{"title":"经直肠超声引导的腔内腔间混合近距离治疗宫颈癌:印度三级癌症中心的可行性研究。","authors":"Harjot Kaur Bajwa, Rohith Singareddy, Anil Kumar Talluri, Heena Kauser, Devender Reddy Boja, G Srikanth, Alluri Krishnam Raju, Nvn Madhusudhana Sresty, Vyshnavi Mytri","doi":"10.5114/jcb.2023.127816","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To report the feasibility of performing hybrid intra-cavitary and interstitial (IC/IS) brachytherapy in patients with carcinoma cervix under trans-rectal ultrasound (TRUS) guidance.</p><p><strong>Material and methods: </strong>All patients who received an external beam radiotherapy (EBRT) dose of 50 Gy in 25 fractions with weekly chemotherapy, followed by a brachytherapy boost (21 Gy in 3 fractions) were prospectively included for analysis. IC/IS brachytherapy was performed using Fletcher style tandem and ovoid applicator with interstitial component under TRUS guidance. Parameters of implant quality analyzed included ability to insert tandem, ratio of needles loaded to the number of needles inserted, and incidence of uterine or organ at risk (OARs) perforation. Dosimetric parameters evaluated were dose to point A*, TRAK, D<sub>90</sub> high-risk clinical target volume (HR-CTV), and D<sub>2cc</sub> to OARs (bladder, rectum, and sigmoid). Width and thickness of the target was compared between TRUS (TRUS<sub>w</sub> and TRUS<sub>t</sub>) and MRI (MRI<sub>w</sub> and MRI<sub>t</sub>).</p><p><strong>Results: </strong>Twenty carcinoma cervix patients treated with IC/IS brachytherapy were included for analysis. The mean HR-CTV volume was 36 cc. The median number of needles used were 6 (range, 2-10 needles). None of the patients had uterine perforation. Two patients had bowel and bladder perforation. The mean D<sub>90</sub> HR-CTV and D<sub>98</sub> HR-CTV were 87.3 Gy and 82 Gy EQD<sub>2</sub>, respectively. The mean D<sub>2cc</sub> to the bladder, rectum, and sigmoid were 80 Gy, 70 Gy, and 64 Gy EQD<sub>2</sub>, respectively. The mean dose to point A* was 70.4 Gy EQD<sub>2</sub>. The mean TRAK was 0.40. The mean TRUS<sub>w</sub> (±SD) and MRI<sub>w</sub> (±SD) were 4.58 cm (±0.44) and 4.49 cm (±0.50), respectively. The mean TRUS<sub>t</sub> (±SD) and MRI<sub>t</sub> (±SD) were 2.7 cm (±0.59) and 2.62 cm (±0.59), respectively. On statistical analysis, there was a significant correlation between TRUS<sub>w</sub> and MRI<sub>w</sub> (<i>r</i> = 0.93), and TRUS<sub>t</sub> and MRI<sub>t</sub> (<i>r</i> = 0.98).</p><p><strong>Conclusions: </strong>TRUS-guided IC/IS brachytherapy is feasible and provides adequate coverage of the target, with acceptable doses to OARs.</p>","PeriodicalId":51305,"journal":{"name":"Journal of Contemporary Brachytherapy","volume":null,"pages":null},"PeriodicalIF":1.1000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/9d/ff/JCB-15-50779.PMC10324591.pdf","citationCount":"0","resultStr":"{\"title\":\"Trans-rectal ultrasound-guided hybrid intra-cavitary and interstitial brachytherapy in carcinoma cervix: A feasibility study from a tertiary cancer center in India.\",\"authors\":\"Harjot Kaur Bajwa, Rohith Singareddy, Anil Kumar Talluri, Heena Kauser, Devender Reddy Boja, G Srikanth, Alluri Krishnam Raju, Nvn Madhusudhana Sresty, Vyshnavi Mytri\",\"doi\":\"10.5114/jcb.2023.127816\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>To report the feasibility of performing hybrid intra-cavitary and interstitial (IC/IS) brachytherapy in patients with carcinoma cervix under trans-rectal ultrasound (TRUS) guidance.</p><p><strong>Material and methods: </strong>All patients who received an external beam radiotherapy (EBRT) dose of 50 Gy in 25 fractions with weekly chemotherapy, followed by a brachytherapy boost (21 Gy in 3 fractions) were prospectively included for analysis. IC/IS brachytherapy was performed using Fletcher style tandem and ovoid applicator with interstitial component under TRUS guidance. Parameters of implant quality analyzed included ability to insert tandem, ratio of needles loaded to the number of needles inserted, and incidence of uterine or organ at risk (OARs) perforation. Dosimetric parameters evaluated were dose to point A*, TRAK, D<sub>90</sub> high-risk clinical target volume (HR-CTV), and D<sub>2cc</sub> to OARs (bladder, rectum, and sigmoid). Width and thickness of the target was compared between TRUS (TRUS<sub>w</sub> and TRUS<sub>t</sub>) and MRI (MRI<sub>w</sub> and MRI<sub>t</sub>).