Hysterectomy with radiotherapy or chemotherapy or both for women with locally advanced cervical cancer.


Journal

The Cochrane database of systematic reviews
ISSN: 1469-493X
Titre abrégé: Cochrane Database Syst Rev
Pays: England
ID NLM: 100909747

Informations de publication

Date de publication:
22 08 2022
Historique:
entrez: 22 8 2022
pubmed: 23 8 2022
medline: 25 8 2022
Statut: epublish

Résumé

This is an update of the Cochrane Review published in Issue 4, 2015. Cervical cancer is one of the most frequent cause of death from gynaecological cancers worldwide. Many new cervical cancer cases in low-income countries present at an advanced stage. Standard care in Europe and the US for locally advanced cervical cancer (LACC) is chemoradiotherapy. In low-income countries, with limited access to radiotherapy, LACC may be treated with chemotherapy and hysterectomy. It is not certain if this improves survival. It is important to assess the value of hysterectomy with radiotherapy or chemotherapy, or both, as an alternative. To determine whether hysterectomy, in addition to standard treatment with radiotherapy or chemotherapy, or both, in women with LACC (Stage IB We searched CENTRAL, MEDLINE via Ovid, Embase via Ovid, LILACS, trial registries and the grey literature up to 3 February 2022. We searched for randomised controlled trials (RCTs) that compared treatments involving hysterectomy versus radiotherapy or chemotherapy, or both, in women with LACC International Federation of Gynecology and Obstetrics (FIGO) Stages IB We used standard methodological procedures expected by Cochrane. We independently assessed study eligibility, extracted data and assessed the risk of bias. Where possible, we synthesised overall (OS) and progression-free (PFS) or disease-free (DFS) survival in a meta-analysis using a random-effects model. Adverse events (AEs) were incompletely reported and we described the results of single trials in narrative form. We used the GRADE approach to assess the certainty of the evidence. From the searches we identified 968 studies. After deduplication, title and abstract screening, and full-text assessment, we included 11 RCTs (2683 women) of varying methodological quality. This update identified four new RCTs and three ongoing RCTs. The included studies compared: hysterectomy (simple or radical) with radiotherapy or chemoradiotherapy or neoadjuvant chemotherapy (NACT) versus radiotherapy alone or chemoradiotherapy (CCRT) alone or CCRT and brachytherapy. There is also one ongoing study comparing three groups: hysterectomy with CCRT versus hysterectomy with NACT versus CCRT. There were two comparison groups for which we were able to do a meta-analysis. Hysterectomy (radical) with neoadjuvant chemotherapy versus chemoradiotherapy alone Two RCTs with similar design characteristics (620 and 633 participants) found no difference in five-year OS between NACT with hysterectomy versus CCRT. Meta-analysis assessing 1253 participants found no evidence of a difference in risk of death (OS) between women who received NACT plus hysterectomy and those who received CCRT alone (HR 0.94, 95% CI 0.76 to 1.16; moderate-certainty evidence). In both studies, the five-year DFS in the NACT plus surgery group was worse (57%) compared with the CCRT group (65.6%), mostly for Stage IIB. Results of single trials reported no apparent difference in long-term severe complications, grade 3 acute toxicity and severe late toxicity between groups (very low-quality evidence). Hysterectomy (simple or radical) with neoadjuvant chemotherapy versus radiotherapy alone Meta-analysis of three trials of NACT with hysterectomy versus radiotherapy alone, assessing 571 participants, found that women who received NACT plus hysterectomy had less risk of death (OS) than those who received radiotherapy alone (HR 0.71, 95% CI 0.55 to 0.93; I From the available RCTs, we found insufficient evidence that hysterectomy with radiotherapy, with or without chemotherapy, improves the survival of women with LACC who are treated with radiotherapy or CCRT alone. The overall certainty of the evidence was variable across the different outcomes and was universally downgraded due to concerns about risk of bias. The certainty of the evidence for NACT and radical hysterectomy versus radiotherapy alone for survival outcomes was moderate. The same occurred for the comparison involving NACT and hysterectomy compared with CCRT alone. Evidence from other comparisons was generally sparse and of low or very low-certainty. This was mainly based on poor reporting and sparseness of data where results were based on single trials. More trials assessing medical management with and without hysterectomy may test the robustness of the findings of this review as further research is likely to have an important impact on our confidence in the estimate of effect.

