Risk of treatment-altering haematological toxicity and its dependence on bone marrow doses in peptide receptor radionuclide therapy.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING EJNMMI Research Pub Date : 2024-02-06 DOI:10.1186/s13550-024-01077-7
Märta Persson, Cecilia Hindorf, Oscar Ardenfors, Martin Larsson, Joachim N Nilsson
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Abstract

Background: Peptide receptor radionuclide therapy is effective in treating neuroendocrine tumours, but treatment may be limited by kidney and bone marrow toxicity. In this work, the absorbed dose burden to the bone marrow was estimated using image-based dosimetry and its potential use for predicting treatment-altering toxicity was studied. Peripheral blood samples taken before and after 229 treatments with 177Lu-DOTATATE in 59 patients were studied. In connection to the treatments, a total of 940 blood sample occasions provided data on white blood cell, neutrophil granulocyte, platelet, erythrocyte and haemoglobin concentrations. SPECT/CT image data were collected at two or three time points after each treatment. Absorbed doses to bone marrow were calculated from the activity concentration in a metastasis-free lumbar vertebra. The rate of delayed and aborted treatments was analysed based on medical records.

Results: The average absorbed dose to the bone marrow was 0.42 Gy (median 0.33 Gy, SD 0.27 Gy) per treatment. Dose-response relationships between white blood cells, neutrophil granulocytes and haemoglobin concentrations were observed, most prominently at 31-45 days after each treatment. The correlations were stronger in patients with skeletal metastases. The rates of haematological toxicity-related delays and aborted treatments were 6% and 12%, respectively. None of the studied bone marrow dosimetric parameters could clearly predict treatment-related toxicity. However, patients with skeletal metastases had higher risk of treatment-altering toxicity (odds ratio = 6.0).

Conclusions: Treatment-altering haematological toxicity in peptide receptor radionuclide therapy is relatively rare and appears difficult to fully predict from post-therapeutic image-based dosimetry. However, for patients with skeletal metastases, the haematological dose-response relationships are stronger. Future studies may focus on this patient group, to further investigate the usefulness of dosimetry in predicting decreases in blood values.

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肽受体放射性核素疗法中改变治疗的血液毒性风险及其与骨髓剂量的关系。
背景:肽受体放射性核素疗法可有效治疗神经内分泌肿瘤,但治疗可能会受到肾脏和骨髓毒性的限制。在这项研究中,利用基于图像的剂量测定法估算了骨髓的吸收剂量负担,并研究了其用于预测改变治疗的毒性的潜力。研究了59名患者在接受229次177Lu-DOTATATE治疗前后采集的外周血样本。在治疗过程中,共有 940 个血液样本场合提供了白细胞、中性粒细胞、血小板、红细胞和血红蛋白浓度数据。在每次治疗后的两个或三个时间点收集 SPECT/CT 图像数据。骨髓吸收剂量是根据无转移的腰椎中的活性浓度计算得出的。根据医疗记录分析了延迟治疗和中止治疗的比例:结果:每次治疗对骨髓的平均吸收剂量为 0.42 Gy(中位数为 0.33 Gy,SD 为 0.27 Gy)。白细胞、中性粒细胞和血红蛋白浓度之间存在剂量反应关系,在每次治疗后 31-45 天最为明显。骨骼转移患者的相关性更强。与血液毒性相关的治疗延迟率和治疗中止率分别为 6% 和 12%。所研究的骨髓剂量学参数都不能明确预测与治疗相关的毒性。然而,骨骼转移患者出现治疗相关毒性的风险更高(几率比=6.0):结论:在肽受体放射性核素治疗中,改变治疗的血液学毒性相对罕见,而且似乎很难通过治疗后基于图像的剂量测定来完全预测。不过,对于骨骼转移患者,血液学剂量-反应关系更为密切。未来的研究可能会关注这一患者群体,进一步研究剂量测量在预测血值下降方面的作用。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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