Ychou Marc, Azria David, Menkarios Cathy, Faurous Patrick, Quenet François, Saint-Aubert Bernard, Rouanet Philippe, Pèlegrin Monique, Bascoul-Mollevi Caroline, Guerreau Dominique, Saccavini Jean-Claude, Mach Jean-Pierre, Artus Jean-Claude, Pèlegrin André
Institut de Recherche en Cancérologie de Montpellier, CRLC Val d'Aurelle-Paul Lamarque, 34298 Montpellier Cedex 5, France.
Clin Cancer Res. 2008 Jun 1;14(11):3487-93. doi: 10.1158/1078-0432.CCR-07-4698.
To evaluate the feasibility of radioimmunotherapy (RIT) with radiolabeled anti-carcinoembryonic antigen antibodies after complete resection of liver metastases (LM) from colorectal cancer.
Twenty-two patients planned for surgery of one to four LM received a preoperative diagnostic dose of a 131I-F(ab')2-labeled anti-carcinoembryonic antigen monoclonal antibody F6 (8-10 mCi/5 mg). 131I-F(ab')2 uptake was analyzed using direct radioactivity counting, and tumor-to-normal liver ratios were recorded. Ten patients with tumor-to-normal liver ratios of >5 and three others were treated with a therapeutic injection [180-200 mCi 131I/50 mg F(ab')2] 30 to 64 days after surgery.
Median 131I-F(ab')2 immunoreactivity in patient serum remained at 91% of initial values for up to 96 hours after injection. The main and dose-limiting-toxicity was hematologic, with 92% and 85% grades 3 to 4 neutropenia and thrombocytopenia, respectively. Complete spontaneous recovery occurred in all patients. No human anti-mouse antibody response was observed after the diagnosis dose; however, 10 of the 13 treated patients developed human anti-mouse antibody approximately 3 months later. Two treated patients presented extrahepatic metastases at the time of RIT (one bone and one abdominal node) and two relapsed within 3 months of RIT (one in the lung and the other in the liver). Two patients are still alive, and one of these is disease-free at 93 months after resection. At a median follow-up of 127 months, the median disease-free survival is 12 months and the median overall survival is 50 months.
RIT is feasible in an adjuvant setting after complete resection of LM from colorectal cancer and should be considered for future trials, possibly in combination with chemotherapy, because of the generally poor prognosis of these patients.
评估在结直肠癌肝转移(LM)完全切除术后,使用放射性标记的抗癌胚抗原抗体进行放射免疫治疗(RIT)的可行性。
计划对1至4个肝转移灶进行手术的22例患者接受了术前诊断剂量的131I-F(ab')2标记的抗癌胚抗原单克隆抗体F6(8 - 10毫居里/5毫克)。使用直接放射性计数分析131I-F(ab')2摄取情况,并记录肿瘤与正常肝脏的比值。10例肿瘤与正常肝脏比值>5的患者以及另外3例患者在术后30至64天接受了治疗性注射[180 - 200毫居里131I/50毫克F(ab')2]。
注射后长达96小时,患者血清中131I-F(ab')2的中位免疫反应性维持在初始值的91%。主要的剂量限制性毒性为血液学毒性,3至4级中性粒细胞减少和血小板减少的发生率分别为92%和85%。所有患者均完全自发恢复。诊断剂量后未观察到人抗鼠抗体反应;然而,13例接受治疗的患者中有10例在约3个月后出现人抗鼠抗体。2例接受治疗的患者在RIT时出现肝外转移(1例骨转移和1例腹部淋巴结转移)且2例在RIT后3个月内复发(1例肺转移和另例肝转移)。2例患者仍存活,其中1例在切除术后93个月无疾病。中位随访127个月时,中位无病生存期为12个月,中位总生存期为50个月。
在结直肠癌肝转移完全切除术后的辅助治疗中,RIT是可行的,鉴于这些患者总体预后通常较差,应考虑在未来试验中使用,可能与化疗联合使用。