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S481

ESTRO 36 2017

_______________________________________________________________________________________________

Conclusion

The availability of MRI images during target delineation of

pancreatic cancer on 3DCT and 4DCT improved the

interobserver variation. Furthermore, delineated volumes

are smaller on CT+MRI than on CT only. An approach of

3DCT GTV delineation with margins may be preferable to

4DCT iGTV delineation since the latter increases

uncertainty.

Poster: Physics track: (Quantitative) functional and

biological imaging

PO-0885 Assess Tumor Voxel Dose Response (SF2) Using

Multiple FDG PET Images

D. Yan

1

, S. Chen

2

, D. Krauss

2

, P. Chen

2

, G. Wilson

2

1

Beaumont Health System, Radiation Oncology, Royal

Oak MI, USA

2

Beaumont Health system, Radiation Oncology, Royal

Oak- MI, USA

Purpose or Objective

To determine human tumor voxel dose response with using

bio-marker (SF2) derived from multiple FDG PET images

and evaluate the pattern of tumor local radioresistance

and failure.

Material and Methods

Multiple FDG PET/CT images obtained at the pre- and

weekly during the treatment (35x2Gy) for 15 HN cancer

patients were used for the study. from 0 to 70Gy, for each

tumor voxel, v, such that TMR(v, d) = SUV(v, d)/SUV(v, 0).

TMR of each patient was constructed following voxel-by-

voxel deformable PET/CT image registration. Assuming

ln(TMR(v, d)) = k

.

ln(SF(v, d)), the optimal linear

regression with unknown break-points was used to

determine the tumor voxel survival fraction, SF at

different treatment dose levels. Therefore, SF2(v, d), the

tumor voxel survival fraction after 2Gy, was obtained and

used as the tumor voxel dose response marker. Tumor

voxel SF2 distribution at different treatment dose level

was analyzed to evaluate the pattern of tumor voxel dose

response, specifically the tumor local radioresistant

pattern; meanwhile the effects of tumor voxel

reoxygennation and proliferation with respect to tumor

local failure were also evaluated. The tumor volumes with

different SF2 cutoffs were also correlated to treatment

outcome.

Results

Human tumor has significant inter- and intra-tumor

variations in their voxel dose response (Table). Tumor

voxels with the mean SF2 > 0.7 shows significant

prediction power (p < 0.01) after the treatment dose of

20~40Gy on tumor local failure. Tumor local recurrence

showed strong correlation to the tumor local

radioresistance determined using SF2 (Figure). Two of 3

failures showed a clear reoxygennation effect after 20Gy,

therefore could be potentially controlled by escalating

dose to destroy the local radioresistant niches. One failure

had a small (< 1cc) local radioresistant sub-volume and

showed the minimal reoxygennation, therefore it may

need a local ablation.

Conclusion

Tumor voxel metabolic ratio determined us ing multiple

FDG PET images can be used to assess tumor voxel dose

response, SF2, which shows an excellent predictive value

for tumor local radioresistance and failure. Our results

demonstrate that a heterogeneous dose distribution in

tumor should be prescribed to optimize cancer

radiotherapy. Tumor voxel TMR determined at the early

treatment will be good bio-parametric matrix to

determine a new tumor dose prescription function at the

voxel level for the treatment of adaptive dose-painting-

by-number.

PO-0886 Early changes of FDG-PET markers predict the

outcome after chemo-radiotherapy for pancreatic

cancer

S. Broggi

1

, P. Passoni

2

, E.G. Vanoli

3

, C. Fiorino

1

, G.M.

Cattaneo

1

, C. Gumina

2

, P. Mapelli

3

, E. Incerti

3

, L.

Gianolli

3

, N. Slim

2

, M. Picchio

3

, R. Calandrino

1

, N.G. Di

Muzio

2