Prognostic Value and Risk Factors of Peritoneal Carcinomatosis Recurrence for Patients with Endometrial Cancer: A Multicenter Study from the FRANCOGYN Group.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 11 03 2020
accepted: 15 06 2020
pubmed: 11 7 2020
medline: 15 5 2021
entrez: 11 7 2020
Statut: ppublish

Résumé

The prognosis for patients with endometrial cancer (EC) peritoneal carcinomatosis (PC) recurrence has received little study. This study aimed to determine specific risk factors and prognosis of EC with PC recurrence (PCR) versus no PC recurrence (NPCR). Data of all patients with EC who received primary surgical treatment between January 2000 and February 2017 were abstracted from the French FRANCOGYN Research Group database. Clinical and pathologic variables were compared between the two groups (PCR vs. NPCR). Multivariate analysis was performed to define prognostic factors for peritoneal recurrence. Overall survivals (OS) of patients after recurrence were compared using the Kaplan-Meier method. The study analyzed 1466 patients, and 257 of these patients (17.5%) had recurrence. At presentation, 63 of these patients had PC. International Federation of Gynecology and Obstetrics (FIGO) stages 3 and 4 disease were significantly associated with PCR versus NPCR (odds ratio 2.24; 95% confidence interval 1.23-4.07; p = 0.008). The death rate for the patients with PC was 47.6%, with a median survival of 12 months after diagnosis of recurrence. According to the histologic subtype, OS was 29 months (Q1-Q3, 13-NA) for endometrioid carcinomas, 7.5 months (Q1-Q3, 4-15) for serous carcinomas, and 10 months (Q1-Q3, 5-15) for clear cell carcinomas. Chemotherapy for treatment of PCR was associated with improved OS after recurrence (OSAR; p = 0.0025). An initial advanced stage of EC is a risk factor for PCR. For women with PCR, a diagnosis of type 1 EC recurrence more than 12 months after the initial treatment and management of PCR with chemotherapy is associated with improved OSAR. Prospective studies are needed to determine the precise optimal management required in this clinical situation and to assess the relevance of biomarkers to predict the risk of PCR for EC patients.

Sections du résumé

BACKGROUND BACKGROUND
The prognosis for patients with endometrial cancer (EC) peritoneal carcinomatosis (PC) recurrence has received little study. This study aimed to determine specific risk factors and prognosis of EC with PC recurrence (PCR) versus no PC recurrence (NPCR).
METHODS METHODS
Data of all patients with EC who received primary surgical treatment between January 2000 and February 2017 were abstracted from the French FRANCOGYN Research Group database. Clinical and pathologic variables were compared between the two groups (PCR vs. NPCR). Multivariate analysis was performed to define prognostic factors for peritoneal recurrence. Overall survivals (OS) of patients after recurrence were compared using the Kaplan-Meier method.
RESULTS RESULTS
The study analyzed 1466 patients, and 257 of these patients (17.5%) had recurrence. At presentation, 63 of these patients had PC. International Federation of Gynecology and Obstetrics (FIGO) stages 3 and 4 disease were significantly associated with PCR versus NPCR (odds ratio 2.24; 95% confidence interval 1.23-4.07; p = 0.008). The death rate for the patients with PC was 47.6%, with a median survival of 12 months after diagnosis of recurrence. According to the histologic subtype, OS was 29 months (Q1-Q3, 13-NA) for endometrioid carcinomas, 7.5 months (Q1-Q3, 4-15) for serous carcinomas, and 10 months (Q1-Q3, 5-15) for clear cell carcinomas. Chemotherapy for treatment of PCR was associated with improved OS after recurrence (OSAR; p = 0.0025).
CONCLUSION CONCLUSIONS
An initial advanced stage of EC is a risk factor for PCR. For women with PCR, a diagnosis of type 1 EC recurrence more than 12 months after the initial treatment and management of PCR with chemotherapy is associated with improved OSAR. Prospective studies are needed to determine the precise optimal management required in this clinical situation and to assess the relevance of biomarkers to predict the risk of PCR for EC patients.

Identifiants

pubmed: 32648177
doi: 10.1245/s10434-020-08812-z
pii: 10.1245/s10434-020-08812-z
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

