Gestational trophoblastic neoplasia: treatment outcomes from a single institutional experience

被引:16
|
作者
Al-Husaini, H. [1 ]
Soudy, H. [1 ,2 ]
Darwish, A. [3 ]
Ahmed, M. [1 ,2 ]
Eltigani, A. [4 ]
Edesa, W. [2 ]
Elhassan, T. [1 ]
Omar, A. [1 ]
Elghamry, W. [5 ]
Al-Hashem, H. [6 ]
Al-Hayli, S. [1 ]
Madkhali, I. [1 ]
Ahmad, S. [7 ]
Al-Badawi, I. A. [1 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, King Faisal Canc Ctr, Riyadh 11211, Saudi Arabia
[2] Cairo Univ, Cairo, Egypt
[3] Dr Soliman Fakeeh Hosp, Dept Oncol, Jeddah, Saudi Arabia
[4] Natl Guard Hosp, Riyadh, Saudi Arabia
[5] Ain Shams Univ, Cairo, Egypt
[6] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[7] Florida Hosp Canc Inst, Orlando, FL 32804 USA
关键词
Gestational trophoblastic disease; Chemotherapy; treatment; Survival; Clinical outcomes; Salvage therapy; ACTINOMYCIN-D; MOLAR PREGNANCY; TUMORS; CHEMOTHERAPY; METHOTREXATE; DISEASE; CYCLOPHOSPHAMIDE; ETOPOSIDE;
D O I
10.1007/s12094-014-1251-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To report the outcomes of gestational trophoblastic neoplasia (GTN) at a single institution and to determine the factors affecting response to chemotherapy and survival. From 1979-2010, we retrospectively reviewed the data of 221 patients treated at our center. GTN Patients were assigned to low-risk (score a parts per thousand currency sign6) or high-risk (score a parts per thousand yen7) based on the WHO risk factor scoring system. Overall survival (OS) probabilities were estimated using Kaplan-Meier method. Logistic regression was applied to study the impact of different factors on the response to initial therapy. Patients' OS rate was 97 %. Median age at diagnosis was 37 year. 131 (59 %) patients had low-risk and 88 (40 %) cases had high-risk GTN. Complete remission rates to initial chemotherapy in low-risk group were 53 % and 87 % for single-agent methotrexate or dactinomycin, respectively. In high-risk group, 94 % achieved complete remission to initial chemotherapy with etoposide, methotrexate, dactinomycin, cyclophosphamide, and vincristine (EMA-CO). Etoposide, cisplatin, and dactinomycin as primary therapy in high-risk patients was successful in 70 %, while bleomycin, etoposide, and cisplatin (BEP) was successful in 53 % of cases. Salvage chemotherapy, surgical intervention or radiation therapy resulted in overall complete remission of 90 % in low-risk and 73 % in high-risk groups. Factors associated with resistance to initial chemotherapy were advanced-stage III/IV (p = 0.005), metastatic site other than lung or vagina (p = 0.005) and high-risk prognostic score (p = 0.05). OS was significantly influenced by the type of antecedent pregnancy (molar 98 % vs. others 93 %; p = 0.04), FIGO stage (I, II 100 % vs. III, IV 94 %; p = 0.02), score (low-risk 100 % vs. high-risk 92 %; p = 0.01), and site of metastasis (lung/vagina 98 % vs. others 85 %; p = 0.002). GTNs have excellent prognosis if properly treated at experienced centers. Single-agent dactinomycin seems more effective for low-risk GTN. EMA-CO remains the preferred primary treatment regimen for high-risk group. The excellent outcome reflects the success of salvage therapy.
引用
收藏
页码:409 / 415
页数:7
相关论文
共 50 条
  • [21] Gestational Trophoblastic Neoplasia: Diagnosis, Management, and Emerging Therapeutic Strategies
    Gupta, Sumedha
    Ahuja, Sana
    Kalwaniya, Dheer Singh
    INDIAN JOURNAL OF GYNECOLOGIC ONCOLOGY, 2025, 23 (01)
  • [22] Low-Risk Gestational Trophoblastic Neoplasia in Manitoba Experience With Alternating Methotrexate and Dactinomycin
    Carlson, Vanessa
    Walters, Leslea
    Lambert, Pascal
    Dean, Erin
    Lotocki, Robert
    Altman, Alon D.
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2018, 28 (08) : 1448 - 1452
  • [23] Weekly intramuscular methotrexate in the treatment of low-risk gestational trophoblastic neoplasia
    Mohit, Mitra
    Sarraf, Zahra
    Sheikhi, Gelavizh
    Robati, Minoo
    Vasheghani-Farahani, Amir
    ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 2009, 280 (05) : 775 - 780
  • [24] Treatment Outcomes of Gestational Trophoblastic Neoplasia in King Chulalongkorn Memorial Hospital over Two Decades
    Lertkhachonsuk, Ruangsak
    Wairachpanich, Varangkana
    JOURNAL OF REPRODUCTIVE MEDICINE, 2016, 61 (5-6) : 238 - 242
  • [25] Challenges in the Treatment of Low-risk Gestational Trophoblastic Neoplasia
    Braga, Antonio
    Elias, Kevin M.
    Horowitz, Neil S.
    Berkowitz, Ross S.
    REVISTA BRASILEIRA DE GINECOLOGIA E OBSTETRICIA, 2021, 43 (07): : 503 - 506
  • [26] Complete Resection Is Essential in the Surgical Treatment of Gestational Trophoblastic Neoplasia
    Essel, Kathleen Gong
    Shafer, Aaron
    Bruegl, Amanda
    Gershenson, David M.
    Drury, Lane K.
    Ramondetta, Lois M.
    Naumann, R. Wendel
    Brown, Jubilee
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2018, 28 (08) : 1453 - 1460
  • [27] Changes in the Management of High-risk Gestational Trophoblastic Neoplasia in the National Trophoblastic Disease Center of Hungary
    Fueloep, Vihnos
    Szigetvari, Ivan
    Szepesi, Janos
    Vegh, Gyoergy
    Berkowitz, Ross S.
    JOURNAL OF REPRODUCTIVE MEDICINE, 2014, 59 (5-6) : 227 - 234
  • [28] Gestational trophoblastic neoplasia with retroperitoneal metastases: A fatal complication
    Thomakos, Nikolaos
    Rodolakis, Alexandros
    Belitsos, Panayiotis
    Zagouri, Flora
    Chatzinikolaou, Ioannis
    Dimopoulos, Athanassios-Meletios
    Papadimitriou, Christos A.
    Antsaklis, Aris
    WORLD JOURNAL OF SURGICAL ONCOLOGY, 2010, 8
  • [29] Single or two drug combination therapy as initial treatment for low risk, gestational trophoblastic neoplasia. A Canadian analysis
    Hoskins, Paul J.
    Le, Nhu
    Kumar, Aalok
    Pina, Annick
    Sabourin, Jeanelle N.
    Kim, Hannah
    Osborne, Ray J.
    GYNECOLOGIC ONCOLOGY, 2020, 157 (02) : 367 - 371
  • [30] Diagnosis and Treatment of High-Risk Metastatic Gestational Trophoblastic Neoplasia in Hungary 40 Years of Experience
    Fulop, Vilmos
    Szigetvari, Ivan
    Szepesi, Janos
    Vegh, Gyorgy
    Demeter, Janos
    Berkowitz, Ross S.
    JOURNAL OF REPRODUCTIVE MEDICINE, 2018, 63 (5-6) : 240 - 248