Department of Medical Oncology, Flinders Centre for Innovation in Cancer, Flinders Medical Centre, Bedford Park, Australia.
Department of Medical Oncology, The Queen Elizabeth Hospital Woodville, Australia; The University of Adelaide, Adelaide, Australia.
Clin Colorectal Cancer. 2014 Jun;13(2):87-93. doi: 10.1016/j.clcc.2013.11.008. Epub 2013 Nov 13.
Whether metastatic colorectal cancer (mCRC) that presents synchronously with the primary lesion behaves differently from mCRC that appears metachronously to the primary disease is not clear.
The South Australian Clinical Registry for mCRC collects data for patients diagnosed after February 2006. Data from 2502 patients, available on October 22, 2012, were analyzed according to stage at initial diagnosis (SAID) to compare outcomes between metachronous tumors (MTs) (stages I, II, III) and synchronous tumors (STs) (stage IV). Overall survival (OS) was calculated from the date of mCRC diagnosis.
Patients with ST had more liver-only metastases, and patients with MT had more lung-only, non-lung and non-liver, and non-lung metastases. The median time to recurrence differed significantly according to SAID: stage I, 49.3 mo (n = 29), stage II, 25.2 mo (n = 346) and stage III, 18.4 mo (n = 497). The median OS was longer for patients with MT than for those with ST (19.0 vs.14.9 mo, P = .003). For patients who received any treatment for mCRC, the OS was longer for patients with MT than for those with ST (19.2 vs. 15.3 mo, P = .005). In patients who received only chemotherapy for mCRC, the median OS was longer for patients with MT than for those with ST (15.2 vs. 9.9 mo, P < .0001). No difference in OS between the MT and ST groups for patients who did not receive treatment for mCRC (1.6 vs. 2.6 mo; P = .95).
Patients with MT have a longer OS than those with ST, independent of treatment. Classification of patients according to whether they have metachronous or synchronous presentation of mCRC is prognostic. These results may add further support for population screening with the aim to reduce de novo metastatic disease.
同时性原发灶结直肠癌(mCRC)与异时性原发灶 mCRC 的行为是否不同尚不清楚。
南澳大利亚 mCRC 临床登记处收集 2006 年 2 月后诊断患者的数据。截至 2012 年 10 月 22 日,分析了 2502 例患者的数据,根据初始诊断的分期(SAID)进行分析,比较异时性肿瘤(MTs)(I 期、II 期、III 期)和同时性肿瘤(STs)(IV 期)之间的结果。总生存期(OS)从 mCRC 诊断日期开始计算。
ST 患者中肝脏转移更多,MT 患者中肺转移、非肺和非肝转移、非肺转移更多。复发中位时间根据 SAID 差异显著:I 期 49.3 个月(n=29)、II 期 25.2 个月(n=346)和 III 期 18.4 个月(n=497)。MT 患者的 OS 明显长于 ST 患者(19.0 比 14.9 个月,P=0.003)。对于接受任何 mCRC 治疗的患者,MT 患者的 OS 长于 ST 患者(19.2 比 15.3 个月,P=0.005)。对于仅接受 mCRC 化疗的患者,MT 患者的中位 OS 长于 ST 患者(15.2 比 9.9 个月,P<0.0001)。未接受 mCRC 治疗的患者 OS 无差异(1.6 比 2.6 个月,P=0.95)。
MT 患者的 OS 长于 ST 患者,与治疗无关。根据 mCRC 是否同时或异时性发生对患者进行分类具有预后意义。这些结果可能为减少新发转移性疾病的人群筛查提供更多支持。