Adiposity may predict survival in patients with advanced stage cancer treated with immunotherapy in phase 1 clinical trials.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 02 2020
Historique:
received: 28 05 2019
revised: 27 07 2019
accepted: 14 08 2019
pubmed: 28 10 2019
medline: 13 8 2020
entrez: 25 10 2019
Statut: ppublish

Résumé

Body mass index (BMI) is used to define obesity, but it is an imperfect measure of body composition. In the current study, the authors explored the association between types of fat and survival in patients treated with immunotherapy. A retrospective analysis of 90 patients who were treated with immunotherapy on phase 1 clinical trials at the Winship Cancer Institute in Atlanta, Georgia, from 2009 through 2017 was performed. Overall survival (OS) and progression-free survival (PFS) were used to measure clinical outcomes. Baseline BMI and radiographic images at the middle of the third lumbar vertebrae were obtained. Fat densities were calculated and converted to indices (subcutaneous fat index [SFI], intermuscular fat index [IFI], and visceral fat index [VFI]) after dividing by height in meters squared. Risk groups were created using recursive partitioning and the regression trees method for SFI and IFI, which were selected by stepwise variable selection among all fat-related variables. The Cox proportional hazards model and Kaplan-Meier method were used for the association with OS and PFS. The majority of patients (59%) were male and diagnosed with melanoma (33%) or gastrointestinal cancers (22%). The median BMI was 27.4 kg/m Increased BMI, increased SFI, and decreased IFI may be associated with prolonged survival in patients with cancer who are treated with immunotherapy. Further studies are needed to elucidate the effect of adiposity on the host immune response to immunotherapy.

Sections du résumé

BACKGROUND
Body mass index (BMI) is used to define obesity, but it is an imperfect measure of body composition. In the current study, the authors explored the association between types of fat and survival in patients treated with immunotherapy.
METHODS
A retrospective analysis of 90 patients who were treated with immunotherapy on phase 1 clinical trials at the Winship Cancer Institute in Atlanta, Georgia, from 2009 through 2017 was performed. Overall survival (OS) and progression-free survival (PFS) were used to measure clinical outcomes. Baseline BMI and radiographic images at the middle of the third lumbar vertebrae were obtained. Fat densities were calculated and converted to indices (subcutaneous fat index [SFI], intermuscular fat index [IFI], and visceral fat index [VFI]) after dividing by height in meters squared. Risk groups were created using recursive partitioning and the regression trees method for SFI and IFI, which were selected by stepwise variable selection among all fat-related variables. The Cox proportional hazards model and Kaplan-Meier method were used for the association with OS and PFS.
RESULTS
The majority of patients (59%) were male and diagnosed with melanoma (33%) or gastrointestinal cancers (22%). The median BMI was 27.4 kg/m
CONCLUSIONS
Increased BMI, increased SFI, and decreased IFI may be associated with prolonged survival in patients with cancer who are treated with immunotherapy. Further studies are needed to elucidate the effect of adiposity on the host immune response to immunotherapy.

Identifiants

pubmed: 31648379
doi: 10.1002/cncr.32576
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

575-582

Subventions

Organisme : NCI NIH HHS
ID : P30 CA138292
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2019 American Cancer Society.

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Auteurs

Dylan J Martini (DJ)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Meredith R Kline (MR)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Yuan Liu (Y)

Department of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia.

Julie M Shabto (JM)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Milton A Williams (MA)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Amir Ishaq Khan (AI)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Colleen Lewis (C)

Winship Cancer Institute of Emory University, Atlanta, Georgia.

Hannah Collins (H)

Winship Cancer Institute of Emory University, Atlanta, Georgia.

Mehmet Akce (M)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Haydn T Kissick (HT)

Winship Cancer Institute of Emory University, Atlanta, Georgia.
Department of Urology, Emory University School of Medicine, Atlanta, Georgia.

Bradley C Carthon (BC)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Walid L Shaib (WL)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Olatunji B Alese (OB)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Rathi N Pillai (RN)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Conor E Steuer (CE)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Christina S Wu (CS)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

David H Lawson (DH)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Ragini R Kudchadkar (RR)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Bassel F El-Rayes (BF)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Suresh S Ramalingam (SS)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Taofeek K Owonikoko (TK)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

R Donald Harvey (RD)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.
Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia.

Viraj A Master (VA)

Department of Urology, Emory University School of Medicine, Atlanta, Georgia.

Mehmet Asim Bilen (MA)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

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