68Ga-PSMA PET/CT 对前列腺癌患者放射治疗计划的影响。

Felix Bock, B. Frerker, Laura Schubert, Hannes Rennau, Jens Kurth, Bernd J. Krause, Guido Hildebrandt, S. Schwarzenböck
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In sRT primary PTV was changed in 16/27 patients extending the PTV to the lymphatic drainage (10/16), PSMA-positive LR (3/16), bone metastases (2/16) and both nodal/bone metastases (1/16). PET-based increase of primary PTV was 116%. PET-based boosts were administered in 19/27 patients (8/19: local, 10/19: nodal, 1/19: both), median boost volume was 31.3 cm3 (range 17.2-80.2) (local) and 19.7 cm3 (range 3.0-109.3) (nodal). PTV was changed in 1/11 (9%) of dRT patients (extension of primary PTV to the lymphatic drainage (RT volume of 644.5 cm3), additional nodal boost (volume of 2.7 cm3, 23.1 Gy)). All patients showed biochemical response (mean PSA decrease 88.8 +/- 14.0%). Nadir PSA was reached 10 months (range 1-17) after end of RT (median 0.07 ng/ml, range 0.002-3.96). 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摘要

目的:本研究旨在评估 68Ga-PSMA PET/CT 对接受挽救性(sRT)或确定性(dRT)放疗的前列腺癌患者的放疗(RT)计划的影响。方法:38 例患者(27 例 sRT,中位 PSA 0.79 ng/ml(范围 0.06-12.1);11 例 dRT,中位 PSA 4.35 ng/ml(范围 1.55-55.5))在 RT 前接受了 68Ga-PSMA PET/CT。评估了68Ga-PSMA PET/CT对规划靶体积(PTV)范围和增加基于PET的增量的影响。结果68Ga-PSMA PET/CT在23/38例患者中显示阳性结果(8/23例:局部复发(LR),11/23例:结节转移,1/23例:LR和结节,2/23例:单发骨转移,1/23例:寡转移结节/骨转移)。在 sRT 中,有 16/27 例患者的原发 PTV 发生变化,PTV 扩展到淋巴引流(10/16)、PSMA 阳性 LR(3/16)、骨转移(2/16)和结节/骨转移(1/16)。基于 PET 的原发 PTV 增量为 116%。19/27例患者接受了基于PET的增强治疗(8/19例:局部,10/19例:结节,1/19例:两者),中位增强体积为31.3立方厘米(范围17.2-80.2)(局部)和19.7立方厘米(范围3.0-109.3)(结节)。1/11(9%)名 dRT 患者的 PTV 发生了改变(原发 PTV 扩展到淋巴引流(RT 容量为 644.5 立方厘米),额外的结节增强(容量为 2.7 立方厘米,23.1 Gy))。所有患者都出现了生化反应(PSA平均下降88.8 +/- 14.0%)。PSA 在 RT 结束后 10 个月(1-17 个月)达到最低水平(中位数为 0.07 ng/ml,范围为 0.002-3.96)。在中位 12 个月的随访期间(sRT/dRT 的范围为 3-22/8-24 个月),PSA 中位值为 0.05 ng/ml(范围为 0.002-8.5)(sRT)和 0.26 ng/ml(范围为 0.02-2.68)(dRT)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of 68Ga-PSMA PET/CT on radiation treatment planning of prostate cancer patients.
AIM This study aimed to assess the impact of 68Ga-PSMA PET/CT on radiation treatment (RT) planning in prostate cancer patients with salvage (sRT) or definitive (dRT) radiotherapy. METHODS 38 patients (27 sRT, median PSA 0.79 ng/ml (range 0.06-12.1); 11 dRT, median PSA 4.35 ng/ml (range 1.55-55.5) underwent 68Ga-PSMA PET/CT before RT. Influence of 68Ga-PSMA PET/CT on the extent of planning target volume (PTV) and addition of PET-based boosts were assessed. Median follow up was 12 months (range 3-24). RESULTS 68Ga-PSMA PET/CT showed positive findings in 23/38 patients (8/23: local recurrence (LR), 11/23: nodal metastasis, 1/23: LR and nodal, 2/23: solitary bone metastasis, 1/23: oligometastatic nodal/ bone metastases). In sRT primary PTV was changed in 16/27 patients extending the PTV to the lymphatic drainage (10/16), PSMA-positive LR (3/16), bone metastases (2/16) and both nodal/bone metastases (1/16). PET-based increase of primary PTV was 116%. PET-based boosts were administered in 19/27 patients (8/19: local, 10/19: nodal, 1/19: both), median boost volume was 31.3 cm3 (range 17.2-80.2) (local) and 19.7 cm3 (range 3.0-109.3) (nodal). PTV was changed in 1/11 (9%) of dRT patients (extension of primary PTV to the lymphatic drainage (RT volume of 644.5 cm3), additional nodal boost (volume of 2.7 cm3, 23.1 Gy)). All patients showed biochemical response (mean PSA decrease 88.8 +/- 14.0%). Nadir PSA was reached 10 months (range 1-17) after end of RT (median 0.07 ng/ml, range 0.002-3.96). Within a median 12 months follow-up (range 3-22/8-24 in sRT/dRT), median PSA was 0.05 ng/ml (range 0.002-8.5) (sRT) and 0.26 ng/ml (range 0.02-2.68) (dRT). CONCLUSIONS 68Ga-PSMA PET/CT influenced sRT planning in almost 63% and dRT in 9% of patients by change of PTV and additional boosts.
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