Establishing a Pediatric Hematology-Oncology Program in Botswana

Jeremy S Slone1, Amanda K Slone1, Oaitse Wally1

  • 1Jeremy S. Slone, Amanda K. Slone, Kamusisi Chinyundo, Judith Margolin, Alan R. Anderson, Michael E. Scheurer, and Parth S. Mehta, Texas Children's Cancer and Hematology Centers; Jeremy S. Slone, Amanda K. Slone, Susan Alisanski, Lisa M. Force, Kamusisi Chinyundo, Judith Margolin, Anurag K. Agrawal, Alan R. Anderson, Michael E. Scheurer, and Parth S. Mehta, Baylor College of Medicine, Houston, TX; Oaitse Wally, University of Botswana; Oaitse Wally, Pearl Semetsa, and Mpho Raletshegwana, Princess Marina Hospital, Gaborone, Botswana; and Anurag K. Agrawal, Children's Hospital and Research Center, Oakland, CA.

Journal of Global Oncology
|September 23, 2018
PubMed

Insights

Pediatric cancer survival in Botswana reached 52.4% over two years, demonstrating successful diagnosis and treatment for childhood cancers through a collaborative program. This highlights progress in managing pediatric malignancies in low-resource settings.

Area of Science:

  • Pediatric Oncology
  • Global Health
  • Cancer Epidemiology

Background:

  • 300,000 children diagnosed with cancer annually, predominantly in low- and middle-income countries (LMICs).
  • Limited data exists on pediatric cancer incidence, diagnosis, and outcomes in Africa.
  • A pediatric hematology-oncology program established in Botswana in 2007 through international partnership.

Purpose of the Study:

  • To assess patient characteristics and treatment outcomes at Botswana's sole pediatric cancer program.
  • To establish a hospital-based database, the Botswana Pediatric Oncology Database, for comprehensive data collection.
  • To analyze data from children diagnosed between 2008 and 2015.

Main Methods:

  • Utilized the Botswana Pediatric Oncology Database, established in 2014.
  • Included children under 18 diagnosed between 2008 and 2015.
  • Extracted data in February 2016 for 185 eligible children (77% of potential enrollees).

Main Results:

  • Leukemia was the most frequent malignancy (18.9%); 88.1% had histopathologic diagnosis.
  • HIV seropositivity was present in 13.5% of the pediatric cancer cohort.
  • The 2-year overall survival rate for all pediatric cancers was 52.4%; treatment abandonment was 3.8%.

Conclusions:

  • A Botswana-based pediatric cancer program, supported by international partnerships, has successfully provided care for children with cancer and blood disorders.
  • Outcomes demonstrate that children with cancer in Botswana can be effectively diagnosed and treated.
  • Continued improvements are necessary, but current results show significant progress in pediatric oncology care in LMICs.
Abstract

Related Concept Videos

Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
264
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
311
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
233
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
301
Clinically Relevant Drug Product Specifications: Methods of Establishment01:29

Clinically Relevant Drug Product Specifications: Methods of Establishment

Product specifications define the acceptable quality of a pharmaceutical product by ensuring identity, purity, potency, and strength. These specifications serve as benchmarks during development, manufacturing, and post-approval quality control. Clinically relevant specifications are particularly important because they directly relate to a drug's safety and efficacy in clinical use.Dissolution studies are critical biopharmaceutic tools that link in vitro behavior to in vivo performance. They...
220
The Nernst Equation02:59

The Nernst Equation

Nonstandard Reaction Conditions
The interconnection between standard cell potentials and various thermodynamic parameters such as the standard free energy change ΔG° and equilibrium constant K has been previously explored. For example, a redox reaction involving zinc(II) and tin(II) ions at 1 M concentration with Eºcell = +0.291 V and ΔG° = −56.2 kJ is spontaneous.
47.0K