Lymphadenectomy in elderly patients with high-intermediate-risk, high-risk or advanced endometrial cancer: Time to move from personalized cancer medicine to personalized patient medicine!


Journal

European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
ISSN: 1532-2157
Titre abrégé: Eur J Surg Oncol
Pays: England
ID NLM: 8504356

Informations de publication

Date de publication:
08 2019
Historique:
received: 15 07 2018
revised: 02 02 2019
accepted: 14 02 2019
pubmed: 9 3 2019
medline: 12 6 2020
entrez: 9 3 2019
Statut: ppublish

Résumé

Pelvic and paraaortic lymphadenectomy are recommended for women with high-intermediate, high-risk and advanced endometrial cancer (EC). Lymphadenectomy is less frequently performed in elderly patients than in younger patients. We examined the survival of elderly women diagnosed with high-risk EC according to whether lymphadenectomy was performed or not. We selected women over 70 years with high-intermediate risk, high-risk or advanced EC from a multicenter retrospective cohort of women diagnosed between 2001 and 2013. Multivariate logistic regression models and Cox proportional hazards survival methods for overall survival (OS), disease-free survival (DFS) and cancer-specific survival (CSS) were used for analyses. 71 women had lymphadenectomy and were compared with the 213 who did not. Recurrence was similar in both groups (42% vs 33%, respectively, p = 0.17) but more deaths were reported in the group without lymphadenectomy (38% vs 23%, respectively, p < 0.001). There was no difference in adjuvant treatment in the two groups (17% vs 27%, respectively, p = 0.27). Elderly patients without lymphadenectomy had lower 3-year DFS (56% vs 71%, p = 0.076), CSS (67% vs 85%, p < 0.001) and OS (50% vs 71% p < 0.001). The Cox proportional hazard models showed independently poorer prognosis in women without lymphadenectomy (3.027, 95% CI 1.58-5.81, p < 0.001), histology type 2 (3.46, 95% CI 1.51-7.97, p = 0.003) and lymphovascular space involvement (3.47, 95% CI 1.35-8.98, p = 0.01) on 3-year CSS. No lymphadenectomy in elderly patients with high-risk or advanced EC is independently associated with poorer prognosis. Elderly patients with EC should benefit from lymphadenectomy when indicated.

Sections du résumé

BACKGROUND
Pelvic and paraaortic lymphadenectomy are recommended for women with high-intermediate, high-risk and advanced endometrial cancer (EC). Lymphadenectomy is less frequently performed in elderly patients than in younger patients. We examined the survival of elderly women diagnosed with high-risk EC according to whether lymphadenectomy was performed or not.
METHODS
We selected women over 70 years with high-intermediate risk, high-risk or advanced EC from a multicenter retrospective cohort of women diagnosed between 2001 and 2013. Multivariate logistic regression models and Cox proportional hazards survival methods for overall survival (OS), disease-free survival (DFS) and cancer-specific survival (CSS) were used for analyses.
RESULTS
71 women had lymphadenectomy and were compared with the 213 who did not. Recurrence was similar in both groups (42% vs 33%, respectively, p = 0.17) but more deaths were reported in the group without lymphadenectomy (38% vs 23%, respectively, p < 0.001). There was no difference in adjuvant treatment in the two groups (17% vs 27%, respectively, p = 0.27). Elderly patients without lymphadenectomy had lower 3-year DFS (56% vs 71%, p = 0.076), CSS (67% vs 85%, p < 0.001) and OS (50% vs 71% p < 0.001). The Cox proportional hazard models showed independently poorer prognosis in women without lymphadenectomy (3.027, 95% CI 1.58-5.81, p < 0.001), histology type 2 (3.46, 95% CI 1.51-7.97, p = 0.003) and lymphovascular space involvement (3.47, 95% CI 1.35-8.98, p = 0.01) on 3-year CSS.
CONCLUSION
No lymphadenectomy in elderly patients with high-risk or advanced EC is independently associated with poorer prognosis. Elderly patients with EC should benefit from lymphadenectomy when indicated.

