Trans-rectal ultrasound-guided hybrid intra-cavitary and interstitial brachytherapy in carcinoma cervix: A feasibility study from a tertiary cancer center in India

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. All patients who received an external beam radiotherapy (EBRT) dose of 50 Gy in 25 fractions with weekly chemotherapy,...

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Published in:Journal of contemporary brachytherapy Vol. 15; no. 3; pp. 198 - 205
Main Authors: Bajwa, Harjot Kaur, Singareddy, Rohith, Talluri, Anil Kumar, Kauser, Heena, Boja, Devender Reddy, Srikanth, G, Raju, Alluri Krishnam, Sresty, Nvn Madhusudhana, Mytri, Vyshnavi
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Published: Poland Termedia Publishing House 01-06-2023
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Abstract 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. 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 high-risk clinical target volume (HR-CTV), and D to OARs (bladder, rectum, and sigmoid). Width and thickness of the target was compared between TRUS (TRUS and TRUS ) and MRI (MRI and MRI ). 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 HR-CTV and D HR-CTV were 87.3 Gy and 82 Gy EQD , respectively. The mean D to the bladder, rectum, and sigmoid were 80 Gy, 70 Gy, and 64 Gy EQD , respectively. The mean dose to point A* was 70.4 Gy EQD . The mean TRAK was 0.40. The mean TRUS (±SD) and MRI (±SD) were 4.58 cm (±0.44) and 4.49 cm (±0.50), respectively. The mean TRUS (±SD) and MRI (±SD) were 2.7 cm (±0.59) and 2.62 cm (±0.59), respectively. On statistical analysis, there was a significant correlation between TRUS and MRI ( = 0.93), and TRUS and MRI ( = 0.98). TRUS-guided IC/IS brachytherapy is feasible and provides adequate coverage of the target, with acceptable doses to OARs.
AbstractList 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. 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 high-risk clinical target volume (HR-CTV), and D to OARs (bladder, rectum, and sigmoid). Width and thickness of the target was compared between TRUS (TRUS and TRUS ) and MRI (MRI and MRI ). 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 HR-CTV and D HR-CTV were 87.3 Gy and 82 Gy EQD , respectively. The mean D to the bladder, rectum, and sigmoid were 80 Gy, 70 Gy, and 64 Gy EQD , respectively. The mean dose to point A* was 70.4 Gy EQD . The mean TRAK was 0.40. The mean TRUS (±SD) and MRI (±SD) were 4.58 cm (±0.44) and 4.49 cm (±0.50), respectively. The mean TRUS (±SD) and MRI (±SD) were 2.7 cm (±0.59) and 2.62 cm (±0.59), respectively. On statistical analysis, there was a significant correlation between TRUS and MRI ( = 0.93), and TRUS and MRI ( = 0.98). TRUS-guided IC/IS brachytherapy is feasible and provides adequate coverage of the target, with acceptable doses to OARs.
PurposeTo 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 methodsAll 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). ResultsTwenty 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). ConclusionsTRUS-guided IC/IS brachytherapy is feasible and provides adequate coverage of the target, with acceptable doses to OARs.
Author Singareddy, Rohith
Sresty, Nvn Madhusudhana
Talluri, Anil Kumar
Raju, Alluri Krishnam
Mytri, Vyshnavi
Kauser, Heena
Boja, Devender Reddy
Srikanth, G
Bajwa, Harjot Kaur
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Keywords carcinoma cervix
hybrid brachytherapy
trans-rectal ultrasound
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Snippet To report the feasibility of performing hybrid intra-cavitary and interstitial (IC/IS) brachytherapy in patients with carcinoma cervix under trans-rectal...
PurposeTo report the feasibility of performing hybrid intra-cavitary and interstitial (IC/IS) brachytherapy in patients with carcinoma cervix under...
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SubjectTerms carcinoma cervix
hybrid brachytherapy
Original Paper
trans-rectal ultrasound
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Title Trans-rectal ultrasound-guided hybrid intra-cavitary and interstitial brachytherapy in carcinoma cervix: A feasibility study from a tertiary cancer center in India
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