Sections du résumé

BACKGROUND
This is an update of the Cochrane Review published in Issue 4, 2015. Cervical cancer is one of the most frequent cause of death from gynaecological cancers worldwide. Many new cervical cancer cases in low-income countries present at an advanced stage. Standard care in Europe and the US for locally advanced cervical cancer (LACC) is chemoradiotherapy. In low-income countries, with limited access to radiotherapy, LACC may be treated with chemotherapy and hysterectomy. It is not certain if this improves survival. It is important to assess the value of hysterectomy with radiotherapy or chemotherapy, or both, as an alternative.
OBJECTIVES
To determine whether hysterectomy, in addition to standard treatment with radiotherapy or chemotherapy, or both, in women with LACC (Stage IB
SEARCH METHODS
We searched CENTRAL, MEDLINE via Ovid, Embase via Ovid, LILACS, trial registries and the grey literature up to 3 February 2022.
SELECTION CRITERIA
We searched for randomised controlled trials (RCTs) that compared treatments involving hysterectomy versus radiotherapy or chemotherapy, or both, in women with LACC International Federation of Gynecology and Obstetrics (FIGO) Stages IB
DATA COLLECTION AND ANALYSIS
We used standard methodological procedures expected by Cochrane. We independently assessed study eligibility, extracted data and assessed the risk of bias. Where possible, we synthesised overall (OS) and progression-free (PFS) or disease-free (DFS) survival in a meta-analysis using a random-effects model. Adverse events (AEs) were incompletely reported and we described the results of single trials in narrative form. We used the GRADE approach to assess the certainty of the evidence.
MAIN RESULTS
From the searches we identified 968 studies. After deduplication, title and abstract screening, and full-text assessment, we included 11 RCTs (2683 women) of varying methodological quality. This update identified four new RCTs and three ongoing RCTs. The included studies compared: hysterectomy (simple or radical) with radiotherapy or chemoradiotherapy or neoadjuvant chemotherapy (NACT) versus radiotherapy alone or chemoradiotherapy (CCRT) alone or CCRT and brachytherapy. There is also one ongoing study comparing three groups: hysterectomy with CCRT versus hysterectomy with NACT versus CCRT. There were two comparison groups for which we were able to do a meta-analysis. Hysterectomy (radical) with neoadjuvant chemotherapy versus chemoradiotherapy alone Two RCTs with similar design characteristics (620 and 633 participants) found no difference in five-year OS between NACT with hysterectomy versus CCRT. Meta-analysis assessing 1253 participants found no evidence of a difference in risk of death (OS) between women who received NACT plus hysterectomy and those who received CCRT alone (HR 0.94, 95% CI 0.76 to 1.16; moderate-certainty evidence). In both studies, the five-year DFS in the NACT plus surgery group was worse (57%) compared with the CCRT group (65.6%), mostly for Stage IIB. Results of single trials reported no apparent difference in long-term severe complications, grade 3 acute toxicity and severe late toxicity between groups (very low-quality evidence). Hysterectomy (simple or radical) with neoadjuvant chemotherapy versus radiotherapy alone Meta-analysis of three trials of NACT with hysterectomy versus radiotherapy alone, assessing 571 participants, found that women who received NACT plus hysterectomy had less risk of death (OS) than those who received radiotherapy alone (HR 0.71, 95% CI 0.55 to 0.93; I
AUTHORS' CONCLUSIONS
From the available RCTs, we found insufficient evidence that hysterectomy with radiotherapy, with or without chemotherapy, improves the survival of women with LACC who are treated with radiotherapy or CCRT alone. The overall certainty of the evidence was variable across the different outcomes and was universally downgraded due to concerns about risk of bias. The certainty of the evidence for NACT and radical hysterectomy versus radiotherapy alone for survival outcomes was moderate. The same occurred for the comparison involving NACT and hysterectomy compared with CCRT alone. Evidence from other comparisons was generally sparse and of low or very low-certainty. This was mainly based on poor reporting and sparseness of data where results were based on single trials. More trials assessing medical management with and without hysterectomy may test the robustness of the findings of this review as further research is likely to have an important impact on our confidence in the estimate of effect.

