Comparison of weekly methotrexate regimen versus methotrexate folinic acid 8-day regimen for treatment of low-risk gestational trophoblastic neoplasia

被引:1
作者
Korkmaz, Vakkas [1 ]
Sunar, Veli [2 ]
Akar, Serra [1 ]
Alinca, Cihat Murat [1 ]
Arik, Zafer [3 ]
Boran, Nurettin [1 ]
Ozdal, Bulent [4 ]
Ustun, Yaprak Engin [5 ]
机构
[1] Univ Hlth Sci, Fac Med, Etlik Zubeyde Hanim Womens Hlth Training & Res Ho, Dept Gynecol Oncol, Ankara, Turkey
[2] Univ Hlth Sci, Fac Med, Zekai Tahir Burak Womens Hlth Training & Res Hosp, Dept Med Oncol, Ankara, Turkey
[3] Hacettepe Univ, Inst Canc, Dept Med Oncol, Ankara, Turkey
[4] Univ Hlth Sci, Fac Med, Zekai Tahir Burak Womens Hlth Training & Res Hosp, Dept Gynecol Oncol, Ankara, Turkey
[5] Univ Hlth Sci, Fac Med, Etlik Zubeyde Hanim Womens Hlth Training & Res Ho, Dept Gynecol & Obstet, Ankara, Turkey
关键词
gestational trophoblastic neoplasms; methotrexate; response rate; WEEKLY INTRAMUSCULAR METHOTREXATE; DISEASE; CHEMOTHERAPY; MANAGEMENT; CHORIOCARCINOMA; RESISTANCE; DIAGNOSIS;
D O I
10.1111/ajco.13623
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim We aimed to compare weekly methotrexate (MTX) regimen and methotrexate-folinic acid (MTX-FA) 8-day regimen in the first line treatment of low-risk gestational trophoblastic neoplasia (GTN). Methods The study included 73 patients with low-risk GTN according to FIGO risk score (FIGO risk score < 7). All patients received either weekly MTX (30-50 mg/m(2) intramuscular weekly) or MTX-FA 8-day (MTX 1 mg/kg IV on day 1, 3, 5, and 7, FA 15 mg orally on day 2, 4, 6, and 8 given 24 h after each MTX dose, every 14 days) regimens in the first-line treatment of low-risk GTN. The baseline clinicopathological characteristics and treatment outcomes were analyzed retrospectively. Results The median age of all patients was 29 (18-51) years, and the median FIGO risk score was 3 (1-6). Of the patients recruited, 53 received MTX-FA 8-day, and 20 had MTX weekly regimens. There was a significant difference between the two groups with respect to FIGO risk scores (3 [1-6] vs. 2 [1-5], p = 0.023, MTX-FA 8-day vs. MTX weekly, respectively). The complete response rate was significantly higher in MTX-FA 8-day group compared to MTX weekly group (83% [44/53] vs. 60% [12/20] p = 0.038). In univariate and multivariate regression analyses, only presence of lung metastasis was found to be an independent risk factor for treatment resistance (OR: 3.959, 95% CI 1.105-14.179, p = 0.035). Conclusion MTX-FA 8-day regimen is more effective than weekly MTX regimen in the first line treatment of low-risk GTN including patients even with higher FIGO risk scores. Treatment resistance may develop especially in patients with lung metastasis.
引用
收藏
页码:326 / 332
页数:7
相关论文
共 50 条
[21]   Treatment of low-risk gestational trophoblastic neoplasia [J].
Winter, Matthew C. .
BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY, 2021, 74 :67-80
[22]   Relapse rates after two versus three consolidation courses of methotrexate in the treatment of low-risk gestational trophoblastic neoplasia [J].
Lybol, C. ;
Sweep, F. C. G. J. ;
Harvey, R. ;
Mitchell, H. ;
Short, D. ;
Thomas, C. M. G. ;
Ottevanger, P. B. ;
Savage, P. M. ;
Massuger, L. F. A. G. ;
Seckl, M. J. .
GYNECOLOGIC ONCOLOGY, 2012, 125 (03) :576-579
[23]   Comparison of pulse methotrexate and pulse dactinomycin in the treatment of low-risk gestational trophoblastic neoplasia [J].
Gilani, MM ;
Yarandi, F ;
Eftekhar, Z ;
Hanjani, P .
AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, 2005, 45 (02) :161-164
[24]   Five-Day Intravascular Methotrexate Versus Biweekly Actinomycin-D in the Treatment of Low-Risk Gestational Trophoblastic Neoplasia A Clinical Randomized Trial [J].
Yarandi, Fariba ;
Mousavi, Azamsadat ;
Abbaslu, Fereshteh ;
Aminimoghaddam, Soheila ;
Nekuie, Sepideh ;
Adabi, Khadijeh ;
Hanjani, Parviz .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2016, 26 (05) :971-976
[25]   Actinomycin D for Methotrexate-Failed Low-Risk Gestational Trophoblastic Neoplasia [J].
Lurain, John R. ;
Chapman-Davis, Eloise ;
Hoekstra, Anna V. ;
Schink, Julian C. .
JOURNAL OF REPRODUCTIVE MEDICINE, 2012, 57 (7-8) :283-287
[26]   Low-Risk Gestational Trophoblastic Neoplasia in Manitoba Experience With Alternating Methotrexate and Dactinomycin [J].
Carlson, Vanessa ;
Walters, Leslea ;
Lambert, Pascal ;
Dean, Erin ;
Lotocki, Robert ;
Altman, Alon D. .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2018, 28 (08) :1448-1452
[27]   Efficacy of Combination Therapy with Actinomycin D and Methotrexate in the Treatment of Low-Risk Gestational Trophoblastic Neoplasia [J].
Kang, Hai-Li ;
Zhao, Qun ;
Yang, Shu-Li ;
Duan, Wei .
CHEMOTHERAPY, 2019, 64 (01) :42-47
[28]   Predictive factors of relapse in low-risk gestational trophoblastic neoplasia patients successfully treated with methotrexate alone [J].
Couder, Florence ;
Massardier, Jerome ;
You, Benoit ;
Abbas, Fatima ;
Hajri, Touria ;
Lotz, Jean-Pierre ;
Schott, Anne-Marie ;
Golfier, Francois .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2016, 215 (01) :80.e1-80.e7
[29]   Pulse methotrexate versus pulse actinomycin D in the treatment of low-risk gestational trophoblastic neoplasia [J].
Yarandi, Fariba ;
Eftekhar, Zahra ;
Shojaei, Hadi ;
Kanani, Soheyla ;
Sharifi, Ali ;
Hanjani, Parviz .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2008, 103 (01) :33-37
[30]   Comparison of pulsed actinomycin D versus 5-day methotrexate for the treatment of low-risk gestational trophoblastic disease [J].
Mousavi, Azamsadat ;
Cheraghi, Fatemeh ;
Yarandi, Fariba ;
Gilani, Mitra Modaress ;
Shojaei, Hadi .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2012, 116 (01) :39-42