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S366

ESTRO 36 2017

_______________________________________________________________________________________________

Of the 156 eligible patients, 133 (85.3%) responded to at

least one of the questionnaires. Non-response included

patients who didn’t return the questionnaires (8.3%) or

had missing values in the WAI questionnaire (6.4%). Of the

responders, 107 patients (80.5%) had paid employment.

These patients had a mean age of 56.2 years and 73.8%

were male. All patients underwent neoadjuvant therapy

of which 64.5% chemoradiation, 30.8% short-course

radiation and 4.7% other regimes. Surgery was performed

in 89.7% of the patients, mostly by low anterior (50.5%) or

abdominoperineal resection (33.6%). At baseline, the

mean WAI score was 32.3, which was substantially lower

than the reference population score of 40.9. Workability

was poor in 27.5% of the patients, and moderate, good and

excellent in resp. 34.1%, 34.1% and 4.4% (Figure 1).

Corresponding scores of the Dutch reference population

were 2.8%, 14.2%, 47.2% and 35,8% resp. Workability was

limited by illness in 82.4% of the patients, and 23.1%

completely stopped working. At 3 months, the mean WAI

score decreased significantly to 27.1 (p<.001) and was

poor in 54.7% of the patients. Here after, at 6 and 12

months, the mean WAI score increased to resp. 29.1 and

34.6. At 12 months, 55.3% of the patients reported

absenteeism of 100-365 days as result of health problems

in the past year compared to 2.3% in the reference

population. Only 14.9% of the patients reported no

absenteeism. Stratification by neoadjuvant regimen and

surgical procedure did not modify the results.

Conclusion

Workability in patients with rectal cancer is negatively

affected by treatment but seems to recover towards

baseline levels at 12 months after diagnosis. Compared to

the Dutch population, rectal cancer patients report a

much lower workability and a higher level of absenteeism.

PO-0706 Assessing the impact of sentinel lymph-node

and inguinal irradiation in patients with anal cancer

C. Gumina

1

, N. Slim

1

, G.M. Cattaneo

2

, P. De Nardi

3

, C.

Canevari

4

, M. Ronzoni

5

, A. Fasolo

5

, C. Fiorino

2

, L. Perna

2

,

A.M. Tamburini

3

, R. Rosati

3

, P. Passoni

1

, N. Di Muzio

1

1

San Raffaele Scientific Institute, Radiotherapy, Milan,

Italy

2

San Raffaele Scientific Institute, Medical Physics, Milan,

Italy

3

San Raffaele Scientific Institute, Surgery, Milan, Italy

4

San Raffaele Scientific Institute, Nuclear Medicine,

Milan, Italy

5

San Raffaele Scientific Institute, Medical Oncology,

Milan, Italy

Purpose or Objective

To evaluate the role of sentinel lymph-node biopsy (SLNB)

in staging and the impact of inguinal irradiation.

Material and Methods

Patients with anal squamous cell carcinoma and without

gross inguinal lymph-nodes metastases were considered

for SLNB after staging with standard imaging procedures

and FDG-PET. The Clinical Target Volume (CTV) included

the Gross Tumor Volume (GTV: primary tumour and

positive lymph-nodes) and pelvic ± inguinal lymph-nodes.

Planning Target Volume (PTV)1 and PTV2 corresponded to

GTV and CTV, respectively, with a margin of 0.5-1.0 cm.

Prescribed dose was 50.4 Gy in 28 fractions to the PTV2

and 64.8 Gy in 36 fractions to the PTV1, delivered with

IMRT or VMAT. Concomitant chemotherapy consisted of

Mito-C 10 mg/m

2

and continuous infusion 5-FU 1000 mg/m

2

for 4 consecutive days.

Results

From 03/2008 to 02/2014, 48 consecutive patients were

treated. FDG-PET was performed in 42 out of 48 patients.

Pathologic inguinal uptake was shown in 15/42 (36%) and

9 of them underwent lymphoscintigraphy: SLNB confirmed

inguinal metastases only in 3/8 (37.5 %) (SLN not found in

1 patient). FDG-PET did not show inguinal uptake in 27/42

(64%) patients and 17 of them underwent

lymphoscintigraphy: SLNB found metastases in 2/17 (12%).

Thirty-one patients received prophylactic or curative

radiotherapy to the groins (Inguinal RT group) and 17

patients did not (No inguinal RT group). Sixteen/17

patients of the No inguinal RT group had a negative SLNB.

At a median follow-up of 41 months no relapse was

observed in the “No inguinal RT”. No significant

differences in terms of toxicities, apart from inguinal

dermatitis, were observed between the two groups.

Conclusion

SLNB improves the PET-based staging and is highly

accurate in identifying the true negative patients for

which the inguinal irradiation could be avoided. The use

of advanced radiotherapy techniques, sparing inguinal

lymph-nodes reduces dramatically the inguinal skin

toxicity while no differences were found for other side

effects.

PO-0707 Magnetic Resonance Imaging Texture Analysis

Parameters for predicting risk of Anal Cancer

recurrence

K. Owczarczyk

1

, D. Prezzi

1

, M. Siddique

1

, J. Stirling

1

, G.

Cook

1

, R. Glynne-Jones

2

, A. Gaya

1

, M. Leslie

1

, V. Goh

1

1

Guy's and St.Thomas' Hospital NHS Foundation Trust,

Department of Cancer Imaging, LONDON, United Kingdom

2

Mount Vernon Cancer Center, Department of Oncology,

London, United Kingdom

Purpose or Objective

Despite advances in the management of anal squamous

cell carcinoma (ASCC), roughly 25% of patients undergoing

standard chemoradiotherapy (CRT) will experience

disease recurrence. Currently, there is no established way

of predicting disease outcome. Quantitative magnetic

resonance (MR) imaging texture analysis (TA) parameters

have shown promise in assessing the risk of recurrence in

other cancer types. This study was carried out to assess

their role in evaluating recurrence risk in patients with

ASCC undergoing CRT.

Material and Methods

We used baseline high-resolution T2-weighted MR images

from 42 patients with ASCC undergoing CRT to identify TA

parameters with the best ability to predict disease

recurrence. Multi-slice regions of interest (ROI) were

drawn around the tumours, generating a whole tumour

volume. 3D volume statistical and fractal heterogeneity

parameters were derived using in-house

software.We

calculated False Discovery Rate (FDR)

p

-value for all TA

parameters using the Benjamini-Hochberg correction to

adjust for multiple tests and used a FDR p-value cut-off of

0.15 to identify candidate

parameters.We

then analysed

baseline T2-W MR images from further 33 patients to

independently cross-validate performance of the

identified TA parameters. We calculated replication FDR

p-values for the validation cohort as well as p values for

the pooled cohort.

Results

Two patients in the test cohort and three patients in the

replication cohort had to be excluded based on lack of

visible tumour (n=2) and palliative treatment intent (n=3).

40 patients in the test cohort and 30 patients in the

replication cohort were included in the final analysis. All