Lehtomäki Kaisa, Mustonen Harri, Kellokumpu-Lehtinen Pirkko-Liisa, Joensuu Heikki, Hermunen Kethe, Soveri Leena-Maija, Boisen Mogens Karsbøl, Dehlendorff Christian, Johansen Julia Sidenius, Haglund Caj, Osterlund Pia
Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön katu 34, 33520 Tampere, Finland.
Department of Oncology: Tays Cancer Center, Tampere University Hospital, Teiskontie 35, 33520 Tampere, Finland.
Cancers (Basel). 2021 Aug 2;13(15):3892. doi: 10.3390/cancers13153892.
In colorectal cancer (CRC), 20-50% of patients relapse after curative-intent surgery with or without adjuvant therapy. We investigated the lead times and prognostic value of post-adjuvant (8 months from randomisation to adjuvant treatment) serum CEA, CA19-9, IL-6, CRP, and YKL-40. We included 147 radically resected stage II-IV CRC treated with 24 weeks of adjuvant 5-fluorouracil-based chemotherapy in the phase III LIPSYT-study (ISRCTN98405441). All 147 were included in lead time analysis, but 12 relapsing during adjuvant therapy were excluded from post-adjuvant analysis. Elevated post-adjuvant CEA, IL-6, and CRP were associated with impaired disease-free survival (DFS) with hazard ratio (HR) 5.21 (95% confidence interval 2.32-11.69); 3.72 (1.99-6.95); 2.58 (1.18-5.61), respectively, and elevated IL-6 and CRP with impaired overall survival (OS) HR 3.06 (1.64-5.73); 3.41 (1.55-7.49), respectively. Elevated post-adjuvant IL-6 in CEA-normal patients identified a subgroup with impaired DFS. HR 3.12 (1.38-7.04) and OS, HR 3.20 (1.39-7.37). The lead times between the elevated biomarker and radiological relapse were 7.8 months for CEA and 10.0-53.1 months for CA19-9, IL-6, CRP, and YKL-40, and the lead time for the five combined was 27.3 months. Elevated post-adjuvant CEA, IL-6, and CRP were associated with impaired DFS. The lead time was shortest for CEA.
在结直肠癌(CRC)中,20%-50%的患者在接受根治性手术(无论是否接受辅助治疗)后会复发。我们研究了辅助治疗后(从随机分组到辅助治疗8个月)血清癌胚抗原(CEA)、糖类抗原19-9(CA19-9)、白细胞介素-6(IL-6)、C反应蛋白(CRP)和YKL-40的提前期及预后价值。我们纳入了147例在III期LIPSYT研究(ISRCTN98405441)中接受了24周基于5-氟尿嘧啶辅助化疗的II-IV期根治性切除的CRC患者。147例患者均纳入提前期分析,但12例在辅助治疗期间复发的患者被排除在辅助治疗后分析之外。辅助治疗后CEA、IL-6和CRP升高与无病生存期(DFS)受损相关,风险比(HR)分别为5.21(95%置信区间2.32-11.69)、3.72(1.99-6.95)、2.58(1.18-5.61),IL-6和CRP升高与总生存期(OS)受损相关,HR分别为3.06(1.64-5.73)、3.41(1.55-7.49)。CEA正常的患者中辅助治疗后IL-6升高确定了一个DFS受损的亚组,HR为3.12(1.38-7.04),OS的HR为3.20(1.39-7.37)。生物标志物升高与影像学复发之间的提前期,CEA为7.8个月,CA19-9、IL-6、CRP和YKL-40为10.0-53.1个月,五项联合的提前期为27.3个月。辅助治疗后CEA、IL-6和CRP升高与DFS受损相关。CEA的提前期最短。