和OS。对每组内各研究的3年生存率加权估计值进行合并,并使用二项检验比较各组的合并生存估计值。
所有IHC研究均检测到微转移;32%(179/566例患者)实现了分期上调,包括N1、N1mi和N0(i+)。所有RT-PCR研究均检测到微转移;37%(64/173例患者)实现了分期上调至N0(mol+)。RT-PCR阳性的N0(mol+)患者与未检测到微转移的患者相比,3年OS存在统计学显著差异(77.8%对96.6%,P <.001)。
RT-PCR回顾性检测到的微转移对美国癌症联合委员会(AJCC)II期结直肠癌患者具有显著的预后价值。与使用IHC技术的研究相比,采用RT-PCR的研究进行了更全面的淋巴结分析。与IHC检测细胞角蛋白相比,RT-PCR对检测临床相关微转移可能也更具特异性。需要进行前瞻性研究来评估分子转移患者全身化疗的潜在益处。