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Neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages IB3 and IIA2 cervical cancer: a multicenter prospective trial
BACKGROUND: Preoperative neoadjuvant chemotherapy (NACT) has been widely used in developing countries for the treatment of patients with International Federation of Gynecology and Obstetrics (FIGO) stages IB3 and IIA2 cervical cancer. However, the effectiveness of NACT and treatment options for NACT...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724322/ https://www.ncbi.nlm.nih.gov/pubmed/36471257 http://dx.doi.org/10.1186/s12885-022-10355-3 |
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author | Hu, Yingjie Han, Yingyan Shen, Yuanming Chen, Jing Chen, Yaheng Chen, Yile Tang, Junying Xue, Min Hong, Li Cheng, Wenjun Wang, Danbo Liang, Zhiqing Wang, Yifeng Zhang, Qinghua Xing, Hui Zhang, Yu Yi, Cunjian Yu, Zhiying Chen, Youguo Cui, Manhua Ma, Cailing Yang, Hongying Li, Ruizhen Long, Ping Zhao, Yu Qu, Pengpeng Tao, Guangshi Yang, Lihua Wu, Sufang Liu, Zhihua Yang, Ping Lv, Weiguo Xie, Xing Ma, Ding Wang, Hui Li, Kezhen |
author_facet | Hu, Yingjie Han, Yingyan Shen, Yuanming Chen, Jing Chen, Yaheng Chen, Yile Tang, Junying Xue, Min Hong, Li Cheng, Wenjun Wang, Danbo Liang, Zhiqing Wang, Yifeng Zhang, Qinghua Xing, Hui Zhang, Yu Yi, Cunjian Yu, Zhiying Chen, Youguo Cui, Manhua Ma, Cailing Yang, Hongying Li, Ruizhen Long, Ping Zhao, Yu Qu, Pengpeng Tao, Guangshi Yang, Lihua Wu, Sufang Liu, Zhihua Yang, Ping Lv, Weiguo Xie, Xing Ma, Ding Wang, Hui Li, Kezhen |
author_sort | Hu, Yingjie |
collection | PubMed |
description | BACKGROUND: Preoperative neoadjuvant chemotherapy (NACT) has been widely used in developing countries for the treatment of patients with International Federation of Gynecology and Obstetrics (FIGO) stages IB3 and IIA2 cervical cancer. However, the effectiveness of NACT and treatment options for NACT-insensitive patients have been concerning. This study will assess prognostic differences between NACT and primary surgery treatment (PST), determine factors associated with prognosis, and explore better adjuvant treatment modalities for NACT-insensitive patients. METHODS: This study analyzed clinical characteristics, pathological characteristics, treatment options, and follow-up information of 774 patients with FIGO stages IB3 and IIA2 cervical cancer from 28 centers from January 2016 to October 2019 who participated in a multicenter, prospective, randomized controlled trial. RESULTS: For patients undergoing NACT, the 5-year OS and PFS rate was 85.8 and 80.5% respectively. They were similar in the PST group. There was no significant difference in OS and PFS between clinical response (CR)/partial response (PR) groups and stable disease (SD)/progressive disease (PD) groups. Apart from deep cervical invasion (p = 0.046) affecting OS for patients undergoing NACT, no other clinical and pathological factors were associated with OS. 97.8% of NACT-insensitive patients opted for surgery. If these patients did not have intermediate- or high-risk factors, whether they had undergone postoperative adjuvant therapy was irrelevant to their prognosis, whereas for patients with intermediate- or high-risk factors, adjuvant chemotherapy resulted in better PFS (chemotherapy vs. no therapy, p < 0.001; chemotherapy vs. radiotherapy, p = 0.019) and OS (chemotherapy vs. no therapy, p < 0.001; chemotherapy vs. radiotherapy, p = 0.002). CONCLUSIONS: NACT could be a choice for patients with FIGO stages IB3 and IIA2 cervical cancer. The main risk factor influencing prognosis in the NACT group is deep cervical invasion. After systematic treatment, insensitivity to NACT does not indicate a poorer prognosis. For NACT-insensitive patients, Chinese prefer surgery. Postoperative adjuvant therapy in patients with no intermediate- or high-risk factors does not improve prognosis, and chemotherapy in patients with intermediate- and high-risk factors is more effective than radiation therapy and other treatments. TRIAL REGISTRATION: The study was prospectively registered on ClinicalTrials.gov (NCT03308591); date of registration: 12/10/2017. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10355-3. |
format | Online Article Text |
