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The systematic surgical staging in patients with SPEOC can be
accomplished either with laparotomy or laparoscopy. Laparotomy
is the preferable treatment approach for systematic surgical staging
especially in patients with advanced stage disease. Minimally invasive
techniques (laparoscopy and robotic‒assisted surgery) offer essential
advantages mainly in overweight and elderly patients (smaller
incisions, better visualization, shorter hospital stay, less postoperative
pain, quick recovery and low risk for postoperative complications).
However, they are significantly more difficult and time consuming
and require advanced surgical skills. This is the reason why, minimally
invasive techniques are less popular and are mainly implemented in
patients with early stage disease.3‒8,11,13,17‒19,23,24,27,31
It is interesting to note, that pelvic and para‒aortic
lymphadenectomy plays a crucial role in the systematic surgical
staging of patients with SPEOC. Moreover pelvic and para‒aortic
lymphadenectomy represents the only way to diagnose patients
with stage III disease. 3‒8,27,31 The radical extent of pelvic and para‒
aortic lymph node dissection (more than 14 lymph nodes) in patients
with SPEOC, increases significantly the risk for postoperative
complications.3‒8,23‒25,32,34 Consequently, in elderly patients and in
patients with comorbidities (obesity, diabetes mellitus and coronary
artery disease), the surgeon should carefully weigh the increased
morbidity with any survival advantage.3‒8,26,35,36
On the other hand, according to the recommendations of the
international scientific societies (ACOG, FIGO and ESMO),
postoperative adjuvant treatment (radiotherapy and/or chemotherapy)
plays an equally important role in patients with malignancies of
the female genital tract and either increased risk for recurrence or
at advanced disease stage. 3,4,7,8,10,11,13,17‒20,23‒29 However, in patients
with SPEOC, postoperative adjuvant treatment has a controversial
role.17,20,37 In this light, postoperative adjuvant treatment should be
individualized based on the risk of recurrence of each individual
primary cancer [3‒8,37,38]. Additionally, the postoperative adjuvant
treatment of each primary cancer should not affect the postoperative
adjuvant treatment of the other neoplasm.3‒8,10,13,18‒20,22‒24,37,39‒42
The postoperative adjuvant radiotherapy in patients with SPEOC
includes vaginal brachytherapy and external radiotherapy. 3‒8,23‒25
Vaginal brachytherapy is the adjuvant treatment of choice for
intermediate risk endometrial cancer (EC) patients (stage IA grade
3 endometrioid type EC, stage IB grade 1‒2 endometrioid type
EC).3‒8,28,43‒48 It is well tolerated and minimizes the risk of local
recurrences but has no impact on overall survival. 43,45,47,49 Moreover,
it is associated with well‒tolerated side effects and improved quality
of life.3‒8,43,45,47,49 Especially for intermediate risk EC patients, vaginal
brachytherapy and external pelvic radiotherapy are equivalent in
achieving local control of the disease.28,43‒46
Likewise, external pelvic radiotherapy represents the adjuvant
treatment of choice in high risk EC patients (stage IB grade 3
endometrioid type EC, stage I non‒endometrioid type EC). 3‒8,28,44,46,49
It is not well tolerated, being associated with significant morbidity and
impairment in the quality of life. 3‒8,43,50 Despite the fact that external
pelvic radiotherapy reduces the risk for local recurrences, it has no
impact on overall survival.3‒8,43,45,47,50,51
In contrast, postoperative adjuvant chemotherapy is the
adjuvant treatment of choice in patients with SPEOC and advanced
stage disease. 3‒8,38 The most common used chemotherapeutic
agents in patients with SPEOC, are taxanes, anthracyclines
Obstet Gynecol Int J. 2016;4(6):216‒218. 216
©2016 Androutsopoulos et al. This is an open access article distributed under the terms of the Creative Commons Attribution
License, which permits unrestricted use, distribution, and build upon your work non-commercially.