Identifiants

pubmed: 35994243
doi: 10.1002/14651858.CD010260.pub3
pmc: PMC9394583
doi:

Types de publication

Journal Article Meta-Analysis Review Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

CD010260

Commentaires et corrections

Type : UpdateOf

Informations de copyright

Copyright © 2022 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

Références

Gynecol Oncol. 2016 May;141(2):231-239
pubmed: 26115978
Syst Rev. 2014 Jul 24;3:82
pubmed: 25056145
Ann Chir. 1998;52(5):425-33
pubmed: 9752481
Gynecol Oncol. 2006 Sep;102(3):523-9
pubmed: 16504274
Eur J Surg Oncol. 2013 Dec;39(12):1428-34
pubmed: 24183796
Int J Gynaecol Obstet. 2014 May;125(2):111-5
pubmed: 24548892
PLoS One. 2009 Oct 05;4(10):e7340
pubmed: 19806210
Int J Gynaecol Obstet. 2009 May;105(2):107-8
pubmed: 19342051
J Clin Oncol. 1999 May;17(5):1339-48
pubmed: 10334517
Control Clin Trials. 1986 Sep;7(3):177-88
pubmed: 3802833
J Surg Oncol. 2013 Jul;108(1):63-9
pubmed: 23737035
J Clin Oncol. 2018 Jun 1;36(16):1548-1555
pubmed: 29432076
N Engl J Med. 1999 Apr 15;340(15):1144-53
pubmed: 10202165
Eur J Surg Oncol. 2007 May;33(4):498-503
pubmed: 17156969
Oncologist. 2012;17(1):64-71
pubmed: 22234626
Lancet. 2001 Sep 8;358(9284):781-6
pubmed: 11564482
South Asian J Cancer. 2013 Jul;2(3):137-9
pubmed: 24455590
Acta Oncol. 1996;35 Suppl 8:99-107
pubmed: 9073055
Gynecol Oncol. 1987 Jun;27(2):129-40
pubmed: 3570053
J Clin Oncol. 2000 Apr;18(8):1740-7
pubmed: 10764435
Ann Oncol. 2013 Aug;24(8):2043-7
pubmed: 23609186
Gynecol Oncol. 2009 Sep;114(3):404-9
pubmed: 19555996
Cell Physiol Biochem. 2013;32(5):1528-40
pubmed: 24335178
J BUON. 2019 Sep-Oct;24(5):2028-2034
pubmed: 31786871
CA Cancer J Clin. 2021 May;71(3):209-249
pubmed: 33538338
Ann Surg Oncol. 2007 Sep;14(9):2643-8
pubmed: 17562114
Int J Radiat Oncol Biol Phys. 2019 Apr 1;103(5):1088-1097
pubmed: 30445171
Best Pract Res Clin Obstet Gynaecol. 2012 Jun;26(3):293-309
pubmed: 22353492
J Clin Oncol. 2000 Apr;18(8):1606-13
pubmed: 10764420
Br J Cancer. 2013 May 28;108(10):1957-63
pubmed: 23640393
N Engl J Med. 1999 Apr 15;340(15):1154-61
pubmed: 10202166
Curr Opin Oncol. 2018 Sep;30(5):323-329
pubmed: 29994902
Gynecol Oncol. 1989 Nov;35(2):130-5
pubmed: 2807001
J Clin Oncol. 2002 Jan 1;20(1):179-88
pubmed: 11773168
Int J Gynaecol Obstet. 2018 Oct;143 Suppl 2:22-36
pubmed: 30306584
Int J Gynaecol Obstet. 2017 Nov;139(2):185-191
pubmed: 28755426
