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      Helical tomotherapy for asymptomatic chemotherapy-refractory or -unfit multiple (3 or more) metastases

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          Abstract

          Background

          Despite chemotherapy innovations, prognosis of patients with chemotherapy-refractory or -unfit multiple metastases (CRMM/CUMM) remains poor. In this prospective study, the efficacy and toxicity of helical tomotherapy for CRMM/CUMM were evaluated.

          Materials and methods

          Between 2014 and 2020, asymptomatic patients with CRMM/CUMM with ≥ 3 lesions and no prior radiotherapy of the targets were enrolled. Patients who had intolerable toxicities to chemotherapy and those who refused chemotherapy were included in the CRMM and CUMM groups, respectively. Prostate cancer patients and patients with metastases mainly localized in the liver, lung, or brain were excluded. By helical tomotherapy, up to 10 lesions per patient were irradiated in order of volume. The standard dose was 50–60 Gy in 25–30 fractions.

          Results

          Forty-five patients (median age, 63 years; 35 CRMM/10 CUMM) were enrolled. Primary tumors included lung, gynecological, and gastrointestinal cancers. The most frequently treated targets were lymph node metastases, followed by peritoneal/pleural disseminations and bone tumors. The 1-year survival rate was 51% (median, 12.5 months). In the 35 patients with CRMM, the median survival time was 12.5 months, and the median pre-radiation chemotherapy period was 8.8 months (p > 0.05). The 6-month target control rate was 78%. Acute adverse events (grade ≥ 2) occurred in 33 patients: hematologic toxicities in 23, dermatitis in 6, and others in 8. Late grade ≥ 2 toxicities occurred in 6 patients: pneumonitis in 4 and gastric hemorrhage in 2.

          Conclusion

          Tomotherapy for CRMM/CUMM resulted in median survival times > 1 year. This treatment should be investigated further in larger prospective studies.

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          Most cited references26

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          Stereotactic ablative radiotherapy versus standard of care palliative treatment in patients with oligometastatic cancers (SABR-COMET): a randomised, phase 2, open-label trial

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            The dendritic cell lineage: ontogeny and function of dendritic cells and their subsets in the steady state and the inflamed setting.

            Dendritic cells (DCs) form a remarkable cellular network that shapes adaptive immune responses according to peripheral cues. After four decades of research, we now know that DCs arise from a hematopoietic lineage distinct from other leukocytes, establishing the DC system as a unique hematopoietic branch. Recent work has also established that tissue DCs consist of developmentally and functionally distinct subsets that differentially regulate T lymphocyte function. This review discusses major advances in our understanding of the regulation of DC lineage commitment, differentiation, diversification, and function in situ.
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              Tolerance of normal tissue to therapeutic irradiation

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                Author and article information

                Journal
                Rep Pract Oncol Radiother
                Rep Pract Oncol Radiother
                Reports of Practical Oncology and Radiotherapy
                Via Medica
                1507-1367
                2083-4640
                2022
                22 March 2022
                : 27
                : 1
                : 125-133
                Affiliations
                [1 ]Department of Radiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
                [2 ]Department of Radiology, Kasugai Municipal Hospital, Kasugai, Japan
                [3 ]Narita Memorial Proton Center, Toyohashi, Japan
                [4 ]Department of Radiation Oncology, Hokkaido Ohno Memorial Hospital, Sapporo, Japan
                [5 ]Department of Radiology, Narita Memorial Hospital, Toyohashi, Japan
                [6 ]Department of Radiology, Nagoya Daini Red Cross Hospital, Nagoya, Japan
                Author notes
                Address for correspondence: Yuta Shibamoto, MD, Department of Radiology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan, tel: +81-52-853-8274, fax: +81-52-852-5244; e-mail: yshiba@ 123456med.nagoya-cu.ac.jp
                Article
                rpor-27-1-125
                10.5603/RPOR.a2022.0016
                8989439
                dadaf1e8-9c79-4e17-ab0e-85f6400aa4a7
                © 2022 Greater Poland Cancer Centre

                This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially

                History
                : 20 October 2021
                : 16 January 2022
                Categories
                Research Paper

                multiple metastases,chemotherapy-refractory,chemotherapy-unfit,intensity-modulated radiotherapy,tomotherapy

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