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Therapeutic effects of surgical debulking of metastatic lymph nodes in cervical cancer IIICr: a trial protocol for a phase III, multicenter, randomized controlled study (KGOG1047/DEBULK trial)open access

Authors
Yun, Bo SeongLee, Kwang-BeomLee, Keun HoChang, Ha KyunKim, Joo-YoungLim, Myong CheolChoi, Chel HunCho, HanbyoulKim, Dae-YeonKim, Yun HwanChoi, Joong SubLee, Chae HyeongKim, Jae-WeonKim, Sang WunKim, Yong BaeCho, Chi-HeumHong, Dae GySong, Yong JungJeon, SeobKim, Min KyuJeong, Dae HoonPark, HyunKim, Seok MoPark, Sang-IlSong, Jae-YunMukhopadhyay, AsimaThinh, Dang Huy QuocKampan, Nirmala ChandralegaLee, Grace J.Kim, Jae-HoonEom, Keun-YongRoh, Ju-Won
Issue Date
Sep-2024
Publisher
대한부인종양학회
Keywords
Bulky Lymph Node; Cervical Cancer; Concurrent Chemoradiotherapy; Lymph Node Excision; Lymph Node Metastasis; Progression-Free Survival
Citation
Journal of Gynecologic Oncology, v.35, no.5, pp 1 - 11
Pages
11
Indexed
SCIE
SCOPUS
KCICANDI
Journal Title
Journal of Gynecologic Oncology
Volume
35
Number
5
Start Page
1
End Page
11
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/26437
DOI
10.3802/jgo.2024.35.e57
ISSN
2005-0380
2005-0399
Abstract
Background: Bulky or multiple lymph node (LN) metastases are associated with poor prognosiin cervical cancer, and the size or number of LN metastases is not yet reflected in the staging system and therapeutic strategy. Although the therapeutic effects of surgical resection of bulky LNs before standard treatment have been reported in several retrospective studies, well-planned randomized clinical studies are lacking. Therefore, the aim of the Korean Gynecologic Oncology Group (KGOG) 1047/DEBULK trial is to investigate whether the debulking surgery of bulky or multiple LNs prior to concurrent chemoradiation therapy (CCRT) improves the survival rate of patients with cervical cancer IIICr diagnosed by imaging tests. Methods: The KGOG 1047/DEBULK trial is a phase III, multicenter, randomized clinical trial involving patients with bulky or multiple LN metastases in cervical cancer IIICr. This study will include patients with a short-axis diameter of a pelvic or para-aortic LN ≥2 cm or ≥3 LNs with a short-axis diameter ≥1 cm and for whom CCRT is planned. The treatment arms will be randomly allocated in a 1:1 ratio to either receive CCRT (control arm) or undergo surgical debulking of bulky or multiple LNs before CCRT (experimental arm). CCRT consists of extended-field external beam radiotherapy/pelvic radiotherapy, brachytherapy and LN boost, and weekly chemotherapy with cisplatin (40 mg/m2), 4–6 times administered intravenously. The primary endpoint will be 3-year progression-free survival rate. The secondary endpoints will be 3-year overall survival rate, treatment-related complications, and accuracy of radiological diagnosis of bulky or multiple LNs. © 2024. Asian Society of Gynecologic Oncology, Korean Society of Gynecologic Oncology, and Japan Society of Gynecologic Oncology.
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