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S48

A B S T R A C T S

Thus, risk benefit in elderly pts might be questionable when

using AA which prolong survival, but might alter quality of life.

Objectives:

The aim of our study was to describe the

treatment of elderlymRCC patients withAA in routine practice

compared to a younger population in order to assess whether

age can influence treatment patterns, patients outcomes and

to identify specific toxicity profiles.

Methods:

We performed a retrospective review of all

medical records of patients treated with AA for mRCC

in 2 French institutions between June 2006 and 2015. Pts

70 y.o. were considered as elderly and pts <70 y.o. formed

the control group of young pts. Recorded variables included:

age, comorbidities, first to third-line therapies, treatment

schedules, and survival data. We assessed toxicity data by

recording toxicity-related treatment discontinuation, hemato-

logical and non-hematological grade 3-4 adverse events.

Results:

A total of 170 patients were identified, median age

was 65.2 y.o. (range 26.2-89.7). According to IMDC prognostic

model, 27.8% patients had favorable risk, 51.3% intermediate

risk and 20.9% poor risk. Both study groups were well balanced

according to IMDC risk groups. Among the whole population,

60 patients were

70 y.o.. Elderly pts were treated with

sunitinib (N=40, 66.7%), sorafenib (N=11, 18.3%) or pazopanib

(N=9, 15%). First-line median progression-free survival (PFS)

was shorter for pts

70 y.o.: 10.0 months (IC 95% [8.4-12.2])

versus 14.8 months (IC 95% [10.2-19.0]) for younger pts (p =

0.033). Median overall survival was 21.2 months (IC 95% [14.6-

46.9]) for the elderly versus 41.2 months (IC 95% [35.4-57.9]) for

younger pts (p = 0.016). In the elderly group, 35 pts received

a second-line treatment and 11 pts a third-line treatment.

The median PFS for elderly pts was 5.4 months (IC 95% [4.1-

11.4]) in second-line and 4.3 months (IC 95% [2.2-NA]) in third-

line. Grade 3-4 non-hematological toxicities were observed

in 35/60 elderly pts (58.3%), including skin toxicity (n=9),

mucositis (n=4), hypertension (n=8), fatigue (n=13), diarrhea

(n=8). No difference was found between the two groups for

grade 3-4 hypertension, skin toxicity and diarrhea. There

were significantly more grade 3-4 cardiovascular toxicities

(excluding hypertension) in the group

70 y.o. (p = 0.015).

21.6% of elderly pts definitively stopped treatment due to

toxicity versus 9.1% in younger pts (p = 0.04). Further results

on treatment schedules will be presented at the meeting.

Conclusion:

This retrospective study shows that treatment

with AA is feasible with good efficacy in elderly pts. Efficacy

observed supports the use of AA in elderly pts. However, age

appears to be a prognostic factor for patients with mRCC

treated by AA. Finally, physicians should be aware of toxicity

that seems to be more frequently limiting for elderly pts

treated with antiangiogenic therapies.

Reference

[1] Bellmunt J, Négrier S, Escudier B, Awada A, Aapro M. The

medical treatment of metastatic renal cell cancer in the

elderly: Position paper of a SIOG Taskforce. Crit Rev Oncol

Hematol. 2009 Jan;69(1):64–72.

Disclosure of interest:

L. Pierard: None declared, F.

Schaff-Wendling: None declared, A. Thiéry: None declared,

C. Korenbaum: None declared, J. Gantzer: None declared,

D. Heitz: None declared, B. Duclos Consultant for: Novartis,

Pfizer, C. Borel: None declared, J.-E. Kurtz: None declared, P.

Barthélémy Consultant for: Novartis, Pfizer

Keywords:

Antiangiogenic therapies, elderly, metastatic renal

cell carcinoma

P023

TOLERANCE AND EFFICACY OF FOLFIRINOX IN ELDERLY

PATIENTS WITH PANCREACTIC OR COLORECTAL CANCER.

A MONOCENTRIC RETROSPECTIVE STUDY ON 52 PATIENTS

J. F. Guion-Dussere

1

, A. Bertaut

2

, F. Ghiringhelli

1

, J. Vincent

1

,

V. Quipourt

3,4

, S. Marilier

3,4

, L. Bengrine Lefevre

1,4,

*

1

Medical oncology,

2

statistic department, Centre Georges François

Leclerc,

3

geriatric department, CHU Champmaillot,

4

UCOG

Bourgogne, Dijon, France

Introduction:

Chemotherapy regimen proposed in

metastatic colorectal cancer are discussed function of general

status health and cancer prognostic criteria. Data are in favor

of efficacy of Folfirinox in these pathologies for patient under

75 years old. Efficacy and tolerance are not clearly evaluated

in elderly patients.

Objectives:

The main objective of this retrospective study

was to evaluate tolerance and efficacy of Folfirinox regimen

in elderly patients diagnosed and treated for metastatic

colorectal or pancreatic cancer in the French anticancer

center Georges Francois Leclerc.

Methods:

Patients over 70 years old treated at CGFL

between January 2009 and January 2015 were included.

Histologically proved pancreatic or colorectal cancers were

required. Demographic, clinical data were recorded and

geriatric parameters as Charlson Comorbidity index (CCI) and

functional assessment. Toxicities were evaluated using the

CTCAE 4.03. Treatment continued until disease progression,

unacceptable toxicities or patient refusal. Primary endpoint

was overall survival (OS).

Results:

On the whole, 52 patients (46 men and 6 women)

were treated by Folfirinox regimen, 34 for colorectal cancer

and 18 for pancreatic cancer. Thirty seven patients had

comorbidities, 30 took 4 or more medications, 43 were 0-1

performance status, and 32 had a CCI under 10. Most of

patients had no home help at the beginning but 34 had one

at 3 months. Half of patients had at least 2 metastasis sites.

Seventy five percent had a “modified” Folfirinox at

beginning, which consist on a 5FU reduction (bolus or

continuous infusion) and irinotecan (67%) reduction. Only

26% had an adapted regimen after beginning.

Regarding adverse events, 32% (n=42) had grade 3-4

neutropenia, 9% grade 3-4 anemia, 25% grade 3-4 diarrhea.

Seven percent had grade 3-4 neuropathy and 26% of patients

had a dose adjustment after the beginning.

Twenty four patients (46%) had a stable disease or partial

response and 21% had progressive disease at 6 courses.

At progression 23 patients had a second line of treatment.

Most patients died from cancer.

In univariate analysis and in multivariate analysis, no

geriatric parameters were linked to OS (age, comorbidities,

independence, CCI, medication number or OMS status).

Primary tumor was the only factor linked to OS in univariate

and multivariate analysis.