Cargando…
Neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer
BACKGROUND: Currently, the standard treatment for locally advanced cervical cancer is concurrent chemoradiation (CCRT). Forty percent of patients present with disease recurrence. This study aims to investigate the feasibility, safety and efficacy of neoadjuvant chemotherapy (NACT) with weekly cispla...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840535/ https://www.ncbi.nlm.nih.gov/pubmed/36641433 http://dx.doi.org/10.1186/s12885-023-10517-x |
_version_ | 1784869654896836608 |
---|---|
author | Li, Jing Li, Ya Wang, Huafeng Shen, Lifei Wang, Qun Shao, Siqi Shen, Yuhong Xu, Haoping Liu, Hua Cai, Rong Feng, Weiwei |
author_facet | Li, Jing Li, Ya Wang, Huafeng Shen, Lifei Wang, Qun Shao, Siqi Shen, Yuhong Xu, Haoping Liu, Hua Cai, Rong Feng, Weiwei |
author_sort | Li, Jing |
collection | PubMed |
description | BACKGROUND: Currently, the standard treatment for locally advanced cervical cancer is concurrent chemoradiation (CCRT). Forty percent of patients present with disease recurrence. This study aims to investigate the feasibility, safety and efficacy of neoadjuvant chemotherapy (NACT) with weekly cisplatin and paclitaxel (TP) followed by CCRT. METHODS: We are conducting a phase III trial comparing the efficacy and side effects of patients with cervical cancer (FIGO 2018 stage IIB to IVA) who were assigned to four cycles of NACT with cisplatin (40 mg/m(2)) and paclitaxel (60 mg/m(2)) weekly followed by CCRT or CCRT alone. In this report, we studied the medium-term effect of 50 patients enrolled in the NACT + CCRT arm. The primary endpoints were the response rate post-NACT and 12 weeks post-CCRT evaluated by MR/CT based on RECIST v 1.1. The secondary endpoints were 3-year OS (overall survival) and PFS (progression-free survival) measured by the Kaplan–Meier method. RESULTS: Among 50 patients enrolled in the NACT + CCRT arm, the complete and partial response rates were 10.4% and 68.8%, post-NACT. Twelve weeks after treatment completion, the complete response rate was 72.0%, whereas the total response rate (complete and partial response) was 90.0%. After a median follow-up of 28 months, the 3-year OS rate was 83.9%, and the 3-year PFS rate was 73.6%. NACT response was related to superior PFS and OS compared with NACT nonresponse (P < 0.01). Late AEs were exiguous, while early AEs mainly included myelosuppression and gastrointestinal AEs. CONCLUSIONS: This study showed a good response rate achieved by dose-dense weekly cisplatin and paclitaxel followed by standard CCRT. The treatment regimen is feasible, as evidenced by the acceptable toxicity of NACT and by the high compliance with radiotherapy. TRIAL REGISTRATION: Protocol version number and date. Chinese clinical trial registry, ChiCTR1900025327; http://www.chictr.org.cn. Registered 24 August 2019. Retrospectively registered, medresman.org.cn/ChiCTR1900025326. The date recruitment began 01–01-2019. |
format | Online Article Text |
id | pubmed-9840535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98405352023-01-16 Neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer Li, Jing Li, Ya Wang, Huafeng Shen, Lifei Wang, Qun Shao, Siqi Shen, Yuhong Xu, Haoping Liu, Hua Cai, Rong Feng, Weiwei BMC Cancer Research BACKGROUND: Currently, the standard treatment for locally advanced cervical cancer is concurrent chemoradiation (CCRT). Forty percent of patients present with disease recurrence. This study aims to investigate the feasibility, safety and efficacy of neoadjuvant chemotherapy (NACT) with weekly cisplatin and paclitaxel (TP) followed by CCRT. METHODS: We are conducting a phase III trial comparing the efficacy and side effects of patients with cervical cancer (FIGO 2018 stage IIB to IVA) who were assigned to four cycles of NACT with cisplatin (40 mg/m(2)) and paclitaxel (60 mg/m(2)) weekly followed by CCRT or CCRT alone. In this report, we studied the medium-term effect of 50 patients enrolled in the NACT + CCRT arm. The primary endpoints were the response rate post-NACT and 12 weeks post-CCRT evaluated by MR/CT based on RECIST v 1.1. The secondary endpoints were 3-year OS (overall survival) and PFS (progression-free survival) measured by the Kaplan–Meier method. RESULTS: Among 50 patients enrolled in the NACT + CCRT arm, the complete and partial response rates were 10.4% and 68.8%, post-NACT. Twelve weeks after treatment completion, the complete response rate was 72.0%, whereas the total response rate (complete and partial response) was 90.0%. After a median follow-up of 28 months, the 3-year OS rate was 83.9%, and the 3-year PFS rate was 73.6%. NACT response was related to superior PFS and OS compared with NACT nonresponse (P < 0.01). Late AEs were exiguous, while early AEs mainly included myelosuppression and gastrointestinal AEs. CONCLUSIONS: This study showed a good response rate achieved by dose-dense weekly cisplatin and paclitaxel followed by standard CCRT. The treatment regimen is feasible, as evidenced by the acceptable toxicity of NACT and by the high compliance with radiotherapy. TRIAL REGISTRATION: Protocol version number and date. Chinese clinical trial registry, ChiCTR1900025327; http://www.chictr.org.cn. Registered 24 August 2019. Retrospectively registered, medresman.org.cn/ChiCTR1900025326. The date recruitment began 01–01-2019. BioMed Central 2023-01-14 /pmc/articles/PMC9840535/ /pubmed/36641433 http://dx.doi.org/10.1186/s12885-023-10517-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Li, Jing Li, Ya Wang, Huafeng Shen, Lifei Wang, Qun Shao, Siqi Shen, Yuhong Xu, Haoping Liu, Hua Cai, Rong Feng, Weiwei Neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer |
title | Neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer |
title_full | Neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer |
title_fullStr | Neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer |
title_full_unstemmed | Neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer |
title_short | Neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer |
title_sort | neoadjuvant chemotherapy with weekly cisplatin and paclitaxel followed by chemoradiation for locally advanced cervical cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840535/ https://www.ncbi.nlm.nih.gov/pubmed/36641433 http://dx.doi.org/10.1186/s12885-023-10517-x |
work_keys_str_mv | AT lijing neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT liya neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT wanghuafeng neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT shenlifei neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT wangqun neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT shaosiqi neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT shenyuhong neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT xuhaoping neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT liuhua neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT cairong neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer AT fengweiwei neoadjuvantchemotherapywithweeklycisplatinandpaclitaxelfollowedbychemoradiationforlocallyadvancedcervicalcancer |