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      Impact of target area selection in 125 Iodine seed brachytherapy on locoregional recurrence in patients with non‐small cell lung cancer

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          Abstract

          Background

          Computed tomography (CT)‐guided percutaneous implantation of 125Iodine radioactive seeds requires the precise arrangement of seeds by tumor shape. We tested whether selecting target areas, including subclinical areas around tumors, can influence locoregional recurrence in patients with non‐small cell lung cancer ( NSCLC).

          Method

          We divided 82 patients with NSCLC into two groups. Target areas in group 1 ( n = 40) were defined along tumor margins based on lung‐window CT. Target areas in group 2 ( n = 42) were extended by 0.5 cm in all dimensions outside tumor margins. Preoperative plans for both groups were based on a treatment plan system, which guided 125 I seed implantation. Six months later, patients underwent chest CT to evaluate treatment efficacy (per Response Evaluation Criteria in Solid Tumors version 1). We compared locoregional recurrences between the groups after a year of follow‐up. We then used the treatment plan system to extend target areas for group 1 patients by 0.5 cm (defined as group 3 data) and compared these hypothetical group 3 planned seeds with the actual seed numbers used in group 1 patients.

          Results

          All patients successfully underwent implantation; none died during the follow‐up period. Recurrence was significantly lower in group 2 than in group 1 ( P  < 0.05). Group 1 patients and group 3 data significantly differed in seed numbers ( P  < 0.01).

          Conclusion

          Our results imply that extending the implantation area for 125 I seeds can decrease recurrence risk by eradicating cancerous lymph‐duct blockades within the extended areas.

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          Most cited references11

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          The American Brachytherapy Society recommendations for permanent prostate brachytherapy postimplant dosimetric analysis.

          The purpose of this report is to establish guidelines for postimplant dosimetric analysis of permanent prostate brachytherapy. Members of the American Brachytherapy Society (ABS) with expertise in prostate dosimetry evaluation performed a literature review and supplemented with their clinical experience formulated guidelines for performing and analyzing postimplant dosimetry of permanent prostate brachytherapy. The ABS recommends that postimplant dosimetry should be performed on all patients undergoing permanent prostate brachytherapy for optimal patient care. At present, computed tomography (CT)-based dosimetry is recommended, based on availability cost and the ability to image the prostate as well as the seeds. Additional plane radiographs should be obtained to verify the seed count. Until the ideal postoperative interval for CT scanning has been determined, each center should perform dosimetric evaluation of prostate implants at a consistent postoperative interval. This interval should be reported. Isodose displays should be obtained at 50%, 80%, 90%, 100%, 150%, and 200% of the prescription dose and displayed on multiple cross-sectional images of the prostate. A dose-volume histogram (DVH) of the prostate should be performed and the D90 (dose to 90% of the prostate gland) reported by all centers. Additionally, the D80, D100, the fractional V80, V90, V100, V150 and V200 (i.e., the percentage of prostate volume receiving 80%, 90%, 100%, 150%, and 200% of the prescribed dose, respectively), the rectal, and urethral doses should be reported and ultimately correlated with clinical outcome in the research environment. On-line real-time dosimetry, the effects of dose heterogeneity, and the effects of tissue heterogeneity need further investigation. It is essential that postimplant dosimetry should be performed on all patients undergoing permanent prostate brachytherapy. Guidelines were established for the performance and analysis of such dosimetry.
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            Rectal-wall dose dependence on postplan timing after permanent-seed prostate brachytherapy.

            Dose to rectal wall after permanent-seed prostate brachytherapy is dependent on distance between posterior prostatic seeds and anterior rectal wall and is influenced by postimplant periprostatic edema. We analyzed the effect of postplan timing on anterior rectal-wall dose. Twenty patients received permanent seed 125I brachytherapy as monotherapy (145 Gy). Implants were preplanned by use of transrectal ultrasound (TRUS) and carried out by use of preloaded needles. Postimplant dosimetry was calculated by use of magnetic resonance imaging-computed tomography fusion on Days 1, 8, and 30. The anterior rectal-wall dose is reported as the isodose enclosing 1.0 or 2.0 cc of rectal wall and as the RV100 in cc. The dose to rectal wall increased progressively over time. The median increase in dose to 1.0 cc of rectal wall (RD [1 cc]) from Day 1 to 30 was 39.2 Gy (p < 0.001). RV100 increased from a median of 0.07 cc on Day 1 to 0.67 cc on Day 30. The most significant predictor of rectal-wall dose (RD [1 cc], RD [2 cc], or RV100) was the time of evaluation (p < 0.001). Although periprostatic edema cannot be quantified by postimplant imaging, the dose to the anterior rectal wall increases significantly over time as prostatic and periprostatic edema resolve. Critical-organ dose reporting and guidelines for minimizing toxicity must take into account the time of the assessment.
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              Limited resection followed by intraoperative seed implantation is comparable to stereotactic body radiotherapy for solitary lung cancer.

              The objective of this study was to compare the outcomes of patients who underwent wedge resection plus intraoperative brachytherapy versus patients who received stereotactic body radiotherapy (SBRT) for single malignant lung nodules.
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                Author and article information

                Contributors
                xxwtj@sina.com
                Journal
                Thorac Cancer
                Thorac Cancer
                10.1111/(ISSN)1759-7714
                TCA
                Thoracic Cancer
                John Wiley & Sons Australia, Ltd (Melbourne )
                1759-7706
                1759-7714
                20 February 2017
                May 2017
                : 8
                : 3 ( doiID: 10.1111/tca.2017.8.issue-3 )
                : 147-152
                Affiliations
                [ 1 ] Department of Thoracic SurgeryThe Second Hospital of Tianjin Medical University TianjinChina
                [ 2 ] Faculty of MedicineUniversity of Southampton SouthamptonUK
                Author notes
                [*] [* ] Correspondence Zhi‐Yu Guan, Department of Thoracic Surgery, The Second Hospital of Tianjin Medical University, Pingjiang Road, Hexi District, Tianjin 300211, China. Tel: +86 22 8832 8526 Fax: +86 22 8832 8792 Email: xxwtj@ 123456sina.com
                Article
                TCA12415
                10.1111/1759-7714.12415
                5415452
                28217920
                cafb2cc0-dfdb-4a0c-9776-84373373af69
                © 2017 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 16 August 2016
                : 24 December 2016
                : 27 December 2016
                Page count
                Figures: 8, Tables: 2, Pages: 1, Words: 2960
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                tca12415
                May 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.0.9 mode:remove_FC converted:03.05.2017

                125iodine radioactive seed,non‐small cell lung cancer,radioactive seed brachytherapy,target area selection,treatment plan system (tps)

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