Literature DB >> 34396643

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

Yuan Li1, Yujia Kong1, Xirun Wan1, Fengzhi Feng1, Tong Ren1, Jun Zhao1, Junjun Yang1, Yang Xiang1.   

Abstract

BACKGROUND: 5-fluorouracil-based multiagent chemotherapy has been used as the primary treatment for high-risk gestational trophoblastic neoplasia (GTN) in China for a few decades. This study aims to assess the efficacy and toxicity of floxuridine, actinomycin D, etoposide, and vincristine (FAEV) as a primary treatment for patients with GTN who had International Federation of Gynecology and Obstetrics (FIGO) scores ≥5.
MATERIALS AND METHODS: A total of 207 patients with GTN who had FIGO scores ≥5 were treated with FAEV as first-line chemotherapy at Peking Union Medical College Hospital between January 2002 and December 2017. Complete remission (CR), resistance, survival, toxicity, and reproductive outcomes were analyzed.
RESULTS: Of the 207 patients treated with FAEV, 9 (4.3%) required a change of chemotherapy owing to toxicity and 1 (0.5%) died of cerebral hernia 5 weeks after commencing treatment. The remaining 197 patients were assessable to determine the response to FAEV; among them, 168 (85.3%) achieved CR with FAEV and 29 (14.7%) developed resistance to FAEV. The 5-year overall survival rate of the entire cohort was 97.4%. Grade 3-4 neutropenia, thrombocytopenia, and anemia occurred in 28.4%, 6.8%, and 6.2% of cycles, respectively. No acute toxicity-related deaths occurred. Five patients developed acute myeloid leukemia 10-50 months after exposure to chemotherapy; another patient developed duodenal cancer 2 years after completing therapy. Sixty-one patients who preserved fertility wanted to become pregnant; 56 of them conceived.
CONCLUSION: The FAEV regimen is an effective primary treatment for patients with GTN who have FIGO scores ≥5 and has predictable and manageable toxicity. IMPLICATIONS FOR PRACTICE: The most commonly used multiagent chemotherapy for high-risk gestational trophoblastic neoplasia (GTN) is etoposide, methotrexate and actinomycin D/cyclophosphamide and vincristine (EMA/CO) worldwide. However, 5-fluorouracil-based multiagent chemotherapy has been used as a primary treatment for high-risk GTN in China for a few decades. This study evaluated the efficacy and toxicity of floxuridine, actinomycin D, etoposide, and vincristine (FAEV) as a primary treatment for patients with GTN who have International Federation of Gynecology and Obstetrics (FIGO) scores ≥5. The study's data demonstrated that FAEV as a primary treatment achieved favorable outcomes for patients with FIGO scores ≥5. Toxicities that result from the FAEV regimen are predictable and manageable. The FAEV regimen may provide another option for the treatment of GTN.
© 2021 AlphaMed Press.

Entities:  

Keywords:  Actinomycin D; Etoposide; Floxuridine; Gestational trophoblastic neoplasia; Treatment efficacy; Vincristine

Mesh:

Substances:

Year:  2021        PMID: 34396643      PMCID: PMC8649027          DOI: 10.1002/onco.13943

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  33 in total

1.  Clinical characteristics and prognosis of ultra high-risk gestational trophoblastic neoplasia patients: A retrospective cohort study.

Authors:  Yujia Kong; Junjun Yang; Fang Jiang; Jun Zhao; Tong Ren; Jie Li; Xiaoyu Wang; Fengzhi Feng; Xirun Wan; Yang Xiang
Journal:  Gynecol Oncol       Date:  2017-04-29       Impact factor: 5.482

2.  Treatment of high-risk gestational trophoblastic disease with methotrexate, actinomycin D, and cyclophosphamide chemotherapy.

Authors:  J R Lurain; J I Brewer
Journal:  Obstet Gynecol       Date:  1985-06       Impact factor: 7.661

3.  Results with EMA/CO (etoposide, methotrexate, actinomycin D, cyclophosphamide, vincristine) chemotherapy in gestational trophoblastic neoplasia.

Authors:  T Turan; O Karacay; G Tulunay; N Boran; S Koc; S Bozok; M F Kose
Journal:  Int J Gynecol Cancer       Date:  2006 May-Jun       Impact factor: 3.437

4.  Salvage combination chemotherapy with floxuridine, dactinomycin, etoposide, and vincristine (FAEV) for patients with relapsed/chemoresistant gestational trophoblastic neoplasia.

Authors:  F Feng; Y Xiang; X Wan; S Geng; T Wang
Journal:  Ann Oncol       Date:  2011-01-13       Impact factor: 32.976

5.  EMA/CO for high-risk gestational trophoblastic neoplasia: good outcomes with induction low-dose etoposide-cisplatin and genetic analysis.

Authors:  Constantine Alifrangis; Roshan Agarwal; Delia Short; Rosemary A Fisher; Neil J Sebire; Richard Harvey; Philip M Savage; Michael J Seckl
Journal:  J Clin Oncol       Date:  2012-12-10       Impact factor: 44.544

6.  Feasibility of central co-ordinated EMA/CO for gestational trophoblastic disease in the Netherlands.

Authors:  Clasien van der Houwen; Ron C Rietbroek; Christianne A R Lok; Marianne J Ten Kate-Booij; Frits B Lammes; Anca C Ansink
Journal:  BJOG       Date:  2004-02       Impact factor: 6.531

7.  Results with the EMA/CO (etoposide, methotrexate, actinomycin D, cyclophosphamide, vincristine) regimen in high risk gestational trophoblastic tumours, 1979 to 1989.

Authors:  E S Newlands; K D Bagshawe; R H Begent; G J Rustin; L Holden
Journal:  Br J Obstet Gynaecol       Date:  1991-06

8.  The role of VP16-213 (etoposide; NSC-141540) in gestational choriocarcinoma.

Authors:  E S Newlands; K D Bagshawe
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

Review 9.  Comparison of 5-fluoro-2'-deoxyuridine with 5-fluorouracil and their role in the treatment of colorectal cancer.

Authors:  J A van Laar; Y M Rustum; S P Ackland; C J van Groeningen; G J Peters
Journal:  Eur J Cancer       Date:  1998-02       Impact factor: 9.162

10.  Update on the diagnosis and management of gestational trophoblastic disease.

Authors:  Hextan Y S Ngan; Michael J Seckl; Ross S Berkowitz; Yang Xiang; François Golfier; Paradan K Sekharan; John R Lurain; Leon Massuger
Journal:  Int J Gynaecol Obstet       Date:  2018-10       Impact factor: 3.561

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