A prospective multicenter trial on sentinel lymph node biopsy in patients with early-stage cervical cancer (SENTIX).
Adenocarcinoma
/ pathology
Adolescent
Adult
Aged
Carcinoma, Squamous Cell
/ pathology
Female
Follow-Up Studies
Humans
Hysterectomy
/ mortality
Incidence
International Agencies
Lymph Node Excision
/ mortality
Middle Aged
Neoplasm Recurrence, Local
/ diagnosis
Neoplasm Staging
Prospective Studies
Sentinel Lymph Node
/ pathology
Sentinel Lymph Node Biopsy
/ mortality
Survival Rate
Uterine Cervical Neoplasms
/ pathology
Young Adult
cervical cancer
lower leg lymphedema
lymphocele
pelvic lymphadenectomy
sentinel lymph node
Journal
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
ISSN: 1525-1438
Titre abrégé: Int J Gynecol Cancer
Pays: England
ID NLM: 9111626
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
accepted:
01
10
2018
entrez:
15
1
2019
pubmed:
15
1
2019
medline:
7
1
2020
Statut:
ppublish
Résumé
Sentinel lymph node (SLN) biopsy has been increasingly used in the management of early-stage cervical cancer. It appears in guidelines as an alternative option to systematic pelvic lymphadenectomy. The evidence about safety is, however, based mostly on retrospective studies, in which SLN was combined with systematic lymphadenectomy. SENTIX is a prospective multicenter trial aiming to prove that less-radical surgery with SLN is non-inferior to treatment with systematic pelvic lymphadenectomy. The primary end point is recurrence rate; the secondary end point is the prevalence of lower-leg lymphedema and symptomatic pelvic lymphocele. The reference recurrence rate was set up conservatively at 7% at 24 months after treatment. With a sample size of 300 patients treated per protocol, the trial is powered to detect a non-inferiority margin of 5% (90% power, p = 0.05) for recurrence rate, 30% reduction in the prevalence of symptomatic lymphocele or lower-leg lymphedema, with reference rates of 30% and 6% at 12 months (p = 0.025, Bonferroni correction). The patients eligible for SENTIX have stage IA1/LVSI+, IA2, IB1 (<2 cm for fertility sparing), with negative LN on pre-operative imaging. Intra-operatively, patients are excluded when there is a failure to detect SLN on both sides of the pelvis in cases of more advanced cancer (stage >IB1), or a positive intra-operative SLN assessment. The quality of SLN pathology evaluation will be assessed by central review. Three interim safety analyses are pre-planned when 30, 60, 150 patients complete 12 months' follow-up. The first patient was enrolled into the study in June 2016 and, by June 2018, 340 patients had been enrolled. The first analysis of secondary outcomes should be available in 2019 and the oncological outcome of 300 patients at the end of 2021. The trial is registered as a CEEGOG trial (CEEGOG CX-01), ENGOT trial (ENGOT-Cx 2), and at the ClinicalTrials.gov database (NCT02494063).
Identifiants
pubmed: 30640706
pii: ijgc-2018-000010
doi: 10.1136/ijgc-2018-000010
doi:
Banques de données
ClinicalTrials.gov
['NCT02494063']
Types de publication
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
212-215Informations de copyright
© IGCS and ESGO 2019. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.