TY - JOUR
T1 - The Influence of Obesity on Outcomes with Immune Checkpoint Blockade
T2 - Clinical Evidence and Potential Biological Mechanisms
AU - Hahn, Andrew W.
AU - Venkatesh, Neha
AU - Msaouel, Pavlos
AU - McQuade, Jennifer L.
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/11
Y1 - 2023/11
N2 - Immune checkpoint blockade (ICB) is a mainstay of treatment for advanced cancer, yet tumor response and host toxicity are heterogenous in those patients who receive ICB. There is growing interest in understanding how host factors interact with tumor intrinsic properties and the tumor microenvironment to influence the therapeutic index with ICB. Obesity, defined by body mass index, is a host factor associated with improved outcomes in select cancers when treated with ICB. While the biological mechanism for this obesity paradox is not fully understood, pre-clinical and translational studies suggest obesity may potentially impact tumor metabolism, inflammation, and angiogenesis. Herein, we summarize clinical studies that support an obesity paradox with ICB, explore potential biological mechanisms that may account for the obesity paradox, and address methodological challenges to consider when studying obesity and treatment outcomes.
AB - Immune checkpoint blockade (ICB) is a mainstay of treatment for advanced cancer, yet tumor response and host toxicity are heterogenous in those patients who receive ICB. There is growing interest in understanding how host factors interact with tumor intrinsic properties and the tumor microenvironment to influence the therapeutic index with ICB. Obesity, defined by body mass index, is a host factor associated with improved outcomes in select cancers when treated with ICB. While the biological mechanism for this obesity paradox is not fully understood, pre-clinical and translational studies suggest obesity may potentially impact tumor metabolism, inflammation, and angiogenesis. Herein, we summarize clinical studies that support an obesity paradox with ICB, explore potential biological mechanisms that may account for the obesity paradox, and address methodological challenges to consider when studying obesity and treatment outcomes.
KW - body composition
KW - immunotherapy
KW - melanoma
KW - obesity
KW - renal cell carcinoma
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U2 - 10.3390/cells12212551
DO - 10.3390/cells12212551
M3 - Review article
C2 - 37947629
AN - SCOPUS:85176403476
SN - 2073-4409
VL - 12
JO - Cells
JF - Cells
IS - 21
M1 - 2551
ER -