Cargando…

Preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase III clinical trial

BACKGROUND: To explore the hematological toxicity (HT) induced by neoadjuvant chemoradiotherapy (nCRT) compared with neoadjuvant chemotherapy (nCT) and to identify the appropriate vertebral body (VB) dosimetric parameters for predicting HT in patients with locally advanced gastric cancer (GC). METHO...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Ji-jin, Shao, Han, Zhang, Li, Jing, Ming, Xu, Wen-jing, Sun, Heng-wen, Zhou, Zhi-wei, Zhang, Yu-jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294302/
https://www.ncbi.nlm.nih.gov/pubmed/37365597
http://dx.doi.org/10.1186/s13014-023-02269-6
_version_ 1785063164882190336
author Wang, Ji-jin
Shao, Han
Zhang, Li
Jing, Ming
Xu, Wen-jing
Sun, Heng-wen
Zhou, Zhi-wei
Zhang, Yu-jing
author_facet Wang, Ji-jin
Shao, Han
Zhang, Li
Jing, Ming
Xu, Wen-jing
Sun, Heng-wen
Zhou, Zhi-wei
Zhang, Yu-jing
author_sort Wang, Ji-jin
collection PubMed
description BACKGROUND: To explore the hematological toxicity (HT) induced by neoadjuvant chemoradiotherapy (nCRT) compared with neoadjuvant chemotherapy (nCT) and to identify the appropriate vertebral body (VB) dosimetric parameters for predicting HT in patients with locally advanced gastric cancer (GC). METHODS: In the phase III study, 302 patients with GC from an ongoing multi-center randomized clinical trial (NCT 01815853) were included. Patients from two major centers were grouped into training and external validation cohorts. The nCT group received three cycles of XELOX chemotherapy, while the nCRT received the same dose-reduced chemotherapy plus 45 Gy radiotherapy. The complete blood counts at baseline, during neoadjuvant treatment, and in the preoperative period were compared between the nCT and nCRT groups. The VB was retrospectively contoured and the dose-volume parameters were extracted in the nCRT group. Patients’ clinical characteristics, VB dosimetric parameters, and HTs were statistically analyzed. Instances of HT were graded according to the Common Terminology Criteria for Adverse Events v5.0 (CTCAE v5.0). The receiver operating characteristic (ROC) curves were generated to identify the optimal cut-off points for dosimetric variables and verify the prediction efficiency of the dosimetric index in both training and external validation cohorts. RESULTS: In the training cohort, 27.4% Grade 3 + HTs were noted in the nCRT group and 16.2% in the nCT group (P = 0.042). A similar result was exhibited in the validation cohort, with 35.0% Grade 3 + HTs in the nCRT group and 13.2% in the nCT group (P = 0.025). The multivariate analysis of the training cohort revealed that V(5) was associated with Grade 3 + leukopenia (P = 0.000), Grade 3 + thrombocytopenia (P = 0.001), and Grade 3 + total HTs (P = 0.042). The Spearman correlation analysis identified a significant correlation of V(5) with the white blood cell nadir (P = 0.0001) and platelet nadir (P = 0.0002). The ROC curve identified the optimal cut-off points for V(5) and showed that V(5) < 88.75% could indicate a decreased risk of Grade 3 + leukopenia, thrombocytopenia, and total HTs in the training as well as the external validation cohorts. CONCLUSIONS: Compared with nCT, nCRT could increase the risk of Grade 3 + HT in patients with locally advanced GC. Dose constraints of V(5) < 88.75% in irradiated VB could reduce the incidence of Grade 3 + HT.
