Radiation Dosimetry of 89Zr-Labeled Chimeric Monoclonal Antibody U36 as Used for Immuno-PET in Head and Neck Cancer Patients

被引:137
作者
Boerjesson, Pontus K. E. [2 ]
Jauw, Yvonne W. S. [2 ]
de Bree, Remco [2 ]
Roos, Jan C. [1 ]
Castelijns, Jonas A. [3 ]
Leemans, C. Rene [2 ]
van Dongen, Guus A. M. S. [1 ,2 ]
Boellaard, Ronald [1 ]
机构
[1] Vrije Univ Amsterdam, Dept Nucl Med & PET Res, Med Ctr, NL-1081 HV Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Dept Otolaryngol Head & Neck Surg, Med Ctr, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Dept Radiol, Med Ctr, NL-1081 HV Amsterdam, Netherlands
关键词
immuno-PET; molecular imaging; head and neck cancer patients; Zr-89-labeled monoclonal antibody; dosimetry; POSITRON-EMISSION-TOMOGRAPHY; SQUAMOUS-CELL CARCINOMA; MARROW DOSIMETRY; IMAGE QUALITY; BIODISTRIBUTION; RADIOIMMUNOSCINTIGRAPHY; RADIOIMMUNOTHERAPY; EXPRESSION; CETUXIMAB; THERAPY;
D O I
10.2967/jnumed.109.065862
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Immuno-PET is an appealing concept in the detection of tumors and planning of antibody-based therapy. For this purpose, the long-lived positron emitter Zr-89 (half-life, 78.4 h) recently became available. The aim of the present first-in-humans Zr-89 immuno-PET study was to assess safety, biodistribution, radiation dose, and quantification of the Zr-89-labeled chimeric monoclonal antibody (cmAb) U36 in patients with head and neck squamous cell carcinoma (HNSCC). In addition, the performance of immuno-PET for detecting lymph node metastases was evaluated, as described previously. Methods: Twenty HNSCC patients, scheduled to undergo surgical tumor resection, received 75 MBq of Zr-89-cmAb U36 (10 mg). Immuno-PET scans were acquired at 1, 24, 72, or 144 h after injection. The biodistribution of the radioimmunoconjugate was evaluated by ex vivo radioactivity measurement in blood and in biopsies from the surgical specimen obtained at 168 h after injection. Uptake levels and residence times in blood, tumors, and organs of interest were derived from quantitative immuno-PET studies, and absorbed doses were calculated using OLINDA/EXM 1.0. The red marrow dose was calculated using the residence time for blood. Results: Zr-89-cmAb U36 was well tolerated by all subjects. PET quantification of blood-pool activity in the left ventricle of the heart showed a good agreement with sampled blood activity (difference equals 0.2% +/- 16.9% [mean +/- SD]) except for heavyweight patients (>100 kg). A good agreement was also found for the assessment of mAb uptake in primary tumors (mean deviation, 28.4% +/- 34.5%). The mean absorbed red marrow dose was 0.07 +/- 0.02 mSv/MBq and 0.09 +/- 0.01 mSv/MBq in men and women, respectively. The normal organ with the highest absorbed dose was the liver (mean dose, 1.25 +/- 0.27 mSv/MBq in men and 1.3560.21 mSv/MBq in women), thereafter followed by kidneys, thyroid, lungs, and spleen. The mean effective dose was 0.53 +/- 0.03 mSv/MBq in men and 0.66 +/- 0.03 mSv/MBq in women. Measured excretion via the urinary tract was less than 3% during the first 72 h. Conclusion: Zr-89 immuno-PET can be safely used to quantitatively assess biodistribution, uptake, organ residence times, and radiation dose, justifying its further clinical exploitation in the detection of tumors and planning of mAb-based therapy.
引用
收藏
页码:1828 / 1836
页数:9
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