Current treatment options in patients with
synchronous primary endometrial and ovarian
cancers
Volume 4 Issue 6 - 2016
Georgios Androutsopoulos, Georgios
Michail, Georgios Decavalas
Department of Obstetrics and Gynecology, University of Patras,
Greece
Correspondence: Georgios Androutsopoulos, Department of
Obstetrics and Gynecology, University of Patras, Medical School,
Rion 26504, Greece, T el 306974088092,
Email
Received: July 08, 2016 | Published: July 18, 2016
Obstetrics & Gynecology International Journal
Editorial
Open Access
Editorial
Nowadays, synchronous primary cancers represent a very rare
clinical entity. 1‒9 Especially in patients with malignancies of the
female genital tract, only 0.5‒1.7% of them harbour synchronous
primary cancers.10‒15 Among them, synchronous primary endometrial
and ovarian cancers (SPEOC) is the most common combination of
cancers of the female genital tract. 1,6,10,11,13 They usually develop in
young, obese, premenopausal and nulliparous women and the average
age at diagnosis is approximately 50 years. 10,15‒21 Those patients are
commonly 10 ‒ 20 years younger than patients with single primary
endometrial or ovarian cancer.11,18,19,21,22
To begin with, most international scientific societies (ACOG, FIGO
and ESMO) recommend the systematic surgical staging as the initial
treatment approach in patients with malignancies of the female genital
tract.3,4,7,8,10,11,13,17‒20,23‒30 In particular, the systematic surgical staging in
those patients with SPEOC includes: total abdominal hysterectomy
with bilateral salpingo‒oophorectomy, total omentectomy,
appendectomy, pelvic and para‒aortic lymphadenectomy, complete
resection of all disease, biopsies of any suspicious lesions and pelvic
washings.3‒8,11,13,17‒19,23,24,27,21
Current treatment options in patients with synchronous primary endometrial and ovarian cancers
217
Copyright:
©2016 Androutsopoulos et al.
Citation: Androutsopoulos G, Michail G, Decavalas G. Current treatment options in patients with synchronous primary endometrial and ovarian cancers.
Obstet Gynecol Int J. 2016;4(6):216‒218. DOI: 10.15406/ogij.2016.04.00134
and platinum compounds. The administration of postoperative
adjuvant chemotherapy achieves high response rates in patients
with SPEOC. 3‒8,18,20 Nowadays, the postoperative combination of
adjuvant radiotherapy with adjuvant chemotherapy shows promising
results, especially in high risk or at advanced stage SPEOC patients.
The combined application of adjuvant radiotherapy and adjuvant
chemotherapy reduces the risk of relapse or death and increases
overall survival in SPEOC patients.3‒8,18,20,28,44,46,49
In conclusion, the systematic surgical staging plays a crucial role
in the treatment of SPEOC and offers many diagnostic, prognostic
and therapeutic advantages. 3‒8,10,11,13,17‒20,23,24,26 Additionally, it allows
more sound and objective decisions on the necessity of postoperative
adjuvant treatment in patients with SPEOC, in order to maximize
survival and minimize the morbidity of over‒treatment (radiation
injury, regimen‒related toxicity) and the effects of under‒treatment
(recurrent disease, increased mortality).3‒8,23‒26
Acknowledgments
None.
Conflicts of interest
None.
References
1. Decavalas G, Adonakis G, Androutsopoulos G, et al. Synchronous
primary endometrial and ovarian cancers: a case report. Eur J Gynaecol
Oncol. 2006;27(4):434‒436.
2. Terzakis E, Androutsopoulos G, Adonakis G, et al. Fallopian tube
primary cancer: report of 5 cases and review of the literature. Eur J
Gynaecol Oncol. 2011;32(1):95‒98.
3. Androutsopoulos G, Decavalas G. Synchronous primary endometrial
and ovarian cancers. J Community Med Health Educ. 2013;3(7):e120.
4. Androutsopoulos G, Decavalas G. Synchronous primary endometrial
and ovarian cancers: pathogenesis, treatment and prognosis. Int J Clin
Ther Diagn. 2(601):2014.
5. Androutsopoulos G, Decavalas G. Synchronous primary endometrial
and ovarian cancers: a critical update. Int J Gynecol Clin Pract .
2015;2:106‒109.
6. Androutsopoulos G, Adonakis G, Tsamantas A, et al. Synchronous
primary cancers in a woman with scleroderma: a case report. Eur J
Gynaecol Oncol. 2008;29(5):548‒550.
7. Androutsopoulos G, Michail G, Adonakis G, et al. Current treatment
approach of endometrial cancer. Int J Clin Ther Diagn. 2015;S1(3):8‒11.
8. Androutsopoulos G, Adonakis G, Tsamandas A, et al. Systemic
sclerosis and multiple cancers of the female genital tract: prolonged
survival following current treatment strategies. Case Rep Rheumatol .
2011;392068.
9. Grigoriadis C, Androutsopoulos G, Zygouris D, et al. Synchronous
squamous cell carcinoma of the endometrium and endometrioid
adenocarcinoma of the ovary. Eur J Gynaecol Oncol. 2012;33(6):666‒668.
