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DOI 10.2967/jnumed.113.132761

Медицинская библиотека · Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2014

Targeted chemoradiation in metastatic colorectal cancer: a phase I trial of 131I-huA33 with concurrent capecitabine.

Herbertson Rebecca A, Tebbutt Niall C, Lee Fook-Thean, Gill Sanjeev, Chappell Bridget, Cavicchiolo Tina, Saunder Tim, O'Keefe Graeme J, Poon Aurora, Lee Sze Ting, Murphy Roger, Hopkins Wendie, Scott Fiona E, Scott Andrew M

Клиническое исследование I фазыСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: 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.

METHODS

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.

RESULTS

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.

CONCLUSION

(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.

Для цитирования: Herbertson Rebecca A, Tebbutt Niall C, Lee Fook-Thean, Gill Sanjeev, Chappell Bridget, Cavicchiolo Tina, Saunder Tim, O'Keefe Graeme J, Poon Aurora, Lee Sze Ting, Murphy Roger, Hopkins Wendie, Scott Fiona E, Scott Andrew M. Targeted chemoradiation in metastatic colorectal cancer: a phase I trial of 131I-huA33 with concurrent capecitabine.. Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 2014. DOI: 10.2967/jnumed.113.132761.

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