Improved outcomes with dose-dense paclitaxel-based neoadjuvant chemotherapy in advanced epithelial ovarian carcinoma

被引:20
作者
Becker, David A. [1 ]
Thomas, Eric D. [1 ]
Gilbert, Allison L. [1 ]
Boone, Jonathan D. [1 ]
Straughn, J. Michael, Jr. [1 ]
Huh, Warner K. [1 ]
Bevis, Kerri S. [1 ]
Leath, Charles A., III [1 ]
Alvarez, Ronald D. [1 ]
机构
[1] Univ Alabama Birmingham, Div Gynecol Oncol, Birmingham, AL USA
关键词
Dose-dense paclitaxel; Neoadjuvant chemotherapy; Ovarian cancer; ADVANCED-STAGE OVARIAN; OPEN-LABEL; DOCETAXEL-CARBOPLATIN; PRIMARY SURGERY; CANCER; SURVIVAL; TRIAL; CYTOREDUCTION; BEVACIZUMAB; MULTICENTER;
D O I
10.1016/j.ygyno.2016.04.539
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. We compared tolerability, toxicity, response, and interval debulking surgery (IDS) outcomes between patients who received weekly dose-dense paclitaxel (DDP) and every three-week platinum to standard every three-week taxane plus platinum neoadjuvant chemotherapy (NACT) for advanced epithelial ovarian cancer (EOC). Methods. We conducted a retrospective study of patients receiving NACT at our center between June 1, 2012 and July 31, 2015. Patients with stage III/IV EOC who received at least one cycle of DDP (weekly paclitaxel plus every three-week carboplatin) or standard taxane (every three-week paclitaxel or docetaxel plus carboplatin) therapy were included. Abstracted data included demographics, tolerability, grade 3/4 toxicity, response, and IDS outcomes. Fisher's exact and student t-test were used for statistical significance. Results. Twenty-one patients received DDP and 40 received standard taxane. Tolerability was comparable. More patients receiving DDP experienced grade 3 or 4 toxicity when considered in aggregate (86% vs. 40%; p = 0.001). Pathologic complete response (pCR) was achieved in 14% of DDP patients versus 3% of standard (p = 0.11). 48% of patients in the DDP group were debulked to no residual disease (NRD) versus 28% in the standard group (p = 0.16). Conclusions. While associated with an increase in severe toxicity compared to standard three-week taxane, DDP appears to facilitate higher rates of pCR and NRD for patients receiving NACT in this preliminary study. These results warrant further investigation of DDP for patients with advanced EOC and assessment of impact on long-term survival outcomes. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:25 / 29
页数:5
相关论文
共 33 条
[1]   Aggressive surgical effort and improved survival in advanced-stage ovarian cancer [J].
Aletti, GD ;
Dowdy, SC ;
Gostout, BS ;
Jones, MB ;
Stanhope, CR ;
Wilson, TO ;
Podratz, KC ;
Cliby, WA .
OBSTETRICS AND GYNECOLOGY, 2006, 107 (01) :77-85
[2]   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
[3]   Survival effect of maximal cytoreductive surgery for advanced ovarian carcinoma during the platinum era: A meta-analysis [J].
Bristow, RE ;
Tomacruz, RS ;
Armstrong, DK ;
Trimble, EL ;
Montz, FJ .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (05) :1248-1259
[4]   Incorporation of Bevacizumab in the Primary Treatment of Ovarian Cancer [J].
Burger, Robert A. ;
Brady, Mark F. ;
Bookman, Michael A. ;
Fleming, Gini F. ;
Monk, Bradley J. ;
Huang, Helen ;
Mannel, Robert S. ;
Homesley, Howard D. ;
Fowler, Jeffrey ;
Greer, Benjamin E. ;
Boente, Matthew ;
Birrer, Michael J. ;
Liang, Sharon X. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (26) :2473-2483
[5]   Cancer of the ovary [J].
Cannistra, SA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (24) :2519-2529
[6]   Weekly vs. Every-3-Week Paclitaxel and Carboplatin for Ovarian Cancer [J].
Chan, J. K. ;
Brady, M. F. ;
Penson, R. T. ;
Huang, H. ;
Birrer, M. J. ;
Walker, J. L. ;
DiSilvestro, P. A. ;
Rubin, S. C. ;
Martin, L. P. ;
Davidson, S. A. ;
Huh, W. K. ;
O'Malley, D. M. ;
Boente, M. P. ;
Michael, H. ;
Monk, B. J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 374 (08) :738-748
[7]   Survival impact of complete cytoreduction to no gross residual disease for advanced-stage ovarian cancer: A meta-analysis [J].
Chang, Suk-Joon ;
Hodeib, Melissa ;
Chang, Jenny ;
Bristow, Robert E. .
GYNECOLOGIC ONCOLOGY, 2013, 130 (03) :493-498
[8]   An analysis of patients with bulky advanced stage ovarian, tubal, and peritoneal carcinoma treated with primary debulking surgery (PDS) during an identical time period as the randomized EORTC-NCIC trial of PDS vs neoadjuvant chemotherapy (NACT) [J].
Chi, Dennis S. ;
Musa, Fernanda ;
Dao, Fanny ;
Zivanovic, Oliver ;
Sonoda, Yukio ;
Leitao, Mario M. ;
Levine, Douglas A. ;
Gardner, Ginger J. ;
Abu-Rustum, Nadeem R. ;
Barakat, Richard R. .
GYNECOLOGIC ONCOLOGY, 2012, 124 (01) :10-14
[9]   The effect of maximal surgical cytoreduction on sensitivity to platinum-taxane chemotherapy and subsequent survival in patients with advanced ovarian cancer [J].
Eisenhauer, Eric L. ;
Abu-Rustum, Nadeem R. ;
Sonoda, Yukio ;
Aghajanian, Carol ;
Barakat, Richard R. ;
Chi, Dennis S. .
GYNECOLOGIC ONCOLOGY, 2008, 108 (02) :276-281
[10]   Comparative effectiveness of gemcitabine plus cisplatin versus methotrexate, vinblastine, doxorubicin, plus cisplatin as neoadjuvant therapy for muscle-invasive bladder cancer [J].
Galsky, Matthew D. ;
Pal, Sumanta K. ;
Chowdhury, Simon ;
Harshman, Lauren C. ;
Crabb, Simon J. ;
Wong, Yu-Ning ;
Yu, Evan Y. ;
Powles, Thomas ;
Moshier, Erin L. ;
Ladoire, Sylvain ;
Hussain, Syed A. ;
Agarwal, Neeraj ;
Vaishampayan, Ulka N. ;
Recine, Federica ;
Berthold, Dominik ;
Necchi, Andrea ;
Theodore, Christine ;
Milowsky, Matthew I. ;
Bellmunt, Joaquim ;
Rosenberg, Jonathan E. .
CANCER, 2015, 121 (15) :2586-2593