PMID- 38023226 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231201 IS - 2234-943X (Print) IS - 2234-943X (Electronic) IS - 2234-943X (Linking) VI - 13 DP - 2023 TI - The efficacy and safety of 5-fluorouracil/cisplatin/vincristine as a multi-agent chemotherapy regimen in gestational trophoblastic neoplasia. PG - 1240972 LID - 10.3389/fonc.2023.1240972 [doi] LID - 1240972 AB - OBJECTIVE: To determine the efficacy and safety of the 5-fluorouracil (5-FU), cisplatin, and vincristine (FPV) chemotherapy regimen in patients with gestational trophoblastic neoplasia (GTN). METHODS: We performed a retrospective study of 96 GTN patients with International Federation of Gynecology and Obstetrics (FIGO) scores of 5 or greater in the Second Affiliated Hospital of Zhengzhou University from October 2013 to October 2019, including 54 patients who received FPV chemotherapy and 42 who received 5-FU/actinomycin D/vincristine (FAV) chemotherapy. A pulsed intravenous device was used to administer 5-FU. The clinical characteristics, adverse events, and response rates were compared between the groups. RESULTS: The patients in the FPV and FAV groups received a total of 228 and 190 courses of chemotherapy, respectively. Complete response (CR) was found in 88.89% (48/54) and 90.48% (38/42) of patients in the FPV group and FAV group, respectively (p = 0.801). Both chemotherapy regimens yielded CR in all low-risk patients (100% vs. 100%), whereas 86.67% and 88.24% of high-risk patients achieved CR (FPV vs. FAV, p = 0.836), respectively. The most common adverse events (AEs) were myelosuppression and gastrointestinal reactions including neutropenia (83.97%), anemia (60.05%), and nausea (46.41%). In comparison to those in the FAV group, patients in the FPV group reported higher rates of grade 1/2 nausea (53.51% vs. 37.89%, p = 0.001), hepatotoxicity (28.95% vs. 17.89%, p = 0.008), oral mucositis (23.25% vs. 10.53%, p = 0.001), and grade 3/4 neutropenia (47.37% vs. 27.37%, p < 0.001), while grade 1/2 diarrhea (7.46% vs. 13.68%, p = 0.037) and grade 3/4 oral mucositis (0 vs. 6.32%, p < 0.001) were much more common in the FAV group. The rate of overall survival at 5 years was 96.8% in the FPV group and 97.3% in the FAV group (p = 0.760), whereas the 5-year disease-free survival rates were 95.9% and 93.9% (p = 0.754), respectively. CONCLUSION: The FPV and FAV regimens with pulsed intravenous 5-FU yielded comparable CR rates and tolerability in patients with GTN with FIGO scores of >5. Further randomized controlled trials are warranted to validate their efficacy. CI - Copyright (c) 2023 Wang, Wang, Xu, Yang and Wang. FAU - Wang, Lu AU - Wang L AD - Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China. AD - Henan Provincial Clinical Research Center for Gynecological and Obstetrical Disease (Gynecological Oncology), Zhengzhou, China. FAU - Wang, Qian AU - Wang Q AD - Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China. AD - Henan Provincial Clinical Research Center for Gynecological and Obstetrical Disease (Gynecological Oncology), Zhengzhou, China. FAU - Xu, Zhen AU - Xu Z AD - Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China. AD - Henan Provincial Clinical Research Center for Gynecological and Obstetrical Disease (Gynecological Oncology), Zhengzhou, China. FAU - Yang, Linli AU - Yang L AD - Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China. AD - Henan Provincial Clinical Research Center for Gynecological and Obstetrical Disease (Gynecological Oncology), Zhengzhou, China. FAU - Wang, Wuliang AU - Wang W AD - Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China. AD - Henan Provincial Clinical Research Center for Gynecological and Obstetrical Disease (Gynecological Oncology), Zhengzhou, China. LA - eng PT - Journal Article DEP - 20231031 PL - Switzerland TA - Front Oncol JT - Frontiers in oncology JID - 101568867 PMC - PMC10644366 OTO - NOTNLM OT - FAV OT - efficacy OT - gestational trophoblastic neoplasia OT - multi-agent chemotherapy OT - pulsed intravenous COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2023/11/29 18:42 MHDA- 2023/11/29 18:43 PMCR- 2023/01/01 CRDT- 2023/11/29 15:42 PHST- 2023/06/29 00:00 [received] PHST- 2023/10/10 00:00 [accepted] PHST- 2023/11/29 18:43 [medline] PHST- 2023/11/29 18:42 [pubmed] PHST- 2023/11/29 15:42 [entrez] PHST- 2023/01/01 00:00 [pmc-release] AID - 10.3389/fonc.2023.1240972 [doi] PST - epublish SO - Front Oncol. 2023 Oct 31;13:1240972. doi: 10.3389/fonc.2023.1240972. eCollection 2023.