A Bibliometric Analysis of Drug Resistance in Pediatric Acute Lymphoblastic Leukemia

Alireza Khanahmad1,2, Mohammad Hossein Khazaee-Nasirabadi3, Mahshid Lotfi4

  • 1Student Research Committee, Afzalipour Faculty of Medicine, Kerman University of Medical Sciences, Kerman, Iran.

PubMed

Insights

Drug resistance in pediatric acute lymphoblastic leukemia (ALL) is a significant challenge. This bibliometric analysis maps global research trends, identifying key biological mechanisms and therapeutic agents for future study.

Area of Science:

  • Hematology
  • Oncology
  • Pediatric Medicine

Background:

  • Drug resistance remains a critical obstacle in treating acute lymphoblastic leukemia (ALL), despite therapeutic advancements.
  • Pediatric ALL presents unique challenges in overcoming treatment resistance.
  • Understanding global research trends is crucial for addressing pediatric ALL drug resistance.

Purpose of the Study:

  • To provide a comprehensive bibliometric overview of global research on drug resistance in pediatric ALL.
  • To identify emerging research directions and key contributors in the field.
  • To highlight significant biological mechanisms and therapeutic agents related to pediatric ALL drug resistance.

Main Methods:

  • Bibliometric analysis of papers from the Web of Science Core Collection.
  • Keywords such as 'acute lymphoblastic leukemia,' 'pediatric,' and 'drug resistance' were utilized.
  • Data visualization and analysis were performed using Biblioshiny and VOSviewer.

Main Results:

  • Analysis of 432 original and 94 review articles from 48 countries.
  • The United States led in publications (148 articles) and citations (9569).
  • Key research themes included altered glucocorticoid response, P-gp overexpression, microRNA roles, and specific agents like clofarabine and nelarabine.

Conclusions:

  • Research on pediatric ALL drug resistance is multifaceted, attracting significant global attention.
  • This bibliometric analysis maps the current research landscape and identifies critical areas for future investigation.
  • Further research is needed on the clinical applications and resistance mechanisms of agents like clofarabine, nelarabine, daunorubicin, vincristine, and microRNA.
Abstract

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