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Examining Immunotherapy Response Using Multiple Radiotracers.

Authors :
Goggi JL
Hartimath SV
Hwang Y
Tan YX
Khanapur S
Ramasamy B
Jiang L
Yong FF
Cheng P
Tan PW
Husaini MA
Yuen TY
Jieu B
Chacko AM
Larbi A
Renia L
Johannes C
Robins EG
Source :
Molecular imaging and biology [Mol Imaging Biol] 2020 Aug; Vol. 22 (4), pp. 993-1002.
Publication Year :
2020

Abstract

Purpose: Cancer immunotherapy has shown huge potential in the fight against cancer, but only a small proportion of patients respond successfully to treatment. Non-invasive methods to stratify responders from non-responders are critically important as immune therapies are often associated with immune-related side effects. Currently, conventional clinical imaging modalities do not provide a useful measure of immune therapy efficacy. Sensitive imaging biomarkers that provide information about the tumoural microenvironment may provide useful insights allowing for improved patient management.<br />Procedures: We have assessed the ability of a number of radiopharmaceuticals to non-invasively measure different aspects of the tumour microenvironment and correlated tumour uptake to immune therapy response in a syngeneic model of colon cancer, CT26-WT. Four radiopharmaceuticals, [ <superscript>18</superscript> F]FDG (a glucose analogue), [ <superscript>18</superscript> F]FEPPA (a marker for macrophage activation), [ <superscript>18</superscript> F]FB-IL2 (a marker for CD25 <superscript>+</superscript> cells) and [ <superscript>68</superscript> Ga] Ga-mNOTA-GZP (a marker for granzyme B, the serine protease downstream effector of cytotoxic T cells), were assessed as potential biomarkers to help stratify response to PD-1 monotherapy or combined anti-PD1 and CLTA4 therapy in vivo correlating tumour uptake with changes in tumour-associated immune cell populations.<br />Results: [ <superscript>18</superscript> F]FDG, [ <superscript>18</superscript> F]FEPPA and [ <superscript>18</superscript> F]FB-IL2 (a marker for CD25 <superscript>+</superscript> cells) showed limited ability to determine therapy response and showed little correlation to tumour-associated immune cell changes. However, [ <superscript>68</superscript> Ga] Ga-mNOTA-GZP showed good predictive ability and correlated well with changes in tumour-associated T cells, especially CD8 <superscript>+</superscript> T cells.<br />Conclusions: [ <superscript>68</superscript> Ga]Ga-mNOTA-GZP uptake correlates well with changes in CD8 <superscript>+</superscript> T cell populations supporting continued development of granzyme B-based imaging agents for stratification of response to immunotherapy. Early assessment of immunotherapy efficacy with [ <superscript>68</superscript> Ga]Ga-mNOTA-GZP may allow for the reduction of unnecessary side effects while significantly improving patient management.

Details

Language :
English
ISSN :
1860-2002
Volume :
22
Issue :
4
Database :
MEDLINE
Journal :
Molecular imaging and biology
Publication Type :
Academic Journal
Accession number :
32006204
Full Text :
https://doi.org/10.1007/s11307-020-01477-w