id | pubmed-9724322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97243222022-12-07 Neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages IB3 and IIA2 cervical cancer: a multicenter prospective trial Hu, Yingjie Han, Yingyan Shen, Yuanming Chen, Jing Chen, Yaheng Chen, Yile Tang, Junying Xue, Min Hong, Li Cheng, Wenjun Wang, Danbo Liang, Zhiqing Wang, Yifeng Zhang, Qinghua Xing, Hui Zhang, Yu Yi, Cunjian Yu, Zhiying Chen, Youguo Cui, Manhua Ma, Cailing Yang, Hongying Li, Ruizhen Long, Ping Zhao, Yu Qu, Pengpeng Tao, Guangshi Yang, Lihua Wu, Sufang Liu, Zhihua Yang, Ping Lv, Weiguo Xie, Xing Ma, Ding Wang, Hui Li, Kezhen BMC Cancer Research BACKGROUND: Preoperative neoadjuvant chemotherapy (NACT) has been widely used in developing countries for the treatment of patients with International Federation of Gynecology and Obstetrics (FIGO) stages IB3 and IIA2 cervical cancer. However, the effectiveness of NACT and treatment options for NACT-insensitive patients have been concerning. This study will assess prognostic differences between NACT and primary surgery treatment (PST), determine factors associated with prognosis, and explore better adjuvant treatment modalities for NACT-insensitive patients. METHODS: This study analyzed clinical characteristics, pathological characteristics, treatment options, and follow-up information of 774 patients with FIGO stages IB3 and IIA2 cervical cancer from 28 centers from January 2016 to October 2019 who participated in a multicenter, prospective, randomized controlled trial. RESULTS: For patients undergoing NACT, the 5-year OS and PFS rate was 85.8 and 80.5% respectively. They were similar in the PST group. There was no significant difference in OS and PFS between clinical response (CR)/partial response (PR) groups and stable disease (SD)/progressive disease (PD) groups. Apart from deep cervical invasion (p = 0.046) affecting OS for patients undergoing NACT, no other clinical and pathological factors were associated with OS. 97.8% of NACT-insensitive patients opted for surgery. If these patients did not have intermediate- or high-risk factors, whether they had undergone postoperative adjuvant therapy was irrelevant to their prognosis, whereas for patients with intermediate- or high-risk factors, adjuvant chemotherapy resulted in better PFS (chemotherapy vs. no therapy, p < 0.001; chemotherapy vs. radiotherapy, p = 0.019) and OS (chemotherapy vs. no therapy, p < 0.001; chemotherapy vs. radiotherapy, p = 0.002). CONCLUSIONS: NACT could be a choice for patients with FIGO stages IB3 and IIA2 cervical cancer. The main risk factor influencing prognosis in the NACT group is deep cervical invasion. After systematic treatment, insensitivity to NACT does not indicate a poorer prognosis. For NACT-insensitive patients, Chinese prefer surgery. Postoperative adjuvant therapy in patients with no intermediate- or high-risk factors does not improve prognosis, and chemotherapy in patients with intermediate- and high-risk factors is more effective than radiation therapy and other treatments. TRIAL REGISTRATION: The study was prospectively registered on ClinicalTrials.gov (NCT03308591); date of registration: 12/10/2017. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10355-3. BioMed Central 2022-12-05 /pmc/articles/PMC9724322/ /pubmed/36471257 http://dx.doi.org/10.1186/s12885-022-10355-3 Text en © The Author(s) 2022 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 Hu, Yingjie Han, Yingyan Shen, Yuanming Chen, Jing Chen, Yaheng Chen, Yile Tang, Junying Xue, Min Hong, Li Cheng, Wenjun Wang, Danbo Liang, Zhiqing Wang, Yifeng Zhang, Qinghua Xing, Hui Zhang, Yu Yi, Cunjian Yu, Zhiying Chen, Youguo Cui, Manhua Ma, Cailing Yang, Hongying Li, Ruizhen Long, Ping Zhao, Yu Qu, Pengpeng Tao, Guangshi Yang, Lihua Wu, Sufang Liu, Zhihua Yang, Ping Lv, Weiguo Xie, Xing Ma, Ding Wang, Hui Li, Kezhen Neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages IB3 and IIA2 cervical cancer: a multicenter prospective trial |
title | Neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages IB3 and IIA2 cervical cancer: a multicenter prospective trial |
title_full | Neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages IB3 and IIA2 cervical cancer: a multicenter prospective trial |
title_fullStr | Neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages IB3 and IIA2 cervical cancer: a multicenter prospective trial |
title_full_unstemmed | Neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages IB3 and IIA2 cervical cancer: a multicenter prospective trial |
title_short | Neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages IB3 and IIA2 cervical cancer: a multicenter prospective trial |
title_sort | neoadjuvant chemotherapy for patients with international federation of gynecology and obstetrics stages ib3 and iia2 cervical cancer: a multicenter prospective trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724322/ https://www.ncbi.nlm.nih.gov/pubmed/36471257 http://dx.doi.org/10.1186/s12885-022-10355-3 |
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