Development of an Adapted Resource and Implementation Application (ARIA) global guideline for the treatment of children with acute lymphoblastic leukemia

J Jessica Boklan (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) G Gita Naidu (3Chris Hani Baragwanath Academic Hospital, Division of Paediatric Oncology, Department of Paediatrics and Child Health, Johannesburg, South Africa) C Caitlyn Duffy (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) H Hannah E. Sauer (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) J Jeffrey Jacobsen (5Institute for Clinical and Experimental Pathology, ARUP Laboratories, Salt Lake City, United States) S Sarah Elitzur (20Schneider Children's Medical Center, Tel Aviv, Israel) S Shawn Lee (3National University of Singapore, Singapore, Singapore) L Liezl du Plessis (10University of the Free State, Department of Pediatric & Child Health, Bloemfontein, South Africa) M Maria Beatriz Gepte (11Philippine Children's Medical Center, Cancer and Hematology Division, Quezon City, Philippines) K Karen Marcus (16Division of Radiation Oncology, Dana-Farber/Boston Children’s Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA) N Nur Melani Sari (13Dr. Hasan Sadikin General Hospital, Department of Child Health, Bandung, Indonesia) D Diriba Hordofa (15Jimma University Medical Center, Department of Pediatric Oncology, Jimma, Ethiopia) L Loyce Hlatywayo (16Parirenyatwa Hospital, Paediatric Oncology Unit, Harare, Zimbabwe) T Trisha Soosay Raj (17Queensland Children's Hospital, Oncology Services Group, Brisbane, Australia) M Mae Concepcion J. Dolendo (18Southern Philippines Medical Center, Children's Cancer Institute, Davao City, Philippines) J Jennifer L. Pauley (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) S Simone Abib (19Pediatric Oncology Institute, GRAACC, Federal University of São Paulo, Pediatric Oncology Surgery, Sao Paulo, Brazil) A Abdelhafeez H. Abdelhafeez (20Golisano Children's Hospital, University of Rochester Medical Center, Division of Pediatric Surgery, Department of Surgery, Rochester, United States) B Bilal Mazhar Qureshi (21Aga Khan University, Radiation Oncology Section, Department of Oncology, Karachi, Pakistan) A Arturo Zapata Lopez (22Instituto Nacional de Enfermedades Neoplásicas, Pediatric Oncology Division, Lima, Peru) M Muhammad Rafie Raza H Hugo Antonio Romo (24Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Department of Pediatric Hematology and Oncology, Guadalajara, Mexico) K Katherine Brusse (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) D Dhwani Babla (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) K Kristina Iligan (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) M Monica Key (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) M Manoo Bhakta (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States) M Miguel Bonilla (1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States)

