Patterns of recurrence in women with advanced and recurrent epithelial ovarian cancer treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy

被引:16
作者
Chambers, Laura M. [1 ]
Yao, Meng [2 ]
Morton, Molly [3 ]
Gruner, Morgan [3 ]
Chichura, Anna [3 ]
Horowitz, Max [1 ]
Costales, Anthony B. [4 ]
Rose, Peter G. [1 ]
Michener, Chad M. [1 ]
Debernardo, Robert [1 ]
机构
[1] Cleveland Clin, Div Gynecol Oncol, Obstet Gynecol Womens Hlth Inst, Desk A81,9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Cleveland Clin, Dept Qualitat Hlth Sci, Cleveland, OH 44195 USA
[3] Cleveland Clin, Obstet Gynecol Womens Hlth Inst, Desk A81,9500, Cleveland, OH 44106 USA
[4] Baylor Coll Med, Dept Gynecol Oncol, Houston, TX 77030 USA
关键词
Epithelial ovarian cancer; Hyperthermic intraperitoneal chemotherapy; Recurrence; PACLITAXEL; CISPLATIN; CARCINOMA; SURVIVAL;
D O I
10.1016/j.ygyno.2021.01.039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective(s). To identify recurrence patterns and outcomes in women with advanced or recurrent epithelial ovarian cancer (EOC) after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). Methods. This is an IRB-approved single-institution cohort study of women who underwent CRS+HIPEC for advanced or recurrent EOC followed in a prospective registry from 1/12/2014-3/1/2020. Recurrence locations were defined as pelvic, upper abdominal (UA) and/or extra-peritoneal (EP). Univariate analysis assessed associations between recurrence location, progression-free survival (PFS), and overall survival (OS). Results. In total, 92 women with EOC underwent interval (56.5%; n=52) or recurrent CRS+HIPEC (43.5%; n= 40). For interval CRS+HIPEC, recurrence locations were pelvic in 50.0% (n=15), UA in 23.3% (n=7) and EP in 56.7% (n=17); 40.0% (n=12) were EP alone. Similarly, for recurrent CRS+HIPEC, recurrence locations were pelvic (22.5%, n=9), UA (5.0%, n=2) and EP (60.0%, n=24); 66.7% (n=20) were EP alone. For both interval and recurrent CRS+HIPEC, median PFS was 10.5 vs. 13.0 months for pelvic and UA vs. EP only recurrences (p=0.02). Similarly, median OS was 29.2 months for pelvic and UA and not reached for EP only (p=0.05). For interval CRS+HIPEC, there was no difference in median PFS (10.6 vs. 11.7 months, p=0.68) and OS (27.1 vs. 24.8 months, p=0.96) for pelvic and UA vs EP alone. However, for recurrent CRS+HIPEC, pelvic and UA sites of recurrence were associated with reduced PFS (10.0 vs. 18.1 months, p=0.03) and OS (33.6 months vs. not reached, p= 0.02) vs. EP only. Conclusions. In women with advanced or recurrent EOC undergoing CRS+HIPEC, one-half of patients experience their first recurrence outside of the peritoneal cavity. Providers must be aware of the risk of EP failure in patients treated with CRS+HIPEC. (c) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:389 / 395
页数:7
相关论文
共 24 条
[1]   Intraperitoneal cisplatin plus intravenous cyclophosphamide versus intravenous cisplatin plus intravenous cyclophosphamide for stage III ovarian cancer [J].
Alberts, DS ;
Liu, PY ;
Hannigan, EV ;
OToole, R ;
Williams, SD ;
Young, JA ;
Franklin, EW ;
ClarkePearson, DL ;
Malviya, VK ;
DuBeshter, B ;
Adelson, MD ;
Hoskins, WJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (26) :1950-1955
[2]   Treatment of Microscopic Disease with Hyperthermic Intraoperative Intraperitoneal Chemotherapy After Complete Cytoreduction Improves Disease-Free Survival in Patients with Stage IIIC/IV Ovarian Cancer [J].
