{"title":"前列腺腺癌患者前列腺特异性膜抗原正电子发射断层扫描(PSMA PET)引导下淋巴组织增强照射的剂量建议。","authors":"K. Martell , C. Kirkby","doi":"10.1016/j.clon.2024.103730","DOIUrl":null,"url":null,"abstract":"<div><h3>Aims</h3><div>Prostrate-specific membrane antigen positron emission tomography (PSMA-PET) imaging has led to an increase in identifiable small volume metastatic disease in prostate adenocarcinoma. There is clinical equipoise in how to treat these using radiotherapy regimens. The aim of this study is to determine an adequate dosing regimen for small volume lymphatic metastases in prostate adenocarcinoma.</div></div><div><h3>Materials and methods</h3><div>The authors first estimated the cell count of small volume metastases in prostate adenocarcinoma and then used a Poisson distribution-based estimation of the tumour control probability distribution, the required doses for 95% and 99% probabilities of tumour sterilisation were calculated using the linear quadratic formula.</div></div><div><h3>Results</h3><div>Lymph node metastases of 3, 5, and 10 mm diameter were estimated to harbour 1.4, 6.5, and 52.3 million clonogens, respectively. When attempting for a 95% tumour control probability, estimated BEDs of 116.5, 127.0, and 141.1Gy were required. This translated to doses of 26.0, 27.3, and 29.0Gy in 5 fraction regimens. When attempting for a 99% tumour control probability, estimated biological effective doses (BEDs) of 127.6, 138.1, and 152.2 Gy were required. This translated to doses of 27.4, 28.6, and 30.2 Gy in 5 fraction regimens.</div></div><div><h3>Conclusion</h3><div>In prostate cancers with small-volume metastatic disease, doses can be adjusted according to tumour size without likely to compromise tumour control. This would have positive implications on radiotherapy planning and possibly lead to decreased risks of toxicity in scenarios where planning difficulty is encountered. Clinical evaluation of efficacy and safety for these dose regimens is warranted.</div></div>","PeriodicalId":10403,"journal":{"name":"Clinical oncology","volume":"38 ","pages":"Article 103730"},"PeriodicalIF":3.2000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dose Recommendations for Prostrate-specific Membrane Antigen Positron Emission Tomography (PSMA PET) Guided Boost Irradiation to Lymphatic Tissue in Prostate Adenocarcinoma\",\"authors\":\"K. Martell , C. Kirkby\",\"doi\":\"10.1016/j.clon.2024.103730\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Aims</h3><div>Prostrate-specific membrane antigen positron emission tomography (PSMA-PET) imaging has led to an increase in identifiable small volume metastatic disease in prostate adenocarcinoma. There is clinical equipoise in how to treat these using radiotherapy regimens. The aim of this study is to determine an adequate dosing regimen for small volume lymphatic metastases in prostate adenocarcinoma.</div></div><div><h3>Materials and methods</h3><div>The authors first estimated the cell count of small volume metastases in prostate adenocarcinoma and then used a Poisson distribution-based estimation of the tumour control probability distribution, the required doses for 95% and 99% probabilities of tumour sterilisation were calculated using the linear quadratic formula.</div></div><div><h3>Results</h3><div>Lymph node metastases of 3, 5, and 10 mm diameter were estimated to harbour 1.4, 6.5, and 52.3 million clonogens, respectively. When attempting for a 95% tumour control probability, estimated BEDs of 116.5, 127.0, and 141.1Gy were required. This translated to doses of 26.0, 27.3, and 29.0Gy in 5 fraction regimens. When attempting for a 99% tumour control probability, estimated biological effective doses (BEDs) of 127.6, 138.1, and 152.2 Gy were required. This translated to doses of 27.4, 28.6, and 30.2 Gy in 5 fraction regimens.</div></div><div><h3>Conclusion</h3><div>In prostate cancers with small-volume metastatic disease, doses can be adjusted according to tumour size without likely to compromise tumour control. This would have positive implications on radiotherapy planning and possibly lead to decreased risks of toxicity in scenarios where planning difficulty is encountered. Clinical evaluation of efficacy and safety for these dose regimens is warranted.</div></div>\",\"PeriodicalId\":10403,\"journal\":{\"name\":\"Clinical oncology\",\"volume\":\"38 \",\"pages\":\"Article 103730\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S093665552400534X\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical oncology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S093665552400534X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
Dose Recommendations for Prostrate-specific Membrane Antigen Positron Emission Tomography (PSMA PET) Guided Boost Irradiation to Lymphatic Tissue in Prostate Adenocarcinoma
Aims
Prostrate-specific membrane antigen positron emission tomography (PSMA-PET) imaging has led to an increase in identifiable small volume metastatic disease in prostate adenocarcinoma. There is clinical equipoise in how to treat these using radiotherapy regimens. The aim of this study is to determine an adequate dosing regimen for small volume lymphatic metastases in prostate adenocarcinoma.
Materials and methods
The authors first estimated the cell count of small volume metastases in prostate adenocarcinoma and then used a Poisson distribution-based estimation of the tumour control probability distribution, the required doses for 95% and 99% probabilities of tumour sterilisation were calculated using the linear quadratic formula.
Results
Lymph node metastases of 3, 5, and 10 mm diameter were estimated to harbour 1.4, 6.5, and 52.3 million clonogens, respectively. When attempting for a 95% tumour control probability, estimated BEDs of 116.5, 127.0, and 141.1Gy were required. This translated to doses of 26.0, 27.3, and 29.0Gy in 5 fraction regimens. When attempting for a 99% tumour control probability, estimated biological effective doses (BEDs) of 127.6, 138.1, and 152.2 Gy were required. This translated to doses of 27.4, 28.6, and 30.2 Gy in 5 fraction regimens.
Conclusion
In prostate cancers with small-volume metastatic disease, doses can be adjusted according to tumour size without likely to compromise tumour control. This would have positive implications on radiotherapy planning and possibly lead to decreased risks of toxicity in scenarios where planning difficulty is encountered. Clinical evaluation of efficacy and safety for these dose regimens is warranted.
期刊介绍:
Clinical Oncology is an International cancer journal covering all aspects of the clinical management of cancer patients, reflecting a multidisciplinary approach to therapy. Papers, editorials and reviews are published on all types of malignant disease embracing, pathology, diagnosis and treatment, including radiotherapy, chemotherapy, surgery, combined modality treatment and palliative care. Research and review papers covering epidemiology, radiobiology, radiation physics, tumour biology, and immunology are also published, together with letters to the editor, case reports and book reviews.