Abstract

Abstract While cure rates for acute lymphoblastic leukemia (ALL) have improved significantly over the last few decades, there remain major disparities in survival outcomes between children in high-income countries (HICs) and those in low- and middle-income countries (LMICs). Using HIC treatment protocols in LMICs without adequate resources for safe administration and supportive care often leads to excessive treatment-related morbidity, mortality, and abandonment, outweighing the anti-cancer benefit. Conversely, over adaptation of protocols to lessen toxicity may significantly reduce treatment efficacy. The Adapted Resource and Implementation Application (ARIA), is a joint initiative between the St. Jude Children's Research Hospital (SJCRH) Department of Global Medicine and the International Society of Paediatric Oncology (SIOP) in partnership with the Paediatric Radiation Oncology Society (PROS), the International Society of Paediatric Surgical Oncology (IPSO), and Childhood Cancer International (CCI), to develop trusted, safe, and effective treatment guidelines for children and adolescents with cancer in all resource settings. These evidence-based global guidelines, incorporating adaptations for local context, are freely available for healthcare providers on a web-based portal which may be used off-line for those with limited internet access. Development of an adapted management guideline (AMG) for ALL involved a rigorous process, starting with a systematic literature search of all publications between January 2000- January 2021 involving treatment of ALL in LMICs, with ongoing alerts for relevant papers subsequently published. A 24-person working group (WG) of pediatric hematologists-oncologists, radiation oncologists, pharmacists, surgeons, and a hematopathologist, from diverse geographic and income level settings was then assembled. WG members attended 27 2-hour meetings between 2023-2024, culminating in an initial guideline draft. Evidence-based recommendations were stratified based upon local resources including presence/absence of blood products, broad-spectrum antimicrobials, radiologic testing modalities, advance intensive care including ventilatory and vasopressor support, and availability of hematopoietic stem cell transplant. Guidance was developed for management of B-cell ALL and T-cell ALL, including the special categories of Philadelphia-chromosome positive ALL, Down syndrome, and infants. A risk classification algorithm was created for assigning risk group based upon whatever diagnostic tests a treating institution has available. Providers can choose between recommendations adapted from a Children's Oncology Group (COG)-backbone or a Berlin-Frankfurt-Münster (BFM)-backbone. Additional treatment modification strategies were generated to address specific chemotherapy unavailability, radiotherapy inaccessibility, malnutrition, and other local challenges. Pharmacy instructions for drug administration, toxicities, and dose adjustments were included. Additional information was provided for general issues of ALL management, important treatment-related complications, and supportive care. Following development by the WG, the AMG draft underwent additional review by a 75-member global representative panel (GRP) of disease experts from 44 countries representing each World Health Organization region and World Bank income level (11 high-income; 12 upper-middle-income; 18 lower-middle-oncome; 3 low-income). Initial feedback from GRP members yielded 603 comments for consideration A modified Delphi method consensus process was employed for issues without sufficient evidence to make solely evidence-based recommendations. For the first iterative review, 24 Delphi statements were distributed to all GRP members with 66 GRP members providing input. In the first round, 17 of 24 statements achieved ≥ 70% agreeance (defined as a score ≥ 7 on a 9-point Likert scale). Full analysis and preparation for the 2nd Delphi round is underway. Following 3 rounds of GRP iterative review, additional external expert input, and patient/family focus group feedback, the final AMG will be made available on the ARIA web-based portal. We anticipate the guideline will be an important tool, helping to maximize survival outcomes for all children with ALL, regardless of where they live.

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 7933-7933
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (28)

J

Jessica Boklan

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

G

Gita Naidu

3Chris Hani Baragwanath Academic Hospital, Division of Paediatric Oncology, Department of Paediatrics and Child Health, Johannesburg, South Africa

C

Caitlyn Duffy

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

H

Hannah E. Sauer

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

J

Jeffrey Jacobsen

5Institute for Clinical and Experimental Pathology, ARUP Laboratories, Salt Lake City, United States

S

Sarah Elitzur

20Schneider Children's Medical Center, Tel Aviv, Israel

S

Shawn Lee

3National University of Singapore, Singapore, Singapore

L

Liezl du Plessis

10University of the Free State, Department of Pediatric & Child Health, Bloemfontein, South Africa

M

Maria Beatriz Gepte

11Philippine Children's Medical Center, Cancer and Hematology Division, Quezon City, Philippines

K

Karen Marcus

16Division of Radiation Oncology, Dana-Farber/Boston Children’s Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA

N

Nur Melani Sari

13Dr. Hasan Sadikin General Hospital, Department of Child Health, Bandung, Indonesia

D

Diriba Hordofa

15Jimma University Medical Center, Department of Pediatric Oncology, Jimma, Ethiopia

L

Loyce Hlatywayo

16Parirenyatwa Hospital, Paediatric Oncology Unit, Harare, Zimbabwe

T

Trisha Soosay Raj

17Queensland Children's Hospital, Oncology Services Group, Brisbane, Australia

M

Mae Concepcion J. Dolendo

18Southern Philippines Medical Center, Children's Cancer Institute, Davao City, Philippines

J

Jennifer L. Pauley

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

S

Simone Abib

19Pediatric Oncology Institute, GRAACC, Federal University of São Paulo, Pediatric Oncology Surgery, Sao Paulo, Brazil

A

Abdelhafeez H. Abdelhafeez

20Golisano Children's Hospital, University of Rochester Medical Center, Division of Pediatric Surgery, Department of Surgery, Rochester, United States

B

Bilal Mazhar Qureshi

21Aga Khan University, Radiation Oncology Section, Department of Oncology, Karachi, Pakistan

A

Arturo Zapata Lopez

22Instituto Nacional de Enfermedades Neoplásicas, Pediatric Oncology Division, Lima, Peru

M

Muhammad Rafie Raza

H

Hugo Antonio Romo

24Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Department of Pediatric Hematology and Oncology, Guadalajara, Mexico

K

Katherine Brusse

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

D

Dhwani Babla

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

K

Kristina Iligan

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

M

Monica Key

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

M

Manoo Bhakta

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States

M

Miguel Bonilla

1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, United States