Caloric and nutrient restriction to augment chemotherapy efficacy for acute lymphoblastic leukemia: the IDEAL trial

Author:

Orgel Etan1ORCID,Framson Celia2,Buxton Rubi3ORCID,Kim Jiyoon4,Li Gang4,Tucci Jonathan5ORCID,Freyer David R.1ORCID,Sun Weili6,Oberley Matthew J.7ORCID,Dieli-Conwright Christina8,Mittelman Steven D.5ORCID

Affiliation:

1. Cancer and Blood Disease Institute,

2. Department of Clinical Nutrition, and

3. Division of Pediatric Rehabilitation Medicine, Children’s Hospital Los Angeles, Los Angeles, CA;

4. Department of Biostatistics and Computational Medicine, Jonathan and Karin Fielding School of Public Health, and

5. Division of Pediatric Endocrinology, UCLA Children’s Discovery and Innovation Institute, David Geffen School of Medicine, University of California Los Angeles (UCLA), Los Angeles, CA;

6. Pediatric Hematology Oncology, Department of Pediatrics, City of Hope National Medical Center, Duarte, CA;

7. Department of Pathology and Laboratory Medicine, Children’s Hospital Los Angeles, Los Angeles, CA; and

8. Division of Population Sciences, Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA

Abstract

Abstract Being overweight or obese (OW/OB) during B-cell acute lymphoblastic leukemia (B-ALL) induction is associated with chemoresistance as quantified by minimal residual disease (MRD). We hypothesized that caloric and nutrient restriction from diet/exercise could lessen gains in fat mass (FM) and reduce postinduction MRD. The Improving Diet and Exercise in ALL (IDEAL) trial enrolled patients 10 to 21 years old, newly diagnosed with B-ALL (n = 40), in comparison with a recent historical control (n = 80). Designed to achieve caloric deficits ≥20% during induction, reduce fat intake/glycemic load, and increase activity, IDEAL’s end points were FM gain (primary), MRD ≥0.01%, and adherence/feasibility. Integrated biology explored biomarkers of OW/OB physiology. IDEAL intervention did not significantly reduce median FM change from baseline overall (+5.1% [interquartile range [IQR], 15.8] vs +10.7% [IQR, 16.0]; P = .13), but stratified analysis showed benefit in those OW/OB (+1.5% [IQR, 6.6] vs +9.7% [IQR, 11.1]; P = .02). After accounting for prognostic factors, IDEAL intervention significantly reduced MRD risk (odds ratio, 0.30; 95% confidence interval, 0.09-0.92; P = .02). The trial exceeded its adherence (≥75% of overall diet) and feasibility (≥80% completed visits) thresholds. Integrated biology found the IDEAL intervention increased circulating adiponectin and reduced insulin resistance. The IDEAL intervention was feasible, decreased fat gain in those OW/OB, and reduced MRD. This is the first study in any hematologic malignancy to demonstrate potential benefit from caloric restriction via diet/exercise to augment chemotherapy efficacy and improve disease response. A prospective, randomized trial is warranted for validation. These trials were registered at www.clinicaltrials.gov as #NCT02708108 (IDEAL trial) and #NCT01317940 (historical control).

Publisher

American Society of Hematology

Subject

Hematology

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