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Introdpatientclinicadoses oMethomicro-0.156xDTPA weightnormalResulton T2- summaBoth Hregion While compa(p< 0.01 and cfrom hWherelow dotreatmeDiscusperfusiconvenradiatio
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Fig. (D) thera
Detecting E
Vickie Zhangrtment of Radiologrsity of California,
duction: Radiationts suffer post-treatmal disease-free survof radiation therapods: A TRAMP moimaging spectrom
x0.312x1mm). [1-1
(Magnevist, Bayeted gradient echo slized to maximumt: Fig. 2 shows lacweighted images
ary from high (14-HP markers showe
decreased by day lac/pyr ratio from
are to day 0 (p< 0.001), and subsequencontinued to increa
high dose region sias DCE AUC from
ose regions initiallyent. ssion: These resultion in tumor exposntional 1H MR maron therapy.
ence: 1. Martinez Aeal, 2011, p3161. owledgments: Thi
2: Lac/pyr (A), urimages from day 0apy
Early Tumor R
g1,2, Robert Bok1, gy and Biomedica, San Francisco -
n therapy remains oment cancer recurr
vival for locally adpy in TRAMP tumoouse tumor (size =
meter (Varian Inc.).3C]pyruvate and 1
er HealthCare), dynsequence (TE/TR=
m HP urea in the kid/pyr ratio, urea, arat baseline, 1, 4, a-8Gy) and low dosd significant dose 1 after treatment alow dose region in
01). HP urea from ntly returned to baase (p< 0.01). AUCgnificantly decream low dose region y decreased and re
ts suggest HP biomsed to varying radirkers. Ongoing stu
AA, et. al. Int. J. R 3. Sukumar S et. s project was fund
rea (B), DCE AUC0, 1, 4, and 8 days
Response of P
Subramaniam Sukl Imaging, UniversUniversity of Calif
S
one of the most corence. Clinical dos
dvanced prostate caors using multi-pa
= 3.5cc) was expos Diffusion weight3C Urea were hypenamic contrast enh
=1.11/39ms, 0.312dney. rea under curve (And 8 days after rade (8-4 Gy) regionsdependent change
and continued to dnitially increased bthe high dose regiseline level. HP urC calculated from se on day 1 after trcontinuously incr
eturned to baseline
markers are sensitiiation dose levels. udies are investigat
Radiation Oncologal. Proceedings of
ded by the grant RO
C (C) and ADC after radiation
Prostate CanceHyperpolari
kumar1, Adam Cunsity of California, fornia, Berkeley, BSan Francisco, San
ommon definite trese-escalation trialsancer patients [1]. arametric 14T 1H &sed to varying doseed imaging (DWI)erpolarized and 3Dhancement imaginx0.312x1mm). Th
AUC) calculated frodiation therapy. Fis of tumor at 1 to 8es over time (p< 0.decrease on day 4 &by day 1, and subsion showed signifirea from low dose 1H DCE showed sreatment and retur
reased over time (pe level and higher b
ive to the early chaHP 13C biomarkerting the ability of
gy Biol. 2011;79(2f the 19th Annual MO1EB007588
Fig 3: % chadays after treSignificantlydose regions
er to Radiatioized 13C MR Inha3, I-C. Hsu3, JeaSan Francisco, Sa
Berkeley, CA, Unitn Francisco, CA, U
eatments for prostas reported that highThe purpose of th
& hyperpolarized (es of radiation as s) data were acquireD imaging data weng (DCE) was acquhe signal intensity o
om DCE and ADCg. 3 provides a qu8 days after treatm01). Lac/pyr ratio & 8 (p< 0.01 comsequently decreaseicant decrease 1 dalevel significantly
similar result as Hrned to baseline levp< 0.01), ADC froby day 8 following
anges in metabolisrs correlated with multi-parametric 1
2):363-370 2. ZhanMeeting of ISMRM
ange from baselineeatment in tumor ry different from ba.
on Therapy usImaging an Pouliot2,3, Danian Francisco, CA, ted States, 3DepartUnited States
ate cancer, but desher radiation doses
his study was to inv(HP) 13C MR imagshown in Fig. 1 [2ed using a spin-echere acquired as desuired using a T1-of HP urea was
C images overlaid uantitative ment.
from high dose mpare to day 0). ed by day 4 & 8 ay after therapy y increased on day
HP urea. DCE AUCevel over time. om both high and g
sm and
1H and HP 13C MR
ng VY et. al. ProcM, Montreal, 2011
Figaxi
e of lac/pyr (A), urregions receiving haseline level. +: Sig
ing Multi-Par
iel B. Vigneron1,2, United States, 2Gtment of Radiation
spite excellent succs significantly impvestigate early resging. 2]. Imaging studiesho pulse sequencescribed previously
y C
R in planning and m
ceedings of the 19t
1, p3531
g. 1: Dose distribual image of TRAM
rea (B), ADC (C) &high (red) and lowgnificantly differe
rametric 14T 1
and John KurhaneGraduate Program n Oncology, Unive
cess rates, a signifprove biochemical ponse to the impac
s were performed oe (TE/TR=20ms/1.y [2,3]. Following i
monitoring of pros
th Annual Meeting
ution diagram overMP mouse tumor
& DCE AUC (D) w (blue) dose radiatent between high an
1H and
ewicz1,2 in Bioengineering
ersity of California
ficant number of control and
ct of increasing
on a 14T, 600WB .2s, injection of Gd-
state cancer
of ISMRM,
rlaid on the MR
from 1-8 tion. *: nd lose
g, a,
4319Proc. Intl. Soc. Mag. Reson. Med. 20 (2012)