</p><p><strong>Results: </strong>Twenty carcinoma cervix patients treated with IC/IS brachytherapy were included for analysis. The mean HR-CTV volume was 36 cc. The median number of needles used were 6 (range, 2-10 needles). None of the patients had uterine perforation. Two patients had bowel and bladder perforation. The mean D<sub>90</sub> HR-CTV and D<sub>98</sub> HR-CTV were 87.3 Gy and 82 Gy EQD<sub>2</sub>, respectively. The mean D<sub>2cc</sub> to the bladder, rectum, and sigmoid were 80 Gy, 70 Gy, and 64 Gy EQD<sub>2</sub>, respectively. The mean dose to point A* was 70.4 Gy EQD<sub>2</sub>. The mean TRAK was 0.40. The mean TRUS<sub>w</sub> (±SD) and MRI<sub>w</sub> (±SD) were 4.58 cm (±0.44) and 4.49 cm (±0.50), respectively. The mean TRUS<sub>t</sub> (±SD) and MRI<sub>t</sub> (±SD) were 2.7 cm (±0.59) and 2.62 cm (±0.59), respectively. On statistical analysis, there was a significant correlation between TRUS<sub>w</sub> and MRI<sub>w</sub> (<i>r</i> = 0.93), and TRUS<sub>t</sub> and MRI<sub>t</sub> (<i>r</i> = 0.98).</p><p><strong>Conclusions: </strong>TRUS-guided IC/IS brachytherapy is feasible and provides adequate coverage of the target, with acceptable doses to OARs.</p>\",\"PeriodicalId\":51305,\"journal\":{\"name\":\"Journal of Contemporary Brachytherapy\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2023-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/9d/ff/JCB-15-50779.PMC10324591.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Contemporary Brachytherapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.5114/jcb.2023.127816\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Contemporary Brachytherapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5114/jcb.2023.127816","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
Trans-rectal ultrasound-guided hybrid intra-cavitary and interstitial brachytherapy in carcinoma cervix: A feasibility study from a tertiary cancer center in India.
Purpose: To report the feasibility of performing hybrid intra-cavitary and interstitial (IC/IS) brachytherapy in patients with carcinoma cervix under trans-rectal ultrasound (TRUS) guidance.
Material and methods: All patients who received an external beam radiotherapy (EBRT) dose of 50 Gy in 25 fractions with weekly chemotherapy, followed by a brachytherapy boost (21 Gy in 3 fractions) were prospectively included for analysis. IC/IS brachytherapy was performed using Fletcher style tandem and ovoid applicator with interstitial component under TRUS guidance. Parameters of implant quality analyzed included ability to insert tandem, ratio of needles loaded to the number of needles inserted, and incidence of uterine or organ at risk (OARs) perforation. Dosimetric parameters evaluated were dose to point A*, TRAK, D90 high-risk clinical target volume (HR-CTV), and D2cc to OARs (bladder, rectum, and sigmoid). Width and thickness of the target was compared between TRUS (TRUSw and TRUSt) and MRI (MRIw and MRIt).
Results: Twenty carcinoma cervix patients treated with IC/IS brachytherapy were included for analysis. The mean HR-CTV volume was 36 cc. The median number of needles used were 6 (range, 2-10 needles). None of the patients had uterine perforation. Two patients had bowel and bladder perforation. The mean D90 HR-CTV and D98 HR-CTV were 87.3 Gy and 82 Gy EQD2, respectively. The mean D2cc to the bladder, rectum, and sigmoid were 80 Gy, 70 Gy, and 64 Gy EQD2, respectively. The mean dose to point A* was 70.4 Gy EQD2. The mean TRAK was 0.40. The mean TRUSw (±SD) and MRIw (±SD) were 4.58 cm (±0.44) and 4.49 cm (±0.50), respectively. The mean TRUSt (±SD) and MRIt (±SD) were 2.7 cm (±0.59) and 2.62 cm (±0.59), respectively. On statistical analysis, there was a significant correlation between TRUSw and MRIw (r = 0.93), and TRUSt and MRIt (r = 0.98).
Conclusions: TRUS-guided IC/IS brachytherapy is feasible and provides adequate coverage of the target, with acceptable doses to OARs.
期刊介绍：
The “Journal of Contemporary Brachytherapy” is an international and multidisciplinary journal that will publish papers of original research as well as reviews of articles. Main subjects of the journal include: clinical brachytherapy, combined modality treatment, advances in radiobiology, hyperthermia and tumour biology, as well as physical aspects relevant to brachytherapy, particularly in the field of imaging, dosimetry and radiation therapy planning. Original contributions will include experimental studies of combined modality treatment, tumor sensitization and normal tissue protection, molecular radiation biology, and clinical investigations of cancer treatment in brachytherapy. Another field of interest will be the educational part of the journal.
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