Identifiants

pubmed: 30846299
pii: S0748-7983(19)30286-0
doi: 10.1016/j.ejso.2019.02.015
pii:
doi:

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1388-1395

Informations de copyright

Copyright © 2019 Elsevier Ltd, BASO ~ The Association for Cancer Surgery, and the European Society of Surgical Oncology. All rights reserved.

Auteurs

Adélaïde Racin (A)

CHU de Rennes, Service de Gynécologie, Hôpital Sud, 16 bd de Bulgarie, Université de Rennes 1, U1242, Chemistry, Oncogenesis, Stress and Signaling, CLCC Eugène Marquis, 35000, Rennes, France.

Emilie Raimond (E)

Department of Obstetrics and Gynaecology, Institute Alix de Champagne University Hospital, Reims, France.

Sofiane Bendifallah (S)

Department of Gynaecology and Obstetrics, Tenon University Hospital, Assistance Publique des Hôpitaux de Paris (AP-HP), University Pierre and Marie Curie, Paris 6, Institut Universitaire de Cancérologie (IUC), France; INSERM UMR_S_707, "Epidemiology, Information Systems, Modeling", University Pierre and Marie Curie, Paris 6, France.

Krystel Nyangoh Timoh (K)

CHU de Rennes, Service de Gynécologie, Hôpital Sud, 16 bd de Bulgarie, Université de Rennes 1, U1242, Chemistry, Oncogenesis, Stress and Signaling, CLCC Eugène Marquis, 35000, Rennes, France.

Lobna Ouldamer (L)

Department of Obstetrics and Gynaecology, Centre Hospitalier Régional Universitaire de Tours, Hôpital Bretonneau, Tours, France.

Geoffroy Canlorbe (G)

INSERM UMR_S_707, "Epidemiology, Information Systems, Modeling", University Pierre and Marie Curie, Paris 6, France.

Nina Hudry (N)

Center de lutte contre le cancer Georges François Leclerc, Dijon, France.

Charles Coutant (C)

Center de lutte contre le cancer Georges François Leclerc, Dijon, France.

Olivier Graesslin (O)

Department of Obstetrics and Gynaecology, Centre Hospitalier Régional Universitaire de Tours, Hôpital Bretonneau, Tours, France.

Cyril Touboul (C)

Department of Obstetrics and Gynaecology, Centre Hospitalier Intercommunal, Créteil, France.

Pierre Collinet (P)

Department of Obstetrics and Gynaecology, Centre Hospitalier Régional Universitaire, Lille, France.

Alexandre Bricou (A)

Department of Gynaecology and Obstetrics, Jean Verdier University Hospital, Assistance Publique des Hôpitaux de Paris (AP-HP), University Paris 13, France.

Cyrille Huchon (C)

Department of Gynaecology and Obstetrics, Centre Hospitalier Intercommunal, Poissy, France.

Martin Koskas (M)

Department of Gynaecology and Obstetrics, Bichat University Hospital, Assistance Publique des Hôpitaux de Paris (AP-HP), France.

Marcos Ballester (M)

Department of Obstetrics and Gynaecology, Institute Alix de Champagne University Hospital, Reims, France; INSERM UMR_S_938, University Pierre et Marie Curie, Paris 6, France.

Emile Daraï (E)

Department of Obstetrics and Gynaecology, Institute Alix de Champagne University Hospital, Reims, France; INSERM UMR_S_938, University Pierre et Marie Curie, Paris 6, France.

Jean Levêque (J)

CHU de Rennes, Service de Gynécologie, Hôpital Sud, 16 bd de Bulgarie, Université de Rennes 1, U1242, Chemistry, Oncogenesis, Stress and Signaling, CLCC Eugène Marquis, 35000, Rennes, France.

Vincent Lavoue (V)

CHU de Rennes, Service de Gynécologie, Hôpital Sud, 16 bd de Bulgarie, Université de Rennes 1, U1242, Chemistry, Oncogenesis, Stress and Signaling, CLCC Eugène Marquis, 35000, Rennes, France. Electronic address: vincent.lavoue@chu-rennes.fr.

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