Clinical advantage and outcomes of computed tomography-based transvaginal hybrid brachytherapy performed only by sedation without general or saddle block anesthesia.


Journal

Cancer reports (Hoboken, N.J.)
ISSN: 2573-8348
Titre abrégé: Cancer Rep (Hoboken)
Pays: United States
ID NLM: 101747728

Informations de publication

Date de publication:
11 2022
Historique:
revised: 30 12 2021
received: 29 07 2021
accepted: 21 01 2022
pubmed: 2 3 2022
medline: 23 11 2022
entrez: 1 3 2022
Statut: ppublish

Résumé

Three-dimensional image-guided brachytherapy is the standard of care in cervical cancer radiotherapy. In addition, the usefulness of the so-called "hybrid brachytherapy (HBT)" has been reported, which involves the addition of needle applicators to conventional intracavitary brachytherapy for interstitial irradiation. To evaluate the clinical outcomes of CT-based HBT consisting of transvaginal insertion of needle applicators (CT-based transvaginal HBT) and only intravenous sedation without general or saddle block anesthesia. This is a retrospective chart review of patients who received definitive radiotherapy, including CT-based transvaginal HBT, between February 2012 and July 2019. The inclusion criteria were as follows: (i) histologically diagnosed disease, (ii) untreated cervical cancer, (iii) International Federation of Gynecology and Obstetrics (FIGO) stage IB1-IVA disease in the 2008 FIGO staging system, and (iv) patients who underwent CT-based transvaginal HBT at least once in a series of intracavitary brachytherapy. Overall, 54 patients fulfilled the eligibility criteria in the present study. The median follow-up period was 32 (IQR, 19-44) months. No patient complained of symptoms such as persistent bleeding or abdominal pain after the treatment. The 3-year local control (LC), disease-free survival, and overall survival rates for all 54 patients were 86.6%, 60.3%, and 90.7% (95% CI [81.3%-100.0%]), respectively. The 3-year LC rate was 87.7% in patients with FIGO III-IVA and 90.4% in tumor size >6.0 cm. The incidence rate of late adverse events, grade ≥3, in the rectum and bladder was 0% and 1.8%, respectively. In the dose-volume histogram analyses, transvaginal HBT increased the dose of HR-CTV Considering the favorable clinical outcomes, CT-based transvaginal HBT may be a good option for treating cervical cancer.

Sections du résumé

BACKGROUND
Three-dimensional image-guided brachytherapy is the standard of care in cervical cancer radiotherapy. In addition, the usefulness of the so-called "hybrid brachytherapy (HBT)" has been reported, which involves the addition of needle applicators to conventional intracavitary brachytherapy for interstitial irradiation.
AIM
To evaluate the clinical outcomes of CT-based HBT consisting of transvaginal insertion of needle applicators (CT-based transvaginal HBT) and only intravenous sedation without general or saddle block anesthesia.
METHODS AND RESULTS
This is a retrospective chart review of patients who received definitive radiotherapy, including CT-based transvaginal HBT, between February 2012 and July 2019. The inclusion criteria were as follows: (i) histologically diagnosed disease, (ii) untreated cervical cancer, (iii) International Federation of Gynecology and Obstetrics (FIGO) stage IB1-IVA disease in the 2008 FIGO staging system, and (iv) patients who underwent CT-based transvaginal HBT at least once in a series of intracavitary brachytherapy. Overall, 54 patients fulfilled the eligibility criteria in the present study. The median follow-up period was 32 (IQR, 19-44) months. No patient complained of symptoms such as persistent bleeding or abdominal pain after the treatment. The 3-year local control (LC), disease-free survival, and overall survival rates for all 54 patients were 86.6%, 60.3%, and 90.7% (95% CI [81.3%-100.0%]), respectively. The 3-year LC rate was 87.7% in patients with FIGO III-IVA and 90.4% in tumor size >6.0 cm. The incidence rate of late adverse events, grade ≥3, in the rectum and bladder was 0% and 1.8%, respectively. In the dose-volume histogram analyses, transvaginal HBT increased the dose of HR-CTV
CONCLUSION
Considering the favorable clinical outcomes, CT-based transvaginal HBT may be a good option for treating cervical cancer.

