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S693

ESTRO 36 2017

_______________________________________________________________________________________________

(11p in progression status and 191p with no evidence of

disease). Anemia monitoring: only 36p (53.7%) of 67p with

anemia detected before RDT, underwent subsequent Hb

control (during or after RDT). Only 27p of 67p with anemia

were previously treated with chemotherapy (40p were

anemic with no systemic treatment). Differences between

mean Hb levels were statistically significant for Hb1-Hb2

(p=,00), Hb1-Hb4 (p=,005), Hb3-Hb4 (p=,004) and Hb2-Hb4

(p=,001).

Patients with pre-treatment Hb level <12g/dL presented

worse overall survival (p=.021, Chi2 5.3), with mean OS of

53.39 months (range 45.5-61.3) vs. 61.4 (range 58.4-64.4)

in patients with ≥ 12g/dL.

Conclusion

Despite evidence that anemia is frequent in patients with

endometrial carcinoma and determine OS, the follow-up

of anemia in cancer patients is still suboptimal. There is a

strong need of guidelines for anemia monitoring in cancer

patients.

EP-1306 New pre-treatment eosinophiles-related

ratios as predictive factors for OS in endometrial

carcinoma.

K. Holub

1

, A. Biete

1

1

Hospital Clínic i Universitari de Barcelona, Radiation

Oncology Dpt., Barcelona, Spain

Purpose or Objective

To analyze the influence eosinophil levels in prognosis of

endometrial carcinoma.

Material and Methods

We retrospectively evaluated 233 patients (p) out of a

total cohort of 248p diagnosed with endometrial

carcinoma and treated with radiotherapy (RDT) in our

center between January 2011 and December 2015. We

analyzed the prognostic value of pretreatment

eosinophiles as well as we described new eosinophils-

related ratios in endometrial cancer: Eosinophil-to-

Lymphocyte Ratio and Eosinophil*Neutrophile-to-

Lymphocyte Ratio. Statistics: Chi-square, Kaplan-Meier

method.

Results

Age at diagnosis (years): mean 64.9 (range 36-90). All

patients underwent surgery before RDT, with pelvic

lymphadenectomy in 187p (80.3%). Histology:

Endometrioid 172p (73.8%), non-endometrioid 61p

(26.2%). FIGO stage (2009): IA-60p (27.8%), IB-92p (39.5%),

II-32p (13.7%), IIIA-9p (3.9%), IIIB-0, IIIC1-20 (8.6%), IIIC2-

8 (3.4%), IVA-9 (3.9%), IVB-3(1.3%). Grade: I-50p (21.5%),

II-91p (39%), III-88p (37.8%). External beam radiotherapy

(EBRT) dose (Gy): mean 44.2 (range 9-65). Brachytherapy

(BT) dose (Gy): mean 10.2 (range 5-20). Majority of

patients was treated with combination of EBRT and BT.

EBRT+BT dose (Gy): mean 41.2 (range 5-75). Mean follow-

up (months): mean 32 (SD 17.5). Progression was observed

in 40p (17.2%): only one patient developed pelvic node

recurrence, 39p developed distant recurrence (4p with

simultaneous vaginal progression, 3p with regional

progression and one 1p with both vaginal and regional

progression, remaining 31p presented exclusively distant

progression). Mortality: 31p (13.3%), including cancer-

specific mortality: 28p (12%) and 3 deaths not related with

endometrial cancer (1.3%). Remaining 202p were alive

(11p in progression status and 191p with no evidence of

disease).

Eosinophiles-

related ratios in

pre-treatment

analysis

Numb

er of

patie

nts

Mean

(rang

e)

Cu

t-

Off

Numb

er of

event

s

(deat

hs)

Overal

l

surviv

al

(mont

hs)

p

(Chi

2)

Eosinophils-to-

Lymphocytes Ratio

(ELR)

131

0.08

(0.0-

0.31)

<0.

1

vs

3 vs 9

64.0

vs

52.0

,001

(12.0

1)

≥0.

1

Eosinophiles*Neutr

ophils-to-

Lymphocytes Ratio

(ENR)

112

4.6

(1.14

-

12.5)

<0.

4

vs

≥0.

4

4 vs 8

63.0

vs

53.6

,015

(5.86

)

Conclusion

Tumor-generated inflammation is considered to be one of

the principal triggers for tumor progression. Several

hypotheses link eosinophilia with cancer, however until

now there has not been any evidence of impact of

eosinophil levels in combination with other immune cells

on prognosis of cancer. To our best knowledge, this is the

first publication describing and analyzing the eosinophil-

related ratios as a predictive factor in cancer

.

EP-1307 New neutrophils-related ratios as a novel

predictive biomarkers for endometrial carcinoma.

K. Holub

1

, A. Biete

1

1

Hospital Clínic i Universitari de Barcelona, Radiation

Oncology Dpt., Barcelona, Spain

Purpose or Objective

To analyze the influence of neutrophils, lymphocytes,

monocytes and platelet-related disorders in pre-

treatment blood analysis on prognosis of endometrial

carcinoma.

Material and Methods

We retrospectively evaluated 233 patients (p) out of a

total cohort of 248p diagnosed with endometrial

carcinoma and treated with radiotherapy (RDT) in our

center between January 2011 and December 2015. We

analyzed the prognostic value of pretreatment neutrophils

and lymphocytes levels as well as Neutrophil-to-

Lymphocyte ratio (NLR), Platelet-to-Lymphocyte ratio

(PLR), Lymphocyte-to-Monocyte ratio (LMR) and

Platelet*Neutrophil-to-Lymphocyte

ratio

(Systemic

Immune-Inflammation Index, SII) in endometrial cancer.

Statistics: Chi2, Kaplan-Meier method.

Results

Age at diagnosis (years): mean 64.9 (range 36-90). All

patients underwent surgery before RDT, with pelvic

lymphadenectomy in 187p (80.3%). Histology:

endometrioid 172p (73.8%), non-endometrioid 61p

(26.2%). FIGO stage (2009): IA-60p (27.8%), IB-92p (39.5%),

II-32p (13.7%), IIIA-9p (3.9%) ,IIIB-0, IIIC1-20 (8.6%), IIIC2-

8 (3.4%), IVA-9 (3.9%), IVB-3(1.3%). Grade: I-50p (21.5%),

II-91p (39%), III-88p (37.8%). Majority of patients was

treated with combination of EBRT and BT. EBRT+BT dose

(Gy): mean 41.2 (range 5-75), median 52. Mean follow-up

(months): mean 32 (SD 17.5). Progression was observed in

40p (17.2%): only one patient developed pelvic node

recurrence, 39p developed distant recurrence (in 4p with

simulates vaginal progression, 3p with regional

progression and one 1p with both vaginal and regional

progression, remaining 31p presented exclusively distant

progression). Mortality: 31p (13.3%), including cancer-

specific mortality: 28p (12%) and 3 deaths not related with

endometrial cancer (1.3%). The remaining 202p were alive

(11p in progression status and 191p with no evidence of

disease). Neutrophils-related ratio were calculated as

follows: NLR-absolute neutrophil count/absolute

lymphocyte count, PLR-platelet count/ absolute

lymphocyte

count,

LMR-absolute

lymphocyte

count/absolute

monocyte

count

and

SII

-

platelet*neutrophil count/lymphocyte count.

Hemogram

parameters in

pre-treatment

blood analysis

Num

ber

of

patie

nts

Mean

(range)

Cut

-Off

Numb

er of

event

s

(deat

hs)

Overa

ll

surviv

al

(mont

hs)

p

(Chi2)