Integrated analysis of long-term growth and bone development in pediatric and adolescent patients receiving bevacizumab.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
02 2019
Historique:
received: 27 06 2018
revised: 13 08 2018
accepted: 09 09 2018
pubmed: 1 11 2018
medline: 7 11 2019
entrez: 1 11 2018
Statut: ppublish

Résumé

We conducted an integrated analysis of clinical data to describe long-term effects of bevacizumab on growth and bone development in pediatric and adolescent patients with solid tumors. Clinical data were pooled from five phase I/II trials of bevacizumab versus chemotherapy: BERNIE, HERBY, and AVF4117s enrolled newly diagnosed patients, AVF3842s and AVF2771s enrolled patients with relapsed/refractory disease. Height, weight, body mass index (BMI), and bone-age data were pooled by treatment group. Growth charts were used to track and monitor growth in relation to a reference population of healthy children. Bone age was measured based on X-ray of the left hand and wrist. Analyses were exploratory/descriptive. Overall, 268 patients received bevacizumab ± chemotherapy and 135 received chemotherapy alone. Baseline characteristics were generally balanced. Median duration of long-term follow-up was 41.8 months (range, 2.4-75.1) with bevacizumab and 22.9 months (range, 2.8-69.2) with chemotherapy alone. Patients had age-appropriate baseline height and weight. Mean height and weight percentiles decreased over time in both treatment groups, but remained within the normal range (height: mean standard deviation score [SDS] range -2 to +3; weight: mean SDS range -2 to +1). Similar trends were seen in BMI. A tendency for reduced growth velocity relative to the reference population was observed at 6 months and 1 year in both groups, but there was no additional decrease for patients receiving bevacizumab. Bevacizumab did not appear to have additional negative effects on growth or development of pediatric and adolescent patients with solid tumors.

Sections du résumé

BACKGROUND
We conducted an integrated analysis of clinical data to describe long-term effects of bevacizumab on growth and bone development in pediatric and adolescent patients with solid tumors.
PROCEDURE
Clinical data were pooled from five phase I/II trials of bevacizumab versus chemotherapy: BERNIE, HERBY, and AVF4117s enrolled newly diagnosed patients, AVF3842s and AVF2771s enrolled patients with relapsed/refractory disease. Height, weight, body mass index (BMI), and bone-age data were pooled by treatment group. Growth charts were used to track and monitor growth in relation to a reference population of healthy children. Bone age was measured based on X-ray of the left hand and wrist. Analyses were exploratory/descriptive.
RESULTS
Overall, 268 patients received bevacizumab ± chemotherapy and 135 received chemotherapy alone. Baseline characteristics were generally balanced. Median duration of long-term follow-up was 41.8 months (range, 2.4-75.1) with bevacizumab and 22.9 months (range, 2.8-69.2) with chemotherapy alone. Patients had age-appropriate baseline height and weight. Mean height and weight percentiles decreased over time in both treatment groups, but remained within the normal range (height: mean standard deviation score [SDS] range -2 to +3; weight: mean SDS range -2 to +1). Similar trends were seen in BMI. A tendency for reduced growth velocity relative to the reference population was observed at 6 months and 1 year in both groups, but there was no additional decrease for patients receiving bevacizumab.
CONCLUSION
Bevacizumab did not appear to have additional negative effects on growth or development of pediatric and adolescent patients with solid tumors.

Identifiants

pubmed: 30378286
doi: 10.1002/pbc.27487
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Bevacizumab 2S9ZZM9Q9V

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e27487

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Hermann L Müller (HL)

Department of Pediatrics and Pediatric Hematology and Oncology, Klinikum Oldenburg AöR, Medical Campus University Oldenburg, Oldenburg, Germany.

Johannes H M Merks (JHM)

Department of Pediatric Oncology, Emma Children's Hospital-Academic Medical Center (EKZ-AMC), Amsterdam, The Netherlands.

Birgit Geoerger (B)

Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, Villejuif, France.

Jacques Grill (J)

Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, Villejuif, France.

Darren Hargrave (D)

Paediatric Oncology Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.

Julia Glade Bender (J)

Division of Pediatric Hematology, Oncology, and Stem Cell Transplant, Columbia University Medical Centre, New York.

Sridharan Gururangan (S)

Department of Neurosurgery, Preston A. Wells Jr. Center for Brain Tumor Therapy, McKnight Brain Institute, University of Florida, Florida.

Fariba Navid (F)

Department of Pediatrics, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, California.

Michael Johnston (M)

Safety Science Lead, Genentech, Inc., 1 DNA Way, South San Francisco, California, 94080, USA.

Jeanette Bachir (J)

Pediatric Oncology, F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, Basel, 4070, Switzerland.

Markus C Elze (MC)

Biostatistics, F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, Basel, 4070, Switzerland.

Sabine Fürst-Recktenwald (S)

Pediatric Oncology, F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, Basel, 4070, Switzerland.

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Classifications MeSH