Impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study

Abstract Background We aimed to comprehensively investigate the optimal cumulative cisplatin dose during concurrent chemoradiotherapy (CC-CCD) for locoregionally advanced nasopharyngeal carcinoma (CA-LANPC) with different tumor responses after neoadjuvant chemotherapy (NAC). Methods Patients with CA...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Ya-Nan Jin, Meng-Yun Qiang, Meng-Meng Liu, Zhi-Bin Cheng, Wang-Jian Zhang, Ian Ryan, Tia Marks, Ji-Jin Yao, Liang-Ping Xia
Formato: article
Lenguaje:EN
Publicado: BMC 2021
Materias:
Acceso en línea:https://doaj.org/article/38dee17f974e4bec8dc16d43f14fe5e0
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:38dee17f974e4bec8dc16d43f14fe5e0
record_format dspace
spelling oai:doaj.org-article:38dee17f974e4bec8dc16d43f14fe5e02021-11-14T12:37:34ZImpact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study10.1186/s12935-021-02281-41475-2867https://doaj.org/article/38dee17f974e4bec8dc16d43f14fe5e02021-11-01T00:00:00Zhttps://doi.org/10.1186/s12935-021-02281-4https://doaj.org/toc/1475-2867Abstract Background We aimed to comprehensively investigate the optimal cumulative cisplatin dose during concurrent chemoradiotherapy (CC-CCD) for locoregionally advanced nasopharyngeal carcinoma (CA-LANPC) with different tumor responses after neoadjuvant chemotherapy (NAC). Methods Patients with CA-LANPC who underwent NAC followed by cisplatin-based concurrent chemoradiotherapy were retrospectively analyzed. Evaluation of tumor response in patients was conducted by Response Evaluation Criteria for Solid Tumor (RECIST) 1.1 after two to four cycles NAC. Multivariate Cox proportional hazards models were used for prognosis. Recursive partitioning analysis (RPA) was conducted to classify participates and predict disease-free survival (DFS). Results One hundred and thirty-two patients with favorable response after NAC were included. The median CC-CCD was 163 mg/m2 (IQR, 145–194 mg/m2), and 160 mg/m2 was selected as the cutoff point to group patients into low and high CC-CCD groups (< 160 vs. ≥ 160 mg/m2). There was significant improvement in 5-year DFS (91.2% vs. 72.6%; P = 0.003) for patients receiving high CC-CCD compared to those receiving low CC-CCD. Multivariate analysis revealed that CC-CCD, T stage, and Epstein–Barr virus (EBV) DNA were independent prognostic factors for DFS (P < 0.05 for all). Patients were further categorized into two prognostic groups by RPA: the low-risk group (T1-3 disease with regardless of EBV DNA, and T4 disease with EBV DNA < 4000 copy/mL), and the high-risk group (T4 disease with EBV DNA ≥ 4000 copy/mL). Significant 5-year DFS improvement was observed for the high-risk group (P = 0.004) with high CC-CCD. However, DFS improvement was relatively insignificant in the low-risk group (P = 0.073). Conclusions CC-CCD was a positive prognostic factor for responders after NAC in CA-LANPC. Furthermore, CC-CCD ≥ 160 mg/m2 could significantly improve DFS in the high-risk group with CA-LANPC, but the benefit of high CC-CCD in the low-risk group needs further study.Ya-Nan JinMeng-Yun QiangMeng-Meng LiuZhi-Bin ChengWang-Jian ZhangIan RyanTia MarksJi-Jin YaoLiang-Ping XiaBMCarticleNasopharyngeal carcinomaCumulative cisplatin doseChildren and adolescentsTumor responseNeoadjuvant chemotherapyNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282CytologyQH573-671ENCancer Cell International, Vol 21, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Nasopharyngeal carcinoma
Cumulative cisplatin dose
Children and adolescents
Tumor response
Neoadjuvant chemotherapy
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Cytology
QH573-671
spellingShingle Nasopharyngeal carcinoma
Cumulative cisplatin dose
Children and adolescents
Tumor response
Neoadjuvant chemotherapy
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Cytology
QH573-671
Ya-Nan Jin
Meng-Yun Qiang
Meng-Meng Liu
Zhi-Bin Cheng
Wang-Jian Zhang
Ian Ryan
Tia Marks
Ji-Jin Yao
Liang-Ping Xia
Impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study
description Abstract Background We aimed to comprehensively investigate the optimal cumulative cisplatin dose during concurrent chemoradiotherapy (CC-CCD) for locoregionally advanced nasopharyngeal carcinoma (CA-LANPC) with different tumor responses after neoadjuvant chemotherapy (NAC). Methods Patients with CA-LANPC who underwent NAC followed by cisplatin-based concurrent chemoradiotherapy were retrospectively analyzed. Evaluation of tumor response in patients was conducted by Response Evaluation Criteria for Solid Tumor (RECIST) 1.1 after two to four cycles NAC. Multivariate Cox proportional hazards models were used for prognosis. Recursive partitioning analysis (RPA) was conducted to classify participates and predict disease-free survival (DFS). Results One hundred and thirty-two patients with favorable response after NAC were included. The median CC-CCD was 163 mg/m2 (IQR, 145–194 mg/m2), and 160 mg/m2 was selected as the cutoff point to group patients into low and high CC-CCD groups (< 160 vs. ≥ 160 mg/m2). There was significant improvement in 5-year DFS (91.2% vs. 72.6%; P = 0.003) for patients receiving high CC-CCD compared to those receiving low CC-CCD. Multivariate analysis revealed that CC-CCD, T stage, and Epstein–Barr virus (EBV) DNA were independent prognostic factors for DFS (P < 0.05 for all). Patients were further categorized into two prognostic groups by RPA: the low-risk group (T1-3 disease with regardless of EBV DNA, and T4 disease with EBV DNA < 4000 copy/mL), and the high-risk group (T4 disease with EBV DNA ≥ 4000 copy/mL). Significant 5-year DFS improvement was observed for the high-risk group (P = 0.004) with high CC-CCD. However, DFS improvement was relatively insignificant in the low-risk group (P = 0.073). Conclusions CC-CCD was a positive prognostic factor for responders after NAC in CA-LANPC. Furthermore, CC-CCD ≥ 160 mg/m2 could significantly improve DFS in the high-risk group with CA-LANPC, but the benefit of high CC-CCD in the low-risk group needs further study.
format article
author Ya-Nan Jin
Meng-Yun Qiang
Meng-Meng Liu
Zhi-Bin Cheng
Wang-Jian Zhang
Ian Ryan
Tia Marks
Ji-Jin Yao
Liang-Ping Xia
author_facet Ya-Nan Jin
Meng-Yun Qiang
Meng-Meng Liu
Zhi-Bin Cheng
Wang-Jian Zhang
Ian Ryan
Tia Marks
Ji-Jin Yao
Liang-Ping Xia
author_sort Ya-Nan Jin
title Impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study
title_short Impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study
title_full Impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study
title_fullStr Impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study
title_full_unstemmed Impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study
title_sort impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study
publisher BMC
publishDate 2021
url https://doaj.org/article/38dee17f974e4bec8dc16d43f14fe5e0
work_keys_str_mv AT yananjin impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
AT mengyunqiang impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
AT mengmengliu impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
AT zhibincheng impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
AT wangjianzhang impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
AT ianryan impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
AT tiamarks impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
AT jijinyao impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
AT liangpingxia impactofcumulativecisplatindoseinchildhoodnasopharyngealcarcinomabasedonneoadjuvantchemotherapyresponseintheintensitymodulatedradiotherapyeraarealworldstudy
_version_ 1718429100243156992