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S292

ESTRO 36

_______________________________________________________________________________________________

Poster Viewing : Session 12: Gynaecology and prostate

PV-0548 The role of adjuvant therapy in stage IA

serous and clear cell uterine cancer: a pooled analysis

M.X. Qu

1

, V. Velker

2

, E. Leung

3

, J. Kwon

4

, M.A. Elshaikh

5

,

I. Kong

6

, N. Logie

7

, L.C. Mendez

3

, L. Van der Putten

4

, E.

Donovan

6

, A.R. Munkarah

8

, E.M. Wiebe

7

, A.V. Louie

2

, D.P.

D'Souza

2

1

Queen's University, Oncology, Kingston, Canada

2

Western University, Radiation Oncology, London,

Canada

3

University of Toronto, Radiation Oncology, Toronto,

Canada

4

University of British Columbia, Obstetrics &

Gynaecology, Vancouver, Canada

5

Henry Ford Hospital, Radiation Oncology, Detroit, USA

6

McMaster University, Oncology, Hamilton, Canada

7

University of Alberta, Oncology, Edmonton, Canada

8

Henry Ford Hospital, Gynecology/Oncology, Detroit,

USA

Purpose or Objective

The optimal adjuvant management of Stage IA

endometrial cancer with serous or clear cell histology is

controversial. The objective of this study is to explore the

role of adjuvant therapy in this population and identify

patient characteristics of those suitable for observation.

Material and Methods

Retrospective chart reviews for consecutive patients who

underwent hysterectomy for FIGO Stage IA endometrial

cancer with serous or clear cell histology between 2004-

2015 were conducted in 6 academic centres. After

excluding patients who were upstaged following surgery,

a pooled analysis was performed for relevant endpoints.

Results

A total of 414 patients with a median age of 67 years(range

41-90) met the inclusion criteria. The most common

histology were pure serous (64%,n=266) followed by mixed

(27%,n=112) and pure clear cell (9%,n=36). Myometrial

invasion was identified in 54%(n=222). Most patients

underwent some surgical staging including sampling of

pelvic lymph node (LN) (81%,n=335), para-aortic LN

(45%,n=146), omentum (58%,n=239) and peritoneal

washing (62%,n=219). Only 23% of patients (n=95) were

considered to have adequate staging (pre-defined as ≥10

pelvic LN, sampled para-aortic LN and omentum). Thirty-

four percent of patients (n=140) received adjuvant

chemotherapy and carboplatin/paclitaxel was most

commonly used (77%, n=108). Adjuvant RT was delivered

to 47%(n=178) of patients (external beam alone 16%,n=29;

brachytherapy alone 56%, n=99; both 28%,n=50). The

median follow-up was 2.7 years (range 0-12). Among

patients who did not received any adjuvant treatment, 5-

year actuarial estimates were as follows: local control(LC)

88%, regional control(RC) 93%, distant failure(DF) 15%,

disease free survival(DFS) 74%, cancer specific

survival(CSS) 91% and overall survival(OS) 82%. Adequate

staging was associated with better CSS in patients who did

not have adjuvant treatment (100% vs. 87%, logrank

p=0.0035). Adjuvant RT was associated with better LC(5-

year 96% vs. 84%, HR 0.32,logrank p=0.014). The 5-year

RC was 93%, which was not found to be significantly

improved by external beam RT. Adjuvant chemotherapy

was associated with better LC(5-year 94% vs. 84%,HR 0.29,

logrank p=0.0079), DFS(5-year 79% vs. 71%, HR 0.47,

logrank p=0.033), but not for RC, DF or CSS. The delivery

of at least 5 cycles of chemotherapy, was associated with

a trend towards better LC (4-year 98% vs. 88%, HR

0.18,logrank p=0.090). Myometrial invasion,

lymphovascular invasion, histological subtypes and the

proportion of type II component were not found to be

significant prognostic factors for LC, RR, DF or CSS.

Conclusion

Adjuvant radiotherapy and chemotherapy were associated

with better LC and DFS but not for RC, DF or CSS for stage

IA serous and clear cell uterine cancer. Observation may

be an acceptable strategy in patients who have had

adequate surgical staging.

PV-0549 National Cancer Data Base Analysis of SBRT,

IMRT, and Brachytherapy Boost for Cervical Cancer

M. Ludwig

1

, M. Bonnen

1

, J. Shiao

2

, B. O'Donnell

3

, T.

Pezzi

1

, N. Waheed

1

, S. Sharma

1

1

Baylor College of Medicine, Radiation Oncology,

Houston, USA

2

University of Texas San Antonio, Radiation Oncology,

San Antonio, USA

3

University of Texas Houston, Radiation Oncology,

Houston, USA

Purpose or Objective

Brachytherapy is a vital component of curative

radiotherapy for cervical cancer, but in certain patients,

brachytherapy is not feasible because of inaccessibility of

brachytherapy comorbidities, patient refusal, or

unfavorable anatomy. Our objective was to determine if