212-221

Références

Ferlay J, Parkin DM, Steliarova-Foucher E. Estimates of cancer incidence and mortality in Europe in 2008. Eur J Cancer. 2010;46:765–81.
doi: 10.1016/j.ejca.2009.12.014
Ferlay J, Steliarova-Foucher E, Lortet-Tieulent J, Rosso S, Coebergh JWW, Comber H, et al. Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012. Eur J Cancer. 2013;49:1374–403.
doi: 10.1016/j.ejca.2012.12.027
Stewart BW, Wild CP. World Cancer Report 2014. 2014 [cité 11 sept 2018]. Disponible sur: http://publications.iarc.fr/Non-Series-Publications/World-Cancer-Reports/World-Cancer-Report-2014 .
Binder-Foucard F, Bossard N, Delafosse P, Belot A, Woronoff A-S, Remontet L. Cancer incidence and mortality in France over the 1980–2012 period: solid tumors. Rev d’Épidémiol Santé Publique. 2014;62:95–108.
doi: 10.1016/j.respe.2013.11.073
Fung-Kee-Fung M, Dodge J, Elit L, Lukka H, Chambers A, Oliver T. Follow-up after primary therapy for endometrial cancer: a systematic review. Gynecol Oncol. 2006;101:520–9.
doi: 10.1016/j.ygyno.2006.02.011
Colombo N, Creutzberg C, Amant F, Bosse T, González-Martín A, Ledermann J, et al. ESMO–ESGO–ESTRO consensus conference on endometrial cancer: diagnosis, treatment, and follow-up. Radiother Oncol. 2015;117:559–81.
doi: 10.1016/j.radonc.2015.11.013
Querleu D, Darai E, Lecuru F, Rafii A, Chereau E, Collinet P, et al. Prise en charge primaire des cancers de l’endomètre: recommandations SFOG-CNGOF. Gynécol Obstét Fertilité Sénologie. 2017;45:715–25.
doi: 10.1016/j.gofs.2017.10.008
Colombo N, Creutzberg C, Amant F, Bosse T, González-Martín A, Ledermann J, et al. ESMO–ESGO–ESTRO Consensus conference on endometrial cancer: diagnosis, treatment, and follow-up. Int J Gynecol Cancer. 2016;26:2–30.
doi: 10.1097/IGC.0000000000000609
Bendifallah S, Canlorbe G, Raimond E, Bazire L, Huguet F, Graesslin O, et al. An external validation study of nomograms designed to predict isolated loco-regional and distant endometrial cancer recurrences: how applicable are they? Br J Cancer. 2013;109:1498–503.
doi: 10.1038/bjc.2013.500
Bendifallah S, Canlorbe G, Raimond E, Hudry D, Coutant C, Graesslin O, et al. External validation of nomograms designed to predict lymphatic dissemination in patients with early-stage endometrioid endometrial cancer: a multicenter study. Am J Obstet Gynecol. 2015;212:56.e1–e7.
doi: 10.1016/j.ajog.2014.06.058
Koskas M, Fournier M, Luton D, Darai E, Rouzier R. Survival impact of lymphadenectomy stratified by nodal metastatic probability in endometrial cancer. Ann Surg Oncol. 2014;21:2376–82.
doi: 10.1245/s10434-014-3589-6
Institut National du Cancer. Cancer de l’endometre, rapport integral. 2010. Disponible sur: http://www.e-cancer.fr/Expertises-et-publications/Catalogue-des-publications/Cancer-de-l-endometre-rapport-integral .
Bendifallah S, Ouldamer L, Lavoue V, Canlorbe G, Raimond E, Coutant C, et al. Patterns of recurrence and outcomes in surgically treated women with endometrial cancer according to ESMO–ESGO–ESTRO consensus conference risk groups: results from the FRANCOGYN study group. Gynecol Oncol. 2017;144:107–12.
doi: 10.1016/j.ygyno.2016.10.025
Ahmed A, Zamba G, DeGeest K, Lynch CF. The impact of surgery on survival of elderly women with endometrial cancer in the SEER program from 1992–2002. Gynecol Oncol. 2008;111:35–40.
doi: 10.1016/j.ygyno.2008.06.026
Hamilton T, Lanuke K, Mack LA, Temple WJ. Long-term follow-up in the treatment of peritoneal carcinomatosis. Am J Surg. 2011;201:650–4.
doi: 10.1016/j.amjsurg.2011.01.013
Bricou A, Bendifallah S, Daix-Moreux M, Ouldamer L, Lavoue V, Benbara A, et al. A proposal for a classification for recurrent endometrial cancer: analysis of a French multicenter database from the FRANCOGYN study group. Int J Gynecol Cancer. 2018;28:1278–84.
doi: 10.1097/IGC.0000000000001296
Frati A, Ballester M, Dubernard G, Bats AS, Heitz D, Mathevet P, et al. Contribution of lymphoscintigraphy for sentinel lymph node biopsy in women with early-stage endometrial cancer: results of the SENTI-ENDO study. Ann Surg Oncol. 2015;22:1980–6.
doi: 10.1245/s10434-014-4203-7
Ballester M, Dubernard G, Lécuru F, Heitz D, Mathevet P, Marret H, et al. Detection rate and diagnostic accuracy of sentinel-node biopsy in early-stage endometrial cancer: a prospective multicentre study (SENTI-ENDO). Lancet Oncol. 2011;12:469–76.
doi: 10.1016/S1470-2045(11)70070-5
Creasman W. Revised FIGO staging for carcinoma of the endometrium. Int J Gynaecol Obstet. 2009;105:109.
doi: 10.1016/j.ijgo.2009.02.010
Albertini A-F, Devouassoux-Shisheboran M, Genestie C. Pathology of endometrioid carcinoma. Bull Cancer. 2012;99:7–12.
doi: 10.1684/bdc.2011.1526