10. Ayhan A, Yalcin OT, Tuncer ZS, et al. Synchronous primary
malignancies of the female genital tract. Eur J Obstet Gynecol Reprod
Biol. 1992;45(1):63‒66.
11. Tong SY , Lee YS, Park JS, et al. Clinical analysis of synchronous
primary neoplasms of the female reproductive tract. Eur J Obstet
Gynecol Reprod Biol. 2008;136(1):78‒82.
12. Deligdisch L, Szulman A. Multiple and multifocal carcinomas in female
genital organs and breast. Gynecol Oncol. 1975;3(3):181‒190.
13. Eisner R, Nieberg R, Berek J. Synchronous primary neoplasms of the
female reproductive tract. Gynecol Oncol. 1989;33(3):335‒339.
14. Matlock D, Salem F, Charles E, et al. Synchronous multiple primary
neoplasms of the upper female genital tract. Gynecol Oncol .
1982;13(2):271‒277.
15. Eser S, Gulhan I, Ozdemir R, et al. Synchronous primary cancers of the
female reproductive tract in Turkish women. Asian Pac J Cancer Prev.
2011;12(4):857‒859.
16. Soliman PT, Slomovitz BM, Broaddus RR, et al. Synchronous primary
cancers of the endometrium and ovary: a single institution review of 84
cases. Gynecol Oncol. 2004;94(2):456‒462.
17. Zaino R, Whitney C, Brady MF, et al. Simultaneously detected
endometrial and ovarian carcinomas‒‒a prospective clinicopathologic
study of 74 cases a gynecologic oncology group study. Gynecol Oncol.
2001;83(2):355‒362.
18. Liu Y , Li J, Jin H, et al. Clinicopathological characteristics of patients
with synchronous primary endometrial and ovarian cancers. A review of
43 cases. Oncol Lett. 2013;5(1):267‒270.
19. Signorelli M, Fruscio R, Lissoni A, et al. Synchronous early‒
stage endometrial and ovarian cancer. Int J Gynaecol Obstet .
2008;102(1):34‒38.
20. Chiang Y , Chen C, Huang C, et al. Synchronous primary cancers of the
endometrium and ovary. Int J Gynecol Cancer. 2008;18(1):159‒164.
21. Rodolakis A, Thomakos N, Akrivos N, et al. Clinicopathologic insight of
simultaneously detected primary endometrial and ovarian carcinomas.
Arch Gynecol Obstet. 2012;285(3):817‒821.
22. Pearl ML, Johnston CM, Frank TS, Synchronous dual primary ovarian
and endometrial carcinomas. Int J Gynaecol Obstet. 1993;43(3):305‒312.
23. Androutsopoulos G, Decavalas G. Management of endometrial cancer.
Int J Translation Community Dis. 2013;1(1):1‒3.
24. Androutsopoulos G. Current treatment options in patients with
endometrial cancer. J Community Med Health Educ. 2012;2(12):e113.
25. Androutsopoulos G, Decavalas G. Endometrial cancer: current treatment
strategies. World J Oncol Res. 2014;1(1):1‒4.
26. ACOG. Management of endometrial cancer. ACOG practice bulletin
#65. 2005;106(2):413‒425.
27. Pecorelli S. Revised FIGO staging for carcinoma of the vulva, cervix,
and endometrium. Int J Gynaecol Obstet. 2009;105(2):103‒104.
28. Colombo N, Preti E, Landoni F, et al. Endometrial cancer: ESMO
Clinical Practice Guidelines for diagnosis, treatment and follow‒up. Ann
Oncol. 2013;24Suppl6:vi 33‒vi38.
29. Burke W, Orr J, Leitao M, et al. Endometrial cancer: a review and current
management strategies: part I. Gynecolgy Oncol. 2014;134(2):385‒392.
30. Androutsopoulos G, Adonakis G, Decavalas G. Present and future in
endometrial cancer treatment. Obstet Gynecol Int J. 2015;2(2):00031.
31. Prat J. Staging classification for cancer of the ovary, fallopian tube, and
peritoneum. Int J Gynaecol Obstet. 2014;124(1):1‒5.
32. Benedetti Panici P, Basile S, Maneschi F, et al. Systematic pelvic
lymphadenectomy vs. no lymphadenectomy in early‒stage
endometrial carcinoma: randomized clinical trial. J Natl Cancer Inst .
2008;100(23):1707‒1716.
33. Franchi M, Ghezzi F, Riva C, et al. Postoperative complications after
pelvic lymphadenectomy for the surgical staging of endometrial cancer.
