Concurrent Chemoradiotherapy With Nedaplatin Versus Cisplatin in Patients With Stage IIB-IVA Cervical Cancer: A Randomized Phase III Trial

BackgroundIn this trial, we aimed to assess the efficacy and safety of radiotherapy with nedaplatin or cisplatin in patients with locally advanced cervical cancer.MethodsWe conducted an open-label, non-inferiority, phase III, randomized, controlled trial. Eligible patients with stage IIB-IVA cervica...

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Main Authors: Shasha He, Yan Wang, Yulin Lai, Xinping Cao, Yufeng Ren, Yong Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-02-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2021.798617/full
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author Shasha He
Yan Wang
Yulin Lai
Xinping Cao
Yufeng Ren
Yong Chen
author_facet Shasha He
Yan Wang
Yulin Lai
Xinping Cao
Yufeng Ren
Yong Chen
author_sort Shasha He
collection DOAJ
description BackgroundIn this trial, we aimed to assess the efficacy and safety of radiotherapy with nedaplatin or cisplatin in patients with locally advanced cervical cancer.MethodsWe conducted an open-label, non-inferiority, phase III, randomized, controlled trial. Eligible patients with stage IIB-IVA cervical carcinoma were randomly assigned to receive either nedaplatin or cisplatin for two cycles concurrently with radiotherapy. We reported the therapy-associated harms and survival. The study was registered with chictr.org.cn, number ChiCTR1800020527.ResultsWe randomly assigned 68 patients to nedaplatin-based or cisplatin-based concurrent chemoradiotherapy. Study treatment was stopped early after a data analysis found a higher number of patients suffered severe hematologic harms in the nedaplatin group than in the cisplatin group. Patients in the nedaplatin group had a significantly higher frequency of grade 3-4 neutropenia (19·4% vs. 13%; P < 0·001), severe thrombocytopenia (16·1% vs. 4·3%), and grade 1-2 anemia (51·6% vs. 43·5%) than patients in the cisplatin group. The 1-year PFS and OS in the nedaplatin and cisplatin groups were similar.ConclusionOur findings showed that nedaplatin-based concurrent chemoradiotherapy expressed remarkably higher severe hematologic harms which were mortal. Though the results were negative, the experiences and lessons we learned from it were important.
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spelling doaj.art-36110399f0fe432ea2f6838e21ce4e3f2022-12-21T17:15:24ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-02-011110.3389/fonc.2021.798617798617Concurrent Chemoradiotherapy With Nedaplatin Versus Cisplatin in Patients With Stage IIB-IVA Cervical Cancer: A Randomized Phase III TrialShasha He0Yan Wang1Yulin Lai2Xinping Cao3Yufeng Ren4Yong Chen5Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, ChinaDepartment of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, ChinaDepartment of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, ChinaDepartment of Radiation Oncology, Sun Yat-sen University Cancer Center (SYSUCC), Guangzhou, ChinaDepartment of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, ChinaDepartment of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, ChinaBackgroundIn this trial, we aimed to assess the efficacy and safety of radiotherapy with nedaplatin or cisplatin in patients with locally advanced cervical cancer.MethodsWe conducted an open-label, non-inferiority, phase III, randomized, controlled trial. Eligible patients with stage IIB-IVA cervical carcinoma were randomly assigned to receive either nedaplatin or cisplatin for two cycles concurrently with radiotherapy. We reported the therapy-associated harms and survival. The study was registered with chictr.org.cn, number ChiCTR1800020527.ResultsWe randomly assigned 68 patients to nedaplatin-based or cisplatin-based concurrent chemoradiotherapy. Study treatment was stopped early after a data analysis found a higher number of patients suffered severe hematologic harms in the nedaplatin group than in the cisplatin group. Patients in the nedaplatin group had a significantly higher frequency of grade 3-4 neutropenia (19·4% vs. 13%; P < 0·001), severe thrombocytopenia (16·1% vs. 4·3%), and grade 1-2 anemia (51·6% vs. 43·5%) than patients in the cisplatin group. The 1-year PFS and OS in the nedaplatin and cisplatin groups were similar.ConclusionOur findings showed that nedaplatin-based concurrent chemoradiotherapy expressed remarkably higher severe hematologic harms which were mortal. Though the results were negative, the experiences and lessons we learned from it were important.https://www.frontiersin.org/articles/10.3389/fonc.2021.798617/fullcervical carcinomanedaplatincisplatintoxicitysurvival
spellingShingle Shasha He
Yan Wang
Yulin Lai
Xinping Cao
Yufeng Ren
Yong Chen
Concurrent Chemoradiotherapy With Nedaplatin Versus Cisplatin in Patients With Stage IIB-IVA Cervical Cancer: A Randomized Phase III Trial
Frontiers in Oncology
cervical carcinoma
nedaplatin
cisplatin
toxicity
survival
title Concurrent Chemoradiotherapy With Nedaplatin Versus Cisplatin in Patients With Stage IIB-IVA Cervical Cancer: A Randomized Phase III Trial
title_full Concurrent Chemoradiotherapy With Nedaplatin Versus Cisplatin in Patients With Stage IIB-IVA Cervical Cancer: A Randomized Phase III Trial
title_fullStr Concurrent Chemoradiotherapy With Nedaplatin Versus Cisplatin in Patients With Stage IIB-IVA Cervical Cancer: A Randomized Phase III Trial
title_full_unstemmed Concurrent Chemoradiotherapy With Nedaplatin Versus Cisplatin in Patients With Stage IIB-IVA Cervical Cancer: A Randomized Phase III Trial
title_short Concurrent Chemoradiotherapy With Nedaplatin Versus Cisplatin in Patients With Stage IIB-IVA Cervical Cancer: A Randomized Phase III Trial
title_sort concurrent chemoradiotherapy with nedaplatin versus cisplatin in patients with stage iib iva cervical cancer a randomized phase iii trial
topic cervical carcinoma
nedaplatin
cisplatin
toxicity
survival
url https://www.frontiersin.org/articles/10.3389/fonc.2021.798617/full
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