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6th ICHNO

6

th

ICHNO Conference

International Conference on innovative approaches in Head and Neck Oncology

16 – 18 March 2017

Barcelona, Spain

__________________________________________________________________________________________

Material and Methods

The study concerned three patients with nasopharyngeal

carcinoma stage N2-3. A first CT dosimetry was performed

for treatment planning using a 3D conformal radiotherapy.

A second CT scan was acquired at 38-40 Gy.

After merging the two scans, we quantified the anatomic

variations in target volumes and organs at risk, and then

we faithfully reproduce the original planned parameters

on the new CT to assess the dosimetric changes and check

constraints to organs at risk.

A new treatment plan was generated based on the new

target volumes and organs at risk. The new dose

distribution and new dose-volume histograms were

calculated and compared to the reference plane.

Results

The average reduction in lymph node and tumor

macroscopic volumes (GTV) after 38-40 Gy was 53% and

40% respectively. Dosimetric coverage of planned target

volume (PTV) and lymph node tumor remained

satisfactory. To organs at risk, we found an increase of the

maximum dose to the spinal cord for the three patients

(1.4 Gy on average) and brainstem (1.5 Gy for a patient).

After adaptation of the treatment plan, The coverage of

PTVs remained satisfactory. For organs at risk, maximum

doses to the spinal cord and brainstem decreased. On

average, the decrease was about 1.15 Gy to the spinal

cord and 6.85 Gy to the brain stem

Conclusion

Ours results demonstrated a dosimetric benefit with the

use of adaptative radiotherapy in nasopharyngeal

patients.

This study should be continued with a greater number of

patients to define a clear procedure especially that the

application of this concept in clinical practice is limited

due to the dependence on human resources.

PO-084 HDR Interstitial Brachytherapy for head and

neck malignancies with Iridium 192 implants

V. Pareek

1

, R. Bhalavat

2

, M. Chandra

2

1

Jupiter Hospital- Thane, Radiation Oncology, Mumbai,

India

2

Jupiter Hospital, Radiation Oncology, Thane, India

Purpose or Objective

To evaluate the treatment outcomes with HDR Interstitial

Brachytherapy in Head and Neck Cancers at our Institute

with use of Angiocatheters as carrier source of Iridium –

192 wire implants.

Material and Methods

58 Patients with Head and Neck malignancies of varying

TNM staging as per AJCC staging criteria were analyzed

retrospectively between 2008 and 2015. 42 patients

(72.41%) received EBRT with HDR – BRT and 26 patients

(27.59%) received BRT alone. The age group ranged from

27 to 81 years (Median age 56 years) with 41 patients

(70.69%) males and 17 patients (29.31%) females. HDR –

BRT was delivered with Iridium – 192 wire implants using

plastic bead techniques with varying dose rates. The

Biological equivalent doses (BED) were calculated for both

BRT and EBRT keeping α/β =10 for tumor and α/β =3 for

normal tissue and subsequently median BED doses were

calculated and similarly 2 Gy equivalent dose (EQD2) were

calculated and loco-regional control and disease free

survival was assessed.

Results

After completion of HDR – BRT, Patients for followed up

one month later and subsequently every 3 months for first

2 years and thereafter every 6 months with median follow

up period of 25 months (Range 2-84 months). The DFS

probability at year 1 was 82.76% and 68.05% at year 7. The

overall survival probability was 91.37% at year 1 and

85.89% at year 5. The local control rate was 67.27% and

the control rates according to the stage of disease and T

size classification are mentioned in

Table 1.

The rate of

local recurrence was 8.62%, Regional Recurrence was

1.72%, Loco-Regional Failure was 3.44% and Distant

metastases following local or regional failure was 17.23%.

The Median BED for α/β =10 was 86.775Gy and DFS was

74.07% in patients receiving more than 86.775Gy and DFS

was 64.82% in patients receiving less than 86.775Gy and

Median BED for α/β =3 was 128.76Gy and DFS was 74.07 in

patients receiving more than 128.76Gy as compared to

64.82% in patients receiving less than 128.76Gy. The

median EQD2 for α/β =10 was 71.6Gy and for α/β =3 was

75.85Gy. The DFS was 75.86% in patients receiving more

than median dose of 71.6Gy compared to 61.53% in those

receiving less than the median dose. The DFS was 78.57%

in patients receiving median dose of 75.85Gy as compared

to 59.26% in those receiving less than the median dose.

Conclusion

The overall outcome in the Patients with oral cavity and

oropharyngeal malignancies was good with implementing

of HDR – Interstitial Brachytherapy and use of

Angiocatheters as carriers of Iridium – 192 wire. The BED10

value of 86.775Gy and BED3 of 128.76Gy showed that the

dose received more than the median showed better

outcomes in the form of DFS. The EQD2 calculated values

suggested the dose received more than 71.6Gy (α/β =10)

and 75.85Gy (α/β =3) showed better outcomes .The role

of HDR Interstitial Brachytherapy in Head and Neck

cancers is a proven, effective and safe treatment method

with excellent long term outcome.

PO-085 Role of L Glutamine in reducing severity of

chemoradiation induced mucositis and improve QoL in

HNC

V. Pareek

1

, R. Bhalavat

2

, M. Chandra

2

1

Jupiter Hospital- Thane, Radiation Oncology, Mumbai,

India

2

Jupiter Hospital, Radiation Oncology, Thane, India

Purpose or Objective

The incidence of mucositis in the oral cavity, pharynx and

larynx is high among patients with head and neck cancer

(HNC) receiving chemo-radiotherapy (CRT), resulting in

significant pain and impairment of quality of life. The

present study investigated whether L-glutamine

(glutamine) decreases the severity of mucositis in the oral

cavity, pharynx and larynx induced by CRT

Material and Methods

Patients were randomized to orally receive either

glutamine or placebo at a dose of 10 g 3 times a day

throughout the CRT course. Mucositis was assessed using

the National Cancer Institute Common Terminology

Criteria for Adverse Events version 3.0. The primary end

point was mucositis severity. Seventy biopsy proven

patients with head and neck cancer receiving primary or

adjuvant radiation therapy were randomized to receive

either oral glutamine suspension daily 2h before radiation

in the study arm (10 g in 1000 ml of water) (

n

= 35) or

placebo before radiation; control arm (

n

= 35)

Results

Total 30 patients in the glutamine arm and total 33

patients in placebo developed mucositis. Grade 3

mucositis and grade 4 mucositis in the study arm (who

received oral glutamine) were significantly less in the

glutamine arm. The mean duration of grade 3 or worse

mucositis (grade 3 and grade 4) was significantly less in

study arm with

P

< 0.001. Mean time of onset of mucositis

was significantly delayed in patients who took glutamine

in comparison to control arm with

P

< 0.001. Overall,

glutamine was associated with a significant reduction of

mucositis, WL, and enteral nutrition.

Conclusion