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Comparison of the Efficacy and Toxicity Between Radiotherapy and Chemotherapy in Nodal and Isolated Nonnodal Recurrence of Ovarian Cancer
  1. Maria Lee, MD*,
  2. Sang Wun Kim, MD, PhD*,
  3. San Hui Lee, MD*,
  4. Jiheum Paek, MD*,
  5. Ga Won Yim, MD*,
  6. Gwi Eon Kim, MD, PhD,
  7. Sunghoon Kim, MD, PhD*,
  8. Jae Hoon Kim, MD, PhD*,
  9. Young Tae Kim, MD, PhD* and
  10. Eun Ji Nam, MD*
  1. *Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, and
  2. Department of Radiation Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea.
  1. Address correspondence and reprint requests to Eun Ji Nam, MD, Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Yonsei University College of Medicine, 250 Seongsanno, 134 Shinchon-dong, Seodaemun-gu, CPO Box 8044, Seoul, Korea 120-752. E-mail: nahmej6{at}yuhs.ac.

Abstract

Objectives: To assess and compare the efficacy and toxicity of radiotherapy (RT) versus chemotherapy (CT) in patients with nodal and isolated nonnodal recurrence of ovarian cancer.

Methods: Records of 67 patients treated for nodal or isolated nonnodal ovarian cancer recurrence (50 treated with RT and 17 treated with CT) between 2001 and 2010 were retrospectively reviewed. Patients' responses to RT and CT were assessed by the Response Evaluation Criteria in Solid Tumors, and toxicity was evaluated according to the National Cancer Institute Common Toxicity Criteria, version 3.0. Progression-free survival and overall survival were calculated using the Kaplan-Meier method.

Results: The overall response rate was 64.0% in the RT group and 16.7% in the CT group (P = 0.003). The median follow-up time was 38 months (range, 3-97 months) for RT and 18 months (range, 70-64 months) for CT. The median progression-free survival was 6 months for radiotherapy and 5 months for chemotherapy (P = 0.212). Median overall survival between the 2 groups was not significantly different (P = 0.246). There was no RT-mediated grade 3 or 4 hematologic toxicity, but overall toxicity was not significantly different between the 2 groups.

Conclusions: Radiotherapy resulted in a better response and tolerable toxicities compared to CT in patients with either nodal or isolated nonnodal ovarian cancer recurrence. However, progression-free survival and overall survival did not differ between RT and CT. A prospective, multicenter, randomized controlled study is needed to evaluate the survival benefits of RT for ovarian cancer.

  • Ovarian cancer
  • Nodal recurrence
  • Isolated recurrence
  • Radiotherapy
  • Chemotherapy

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Footnotes

  • This study was supported by grants from the 2010 Yonsei University Research Fund (6-2010-0006), a 2009 Faculty Research Grant from Yonsei University College of Medicine (6-2009-0127), and a National Research Foundation of Korea Grant funded by the Korean Government (7-2010-0264).

  • The authors declare that there are no conflicts of interest.