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S171

ESTRO 36 2017

_______________________________________________________________________________________________

PV-0328 Factors associated with complete response

after brachytherapy for rectal cancer; the HERBERT

study.

E.C. Rijkmans

1

, R.A. Nout

1

, E.M. Kerkhof

1

, A. Cats

2

, B.

Van Triest

3

, A. Inderson

4

, R.P.J. Van den Ende

1

, M.S.

Laman

1

, M. Ketelaars

1

, C.A.M. Marijnen

1

1

Leiden University Medical Center LUMC, Department of

Radiotherapy, Leiden, The Netherlands

2

The Netherlands Cancer Institute, Department of

Gastroenterology and Hepatology, Amsterdam, The

Netherlands

3

The Netherlands Cancer Institute, Department of

Radiotherapy, Amsterdam, The Netherlands

4

Leiden University Medical Center LUMC, Department of

Gastroenterology and Hepatology, Leiden, The

Netherlands

Purpose or Objective

The HERBERT study was performed to examine the

feasibility of a high hose rate endorectal brachytherapy

(HDREBT) boost after external beam radiotherapy (EBRT)

in elderly patients with rectal cancer who were unfit for

surgery. The primary results and long term clinical

outcomes have been presented at ESTRO 2014 and 2016.

With rising interest for organ preservation, the role of

definitive (chemo)radiotherapy becomes increasingly

important. This current analysis evaluates factors that are

associated with a complete response to treatment.

Material and Methods

A dose finding feasibility study was performed from 2007

to 2013 in inoperable rectal cancer patients. Patients

received 13x3 Gy EBRT followed by three weekly

applications HDREBT of 5 to 8 Gy per fraction. Clinical

target volume (CTV) for HDREBT was defined as residual

scarring or tumor after EBRT. Clinical tumor response was

evaluated based on digital rectal examination and

endoscopy (MRI or biopsy was not routinely performed).

Complete response was determined after serial

assessments.

Patient,

tumor

and

treatment

characteristics of complete responders (CR) were

compared to non-complete responders (nCR) using Chi-

square test and the independent samples t-test.

Results

Of the 38 patients included in the study 33 were evaluable

for response evaluation. Seven were treated with 5 Gy per

fraction, four with 6 Gy, 12 with 7 Gy and 10 with 8 Gy per

fraction. In total 20 patients achieved a complete

response. Baseline patient characteristics (age, ASA, WHO

and co-morbidity) and tumor-characteristics (T-stage, N-

stage, cranio-caudal length of the tumor and distance

from anal verge) were not associated with response to

treatment. A trend was observed in complete response

between dose levels; 2/ 7 treated with 5 Gy per fraction;

1/4 with 6 Gy; 9/12 with 7 Gy and 8/10 with 8 Gy per

fraction (p=0.05). The actual planned D98 (dose to 98% of

the CTV) was however not significantly different between

patient with a complete response and no complete

response: 6.25 Gy (range 3.8-8.3 Gy) vs. 5.98 Gy (range

1.2-8.8 Gy) respectively (p=0.63).

Endoscopic evaluation of response after EBRT was

significantly associated with the overall response rate.

Seven patients already had a CR after EBRT, whereas

13/21 patients (62%) with a partial response after EBRT

achieved a CR. None of the five patients with stable

disease achieved a complete response (p=0.002). Mean

residual volume and thickness of residual scarring or tumor

after EBRT were significantly lower in complete

responders (see Figure). In addition, tumors encompassing

less than 1/3 of the circumference were more likely to

achieve a complete response than larger tumors (70% vs

17% respectively, p=0.025).

Conclusion

Endoscopic response after EBRT and residual tumor

thickness, circumference and volume at time of HDREBT

were significantly associated with achieving a complete

response. This demonstrates that careful selection of

patients for organ preserving strategies can result in a very

high success rate.

Proffered Papers: Head and Neck

OC-0329 Does margin matter? Distribution of loco-

regional failures after primary IMRT for Head &Neck

cancer

R. Zukauskaite

1

, C.R. Hansen

1

, C. Brink

1

, C. Grau

2

, E.

Samsøe

3

, J. Johansen

1

, E. Andersen

3

, J. Petersen

2

, J.

Overgaard

4

, J. Eriksen

1

1

Odense University Hospital, Department of Oncology,

Odense, Denmark

2

Aarhus University Hospital, Department of Oncology,

Aarhus, Denmark

3

Herlev Hospital, Department of Oncology, Copenhagen,

Denmark

4

Aarhus University Hospital, Department of Experimental

Clinical Oncology, Aarhus, Denmark

Purpose or Objective

Head and neck squamous cell carcinoma (HNSCC) often

presents as a local or loco-regional disease. Margins are

often added around the gross tumour volume (GTV) during

the planning of curative radiotherapy to cover microscopic

disease. However, there is little evidence available for the

optimal size of the high dose clinical target volume (CTV1)

margin. Until 2013, different margins from GTV to CTV1

were allowed according to the national treatment

guidelines in Denmark, varying from 0 to up to 10 mm. The

objective of this study was to analyse loco-regional

recurrence pattern in a large cohort of patients with

HNSCC treated with curatively intended IMRT. We aimed

at evaluating how the location of CT verified loco-regional

recurrences (LRR) were influenced by different CTV1

margins.

Material and Methods

Patients with larynx, oro-/hypopharynx or oral cavity

HNSCC treated with primary IMRT during 2006–2012 in

three centres were retrospectively identified from

national database. Treatment was given according to

DAHANCA guidelines, primarily 66-68 Gy in 6

fractions/week with concomitant Nimorazole and weekly

cisplatin in loco-regionally advanced cases. The GTV-CTV1

margin was primarily produced by volumetric expansion

that varied from 0-10 mm and eventually modified

according to anatomy. The origin of recurrence was

estimated for all loco-regional treatment failures with

diagnostic CT or PET/CT images available. Assuming that

loco-regional recurrences arise from a few surviving

cancer cells, the possible points of LRR origin (PO) were

identified on diagnostic scans by two independent

observers, and calculated as mass mid-point (MMP) and a