Antonio Cascales-Campos, Pedro ;
Gil, J. ;
Gil, E. ;
Feliciangeli, E. ;
Gonzalez-Gil, A. ;
Parrilla, J. J. ;
Parrilla, P. .
ANNALS OF SURGICAL ONCOLOGY, 2014, 21 (07) :2383-2389
[3]   Intraperitoneal cisplatin and paclitaxel in ovarian cancer [J].
Armstrong, DK ;
Bundy, B ;
Wenzel, L ;
Huang, HQ ;
Baergen, R ;
Lele, S ;
Copeland, LJ ;
Walker, JL ;
Burger, RA .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (01) :34-43
[4]  
Armstrong DK., 2020, NCCN clinical practice guidelines in oncology (NCCN Guidelines1) ovarian cancer including Fallopian tube cancer and primary peritoneal cancer. version
[5]   Treatment of ovarian cancer with paclitaxel- or carboplatin-based intraperitoneal hyperthermic chemotherapy during secondary surgery [J].
Bae, Jeong Hoon ;
Lee, Joon Mo ;
Ryu, Ki Sung ;
Lee, Yong Seok ;
Park, Yong Gyu ;
Hur, Soo Young ;
Ahn, Woong Shik ;
Namkoong, Seong Eun .
GYNECOLOGIC ONCOLOGY, 2007, 106 (01) :193-200
[6]   Peritoneal carcinomatosis treated with cytoreductive surgery and Hyperthermic Intraperitoneal Chemotherapy (HIPEC) for advanced ovarian carcinoma: A French multicentre retrospective cohort study of 566 patients [J].
Bakrin, N. ;
Bereder, J. M. ;
Decullier, E. ;
Classe, J. M. ;
Msika, S. ;
Lorimier, G. ;
Abboud, K. ;
Meeus, P. ;
Ferron, G. ;
Quenet, F. ;
Marchal, F. ;
Gouy, S. ;
Morice, P. ;
Pomel, C. ;
Pocard, M. ;
Guyon, F. ;
Porcheron, J. ;
Glehen, O. .
EJSO, 2013, 39 (12) :1435-1443
[7]   Incidence and predictors of peritoneal metastases of gynecological origin: a population-based study in the Netherlands [J].
Burg, Lara ;
Timmermans, Maite ;
van der Aa, Maaike ;
Boll, Dorry ;
Rovers, Koen ;
de Hingh, Ignace ;
van Altena, Anne .
JOURNAL OF GYNECOLOGIC ONCOLOGY, 2020, 31 (05) :1-12
[8]   Effect of cytoreductive surgery and hyperthermic intraperitoneal chemotherapy on relapse pattern in primary epithelial ovarian cancer: a propensity score based case-control study [J].
Ceresoli, Marco ;
Verrengia, Apollonia ;
Montori, Giulia ;
Busci, Luisa ;
Coccolini, Federico ;
Ansaloni, Luca ;
Frigerio, Luigi .
JOURNAL OF GYNECOLOGIC ONCOLOGY, 2018, 29 (03)
[9]   A guide to establishing a hyperthermic intraperitoneal chemotherapy program in gynecologic oncology [J].
Chambers, Laura M. ;
Costales, Anthony B. ;
Crean-Tate, Katie ;
Kuznicki, Michelle ;
Morton, Molly ;
Horowitz, Max ;
Jagielo, Tiffany ;
Rose, Peter G. ;
Michener, Chad ;
Vargas, Roberto ;
Debernardo, Robert .
GYNECOLOGIC ONCOLOGY, 2020, 158 (03) :794-802
[10]   Patterns of recurrence in advanced epithelial ovarian, fallopian tube and peritoneal cancers treated with intraperitoneal chemotherapy [J].
Esselen, Katharine M. ;
Rodriguez, Noah ;
Growdon, Whitfield ;
Krasner, Carolyn ;
Horowitz, Neil S. ;
Campos, Susana .
GYNECOLOGIC ONCOLOGY, 2012, 127 (01) :51-54