Lancet. 1997 Aug 23;350(9077):535-40
pubmed: 9284774
Ann Surg Oncol. 2005 Apr;12(4):332-7
pubmed: 15827678
J BUON. 2007 Jan-Mar;12(1):57-63
pubmed: 17436403
Eur J Surg Oncol. 2006 Oct;32(8):832-7
pubmed: 16698223
J Gynecol Obstet Biol Reprod (Paris). 2006 Feb;35(1):23-7
pubmed: 16446608
Front Radiat Ther Oncol. 1993;27:130-42
pubmed: 8504941
Am J Obstet Gynecol. 1980 Nov 1;138(5):550-6
pubmed: 7425018
Ann Chir Gynaecol Suppl. 1994;208:50-3
pubmed: 8092773
Gynecol Oncol. 1990 Sep;38(3):352-7
pubmed: 2227547
N Engl J Med. 1999 Apr 15;340(15):1137-43
pubmed: 10202164
Radiat Oncol. 2012 Nov 23;7:197
pubmed: 23176540
Cochrane Database Syst Rev. 2010 Jan 20;(1):CD008285
pubmed: 20091664
Gynecol Oncol. 1997 Oct;67(1):61-9
pubmed: 9345358
Cochrane Database Syst Rev. 2012 Dec 12;12:CD007406
pubmed: 23235641
BMJ. 2004 Jun 19;328(7454):1490
pubmed: 15205295
Gynecol Oncol. 1990 Aug;38(2):175-80
pubmed: 2387532
Cochrane Database Syst Rev. 2015 Apr 07;(4):CD010260
pubmed: 25847525
Zhonghua Zhong Liu Za Zhi. 2002 Sep;24(5):508-10
pubmed: 12485512
Int J Gynecol Cancer. 2021 Jan;31(1):129-133
pubmed: 32522771
Ann Surg Oncol. 2014 May;21(5):1692-9
pubmed: 24407316
Obstet Gynecol. 1975 Nov;46(5):507-10
pubmed: 1196552
Gynecol Oncol. 2013 Dec;131(3):640-4
pubmed: 24096111
Anticancer Drugs. 2001 Nov;12(10):853-8
pubmed: 11707654
Syst Rev. 2013 Sep 23;2:81
pubmed: 24059250
Stat Med. 1998 Dec 30;17(24):2815-34
pubmed: 9921604
Br J Cancer. 2008 Oct 21;99(8):1216-20
pubmed: 18854823
Gynecol Oncol. 2003 Jun;89(3):343-53
pubmed: 12798694
Obstet Gynecol. 1978 Aug;52(2):138-45
pubmed: 683652
Gynecol Oncol. 2014 Mar;132(3):611-7
pubmed: 24342439
Gynecol Oncol. 1990 Sep;38(3):486-93
pubmed: 1699851
BMJ. 2003 Sep 6;327(7414):557-60
pubmed: 12958120

Auteurs

Fani Kokka (F)

East Kent Gynaecological Oncology Centre, Queen Elizabeth The Queen Mother Hospital, Margate, UK.

Andrew Bryant (A)

Institute of Health & Society, Newcastle University, Newcastle upon Tyne, UK.

Adeola Olaitan (A)

Department of Gynaecological Oncology, University College London, London, UK.

Elly Brockbank (E)

Department of Gynaecological Oncology, St Bartholomew's Hospital, London, UK.

Melanie Powell (M)

Department of Clinical Oncology, St Bartholomew's Hospital, London, UK.

David Oram (D)

Department of Gynaecological Oncology, St. Bartholomew's Hospital, London, UK.

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