Comparative effectiveness and risk of preterm birth of local treatments for cervical intraepithelial neoplasia and stage IA1 cervical cancer: a systematic review and network meta-analysis.
Journal
The Lancet. Oncology
ISSN: 1474-5488
Titre abrégé: Lancet Oncol
Pays: England
ID NLM: 100957246
Informations de publication
Date de publication:
08 2022
08 2022
Historique:
received:
30
01
2022
revised:
23
05
2022
accepted:
25
05
2022
pubmed:
15
7
2022
medline:
2
8
2022
entrez:
14
7
2022
Statut:
ppublish
Résumé
The trade-off between comparative effectiveness and reproductive morbidity of different treatment methods for cervical intraepithelial neoplasia (CIN) remains unclear. We aimed to determine the risks of treatment failure and preterm birth associated with various treatment techniques. In this systematic review and network meta-analysis, we searched MEDLINE, Embase, and the Cochrane Central Register of Controlled Trials database for randomised and non-randomised studies reporting on oncological or reproductive outcomes after CIN treatments from database inception until March 9, 2022, without language restrictions. We included studies of women with CIN, glandular intraepithelial neoplasia, or stage IA1 cervical cancer treated with excision (cold knife conisation [CKC], laser conisation, and large loop excision of the transformation zone [LLETZ]) or ablation (radical diathermy, laser ablation, cold coagulation, and cryotherapy). We excluded women treated with hysterectomy. The primary outcomes were any treatment failure (defined as any abnormal histology or cytology) and preterm birth (<37 weeks of gestation). The network for preterm birth also included women with untreated CIN (untreated colposcopy group). The main reference group was LLETZ for treatment failure and the untreated colposcopy group for preterm birth. For randomised controlled trials, we extracted group-level summary data, and for observational studies, we extracted relative treatment effect estimates adjusted for potential confounders, when available, and we did random-effects network meta-analyses to obtain odds ratios (ORs) with 95% CIs. We assessed within-study and across-study risk of bias using Cochrane tools. This systematic review is registered with PROSPERO, CRD42018115495 and CRD42018115508. 7880 potential citations were identified for the outcome of treatment failure and 4107 for the outcome of preterm birth. After screening and removal of duplicates, the network for treatment failure included 19 240 participants across 71 studies (25 randomised) and the network for preterm birth included 68 817 participants across 29 studies (two randomised). Compared with LLETZ, risk of treatment failure was reduced for other excisional methods (laser conisation: OR 0·59 [95% CI 0·44-0·79] and CKC: 0·63 [0·50-0·81]) and increased for laser ablation (1·69 [1·27-2·24]) and cryotherapy (1·84 [1·33-2·56]). No differences were found for the comparison of cold coagulation versus LLETZ (1·09 [0·68-1·74]) but direct data were based on two small studies only. Compared with the untreated colposcopy group, risk of preterm birth was increased for all excisional techniques (CKC: 2·27 [1·70-3·02]; laser conisation: 1·77 [1·29-2·43]; and LLETZ: 1·37 [1·16-1·62]), whereas no differences were found for ablative methods (laser ablation: 1·05 [0·78-1·41]; cryotherapy: 1·01 [0·35-2·92]; and cold coagulation: 0·67 [0·02-29·15]). The evidence was based mostly on observational studies with their inherent risks of bias, and the credibility of many comparisons was low. More radical excisional techniques reduce the risk of treatment failure but increase the risk of subsequent preterm birth. Although there is uncertainty, ablative treatments probably do not increase risk of preterm birth, but are associated with higher failure rates than excisional techniques. Although we found LLETZ to have balanced effectiveness and reproductive morbidity, treatment choice should rely on a woman's age, size and location of lesion, and future family planning. National Institute for Health and Care Research: Research for Patient Benefit.
Sections du résumé
BACKGROUND
The trade-off between comparative effectiveness and reproductive morbidity of different treatment methods for cervical intraepithelial neoplasia (CIN) remains unclear. We aimed to determine the risks of treatment failure and preterm birth associated with various treatment techniques.
METHODS
In this systematic review and network meta-analysis, we searched MEDLINE, Embase, and the Cochrane Central Register of Controlled Trials database for randomised and non-randomised studies reporting on oncological or reproductive outcomes after CIN treatments from database inception until March 9, 2022, without language restrictions. We included studies of women with CIN, glandular intraepithelial neoplasia, or stage IA1 cervical cancer treated with excision (cold knife conisation [CKC], laser conisation, and large loop excision of the transformation zone [LLETZ]) or ablation (radical diathermy, laser ablation, cold coagulation, and cryotherapy). We excluded women treated with hysterectomy. The primary outcomes were any treatment failure (defined as any abnormal histology or cytology) and preterm birth (<37 weeks of gestation). The network for preterm birth also included women with untreated CIN (untreated colposcopy group). The main reference group was LLETZ for treatment failure and the untreated colposcopy group for preterm birth. For randomised controlled trials, we extracted group-level summary data, and for observational studies, we extracted relative treatment effect estimates adjusted for potential confounders, when available, and we did random-effects network meta-analyses to obtain odds ratios (ORs) with 95% CIs. We assessed within-study and across-study risk of bias using Cochrane tools. This systematic review is registered with PROSPERO, CRD42018115495 and CRD42018115508.
