Effect of BMI on toxicities and survival among adolescents and young adults treated on DFCI Consortium ALL trials

Author:

Shimony Shai12ORCID,Flamand Yael3ORCID,Valtis Yannis K.4,Place Andrew E.5ORCID,Silverman Lewis B.5,Vrooman Lynda M.5,Brunner Andrew M.6,Sallan Stephen E.5,Stone Richard M.1,Wadleigh Martha1,Neuberg Donna S.3,DeAngelo Daniel J.1ORCID,Luskin Marlise R.1ORCID

Affiliation:

1. 1Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

2. 2Hematology Department, Rabin Medical Center and Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

3. 3Department of Data Science, Dana-Farber Cancer Institute, Boston, MA

4. 4Department of Medicine, Memorial Sloan Kettering Cancer Institute, New York, NY

5. 5Department of Pediatric Oncology, Dana-Farber Cancer Institute and Boston Children’s Hospital, Boston, MA

6. 6Leukemia Department, Hematology/Oncology, Massachusetts General Hospital, Boston, MA

Abstract

Abstract Adolescent and young adults (AYAs) with acute lymphoblastic leukemia (ALL) treated with asparaginase-containing pediatric regimens are commonly overweight or obese. We studied the association of body mass index (BMI) on outcomes of 388 AYAs aged 15 to 50 years treated on Dana-Farber Cancer Institute (DFCI) consortium regimens (2008-2021). BMI was normal in 207 (53.3%) and overweight/obese in 181 (46.7%). Patients who were overweight or obese experienced higher nonrelapse mortality (NRM; 4-year, 11.7% vs 2.8%, P = .006), worse event-free survival (4-year, 63% vs 77%, P = .003), and worse overall survival (OS; 4-year, 64% vs 83%, P = .0001). Because younger (aged 15-29 years) AYAs more frequently had a normal BMI (79% vs 20%, P < .0001), we conducted separate analyses in each BMI group. We found excellent OS among younger and older (30-50 years) AYAs with normal BMI (4-year OS, 83% vs 85%, P = .89). Conversely, in AYAs who were overweight/obese, worse outcomes were seen in older AYAs (4-year OS, 55% vs 73%, P = .023). Regarding toxicity, AYAs who were overweight/obese experienced higher rates of grade 3/4 hepatotoxicity and hyperglycemia (60.7% vs 42.2%, P = .0005, and 36.4% vs 24.4%, P = .014, respectively) but had comparable rates of hypertriglyceridemia (29.5% vs 24.4%, P = .29). In a multivariable analysis, higher BMI was associated with worse OS, hypertriglyceridemia was associated with improved OS, and age was not associated with OS. In conclusion, among AYAs treated on DFCI Consortium ALL regimens, elevated BMI was associated with increased toxicity, increased NRM, and decreased OS. The deleterious effect of elevated BMI was more pronounced in older AYAs.

Publisher

American Society of Hematology

Subject

Hematology

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