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Aim of our study was to identify the prognostic factors of secondary cytoreductive surgery on survival in patients with recurrent epithelial ovarian cancer

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J Gynecol Oncol Vol. 20, No. 3:199, September 2009 DOI:10.3802/jgo.2009.20.3.199

199 In reply: Different role of secondary cytoreductive surgery by surgeon’s experience and hospital facility

We appreciate the interest, comments, and questions by Dr.

Kim et al. regarding our recent article.1 We would like to reply and comment on these questions.

Aim of our study was to identify the prognostic factors of secondary cytoreductive surgery on survival in patients with recurrent epithelial ovarian cancer. In our study, recurrent disease in the pelvis which can be easily removed and long dis- ease free interval are independent prognostic factors.1

Kim et al. asked the benefit of secondary cytoreduction for platinum-sensitive and resectable tumors. Our clinical expe- rience and published report support the curative role of secon- dary cytoreductive surgery in such patients.2 As Kim et al. de- scribed, the GOG 213 study may provided the answer for the role of secondary cytoreductive surgery compared to chemo- therapy.3 However, we do not expect that patients should un- dergo secondary cytoreductive surgery from the results of GOG 213, because surgical candidates are determined tenta- tively and arbitrarily by surgeons before the first random- ization in the GOG 213 trial. Before randomization, the sur- geon’s decision is the initial step in deciding which patients should be included and excluded. For example, some surgeons think that resection of a tumor at the porta hepatis or cardio- phrenic lymph node,4 or a diaphragmatic tumor near the hep- atic vein or conglomerated lymph node metastases near great vessel is feasible: they are surgical candidates for the GOG213 trial. Some surgeons do not think so, and they are excluded.

The results from the GOG213 trial may offer clues for the role of secondary cytoreductive surgery but, true benefits at the bottom line we may not find. Every surgical trial has a big bias from surgeons themselves. For ovarian cancer, the bias could be enlarged because extensiveness of cytoreductive surgery quite differs between surgeons and/or hospitals.

We agree the Kim et al.’s comment on external validation of the criteria for secondary cytoreductive surgery. Currently, historical comparison is not allowed because patients’ charac- teristics are quite different as far as we know. Our study in- cluded a significant number of ovarian cancer patients who underwent primary cytoreductive surgery at other hospitals:

therefore the application of extensive cytoreductive surgery is

quite questionable. Application of extensive cytoreductive ef- fort at primary cytoreductive surgery may be another variable in the analysis of the role of secondary cytoreductive surgery.

In conclusion, we believe that extensive cytoreductive effort to remove tumor burden while allowing minimal surgical morbidity may be attempted for patients with recurrent ovar- ian cancer in moderation to the surgeon’s experience and hos- pital facility.

REFERENCES

1. Bae J, Lim MC, Choi JH, Song YJ, Lee KS, Kang S, et al.

Prognostic factors of secondary cytoreductive surgery for pa- tients with recurrent epithelial ovarian cancer. J Gynecol Oncol 2009; 20: 101-6.

2. Chi DS, McCaughty K, Diaz JP, Huh J, Schwabenbauer S, Hummer AJ, et al. Guidelines and selection criteria for secon- dary cytoreductive surgery in patients with recurrent, plati- num-sensitive epithelial ovarian carcinoma. Cancer 2006; 106:

1933-9.

3. National Cancer Institute. Defining Therapy for Recurrent Platinum-sensitive Ovarian Cancer [Internet]. Bethesda: National Cancer Institute; c2009 [cited 2009 Sep 12]. Available from:

http://www.cancer.gov/clinicaltrials/ft-GOG-0213.

4. Lim MC, Lee HS, Jung DC, Choi JY, Seo SS, Park SY. Pathological diagnosis and cytoreduction of cardiophrenic lymph node and pleural metastasis in ovarian cancer patients using video-assisted thoracic surgery. Ann Surg Oncol 2009; 16: 1990-6.

Myong Cheol Lim, Jaeman Bae, Sang-Yoon Park Center for Uterine Cancer, Research Institute and Hospital,

National Cancer Center, Goyang, Korea

Correspondence to Sang-Yoon Park

Center for Uterine Cancer, Research Institute and Hospital, National Cancer Center, 111, Jungbalsan-ro, Ilsandong-gu, Goyang 410-769, Korea

Tel: 82-31-920-2381, Fax: 82-31-920-1238 E-mail: sypark.ncc@hotmail.com

DOI:10.3802/jgo.2009.20.3.199

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