format Online
Article
Text
id pubmed-10294302
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-102943022023-06-28 Preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase III clinical trial Wang, Ji-jin Shao, Han Zhang, Li Jing, Ming Xu, Wen-jing Sun, Heng-wen Zhou, Zhi-wei Zhang, Yu-jing Radiat Oncol Research BACKGROUND: To explore the hematological toxicity (HT) induced by neoadjuvant chemoradiotherapy (nCRT) compared with neoadjuvant chemotherapy (nCT) and to identify the appropriate vertebral body (VB) dosimetric parameters for predicting HT in patients with locally advanced gastric cancer (GC). METHODS: In the phase III study, 302 patients with GC from an ongoing multi-center randomized clinical trial (NCT 01815853) were included. Patients from two major centers were grouped into training and external validation cohorts. The nCT group received three cycles of XELOX chemotherapy, while the nCRT received the same dose-reduced chemotherapy plus 45 Gy radiotherapy. The complete blood counts at baseline, during neoadjuvant treatment, and in the preoperative period were compared between the nCT and nCRT groups. The VB was retrospectively contoured and the dose-volume parameters were extracted in the nCRT group. Patients’ clinical characteristics, VB dosimetric parameters, and HTs were statistically analyzed. Instances of HT were graded according to the Common Terminology Criteria for Adverse Events v5.0 (CTCAE v5.0). The receiver operating characteristic (ROC) curves were generated to identify the optimal cut-off points for dosimetric variables and verify the prediction efficiency of the dosimetric index in both training and external validation cohorts. RESULTS: In the training cohort, 27.4% Grade 3 + HTs were noted in the nCRT group and 16.2% in the nCT group (P = 0.042). A similar result was exhibited in the validation cohort, with 35.0% Grade 3 + HTs in the nCRT group and 13.2% in the nCT group (P = 0.025). The multivariate analysis of the training cohort revealed that V(5) was associated with Grade 3 + leukopenia (P = 0.000), Grade 3 + thrombocytopenia (P = 0.001), and Grade 3 + total HTs (P = 0.042). The Spearman correlation analysis identified a significant correlation of V(5) with the white blood cell nadir (P = 0.0001) and platelet nadir (P = 0.0002). The ROC curve identified the optimal cut-off points for V(5) and showed that V(5) < 88.75% could indicate a decreased risk of Grade 3 + leukopenia, thrombocytopenia, and total HTs in the training as well as the external validation cohorts. CONCLUSIONS: Compared with nCT, nCRT could increase the risk of Grade 3 + HT in patients with locally advanced GC. Dose constraints of V(5) < 88.75% in irradiated VB could reduce the incidence of Grade 3 + HT. BioMed Central 2023-06-09 /pmc/articles/PMC10294302/ /pubmed/37365597 http://dx.doi.org/10.1186/s13014-023-02269-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Wang, Ji-jin
Shao, Han
Zhang, Li
Jing, Ming
Xu, Wen-jing
Sun, Heng-wen
Zhou, Zhi-wei
Zhang, Yu-jing
Preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase III clinical trial
title Preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase III clinical trial
title_full Preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase III clinical trial
title_fullStr Preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase III clinical trial
title_full_unstemmed Preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase III clinical trial
title_short Preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase III clinical trial
title_sort preoperative chemoradiation-induced hematological toxicity and related vertebral dosimetry evaluations in patients with locally advanced gastric cancer: data from a phase iii clinical trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294302/
https://www.ncbi.nlm.nih.gov/pubmed/37365597
http://dx.doi.org/10.1186/s13014-023-02269-6
work_keys_str_mv AT wangjijin preoperativechemoradiationinducedhematologicaltoxicityandrelatedvertebraldosimetryevaluationsinpatientswithlocallyadvancedgastriccancerdatafromaphaseiiiclinicaltrial
AT shaohan preoperativechemoradiationinducedhematologicaltoxicityandrelatedvertebraldosimetryevaluationsinpatientswithlocallyadvancedgastriccancerdatafromaphaseiiiclinicaltrial
AT zhangli preoperativechemoradiationinducedhematologicaltoxicityandrelatedvertebraldosimetryevaluationsinpatientswithlocallyadvancedgastriccancerdatafromaphaseiiiclinicaltrial
AT jingming preoperativechemoradiationinducedhematologicaltoxicityandrelatedvertebraldosimetryevaluationsinpatientswithlocallyadvancedgastriccancerdatafromaphaseiiiclinicaltrial
AT xuwenjing preoperativechemoradiationinducedhematologicaltoxicityandrelatedvertebraldosimetryevaluationsinpatientswithlocallyadvancedgastriccancerdatafromaphaseiiiclinicaltrial
AT sunhengwen preoperativechemoradiationinducedhematologicaltoxicityandrelatedvertebraldosimetryevaluationsinpatientswithlocallyadvancedgastriccancerdatafromaphaseiiiclinicaltrial
AT zhouzhiwei preoperativechemoradiationinducedhematologicaltoxicityandrelatedvertebraldosimetryevaluationsinpatientswithlocallyadvancedgastriccancerdatafromaphaseiiiclinicaltrial
AT zhangyujing preoperativechemoradiationinducedhematologicaltoxicityandrelatedvertebraldosimetryevaluationsinpatientswithlocallyadvancedgastriccancerdatafromaphaseiiiclinicaltrial