TY - JOUR
T1 - c-Met PET Imaging Detects Early-Stage Locoregional Recurrence of Basal-Like Breast Cancer
AU - Arulappu, Appitha
AU - Battle, Mark
AU - Eisenblaetter, Michel
AU - McRobbie, Graeme
AU - Khan, Imtiaz
AU - Monypenny, James
AU - Weitsman, Gregory
AU - Galazi, Myria
AU - Hoppmann, Susan
AU - Gazinska, Patrycja
AU - Wulaningsih, Wulan
AU - Dalsgaard, Grethe Tang
AU - Macholl, Sven
AU - Ng, Tony
N1 - © 2016 by the Society of Nuclear Medicine and Molecular Imaging, Inc.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Locoregional recurrence of breast cancer poses significant clinical
problems because of frequent inoperability once the chest
wall is involved. Early detection of recurrence by
molecular imaging agents against therapeutically targetable receptors,
such as c-Met, would be of potential benefit. The
aim of this study was to assess 18F-AH113804, a peptide-based
molecular imaging agent with high affinity for human c-Met, for the
detection of early-stage locoregional
recurrence in a human basal-like breast cancer
model, HCC1954. Methods: HCC1954 tumor–bearing xenograft models were established, and 18F-AH113804
was administered. Distribution of radioactivity was determined via PET
at 60 min after radiotracer injection. PET
and CT images were acquired 10 d after tumor
inoculation, to establish baseline distribution and uptake, and then on
selected
days after surgical tumor resection. CT images and
caliper were used to determine the tumor volume. Radiotracer uptake was
assessed by 18F-AH113804 PET imaging. c-Met expression was assessed by immunofluorescence imaging of tumor samples and correlated with 18F-AH113804 PET imaging results. Results: Baseline uptake of 18F-AH113804,
determined in tumor-bearing animals after 10 d, was approximately
2-fold higher in the tumor than in muscle tissue
or the contralateral mammary fat pad. The tumor
growth rate, determined from CT images, was comparable between the
animals
with recurrent tumors, with detection of tumors of
low volume (<10 mm3) only possible by day 20 after tumor resection. 18F-AH113804
PET detected local tumor recurrence as early as 6 d after surgery in
the recurrent tumor–bearing animals and exhibited
significantly higher 18F-AH113804 uptake (in comparison to mammary fatty tissue), with a target-to-background (muscle) ratio of approximately 3:1
(P < 0.01). The c-Met expression of individual resected tumor samples, determined by immunofluorescence, correlated with the
respective 18F-AH113804 imaging signals (r = 0.82, P < 0.05). Conclusion: 18F-AH113804 PET provides a new diagnostic tool for the detection of c-Met–expressing primary tumor and has potential utility
for the detection of locoregional recurrence from an early stage.
AB - Locoregional recurrence of breast cancer poses significant clinical
problems because of frequent inoperability once the chest
wall is involved. Early detection of recurrence by
molecular imaging agents against therapeutically targetable receptors,
such as c-Met, would be of potential benefit. The
aim of this study was to assess 18F-AH113804, a peptide-based
molecular imaging agent with high affinity for human c-Met, for the
detection of early-stage locoregional
recurrence in a human basal-like breast cancer
model, HCC1954. Methods: HCC1954 tumor–bearing xenograft models were established, and 18F-AH113804
was administered. Distribution of radioactivity was determined via PET
at 60 min after radiotracer injection. PET
and CT images were acquired 10 d after tumor
inoculation, to establish baseline distribution and uptake, and then on
selected
days after surgical tumor resection. CT images and
caliper were used to determine the tumor volume. Radiotracer uptake was
assessed by 18F-AH113804 PET imaging. c-Met expression was assessed by immunofluorescence imaging of tumor samples and correlated with 18F-AH113804 PET imaging results. Results: Baseline uptake of 18F-AH113804,
determined in tumor-bearing animals after 10 d, was approximately
2-fold higher in the tumor than in muscle tissue
or the contralateral mammary fat pad. The tumor
growth rate, determined from CT images, was comparable between the
animals
with recurrent tumors, with detection of tumors of
low volume (<10 mm3) only possible by day 20 after tumor resection. 18F-AH113804
PET detected local tumor recurrence as early as 6 d after surgery in
the recurrent tumor–bearing animals and exhibited
significantly higher 18F-AH113804 uptake (in comparison to mammary fatty tissue), with a target-to-background (muscle) ratio of approximately 3:1
(P < 0.01). The c-Met expression of individual resected tumor samples, determined by immunofluorescence, correlated with the
respective 18F-AH113804 imaging signals (r = 0.82, P < 0.05). Conclusion: 18F-AH113804 PET provides a new diagnostic tool for the detection of c-Met–expressing primary tumor and has potential utility
for the detection of locoregional recurrence from an early stage.
UR - http://www.ncbi.nlm.nih.gov/pubmed/26635342
U2 - 10.2967/jnumed.115.164384
DO - 10.2967/jnumed.115.164384
M3 - Article
C2 - 26635342
SN - 1535-5667
VL - 57
SP - 765
EP - 770
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 5
ER -