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回顾性研究肽受体放射性核素疗法治疗晚期日本神经内分泌肿瘤患者。

Retrospective study of peptide receptor radionuclide therapy for Japanese patients with advanced neuroendocrine tumors.

机构信息

Department of Oncology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Division of Nuclear Medicine, University Hospital Basel, Basel, Switzerland.

出版信息

J Hepatobiliary Pancreat Sci. 2021 Sep;28(9):727-739. doi: 10.1002/jhbp.1014. Epub 2021 Jul 14.

Abstract

BACKGROUND

Peptide receptor radionuclide therapy (PRRT) with radiolabeled somatostatin analogs is an innovative treatment for advanced somatostatin-positive neuroendocrine tumors (NETs). PRRT cannot be performed in Japan because there is no approval or insurance cover so far.

METHODS

We relied on foreign institutions to perform PRRT for Japanese patients with NETs. We retrospectively evaluated the safety and efficacy of PRRT. The inclusion criteria were pathologically confirmed well-differentiated NET and visible tumor uptake on pre-therapeutic somatostatin receptor scintigraphy. Lu-DOTA-TOC was used as the standard treatment, and patients received three infusions every 8 weeks. Until the end of 2017, combination treatment with Y and Lu-DOTA-TOC was performed using the same protocol.

RESULTS

Thirty-five patients were evaluated, and the primary lesions were pancreas, rectum, small intestine, stomach, and other locations. The partial response rate was 42.9%. Progression-free survival (PFS) was 12.8 months and overall survival was 42.8 months. There was no significant difference in PFS between front-line and late-line PRRT (11.0 months vs 28.0 months; P = .383). Severe adverse events included lymphocytopenia (20.0%) and thrombocytopenia (5.7%). Myelodysplastic syndrome occurred in one case.

CONCLUSION

PRRT was effective and safe for Japanese patients with advanced NETs. PRRT was equally effective as front-line and late-line treatment.

摘要

背景

放射性核素肽受体靶向治疗(PRRT)使用放射性标记的生长抑素类似物是治疗晚期生长抑素阳性神经内分泌肿瘤(NETs)的创新方法。由于目前尚未获得批准或保险覆盖,PRRT 无法在日本进行。

方法

我们依靠外国机构为日本 NET 患者进行 PRRT。我们回顾性评估了 PRRT 的安全性和疗效。纳入标准为经病理证实的分化良好的 NET 和治疗前生长抑素受体闪烁显像可见肿瘤摄取。Lu-DOTA-TOC 被用作标准治疗,患者每 8 周接受三次输注。直到 2017 年底,采用相同方案进行 Y 和 Lu-DOTA-TOC 的联合治疗。

结果

共评估了 35 例患者,主要病变位于胰腺、直肠、小肠、胃和其他部位。部分缓解率为 42.9%。无进展生存期(PFS)为 12.8 个月,总生存期为 42.8 个月。一线和晚期 PRRT 的 PFS 无显著差异(11.0 个月比 28.0 个月;P=0.383)。严重不良事件包括淋巴细胞减少症(20.0%)和血小板减少症(5.7%)。一例发生骨髓增生异常综合征。

结论

PRRT 对日本晚期 NET 患者有效且安全。PRRT 作为一线和晚期治疗同样有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/9292713/8b1b4043af44/JHBP-28-727-g001.jpg

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