Adjuvant Chemotherapy for Stage I Ovarian Clear Cell Carcinoma. 2024

Naoki Horikawa, and Yoshihide Inayama, and Miki Otsuki, and Kota Yamauchi, and Yukako Mizuno, and Saya Kiyoshige, and Yukiko Taga, and Kazuki Yamano, and Maki Umemiya, and Motonori Matsubara, and Yukio Yamanishi, and Takahito Ashihara, and Ikuko Emoto, and Masaki Mandai, and Kenzo Kosaka, and Ken Yamaguchi
Departments of Obstetrics and Gynecology, Kurashiki Central Hospital, Okayama, Kyoto University Hospital and Kyoto Medical Center, Kyoto, Kitano Hospital and Osaka Red Cross Hospital, Osaka, Nagahama Red Cross Hospital, Shiga, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Toyooka Hospital, Hyogo, and Shizuoka General Hospital, Shizuoka, Japanese Red Cross Wakayama Medical Center, Wakayama, and the Department of Gynecology, Shiga General Hospital, Shiga, Japan.

OBJECTIVE To assess the association between postoperative chemotherapy and the prognosis of patients with stage I ovarian clear cell carcinoma. METHODS This was a retrospective cohort study of patients with stage I ovarian clear cell carcinoma who underwent surgery, including hysterectomy and bilateral salpingo-oophorectomy, between 2005 and 2019 at 11 affiliated institutions. Patients with preoperative lymph node enlargement, and those who underwent fertility-sparing surgery were excluded. The primary outcome was disease-free survival and overall survival, and was investigated as a secondary outcome. We used propensity score overlap weighting to adjust for confounding factors and estimated the adjusted hazard ratios (HRs) and 95% CIs for the disease-free and overall survival of patients in the control group that did not receive chemotherapy and in the platinum-based multiagent chemotherapy group during the follow-up period. RESULTS In total, 283 patients (64 in the control group and 219 in the chemotherapy group) were included. Five-year disease-free survival was 0.77 (95% CI, 0.66-0.89) in the control group and 0.86 (95% CI, 0.81-0.91) in the chemotherapy group. The unadjusted HR was 0.69 (95% CI, 0.36-1.32; P=.26). After adjustment, patients who received chemotherapy had a significantly lower risk of recurrence than those in the control group (weighted HR for disease-free survival: 0.43; 95% CI, 0.20-0.90; P=.026). There was no difference in overall survival (weighted HR 0.68; 95% CI, 0.27-1.69; P=.40). CONCLUSIONS Postoperative platinum-based multiagent chemotherapy was associated with improved disease-free survival. These findings provide crucial information for shared decision-making regarding whether to undergo adjuvant chemotherapy.

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