Literature DB >> 2846414

EMA/CO regimen in high-risk gestational trophoblastic tumor (GTT).

G Bolis1, C Bonazzi, F Landoni, G Mangili, F Vergadoro, F Zanaboni, C Mangioni.   

Abstract

From June 1980 through December 1985, 36 high-risk GTT patients received Bagshawe's EMA/CO regimen, 22 as first-line, and 14 as second-line treatment, after primary chemotherapy with CHAMOCA, or cyclic regimen, or MTX-CF. All treated patients were metastatic at the start of treatment with EMA/CO; three showed liver metastases and one brain metastasis. Seventeen patients had a high score, greater than 15. Nineteen patients had histologically confirmed diagnosis of choriocarcinoma. The overall response rate was 86% with 81% survival during a median observation time of 32 months. The median number of courses needed to achieve complete remission was 3 (range 3-7). Toxicity was acceptable, and was less than with CHAMOCA and MAC regimens. Only 1 out of 17 high-risk patients developed drug resistance, and 3 needed urgent surgery. The relapse rate of responders was 19% after a median of 5.5 months. The survival rate of high-risk patients was 88%, of which 76% are alive with no evidence of disease, while 12% have still detectable beta-chorionic gonadotrophin. The remission rate in the second-line treatment group was 64%, higher than using other regimens such as MAC or CHAMOCA. In conclusion, we consider EMA/CO to be the best choice for patients with high-risk GTT, because it is effective and well tolerated. In our opinion, the cure rate of high-risk GTT could perhaps be improved by starting trials to establish what salvage treatment to employ after EMA/CO failure and using more aggressive first-line chemotherapy in selected high-risk patients, on the basis of the scoring system.

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Year:  1988        PMID: 2846414     DOI: 10.1016/s0090-8258(88)80029-5

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  7 in total

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2.  Results with Floxuridine, Actinomycin D, Etoposide, and Vincristine in Gestational Trophoblastic Neoplasias with International Federation of Gynecology and Obstetrics Scores ≥5.

Authors:  Yuan Li; Yujia Kong; Xirun Wan; Fengzhi Feng; Tong Ren; Jun Zhao; Junjun Yang; Yang Xiang
Journal:  Oncologist       Date:  2021-09-09

3.  The management and outcome of women with post-hydatidiform mole 'low-risk' gestational trophoblastic neoplasia, but hCG levels in excess of 100 000 IU l(-1).

Authors:  S McGrath; D Short; R Harvey; P Schmid; P M Savage; M J Seckl
Journal:  Br J Cancer       Date:  2010-02-16       Impact factor: 7.640

4.  Current chemotherapeutic management of patients with gestational trophoblastic neoplasia.

Authors:  Taymaa May; Donald P Goldstein; Ross S Berkowitz
Journal:  Chemother Res Pract       Date:  2011-05-11

5.  SLAMF1 Promotes Methotrexate Resistance via Activating Autophagy in Choriocarcinoma Cells.

Authors:  Dazun Shi; Yu Zhang; Yan Tian
Journal:  Cancer Manag Res       Date:  2020-12-30       Impact factor: 3.989

6.  Serum human chorionic gonadotropin ratios for the detection of etoposide, methotrexate, dactinomycin, cyclophosphamide, and vincristine resistance in high-risk gestational trophoblastic neoplasia.

Authors:  Nathapol Sirimusika; Sathana Boonyapipat
Journal:  Health Sci Rep       Date:  2022-07-20

7.  Gestational trophoblastic neoplasia: A 6 year retrospective study.

Authors:  Sushruta Shrivastava; Amal Chandra Kataki; Debabrata Barmon; Pankaj Deka; Chidananda Bhuyan; Saikia J Bhargav
Journal:  South Asian J Cancer       Date:  2014-01
  7 in total

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