The WHO score predicts treatment outcome in low risk gestational trophoblastic neoplasia patients treated with weekly intramuscular methotrexate

被引:18
|
作者
Gillani, Mitra M. [1 ]
Fariba, Behnamfar [1 ,2 ]
Behtash, Nadereh [1 ]
Gaemmaghami, Fatemeh [1 ]
Moosavi, Azam Sadat [1 ]
Rezayof, Elahe [1 ]
机构
[1] Univ Tehran Med Sci, Valie Asr Hosp, Dept Gynecol & Oncol, Tehran, Iran
[2] Beheshti Hosp, Dept Gynecol, Esfahan, Iran
关键词
Gestational trophoblastic neoplasia; Methotrexate; Mole hydatiform; SINGLE-AGENT METHOTREXATE; PULSE METHOTREXATE; FOLINIC ACID; DISEASE; DACTINOMYCIN; ESCALATION; REGIMEN;
D O I
10.4103/0973-1482.110357
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Gestational trophoblastic neoplasia (GTN) includes a spectrum of disease ranging from hydatidifrom mole to choriocarcinoma. Low risk GTN is defined as persistent molar pregnancy with a WHO score lower than seven. The optimal chemotherapeutic regimen still remains controversial. Aim: The objectives of this study was to determine efficacy and safety of weekly intramuscular methotrexte in the treatment of low risk gestational trophoblastic neoplasia.(LRGTN) and also identify prognostic factors associated with treatment failure, necessitating second line chemotherapy. Materials and Methods: Sixty-six women with LRGTN from 2001 to 2009 were treated with weekly intramuscular methotrexate at 40mg/m(2) as first line therapy. Monitoring of treatment was done with weekly checking of beta hCG level. Three consecutive negative beta hCG measurements showed complete response. After first negative beta hCG measurement, one additional dose was administered for consolidation. Results: Of 66 patients, who started the treatment five continued their treatment in other medical centres and were excluded from final analysis for treatment evaluation, and seven discontinued first line therapy because of hepatotoxicity. Of the remaining 54, complete remission occurred in 43 (79.6%) and eleven were resistant to first line therapy. Mean WHO score prior to starting chemotherapy was significantly different between two groups of response and resistance according to our data. Change of treatment to second line Actinomycin-D was necessary in eigtheen cases because of resistance to first line in eleven and liver enzyme elevation in seven patients. Sixteen of these 18 responded to Actinomycin-D as second line and one needed hysterectomy for complete response. One patient received multiagent chemotherapy for complete remission. Conclusion: We recommend this effective and safe method of chemotherapy for women with LRGTN. According to our data, lower mean WHO score predicts a better outcome for this regimen.
引用
收藏
页码:38 / 43
页数:6
相关论文
共 50 条
  • [1] Weekly intramuscular methotrexate in the treatment of low-risk gestational trophoblastic neoplasia
    Mitra Mohit
    Zahra Sarraf
    Gelavizh Sheikhi
    Minoo Robati
    Amir Vasheghani-Farahani
    [J]. Archives of Gynecology and Obstetrics, 2009, 280 : 775 - 780
  • [2] Evaluation of weekly intramuscular methotrexate in the treatment of low risk gestational trophoblastic neoplasia
    Hasanzadeh, Malihe
    Tabari, Azadeh
    Homae, Fatemeh
    Shakeri, Mohammadtaghi
    Bakhshandeh, Tahereh
    MadaniSani, Faezeh
    [J]. JOURNAL OF CANCER RESEARCH AND THERAPEUTICS, 2014, 10 (03) : 646 - 650
  • [3] Weekly intramuscular methotrexate in the treatment of low-risk gestational trophoblastic neoplasia
    Mohit, Mitra
    Sarraf, Zahra
    Sheikhi, Gelavizh
    Robati, Minoo
    Vasheghani-Farahani, Amir
    [J]. ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 2009, 280 (05) : 775 - 780
  • [4] Eight days versus weekly intramuscular methotrexate for the treatment of low-risk gestational trophoblastic neoplasia
    Anfinan, N. M.
    Al Khatieb, M. T.
    Sait, H. K.
    Sait, M. K.
    Baghlaf, O. A.
    Mousa, A. A.
    Sait, K. H.
    [J]. EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY, 2020, 41 (02) : 227 - 232
  • [5] The outcome of patients with low risk gestational trophoblastic neoplasia treated with single agent intramuscular methotrexate and oral folinic acid
    Taylor, F.
    Grew, T.
    Everard, J.
    Ellis, L.
    Winter, M. C.
    Tidy, J.
    Hancock, B. W.
    Coleman, R. E.
    [J]. EUROPEAN JOURNAL OF CANCER, 2013, 49 (15) : 3184 - 3190
  • [6] Outcome of low-risk gestational trophoblastic neoplasia (GTN) treated with methotrexate
    Ahmeed, S.
    [J]. BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2014, 121 : 202 - 202
  • [7] OUTCOME OF LOW-RISK GESTATIONAL TROPHOBLASTIC NEOPLASIA (GTN) TREATED WITH METHOTREXATE
    Alobaid, A.
    Ahmeed, S.
    Saleh, R.
    Mattar, R.
    [J]. INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2013, 23 (08)
  • [8] Evaluating Methotrexate Treatment in Patients With Low-Risk Postmolar Gestational Trophoblastic Neoplasia
    Growdon, Whitfield B.
    Wolfberg, Adam J.
    Goldstein, Donald P.
    Feltmate, Colleen M.
    Chinchilla, Manuel E.
    Lieberman, Ellice S.
    Berkowitz, Ross S.
    [J]. OBSTETRICAL & GYNECOLOGICAL SURVEY, 2009, 64 (05) : 308 - 309
  • [9] Evaluating methotrexate treatment in patients with low-risk postmolar gestational trophoblastic neoplasia
    Growdon, Whitfield B.
    Wolfberg, Adam J.
    Goldstein, Donald P.
    Feltmate, Colleen M.
    Chinchilla, Manuel E.
    Lieberman, Ellice S.
    Berkowitz, Ross S.
    [J]. GYNECOLOGIC ONCOLOGY, 2009, 112 (02) : 353 - 357
  • [10] Differences in Administration of Methotrexate and Impact on Outcome in Low-Risk Gestational Trophoblastic Neoplasia
    Wallin, Emelie
    Niemann, Isa
    Faaborg, Louise
    Fokdal, Lars
    Joneborg, Ulrika
    [J]. CANCERS, 2022, 14 (03)