Chemotherapy in pediatric brain tumor and the challenge of the blood-brain barrier

被引:7
作者
Malik, Johid Reza [1 ,6 ]
Podany, Anthony T. [1 ,2 ]
Khan, Parvez [3 ]
Shaffer, Christopher L. [2 ]
Siddiqui, Jawed A. [3 ]
Baranowska-Kortylewicz, Janina [4 ]
Le, Jennifer [5 ]
Fletcher, Courtney V. [1 ]
Ether, Sadia Afruz [1 ]
Avedissian, Sean N. [1 ,2 ,6 ]
机构
[1] Univ Nebraska Med Ctr, Coll Pharm, Antiviral Pharmacol Lab, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Child Hlth Res Inst, Pediat Clin Pharmacol Program, Omaha, NE 68198 USA
[3] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
[4] Univ Nebraska Med Ctr, Coll Pharm, Dept Pharmaceut Sci, Omaha, NE 68198 USA
[5] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, San Diego, CA USA
[6] Univ Nebraska Med Ctr, Antiviral Pharmacol Lab, 986145 Nebraska Med Ctr, Omaha, NE 68198 USA
关键词
blood-brain barrier; central nervous system; chemotherapy; oncology; pediatric brain tumor; CENTRAL-NERVOUS-SYSTEM; CRANIOSPINAL RADIATION-THERAPY; INTRINSIC PONTINE GLIOMAS; ENDOTHELIAL GROWTH-FACTOR; THAN; YEARS; EARLY-CHILDHOOD MEDULLOBLASTOMA; CANCER RESISTANCE PROTEIN; PHASE-II TRIAL; OF-THE-ART; ADJUVANT CHEMOTHERAPY;
D O I
10.1002/cam4.6647
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundPediatric brain tumors (PBT) stand as the leading cause of cancer-related deaths in children. Chemoradiation protocols have improved survival rates, even for non-resectable tumors. Nonetheless, radiation therapy carries the risk of numerous adverse effects that can have long-lasting, detrimental effects on the quality of life for survivors. The pursuit of chemotherapeutics that could obviate the need for radiotherapy remains ongoing. Several anti-tumor agents, including sunitinib, valproic acid, carboplatin, and panobinostat, have shown effectiveness in various malignancies but have not proven effective in treating PBT. The presence of the blood-brain barrier (BBB) plays a pivotal role in maintaining suboptimal concentrations of anti-cancer drugs in the central nervous system (CNS). Ongoing research aims to modulate the integrity of the BBB to attain clinically effective drug concentrations in the CNS. However, current findings on the interaction of exogenous chemical agents with the BBB remain limited and do not provide a comprehensive explanation for the ineffectiveness of established anti-cancer drugs in PBT.MethodsWe conducted our search for chemotherapeutic agents associated with the blood-brain barrier (BBB) using the following keywords: Chemotherapy in Cancer, Chemotherapy in Brain Cancer, Chemotherapy in PBT, BBB Inhibition of Drugs into CNS, Suboptimal Concentration of CNS Drugs, PBT Drugs and BBB, and Potential PBT Drugs. We reviewed each relevant article before compiling the information in our manuscript. For the generation of figures, we utilized BioRender software.FocusWe focused our article search on chemical agents for PBT and subsequently investigated the role of the BBB in this context. Our search criteria included clinical trials, both randomized and non-randomized studies, preclinical research, review articles, and research papers.FindingOur research suggests that, despite the availability of potent chemotherapeutic agents for several types of cancer, the effectiveness of these chemical agents in treating PBT has not been comprehensively explored. Additionally, there is a scarcity of studies examining the role of the BBB in the suboptimal outcomes of PBT treatment, despite the effectiveness of these drugs for other types of tumors.
引用
收藏
页码:21075 / 21096
页数:22
相关论文
共 244 条
[1]   Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[2]   Dynamics of CNS barriers: Evolution, differentiation, and modulation [J].
Abbott, NJ .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2005, 25 (01) :5-23
[3]   Systemic chemotherapy of pediatric recurrent ependymomas: results from the German HIT-REZ studies [J].
Adolph, Jonas E. ;
Fleischhack, Gudrun ;
Gaab, Christine ;
Mikasch, Ruth ;
Mynarek, Martin ;
Rutkowski, Stefan ;
Schueller, Ulrich ;
Pfister, Stefan M. ;
Pajtler, Kristian W. ;
Milde, Till ;
Witt, Olaf ;
Bison, Brigitte ;
Warmuth-Metz, Monika ;
Kortmann, Rolf-Dieter ;
Dietzsch, Stefan ;
Pietsch, Torsten ;
Timmermann, Beate ;
Tippelt, Stephan .
JOURNAL OF NEURO-ONCOLOGY, 2021, 155 (02) :193-202
[4]   Breast Cancer Resistance Protein and P-Glycoprotein in Brain Cancer: Two Gatekeepers Team Up [J].
Agarwal, Sagar ;
Hartz, Anika M. S. ;
Elmquist, William F. ;
Bauer, Bjoern .
CURRENT PHARMACEUTICAL DESIGN, 2011, 17 (26) :2793-2802
[5]  
Aguilera Dolly G, 2013, J Pediatr Hematol Oncol, V35, pe42, DOI 10.1097/MPH.0b013e318279aed8
[6]   PROGNOSTIC FACTORS IN PEDIATRIC BRAIN-STEM GLIOMAS [J].
ALBRIGHT, AL ;
GUTHKELCH, AN ;
PACKER, RJ ;
PRICE, RA ;
ROURKE, LB .
JOURNAL OF NEUROSURGERY, 1986, 65 (06) :751-755
[7]   Predictors of Survival among Pediatric and Adult Ependymoma Cases: A Study Using Surveillance, Epidemiology, and End Results Data from 1973 to 2007 [J].
Amirian, E. Susan ;
Armstrong, Terri S. ;
Aldape, Kenneth D. ;
Gilbert, Mark R. ;
Scheurer, Michael E. .
NEUROEPIDEMIOLOGY, 2012, 39 (02) :116-124
[8]   Re-programing Chromatin with a Bifunctional LSD1/HDAC Inhibitor Induces Therapeutic Differentiation in DIPG [J].
Anastas, Jamie N. ;
Zee, Barry M. ;
Kalin, Jay H. ;
Kim, Mirhee ;
Guo, Robyn ;
Alexandrescu, Sanda ;
Blanco, Mario Andres ;
Giera, Stefanie ;
Gillespie, Shawn M. ;
Das, Jayanta ;
Wu, Muzhou ;
Nocco, Sarah ;
Bonal, Dennis M. ;
Quang-De Nguyen ;
Suva, Mario L. ;
Bernstein, Bradley E. ;
Alani, Rhoda ;
Golub, Todd R. ;
Cole, Philip A. ;
Filbin, Mariella G. ;
Shi, Yang .
CANCER CELL, 2019, 36 (05) :528-+
[9]   Neurological complications of pediatric cancer [J].
Armstrong, Caren ;
Sun, Lisa R. .
CANCER AND METASTASIS REVIEWS, 2020, 39 (01) :3-23
[10]   Pericytes: Developmental, Physiological, and Pathological Perspectives, Problems, and Promises [J].
Armulik, Annika ;
Genove, Guillem ;
Betsholtz, Christer .
DEVELOPMENTAL CELL, 2011, 21 (02) :193-215