Soslow RA, Tornos C, Park KJ, Malpica A, Matias-Guiu X, Oliva E, et al. Endometrial carcinoma diagnosis: use of FIGO grading and genomic subcategories in clinical practice. Int J Gynecol Pathol. 2019;38:S64–74.
doi: 10.1097/PGP.0000000000000518
Briët JM, Hollema H, Reesink N, Aalders JG, Mourits MJE, ten Hoor KA, et al. Lymphvascular space involvement: an independent prognostic factor in endometrial cancer. Gynecol Oncol. 2005;96:799–804.
doi: 10.1016/j.ygyno.2004.11.033
Institut National du Cancer. Les traitements du cancer de l’endometre. 2013. Disponible sur: http://www.e-cancer.fr/Expertises-et-publications/Catalogue-des-publications/Les-traitements-du-cancer-de-l-endometre .
Baekelandt MM, Castiglione M. ESMO Guidelines Working Group, Endometrial carcinoma: ESMO clinical recommendations for diagnosis, treatment and follow-up. Ann Oncol. 2008;19(Suppl 2):19–20.
doi: 10.1093/annonc/mdn113
Haute Autorité de Santé. Cancer de l’endometre. 2011. Disponible sur: https://www.has-sante.fr/portail/jcms/c_1021574/fr/ald-n-30-cancer-de-l-endometre .
Sartori E, Pasinetti B, Carrara L, Gambino A, Odicino F, Pecorelli S. Pattern of failure and value of follow-up procedures in endometrial and cervical cancer patients. Gynecol Oncol. 2007;107:S241–7.
doi: 10.1016/j.ygyno.2007.07.025
Creutzberg CL, Wárlám-Rodenhuis CC, van de Steen-Banasik E, Beerman H, van Lent M. Surgery and postoperative radiotherapy versus surgery alone for patients with stage-1 endometrial carcinoma: multicentre randomised trial. Lancet. 2000;355:8.
doi: 10.1016/S0140-6736(00)02139-5
Adjuvant external beam radiotherapy in the treatment of endometrial cancer (MRC ASTEC and NCIC CTG EN.5 randomised trials): pooled trial results, systematic review, and meta-analysis. Lancet. 2009;373:137–46.
Kasamatsu T, Shiromizu K, Takahashi M, Matsumoto K, Shirai T. Analysis of initial failure site and spread pattern in endometrial carcinoma: a Japanese experience. Int J Gynecol Cancer. 1999;9:470–6.
doi: 10.1046/j.1525-1438.1999.99070.x
Murphy KT, Rotmensch J, Yamada SD, Mundt AJ. Outcome and patterns of failure in pathologic stages I–IV clear-cell carcinoma of the endometrium: implications for adjuvant radiation therapy. Int J Radiat Oncol Biol Phys. 2003;55:1272–6.
doi: 10.1016/S0360-3016(02)04404-8
Shimamoto K, Saito T, Okadome M, Shimokawa M. Prognostic significance of the treatment-free interval in patients with recurrent endometrial cancer. Eur J Obstet Gynecol Reprod Biol. 2014;175:92–6.
doi: 10.1016/j.ejogrb.2014.01.002
Coleman RL, Brady MF, Herzog TJ, Sabbatini P, Armstrong DK, Walker JL, et al. Bevacizumab and paclitaxel–carboplatin chemotherapy and secondary cytoreduction in recurrent, platinum-sensitive ovarian cancer (NRG Oncology/Gynecologic Oncology Group study GOG-0213): a multicentre, open-label, randomised, phase 3 trial. Lancet Oncol. 2017;18:779–91.
doi: 10.1016/S1470-2045(17)30279-6
Aghajanian C, Goff B, Nycum LR, Wang YV, Husain A, Blank SV. Final overall survival and safety analysis of OCEANS, a phase 3 trial of chemotherapy with or without bevacizumab in patients with platinum-sensitive recurrent ovarian cancer. Gynecol Oncol. 2015;139:10–6.
doi: 10.1016/j.ygyno.2015.08.004
Parmar MKB, Ledermann JA, Colombo N, du Bois A, Delaloye J-F, Kristensen GB, et al. Paclitaxel plus platinum-based chemotherapy versus conventional platinum-based chemotherapy in women with relapsed ovarian cancer: the ICON4/AGO-OVAR-2.2 trial. Lancet. 2003;361:2099–106.
doi: 10.1016/S0140-6736(03)13718-X
Arend RC, Jones BA, Martinez A, Goodfellow P. Endometrial cancer: molecular markers and management of advanced stage disease. Gynecol Oncol. 2018;150:569–80.
doi: 10.1016/j.ygyno.2018.05.015
Sagae S, Susumu N, Viswanathan AN, Aoki D, Backes FJ, Provencher DM, et al. Gynecologic Cancer InterGroup (GCIG) consensus review for uterine serous carcinoma. Int J Gynecol Cancer. 2014;24:S83–9.
doi: 10.1097/IGC.0000000000000264
Mhawech-Fauceglia P, Herrmann RF, Kesterson J, Izevbaye I, Lele S, Odunsi K. Prognostic factors in stages II/III/IV and stages III/IV endometrioid and serous adenocarcinoma of the endometrium. EJSO Eur J Surg Oncol. 2010;36:1195–201.
doi: 10.1016/j.ejso.2010.09.010
Getz G, Gabriel SB, Cibulskis K, Lander E, Sivachenko A, Sougnez C, et al. Integrated genomic characterization of endometrial carcinoma. Nature. 2013;497:67–73.
doi: 10.1038/nature12113
Morice P, Leary A, Creutzberg C, Abu-Rustum N, Darai E. Endometrial cancer. Lancet. 2016;387:1094–108.
doi: 10.1016/S0140-6736(15)00130-0
Phelippeau J, Rouzier R, Koskas M. Adherence to guidelines during follow-up of endometrial cancer: analysis of French Health Insurance Database. Anticancer Res. 2018;38:2977–82.
pubmed: 29715127

