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Vincristine, Irinotecan, and Temozolomide in Patients With Relapsed/Refractory Neuroblastoma

PURPOSE: The combination of irinotecan, temozolomide and vincristine has been proposed as an effective salvage regimen for some pediatric malignancies. Thus, we sought to evaluate this combination for patients with relapsed and refractory neuroblastoma (NB). PATIENTS AND METHODS: In this retrospecti...

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Autores principales: Zhu, Jia, Wang, Juan, Sun, Feifei, Zhen, Zijun, Chen, Tingting, Lu, Suying, Huang, Junting, Zhang, Yizhuo, Sun, Xiaofei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961432/
https://www.ncbi.nlm.nih.gov/pubmed/35359419
http://dx.doi.org/10.3389/fonc.2022.804310
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author Zhu, Jia
Wang, Juan
Sun, Feifei
Zhen, Zijun
Chen, Tingting
Lu, Suying
Huang, Junting
Zhang, Yizhuo
Sun, Xiaofei
author_facet Zhu, Jia
Wang, Juan
Sun, Feifei
Zhen, Zijun
Chen, Tingting
Lu, Suying
Huang, Junting
Zhang, Yizhuo
Sun, Xiaofei
author_sort Zhu, Jia
collection PubMed
description PURPOSE: The combination of irinotecan, temozolomide and vincristine has been proposed as an effective salvage regimen for some pediatric malignancies. Thus, we sought to evaluate this combination for patients with relapsed and refractory neuroblastoma (NB). PATIENTS AND METHODS: In this retrospective study, forty-six patients with relapsed or refractory NB were treated with the combination of vincristine (1.5 mg/m(2) i.v. day 1), irinotecan (50 mg/m(2)/day i.v. days 1–5) and temozolomide (100 mg/m(2)/day p.o. days 1–5) (VIT) during the period 2011–2019. All toxicities were documented. RESULTS: A total of 251 cycles (median 6 cycles/patient) were administered. A complete response (CR) was achieved in 5 patients, partial response (PR) in 27 patients, stable disease (SD) in 8 patients, and progression disease (PD) in 6 patients, with an overall objective response rate (CR+PR) of 69.6%. Eighteen patients developed diarrhea with Grade 3 or less. Grade 1-2 hematologic toxicity occurred in 10 patients. Grade 3-4 hematologic toxicity developed in 32 patients. VIT was an effective regimen for different metastatic sites. UGT1A*28 genotyping performed in 7 patients revealed wild type. Diarrhea occurred in 4 of them. CONCLUSION: The shorter, 5-day VIT regimen is an active and well-tolerated salvage regimen in relapse/refractory NB.
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spelling pubmed-89614322022-03-30 Vincristine, Irinotecan, and Temozolomide in Patients With Relapsed/Refractory Neuroblastoma Zhu, Jia Wang, Juan Sun, Feifei Zhen, Zijun Chen, Tingting Lu, Suying Huang, Junting Zhang, Yizhuo Sun, Xiaofei Front Oncol Oncology PURPOSE: The combination of irinotecan, temozolomide and vincristine has been proposed as an effective salvage regimen for some pediatric malignancies. Thus, we sought to evaluate this combination for patients with relapsed and refractory neuroblastoma (NB). PATIENTS AND METHODS: In this retrospective study, forty-six patients with relapsed or refractory NB were treated with the combination of vincristine (1.5 mg/m(2) i.v. day 1), irinotecan (50 mg/m(2)/day i.v. days 1–5) and temozolomide (100 mg/m(2)/day p.o. days 1–5) (VIT) during the period 2011–2019. All toxicities were documented. RESULTS: A total of 251 cycles (median 6 cycles/patient) were administered. A complete response (CR) was achieved in 5 patients, partial response (PR) in 27 patients, stable disease (SD) in 8 patients, and progression disease (PD) in 6 patients, with an overall objective response rate (CR+PR) of 69.6%. Eighteen patients developed diarrhea with Grade 3 or less. Grade 1-2 hematologic toxicity occurred in 10 patients. Grade 3-4 hematologic toxicity developed in 32 patients. VIT was an effective regimen for different metastatic sites. UGT1A*28 genotyping performed in 7 patients revealed wild type. Diarrhea occurred in 4 of them. CONCLUSION: The shorter, 5-day VIT regimen is an active and well-tolerated salvage regimen in relapse/refractory NB. Frontiers Media S.A. 2022-03-09 /pmc/articles/PMC8961432/ /pubmed/35359419 http://dx.doi.org/10.3389/fonc.2022.804310 Text en Copyright © 2022 Zhu, Wang, Sun, Zhen, Chen, Lu, Huang, Zhang and Sun https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Zhu, Jia
Wang, Juan
Sun, Feifei
Zhen, Zijun
Chen, Tingting
Lu, Suying
Huang, Junting
Zhang, Yizhuo
Sun, Xiaofei
Vincristine, Irinotecan, and Temozolomide in Patients With Relapsed/Refractory Neuroblastoma
title Vincristine, Irinotecan, and Temozolomide in Patients With Relapsed/Refractory Neuroblastoma
title_full Vincristine, Irinotecan, and Temozolomide in Patients With Relapsed/Refractory Neuroblastoma
title_fullStr Vincristine, Irinotecan, and Temozolomide in Patients With Relapsed/Refractory Neuroblastoma
title_full_unstemmed Vincristine, Irinotecan, and Temozolomide in Patients With Relapsed/Refractory Neuroblastoma
title_short Vincristine, Irinotecan, and Temozolomide in Patients With Relapsed/Refractory Neuroblastoma
title_sort vincristine, irinotecan, and temozolomide in patients with relapsed/refractory neuroblastoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961432/
https://www.ncbi.nlm.nih.gov/pubmed/35359419
http://dx.doi.org/10.3389/fonc.2022.804310
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