Sorbonne University, Department of Medical Oncology, Hôpital Saint-Antoine, AP-HP, and INSERM UMRS 938, Équipe Instabilité des Microsatellites et Cancer, Équipe Labellisée par la Ligue Nationale Contre le Cancer, SIRIC CURAMUS, Centre de recherche Saint Antoine, Paris, France.
Statistical Unit, ARCAD Foundation, Paris, France.
Eur J Cancer. 2024 Aug;207:114160. doi: 10.1016/j.ejca.2024.114160. Epub 2024 Jun 10.
The liver is the most frequent site of metastases in colorectal cancer (CRC). This study aimed to assess the response rate and survival outcomes in metastatic CRC patients with non-liver metastases (NLM) compared to those with liver metastases (LM) across different lines of treatment.
A total of 17,924 mCRC patients included in 26 trials from the ARCAD CRC database were analyzed. The analysis was conducted based on the presence or absence of LM across different treatment groups: chemotherapy (CT) alone, CT + anti-VEGF, CT + anti-EGFR in KRAS wild-type tumors, within the first-line (1 L) and second-line (2 L), and patients enrolled in third-line (≥3 L) trials treated with trifluridine/tipiracil or regorafenib or placebo. The endpoints were overall survival (OS), progression-free survival (PFS), and overall response rate (ORR).
Out of the 17,924 patients, 14,066 had LM (30.6 % with only liver involvement and 69.4 % with liver and other metastatic sites), while 3858 patients had NLM. In the CT alone and CT + anti-VEGF subgroups, NLM patients showed better OS and PFS in the 1 L and 2 L settings. However, in the CT + anti-EGFR 1 L and 2 L subgroups, there was no significant difference in OS and PFS between NLM and LM patients. In the ≥ 3 L subgroups, better OS and PFS were observed in NLM patients. ORRs were higher in LM patients than in NLM patients across all cohorts treated in the 1 L and only in the anti-EGFR cohort in the 2 L.
LM is a poor prognostic factor for mCRC increasing from 1 L to ≥ 3 L except for patients in 1 L and 2 L receiving CT+anti-EGFR. These data justify using LM as a stratification factor in future trials for patients with unresectable mCRC.
肝脏是结直肠癌(CRC)转移最常见的部位。本研究旨在评估转移性 CRC 患者中无肝转移(NLM)与肝转移(LM)患者在不同治疗线的缓解率和生存结果。
共分析了来自 ARCAD CRC 数据库的 26 项试验中的 17924 例 mCRC 患者。分析基于不同治疗组中是否存在 LM:单独化疗(CT)、CT+抗 VEGF、KRAS 野生型肿瘤中 CT+抗 EGFR、一线(1L)和二线(2L)、以及接受三氟嘧啶/替匹嘧啶或瑞戈非尼或安慰剂治疗的三线(≥3L)试验中入组的患者。终点是总生存期(OS)、无进展生存期(PFS)和总缓解率(ORR)。
在 17924 例患者中,14066 例有 LM(仅肝脏受累者占 30.6%,肝脏和其他转移部位受累者占 69.4%),3858 例有 NLM。在单独 CT 和 CT+抗 VEGF 亚组中,NLM 患者在 1L 和 2L 时 OS 和 PFS 更好。然而,在 CT+抗 EGFR 1L 和 2L 亚组中,NLM 和 LM 患者的 OS 和 PFS 无显著差异。在≥3L 亚组中,NLM 患者的 OS 和 PFS 更好。ORR 在所有接受 1L 治疗的队列中 LM 患者高于 NLM 患者,仅在 2L 中抗 EGFR 队列中如此。
除了接受 1L 和 2L CT+抗 EGFR 治疗的患者外,LM 是 mCRC 预后不良的因素,从 1L 增加到≥3L。这些数据证明将 LM 作为未来不可切除 mCRC 患者试验的分层因素是合理的。