Auteurs

A Gaudet Chardonnet (A)

AP-HP (Assistance Publique des Hôpitaux de Paris), Department of Gynecological and Breast Surgery and Oncology, Pitié-Salpêtrière University Hospital, Paris, France.

H Azaïs (H)

AP-HP (Assistance Publique des Hôpitaux de Paris), Department of Gynecological and Breast Surgery and Oncology, Pitié-Salpêtrière University Hospital, Paris, France.

M Ballester (M)

Service de Chirurgie Gynécologique et Mammaire, Groupe Hospitalier Diaconesses Croix Saint Simon, Paris, France.

E Raimond (E)

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

S Bendifallah (S)

AP-HP (Assistance Publique des Hôpitaux de Paris), Department of Gynaecology and Obstetrics, Tenon University Hospital, Paris, France.
INSERM UMR_S_938, "Cancer Biology and Therapeutics," Centre de Recherche Saint-Antoine (CRSA), Sorbonne University, Paris, France.
Institut Universitaire de Cancérologie (IUC), Sorbonne University, Paris, France.

L Ouldamer (L)

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

C Coutant (C)

Center de Lutte Contre le Cancer Georges François Leclerc, Dijon, France.

O Graesslin (O)

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

C Touboul (C)

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

P Collinet (P)

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

A Bricou (A)

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

C Huchon (C)

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

E Daraï (E)

AP-HP (Assistance Publique des Hôpitaux de Paris), Department of Gynaecology and Obstetrics, Tenon University Hospital, Paris, France.
INSERM UMR_S_938, "Cancer Biology and Therapeutics," Centre de Recherche Saint-Antoine (CRSA), Sorbonne University, Paris, France.
Institut Universitaire de Cancérologie (IUC), Sorbonne University, Paris, France.

V Lavoue (V)

Service de Gynécologie, INSERM 1242, Oncogenesis, Stress and Signaling, CRLC Eugène Marquis, Université de Rennes 1, Hopital Sud, CHU de Rennes, Rennes, France.

M Koskas (M)

Service de Chirurgie et Oncologie Gynécologique et Mammaire, APHP, Université Paris Diderot Hôpital Bichat, Paris, France.

C Uzan (C)

AP-HP (Assistance Publique des Hôpitaux de Paris), Department of Gynecological and Breast Surgery and Oncology, Pitié-Salpêtrière University Hospital, Paris, France.
INSERM UMR_S_938, "Cancer Biology and Therapeutics," Centre de Recherche Saint-Antoine (CRSA), Sorbonne University, Paris, France.
Institut Universitaire de Cancérologie (IUC), Sorbonne University, Paris, France.

G Canlorbe (G)

AP-HP (Assistance Publique des Hôpitaux de Paris), Department of Gynecological and Breast Surgery and Oncology, Pitié-Salpêtrière University Hospital, Paris, France. geoffroy.canlorbe@aphp.fr.
INSERM UMR_S_938, "Cancer Biology and Therapeutics," Centre de Recherche Saint-Antoine (CRSA), Sorbonne University, Paris, France. geoffroy.canlorbe@aphp.fr.
Institut Universitaire de Cancérologie (IUC), Sorbonne University, Paris, France. geoffroy.canlorbe@aphp.fr.

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