Identifiants

pubmed: 35229494
doi: 10.1002/cnr2.1607
pmc: PMC9675380
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1607

Informations de copyright

© 2022 The Authors. Cancer Reports published by Wiley Periodicals LLC.

Références

Int J Radiat Oncol Biol Phys. 2016 Mar 1;94(3):598-604
pubmed: 26867888
Lancet. 2001 Sep 8;358(9284):781-6
pubmed: 11564482
Radiother Oncol. 2006 Jan;78(1):67-77
pubmed: 16403584
Brachytherapy. 2018 Sep - Oct;17(5):775-781
pubmed: 29941345
Int J Radiat Oncol Biol Phys. 1995 Mar 30;31(5):1341-6
pubmed: 7713792
J Radiat Res. 2019 Jul 1;60(4):490-500
pubmed: 31111896
Int J Radiat Oncol Biol Phys. 2020 Apr 1;106(5):1052-1062
pubmed: 32007365
BMC Cancer. 2014 Jun 17;14:447
pubmed: 24938757
BMC Cancer. 2019 Mar 12;19(1):221
pubmed: 30866877
J Contemp Brachytherapy. 2015 Jun;7(3):259-63
pubmed: 26207117
Radiother Oncol. 2015 Apr;115(1):78-83
pubmed: 25805517
Int J Radiat Oncol Biol Phys. 2007 Jun 1;68(2):491-8
pubmed: 17331668
Cochrane Database Syst Rev. 2005 Jul 20;(3):CD002225
pubmed: 16034873
Cancer Rep (Hoboken). 2022 Nov;5(11):e1607
pubmed: 35229494
Lancet Oncol. 2021 Apr;22(4):538-547
pubmed: 33794207
J Radiat Res. 2017 Jul 1;58(4):543-551
pubmed: 27986859
Radiother Oncol. 2016 Sep;120(3):428-433
pubmed: 27134181
Brachytherapy. 2016 Sep-Oct;15(5):562-9
pubmed: 27474180
J Radiat Res. 2018 Jul 1;59(4):469-476
pubmed: 29986113
Radiother Oncol. 2005 Mar;74(3):235-45
pubmed: 15763303
Oncol Lett. 2020 Sep;20(3):2058-2074
pubmed: 32782524
Radiat Oncol. 2014 Oct 16;9:222
pubmed: 25319341
Int J Radiat Oncol Biol Phys. 2011 Jun 1;80(2):429-36
pubmed: 20542643
Jpn J Clin Oncol. 2010 Aug;40(8):795-9
pubmed: 20444747
Brachytherapy. 2019 Nov - Dec;18(6):771-779
pubmed: 31506225
Acta Oncol. 2013 Oct;52(7):1345-52
pubmed: 23905674
J Radiat Res. 2017 May 1;58(3):341-350
pubmed: 27837120
Radiother Oncol. 2021 Jul;160:273-284
pubmed: 34019918
Int J Clin Oncol. 2011 Aug;16(4):379-86
pubmed: 21331768
Radiother Oncol. 2009 Nov;93(2):311-5
pubmed: 19679365
Brachytherapy. 2017 Jan - Feb;16(1):161-166
pubmed: 27914911
N Engl J Med. 1999 Apr 15;340(15):1198-200
pubmed: 10202172
J Radiat Res. 2021 May 12;62(3):502-510
pubmed: 33532828
J Radiat Res. 2011;52(1):54-8
pubmed: 21293072
Int J Radiat Oncol Biol Phys. 2009 May 1;74(1):140-6
pubmed: 18922646
Int J Radiat Oncol Biol Phys. 2000 Aug 1;48(1):201-11
pubmed: 10924990

Auteurs

Noriyuki Okonogi (N)

QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.

Kazutoshi Murata (K)

QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.

Toshiaki Matsui (T)

QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.

Yuma Iwai (Y)

QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.

Yasumasa Mori (Y)

QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.

Takashi Kaneko (T)

QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.

Masaru Wakatsuki (M)

QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.

Hiroshi Tsuji (H)

QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH