Ludwig Institute for Cancer Research, Melbourne, Australia.
J Nucl Med. 2014 Apr;55(4):534-9. doi: 10.2967/jnumed.113.132761. Epub 2014 Feb 20.
huA33 is a humanized antibody that targets the A33 antigen, which is highly expressed in intestinal epithelium and more than 95% of human colon cancers but not other normal tissues. Previous studies have shown huA33 can target and be retained in a metastatic tumor for 6 wk but eliminated from normal colonocytes within days. This phase I study used radiolabeled huA33 in combination with capecitabine to target chemoradiation to metastatic colorectal cancer. The primary objective was safety and tolerability of the combination of capecitabine and (131)I-huA33. Pharmacokinetics, biodistribution, immunogenicity, and tumor response were also assessed.
Eligibility included measurable metastatic colorectal cancer, adequate hematologic and biochemical function, and informed consent. An outpatient scout (131)I-huA33 dose was followed by a single-therapy infusion 1 wk later, when capecitabine was commenced. Dose escalation occurred over 5 dose levels. Patients were evaluated weekly, with tumor response assessment at the end of the 12-wk trial. Tumor targeting was assessed using a γ camera and SPECT imaging.
Nineteen eligible patients were enrolled. The most frequently observed toxicity included myelosuppression, gastrointestinal symptoms, and asymptomatic hyperbilirubinemia. Biodistribution analysis demonstrated excellent tumor targeting of the known tumor sites, expected transient bowel uptake, but no other normal tissue uptake. (131)I-huA33 demonstrated a mean terminal half-life and serum clearance suited to radioimmunotherapy (T1/2β, 100.24 ± 20.92 h, and clearance, 36.72 ± 8.01 mL/h). The mean total tumor dose was 13.8 ± 7.6 Gy (range, 5.1-26.9 Gy). One patient had a partial response, and 10 patients had stable disease.
(131)I-huA33 achieves specific targeting of radiotherapy to colorectal cancer metastases and can be safely combined with chemotherapy, providing an opportunity to deliver chemoradiation specifically to metastatic disease in colorectal cancer patients.
huA33 是一种针对 A33 抗原的人源化抗体,A33 抗原在肠道上皮细胞中高度表达,超过 95%的人结肠癌,但不在其他正常组织中表达。先前的研究表明,huA33 可以靶向并在转移性肿瘤中保留 6 周,但在数天内从正常结肠细胞中消除。这项 I 期研究使用放射性标记的 huA33 与卡培他滨联合靶向转移性结直肠癌的放化疗。主要目的是评估卡培他滨和 (131)I-huA33 联合应用的安全性和耐受性。还评估了药代动力学、生物分布、免疫原性和肿瘤反应。
入选标准包括可测量的转移性结直肠癌、足够的血液学和生化功能以及知情同意。在门诊进行 (131)I-huA33 剂量探测后,1 周后进行单次治疗输注,同时开始卡培他滨治疗。剂量递增发生在 5 个剂量水平上。患者每周进行评估,在 12 周试验结束时评估肿瘤反应。使用γ相机和 SPECT 成像评估肿瘤靶向。
19 名符合条件的患者入组。最常见的毒性包括骨髓抑制、胃肠道症状和无症状高胆红素血症。生物分布分析显示,已知肿瘤部位的肿瘤靶向性良好,预期的短暂肠道摄取,但无其他正常组织摄取。(131)I-huA33 显示出适合放射免疫治疗的平均终末半衰期和血清清除率(T1/2β,100.24±20.92h,清除率,36.72±8.01mL/h)。平均总肿瘤剂量为 13.8±7.6Gy(范围,5.1-26.9Gy)。1 例患者部分缓解,10 例患者病情稳定。
(131)I-huA33 实现了对结直肠癌转移灶放疗的特异性靶向,可与化疗安全联合,为结直肠癌患者的转移性疾病提供了特异性放化疗的机会。