FINDINGS
7880 potential citations were identified for the outcome of treatment failure and 4107 for the outcome of preterm birth. After screening and removal of duplicates, the network for treatment failure included 19 240 participants across 71 studies (25 randomised) and the network for preterm birth included 68 817 participants across 29 studies (two randomised). Compared with LLETZ, risk of treatment failure was reduced for other excisional methods (laser conisation: OR 0·59 [95% CI 0·44-0·79] and CKC: 0·63 [0·50-0·81]) and increased for laser ablation (1·69 [1·27-2·24]) and cryotherapy (1·84 [1·33-2·56]). No differences were found for the comparison of cold coagulation versus LLETZ (1·09 [0·68-1·74]) but direct data were based on two small studies only. Compared with the untreated colposcopy group, risk of preterm birth was increased for all excisional techniques (CKC: 2·27 [1·70-3·02]; laser conisation: 1·77 [1·29-2·43]; and LLETZ: 1·37 [1·16-1·62]), whereas no differences were found for ablative methods (laser ablation: 1·05 [0·78-1·41]; cryotherapy: 1·01 [0·35-2·92]; and cold coagulation: 0·67 [0·02-29·15]). The evidence was based mostly on observational studies with their inherent risks of bias, and the credibility of many comparisons was low.
INTERPRETATION
More radical excisional techniques reduce the risk of treatment failure but increase the risk of subsequent preterm birth. Although there is uncertainty, ablative treatments probably do not increase risk of preterm birth, but are associated with higher failure rates than excisional techniques. Although we found LLETZ to have balanced effectiveness and reproductive morbidity, treatment choice should rely on a woman's age, size and location of lesion, and future family planning.
FUNDING
National Institute for Health and Care Research: Research for Patient Benefit.
Identifiants
pubmed: 35835138
pii: S1470-2045(22)00334-5
doi: 10.1016/S1470-2045(22)00334-5
pmc: PMC9630146
pii:
doi:
Types de publication
Journal Article
Meta-Analysis
Systematic Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1097-1108Commentaires et corrections
Type : ErratumIn
Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests OE has received consulting fees from Biogen (payments were made to their University). All other authors declare no competing interests.
Références
Hum Vaccin Immunother. 2021 Oct 3;17(10):3562-3576
pubmed: 34506257
Lancet Oncol. 2017 Dec;18(12):1665-1679
pubmed: 29126708
BMJ. 1999 Apr 3;318(7188):904-8
pubmed: 10102852
Cochrane Database Syst Rev. 2013 Dec 04;(12):CD001318
pubmed: 24302546
BMJ. 2016 Oct 12;355:i4919
pubmed: 27733354
J Obstet Gynaecol Can. 2019 Jan;41(1):76-88.e7
pubmed: 30585167
BMJ. 2022 Aug 3;378:e070135
pubmed: 35922074
BMJ Open. 2019 Aug 2;9(8):e028008
pubmed: 31377697
BMC Med Res Methodol. 2015 Jul 31;15:58
pubmed: 26227148
Microbiome. 2016 Nov 1;4(1):58
pubmed: 27802830
PLoS One. 2014 Jul 03;9(7):e99682
pubmed: 24992266
Ann Oncol. 2020 Feb;31(2):213-227
pubmed: 31959338
Stat Med. 2017 Apr 15;36(8):1210-1226
pubmed: 28083901
Stat Med. 2012 Dec 20;31(29):3805-20
pubmed: 22763950
Int J Epidemiol. 2012 Jun;41(3):818-27
pubmed: 22461129
BJOG. 2007 Jan;114(1):3-4
pubmed: 17233854
PLoS One. 2016 Nov 3;11(11):e0163793
pubmed: 27812088
Int J Gynaecol Obstet. 2016 Mar;132(3):266-71
pubmed: 26643302
BMJ. 2008 Sep 18;337:a1284
pubmed: 18801868
BMJ Open. 2019 Oct 21;9(10):e028009
pubmed: 31636110
BMJ. 2014 Jan 14;348:f7361
pubmed: 24423603
BMJ. 2014 Jan 14;348:f7700
pubmed: 24423750
J Low Genit Tract Dis. 2020 Apr;24(2):102-131
pubmed: 32243307
N Engl J Med. 2020 Oct 1;383(14):1340-1348
pubmed: 32997908
BJOG. 2016 Aug;123(9):1426-9
pubmed: 26695087
Eur Rev Med Pharmacol Sci. 2017 Nov;21(21):4747-4754
pubmed: 29164591
Ann Intern Med. 2015 Jun 2;162(11):777-84
pubmed: 26030634
Lancet. 2021 Dec 4;398(10316):2084-2092
pubmed: 34741816
Res Synth Methods. 2021 Jan;12(1):86-95
pubmed: 32524754
Microbiome. 2017 Jan 19;5(1):6
pubmed: 28103952
Res Synth Methods. 2012 Jun;3(2):111-25
pubmed: 26062085
Cochrane Database Syst Rev. 2019 Oct 3;10:ED000142
pubmed: 31643080
BMJ. 1997 Sep 13;315(7109):629-34
pubmed: 9310563
BMJ. 2019 Aug 28;366:l4898
pubmed: 31462531
J Low Genit Tract Dis. 2017 Apr;21(2):129-136
pubmed: 27977541
BMJ. 2014 Oct 28;349:g6192
pubmed: 25352501
Stat Med. 2010 Mar 30;29(7-8):932-44
pubmed: 20213715
BMJ. 2016 Jul 28;354:i3633
pubmed: 27469988
Lancet. 2006 Feb 11;367(9509):489-98
pubmed: 16473126
Eur J Gynaecol Oncol. 2008;29(4):345-9
pubmed: 18714567
Int J Gynaecol Obstet. 2015 Feb;128(2):141-7
pubmed: 25444615
BJOG. 2014 Jul;121(8):929-42
pubmed: 24597779
J Gynecol Oncol. 2021 Sep;32(5):e68
pubmed: 34132067
BMJ. 2012 Aug 16;345:e5174
pubmed: 22899563