Effectiveness and toxicity of first-line methotrexate chemotherapy in low-risk postmolar gestational trophoblastic neoplasia: The New England Trophoblastic Disease Center experience

被引:57
作者
Maesta, Izildinha [1 ,5 ,6 ]
Nitecki, Roni [2 ]
Horowitz, Neil S. [3 ,4 ,7 ,8 ]
Goldstein, Donald P. [3 ,4 ,7 ,8 ]
Segalla Moreira, Marjory de Freitas [1 ,5 ,6 ]
Elias, Kevin M. [3 ,4 ,7 ,8 ]
Berkowitz, Ross S. [3 ,4 ,7 ,8 ]
机构
[1] Sao Paulo State Univ, UNESP, Botucatu Med Sch, Dept Gynecol & Obstet, Botucatu, SP, Brazil
[2] Brigham & Womens Hosp, Dept Obstet & Gynecol, 75 Francis St, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Obstet & Gynecol, Div Gynecol Oncol, 75 Francis St, Boston, MA 02115 USA
[4] New England Trophoblast Dis Ctr, Donald P Goldstein MD Tumor Registry, Boston, MA USA
[5] Sao Paulo State Univ, UNESP, Botucatu Med Sch, Trophoblast Dis Ctr, Botucatu, SP, Brazil
[6] Sao Paulo State Univ, UNESP, Botucatu Med Sch, Postgrad Program Gynecol Obstet & Mastol, Botucatu, SP, Brazil
[7] Harvard Canc Ctr, Dana Farber Canc Inst, Boston, MA USA
[8] Harvard Med Sch, Boston, MA USA
基金
巴西圣保罗研究基金会;
关键词
First-line methotrexate chemotherapy; Effectiveness; Toxicity; Low-risk gestational trophoblastic neoplasia; LOW-DOSE METHOTREXATE; CITROVORUM FACTOR RESCUE; FOLINIC ACID; PRIMARY THERAPY; MANAGEMENT; TUMORS; TIME;
D O I
10.1016/j.ygyno.2017.10.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives. To assess the outcomes and toxicity of first-line methotrexate (MTX) chemotherapy in low-risk postmolar gestational trophoblastic neoplasia (GTN) patients receiving 8-day methotrexate or one-day methotrexate infusion regimens. Methods. This retrospective cohort study was conducted at the New England Trophoblastic Disease Center (NETDC), between 1974 and 2014, and included 325 patients with FIGO-defined low-risk postmolar GTN receiving first-line 8-day MTX/folinic acid (FA) or one-day MTX infusion and FA. Demographics, disease presentation, initial treatment plan, treatment outcome, and treatment-related adverse events were assessed. Results. Sustained remission (84% vs 62%, p < 0.001) and need to switch to second-line therapy due to treatment-related adverse events (53% vs 0%, p = 0.001) were higher for 8-day MTX/FA compared to one-day MIX infusion. MTX resistance, however, was more frequent with one-day MTX (34.5%) than with 8-day MTX/ FA (7.3%, p < 0.001). Relapse rates were similar with both regimens (3.0%). Compared to one-day MTX infusion, 8-day MTX/FA was associated with significantly higher gastrointestinal disorders (48% vs 24%), abnormal laboratory findings (48% vs 28%), eye disorders (37% vs 19%) and general disorders (22% vs 5%) (p < 0.001). Only infection frequency did not differ between 8-day MTX/FA and one-day MTX infusion (20% vs 12%, p = 0.083). Conclusions. This is one of the largest studies to comprehensively catalogue toxicities associated with 8-day MTX/FA and one-day MTX infusion. Although treatment-related adverse events were more frequent with 8 day MTX/FA, these were all self-limited and resolved with no long-term sequelae. Given this and its higher effectiveness, 8-day MTX/FA remains the treatment of choice at NETDC for patients with low-risk postmolar GTN. (C) 2017 Published by Elsevier Inc.
引用
收藏
页码:161 / 167
页数:7
相关论文
共 43 条
[1]   THE ROLE OF LOW-DOSE METHOTREXATE AND FOLINIC ACID IN GESTATIONAL TROPHOBLASTIC TUMORS (GTT) [J].
BAGSHAWE, KD ;
DENT, J ;
NEWLANDS, ES ;
BEGENT, RHJ ;
RUSTIN, GJS .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1989, 96 (07) :795-802
[2]  
BERKOWITZ RS, 1979, OBSTET GYNECOL, V54, P725
[3]  
BERKOWITZ RS, 1982, CANCER-AM CANCER SOC, V50, P2024, DOI 10.1002/1097-0142(19821115)50:10<2024::AID-CNCR2820501008>3.0.CO
[4]  
2-4
[5]   10-YEARS EXPERIENCE WITH METHOTREXATE AND FOLINIC ACID AS PRIMARY THERAPY FOR GESTATIONAL TROPHOBLASTIC DISEASE [J].
BERKOWITZ, RS ;
GOLDSTEIN, DP ;
BERNSTEIN, MR .
GYNECOLOGIC ONCOLOGY, 1986, 23 (01) :111-118
[6]   15 years of progress in gestational trophoblastic disease: Scoring, standardization, and salvage [J].
Brown, Jubilee ;
Naumann, R. Wendel ;
Seckl, Michael J. ;
Schink, Julian .
GYNECOLOGIC ONCOLOGY, 2017, 144 (01) :200-207
[7]   Methotrexate for 2000 FIGO low-risk gestational trophoblastic neoplasia patients: efficacy and toxicity [J].
Chalouhi, Gihad Elias ;
Golfier, Francois ;
Soignon, Pauline ;
Massardier, Jerome ;
Guastalla, Jean-Paul ;
Trillet-Lenoir, Veronique ;
Schott, Anne-Marie ;
Raudrant, Daniel .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2009, 200 (06) :643.e1-643.e6
[8]   Single-dose methotrexate regimen in the treatment of low-risk gestational trophoblastic neoplasia [J].
Chan, Karen K. L. ;
Huang, Yong ;
Tam, Kar Fai ;
Tse, Ka Yu ;
Ngan, Hextan Y. S. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2006, 195 (05) :1282-1286
[9]   Treatment of nonmetastatic and metastatic low-risk gestational trophoblastic neoplasia: Factors associated with resistance to single-agent methotrexate chemotherapy [J].
Chapman-Davis, Eloise ;
Hoekstra, Anna V. ;
Rademaker, Alfred W. ;
Schink, Julian C. ;
Lurain, John R. .
GYNECOLOGIC ONCOLOGY, 2012, 125 (03) :572-575
[10]  
Chaveli-Lopez Begonya, 2016, J Clin Exp Dent, V8, pe201, DOI 10.4317/jced.52917