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A B S T R A C T S

S61

P042

SEGA (SHORT EMERGENCY GERIATRIC ASSESSMENT)

FRAILTY SCORE IN ELDERLY PATIENTS WITH

HAEMATOLOGICAL MALIGNANCIES

N. Carnel

1,

*, J. Poisson, T. Guerekobaya, P. Genet, A. Andreoli,

A. Al Jijakli, B. Poujol, L. Mesbah, L. Sutton, D. Chaoui

1

Haematology unit, Centre hospitalier Victor Dupouy, Argenteuil,

France

Introduction:

Long-termremission canbe achieved inelderly

patients with haematological malignancies. The challenge is

first to identify elderly patients illegible for a curative treatment

and second to prevent complications during the treatment.

In real life, haematological treatment decision does not

include Comprehensive Geriatric Assessment approach

mainly because of time-consuming. SEGA score is an easy tool

to detect frail patients admitted in emergency department.

Objectives:

We report here a real life experience of SEGA

score in elderly patients with haematological malignancies.

Methods:

This study was longitudinal, prospective and

mono-centric. We focused on patients aged 70 or older

who received their first cycle of chemotherapy between

September 1

st

2014 and August 31

th

2015. We recorded the

multidisciplinary treatment decision taken (curative or

palliative treatment). Geriatric tools recorded (G8 score,

CIRS score, sheet A SEGA score, ADL, IADL) were not used

during treatment decision. The first course of chemotherapy

was considered as the standard dose. We analysed during

the following chemotherapy courses: dose reduction,

chemotherapy delaying and early discontinuation. Analysis of

SEGA and other geriatric tools impact on treatment decision

(curative versus palliative), chemotherapy adaptation and

discontinuation was performed.

Results:

During the one year period analysis, 141 patients

70 years old (70-95) were discussed during our weekly

multidisciplinary meeting. Average age was 80. The most

frequent haematological diseases were distributed as follow:

NHL (32%), multiple myeloma (29%), CLL (13%) and MDS

(8%). Twenty one percent of patients and 18% were assigned

to Bendamustine and Bortezomib based chemotherapy,

respectively. Other chemotherapy regimens included (CHOP

and CHOP like treatment ± Rituximab (10%), 5-Azacytidine

(8%), IMID (8%). Palliative treatment decision was taken in

12 patients. At diagnosis, the mean sheet A SEGA score was

6,9 (1-21) indicating that the subjects included were mostly

not frail. CIRS mean total rate excluding haematological

malignancy was 6,19 (0-18).

CIRS score and SEGA score were significantly associated

with palliative treatment, p=0,045 and 0,002 respectively.

Regarding patients assigned to chemotherapy, treatment was

prematurely stopped in 34% of patients, dose reduction in

29% and chemotherapy was delayed in 17%. Only 20% did not

experience any of these events. CIRS grade 3 or 4 and CIRS

score

6 were strongly associated with early chemotherapy

discontinuation (p=0,014 and 0,0021, respectively). In contrast

no impact was observed regarding chemotherapy delaying

or dose reduction. SEGA score was not associated with early

discontinuation, nor dose reduction and chemotherapy

delaying.

Mainly reasons for early chemotherapy discontinuation

were: adverse events (60%) and disease progression (26%).

Conclusion:

SEGA score as well as CIRS could be helpful

in treatment choice. Palliative treatment could be the best

approach in patients with CIRS score

10 and or SEGA score

12. Patients CIRS score more than 6 are at higher risk of early

chemotherapy discontinuation. A special attention is required

for these patients to avoid such events.

Disclosure of interest:

None declared

Keywords:

CIRS, comorbidity, elderly, haematological

malignancy, SEGA

P043

A NEW FRAILTY SCORING IN “CLINICALLY FIT” OLDER

PATIENTS WITH MALIGNANT HEMOPATHIES ADMITTED TO

RECEIVE CHEMOTHERAPY

S. Dubruille

1,2

, C. Kenis

3

, Y. Libert

2

, M. Delforge

4

, J. Alexis Ruiz

1

,

M. Roos

5

, A. Collard

5

, N. Meuleman

1

, M. Maerevoet

1

, D. Razavi

2

,

H. Wildiers

3

, D. Bron

1,

*

1

Department of Hematology,

2

Clinic of Psycho-Oncology, Institut

Jules Bordet, Brussels,

3

Department of Oncology,

4

Department of

Hematology, University Hospitals Leuven, Leuven,

5

Onco-geriatry

Unit, Institut Jules Bordet, Brussels, Belgium

Introduction:

Patients“clinicallyfit”toreceivechemotherapy

suffering frommalignant hemopathies, are an heterogeneous

population covering fit and vulnerable patients. Patients

with geriatric syndromes and/or irreversible comorbidities

are usually excluded from high dose chemotherapy. We

recently reported that neither the G8 screening tool, nor the

CGA total score (

2 impairments) significantly predict overall

survival (OS) in this specific population of patients admitted

for chemotherapy (1). Regarding survival, in a multivariate

analysis, we found that only Mild Cognitive Impairment (MCI)

(MMSE<27 and/or MoCA<26) had a predictive value for one-

year OS [1]. However, a reliable “frailty score” remains urgently

needed to better define the vulnerable population that does

not benefit from chemotherapy.

Objectives:

To determine clinical and biological parameters

associated with unacceptable toxicity defined as 6 months

mortality in order to avoid overtreatment in these vulnerable

patients suffering from malignant hemopathies.

Methods:

This prospective multicentric study was

conducted in three departments of hematology in Belgian

Cancer Centers. A Comprehensive Geriatric Assessment (CGA)

was proposed to 251 consecutive patients (65-90yrs) with

malignant hemopathies admitted to receive chemotherapy.

Clinical data, biological parameters and causes of death were

extracted from medical records. Chi-square test and T-student

test were used to determine relationship between clinical data,

biological parameters and OS. Univariate and multivariate Cox

proportional hazards model were used to predict 6 months OS.

Results:

One hundred and twenty patients were evaluable

for all characteristics (NHL=40%, CLL=8%, MM=12%, AML=25%,

MDS=4%, others=11%). Fifty percent are males. Sixty percent

had a more favorable prognosis (CLL, Lymphoma or Multiple