J Surgery Oncology. 2001;78(4):232‒237.
34. May K, Bryant A, Dickinson H, et al. Lymphadenectomy for the
management of endometrial cancer. Cochrane Database Syst Rev .
2010(1):CD007585.
Current treatment options in patients with synchronous primary endometrial and ovarian cancers
218
Copyright:
©2016 Androutsopoulos et al.
Citation: Androutsopoulos G, Michail G, Decavalas G. Current treatment options in patients with synchronous primary endometrial and ovarian cancers.
Obstet Gynecol Int J. 2016;4(6):216‒218. DOI: 10.15406/ogij.2016.04.00134
35. Lachance J, Darus C, Rice L. Surgical management and postoperative
treatment of endometrial carcinoma. Rev Obstet Gynecolgy .
2008;1(3):97‒105.
36. Lowery W, Gehrig P, Ko E, et al. Surgical staging for endometrial cancer
in the elderly ‒ is there a role for lymphadenectomy? Gynecolgy Oncol.
2012;126(1):12‒15.
37. Ma S, Zhang H, Sun Y , et al. Synchronous primary cancers of the
endometrium and ovary: review of 43 cases. The Chinese‒German
Journal of Clinical Oncology. 2009;8(2):95‒99.
38. Heitz F, Amant F, Fotopoulou C, et al. Synchronous ovarian and
endometrial cancer‒an international multicenter case‒‒control study.
Int J Gynecolgy Cancer. 2014;24(1):54‒60.
39. Castro I, Connell P, Waggoner S, et al. Synchronous ovarian and
endometrial malignancies. Am J Clinical Oncol. 2000;23(5):521‒525.
40. Eifel P, Hendrickson M, Ross J, et al. Simultaneous presentation
of carcinoma involving the ovary and the uterine corpus. Cancer.
1982;50(1):163‒170.
41. Sheu BC, Lin HH, Chen CK, et al. Synchronous primary carcinomas of
the endometrium and ovary. Int J Gynaecol Obstet. 1995;51(2):141‒146.
42. Lim Y , Padma R, Foo L, et al. Survival outcome of women with
synchronous cancers of endometrium and ovary: a 10 year retrospective
cohort study. J Gynecolgy Oncol. 2011;22(4):239‒243.
43. Kong A, Johnson N, Kitchener H, et al. Adjuvant radiotherapy for stage
I endometrial cancer Cochrane Database Syst Rev. 2011;(4):CD003916.
44. Nout R, Smit V , Putter H Jurgenliemk‒Schulz I, et al. Vaginal
broachytherapy versus pelvic external beam radiotherapy for patients
with endometrial cancer of high‒intermediate risk (PORTEC‒2):
an open‒label, non‒inferiority, randomised trial. Lancet.
2010;375(9717):816‒823.
45. Burke W, Orr J, Leitao M, et al. Endometrial cancer: a review and current
management strategies: part II. Gynecolgy Oncol. 2014;134(2):393‒402
46. Chino J, Jones E, Berchuck A, et al. he influence of radiation modality
and lymph node dissection on survival in early‒stage endometrial
cancer. Int J Radiation Oncol Biolgy Phys. 2012;82(5):1872‒1879.
47. Creutzberg C, Nout R. The role of radiotherapy in endometrial cancer:
current evidence and trends. Curr Oncol Rep. 2011;13(6):472‒478.
48. Sorbe B, Horvath G, Andersson H, et al. External pelvic and
vaginal irradiation versus vaginal irradiation alone as postoperative
therapy in medium‒risk endometrial carcinoma: a prospective,
randomized study‒‒quality‒of‒life analysis. Int J Gynecolgy Cancer .
2012;22(7):1281‒1288.
49. Creutzberg C. GOG‒99: ending the controversy regarding pelvic
radiotherapy for endometrial carcinoma? Gynecolgy Oncol .
2004;92(3):740‒743.
50. Creutzberg C, van Putten W, Koper P, et al. Surgery and postoperative
radiotherapy versus surgery alone for patients with stage‒1 endometrial
carcinoma: multicentre randomised trial. PORTEC Study Group. Post
Operative Radiation Therapy in Endometrial Carcinoma. Lancet.
2000;355(9213):1404‒1411.
51. Keys H, Roberts J, Brunetto V , et al. A phase III trial of surgery with or
without adjunctive external pelvic radiation therapy in intermediate risk
endometrial adenocarcinoma: a Gynecologic Oncology Group study.
Gynecolgy Oncol. 2004;92(3):744‒751.
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