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S164

ESTRO 36 2017

_______________________________________________________________________________________________

of ROC=0.80 and not significant deviance in calibration.

Conclusion

Radiomics can be an interesting perspective for detecting

patients with CC who will show PCR and subsequently

could result in better prognosis. Even considering that CRT

followed by surgery is not a standard treatment this

workflow gave us the chance to analyze the relationship

between radiomics signature and pathological findings,

not feasible in CRT alone. An external validation of the

signature is planned to evaluate the stability of this model

by using different MR scanners at diagnosis time.

OC-0318 Hematological toxicity during bowel sparing

IMRT: Exploratory analysis from PARCER Phase III trial.

S. Lewis

1

, S. Chopra

1

, P. Naga

1

, N. Bharadwaj

1

, E.

Dandpani

1

, U. Mahantshetty

1

, R. Engineer

1

, J. Swamidas

1

,

J. Ghosh

2

, S. Gupta

2

, S. Shrivastava

1

1

Tata memorial centre, radiation oncology,

Mumbai,India

2

Tata memorial centre, medical oncology, Mumbai,India

Purpose or Objective

To report acute hematological toxicity (HT) and dose

volume correlates in patients receiving postoperative

bowel sparing intensity-modulated radiotherapy (IMRT)

and cisplatin within a Phase III trial for late bowel toxicity

reduction in patients with cervical cancer.

Material and Methods

Clinical database of Phase III trial (NCT01279135) that

randomizes patients to IMRT (Tomotherapy) and 3DCRT

was searched to select patient strata that received IMRT

(50 Gy/25#/5 wks) and concurrent cisplatin (40 mg/m

2

)

from Jan, 2011 to Jun, 2016. The IMRT planning aimed at

restricting V15 and V40 Small Bowel to ≤ 200 and 100 cc

respectively. No prospective bone marrow (BM)

constraints were applied. The data base was reviewed to

determine worst grade of HT toxicity. IMRT planning scans

were dearchived and pelvic BM was delineated in 2 sets;

whole bone (WB), and freehand (FH) inner cavity of bone

from top of L3 vertebra to ischial tuberosity. Various BM

sub-volumes namely whole pelvis + lumbar (WPL), lumbar

vertebra, sacrum, ilium, ischium, femoral head and neck,

whole pelvis (WP), lower pelvis(LP) were contoured and

dose volume histograms (DVH) parameters (V

5

, V10, V20,

V30, and V40) were obtained. Receiver operating

characteristic (ROC) curve identified DVH thresholds that

predicted for grade≥ II HT toxicity with highest specificity.

All data was dichotomized across these cut-offs.

Univariate and multivariate analysis was performed with

SPSS, version 20.

Results

Of the 94 patients randomized to IMRT arm, 74 received

concurrent cisplatin (median cycles=4). Grades I-V HT was

seen in 55.5%, 32.5%, 5%, 0% and 0% patients, respectively

demonstrating low incidence of HT during bowel sparing

IMRT. Leukopenia, neutropenia, anemia, and

thrombocytopenia ≥ grade II was observed in 24.3%, 5.3%,

17.6%, and 0%, respectively. None of the HT resulted in

treatment break. On comparing BM delineation techniques

the FH sub volumes were 25%-47% of WB sub-volumes. The

mean V

5

, V10, V20, V30, and V40 for WP FH and WB were

99%, 93%, 77%, 60%, and 36%; and 99%, 94%, 80%, 60%, and

36%, respectively suggesting unintended desirable BM

sparing. On univariate analysis WPL FH V30 > 55% (p=0.04)

predicted for overall grade ≥ II HT, WP V10 >95% (p= 0.04)

for grade ≥ II leucopenia and ilium V20 > 90% (p=0.04) for

hemoglobin toxicity. On multivariate analysis, only WP FH

V10 >95% (p value 0.04, OR 3.3 (1-11.5) was statistically

significant for grade ≥ II leucopenia.

Conclusion

The IMRT arm of NCT01279135 (PARCER study) that

employed strict bowel constraints also had unintentional

dosimetrically desirable BM sparing. This was associated

with low absolute rates of HT. Within the setting of bowel

sparing IMRT WP FH V10 should be restricted to ≤95% for

simultaneous bowel and BM sparing. However as none of

the other dosimetric variables predicted for HT, WB

marrow contours could serve as a resource sparing

strategy while planning pelvic IMRT.

OC-0319 Cervix cancer: dose-volume effects in

pathologic lymph nodes

W. Bacorro

1

, R. Mazeron

2

, I. Dumas

3

, A. Escande

2

, A.

Huertas

2

, R. Sun

2

, P. Castelnau-Marchand

2

, C. Haie-

Meder

2

, C. Chargari

2

1

Benavides Cancer Institute- UST Hospital, Radiation

Oncology, Manila, Philippines

2

Gustave Roussy, Radiation Oncology, Villejuif, France

3

Gustave Roussy, Medical Physics, Villejuif, France

Purpose or Objective

Whereas clear dose-volume relationships have been

demonstrated for the tumor and organs at risk in locally

advanced cervix cancer, the optimal threshold to reach

for pathologic lymph nodes remains uncertain. The

objective was to identify planning aim for pathologic

nodes.

Material and Methods

Patients treated with curative intent for a cervical cancer

with nodal involvement were identified. Their treatment

combined external beam radiotherapy (EBRT) and image-

guided brachytherapy (IGABT). Nodal boosts were

performed sequentially or using the simultaneous

integrated boost (SIB) technique depending on the EBRT

technique used. The contributions of EBRT, IGABT (D

98

)

and nodal boosts were converted in 2-Gy equivalent

(α/β=10 Gy) and summed. Each node was considered

individually, and followed from diagnosis to relapse.

Resected nodes during para-aortic node surgical staging

were not considered. Statistical analyses comprised log-

rank tests (univariate analyses), Cox proportional model

(factors with p ≤0.1 in univariate) and probit analyses.

Results

One hundred and fifteen patients were included, with a

total number of nodes of 288 (2.5 per patient). PET-CT

was performed in 90.6% of the patients; para-aortic

dissection in 53.8%. Histologic subtypes comprised

squamous cell carcinomas (SCC) in 88.9%,

adenocarcinomas in 8.5% and adenosquamous in 2.6%. The