TY - JOUR
T1 - Analysis of the relapse patterns and risk factors of endometrial cancer following postoperative adjuvant chemotherapy in a phase III randomized clinical trial
AU - Nomura, Hiroyuki
AU - Aoki, Daisuke
AU - Susumu, Nobuyuki
AU - Mizuno, Mika
AU - Nakai, Hidekatsu
AU - Arai, Masahide
AU - Nishio, Shin
AU - Tokunaga, Hideki
AU - Nakanishi, Toru
AU - Watanabe, Yoh
AU - Yaegashi, Nobuo
AU - Yokoyama, Yoshihito
AU - Takehara, Kazuhiro
N1 - Funding Information:
We thank the Japanese Gynecologic Oncology Group (JGOG) institutions and all investigators participated in the JGOG2043 study. And we also thank the JGOG Data Center (Clinical Trial Coordinating Center, Kitasato Academic Research Organization, Kitasato University) for their role in data management.
Funding Information:
Daisuke Aoki reports grants from Chugai Pharmaceutical, Sanofi, and Taiho Pharmaceutical; personal fees from AstraZeneca, Chugai Pharmaceutical, Daiichi Sankyo, Janssen Pharmaceutical, Kyowa Hakko Kirin, MSD, Nippon Kayaku, Ono Pharmaceutical, Taiho Pharmaceutical, Takeda Pharmaceutical, and Yakult Honsha, outside the submitted work. Kazuhiro Takehara reports personal fees from AstraZeneca, Chugai Pharmaceutical, Eisai, and Ono Pharmaceutical, outside the submitted work. All other authors declare that they have no conflicts of interest.
Funding Information:
This work was partially supported by Health Labour Sciences Research Grant in Japan, which was provided to Daisuke Aoki. JGOG was supported by unrestricted grants from AstraZeneca, Asuka Pharmaceutical, Bristol-Myers Squibb, Chiyoda Technol Corporation, Chugai Pharmaceutical, Daiichi-Sankyo, Eisai, Fuji Pharma, Janssen Pharmaceutical, Kaken Pharmaceutical, Kyowa Hakko Kirin, Nippon Kayaku, Ono Pharmaceutical, Roche-Diagnostics, Sanofi-aventis, Sawai Pharmaceutical, Shionogi, SHISEIDO, Taiho Pharmaceutical, Yakult Honsha, and ZERIA Pharmaceutical.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/12
Y1 - 2019/12
N2 - Objective: This study was to analyze patterns and risk factors of relapse after postoperative adjuvant chemotherapy for endometrial cancer. Methods: Among patients enrolled in a randomized phase III trial (JGOG2043) investigating the efficacy of adjuvant chemotherapy for endometrial cancer at a high risk of progression, the recurrent patients were studied. Clinical information were collected, and correlation between relapse-related factors and clinicopathological factors were analyzed. Results: Among 193 patients analyzed, 50% had local relapse and 63% had distant relapse. Local relapse involved regional lymph nodes in 30%, while distant relapse involved the abdominal cavity in 42%. Imaging was used to confirm relapse in 83%, and the median disease-free interval (DFI) was 11.5 months. Factors showing a significant correlation with DFI ≤12 months were residual tumor at surgery (p < 0.01), Grade 3 histology (p < 0.01), and lymph node metastasis (p = 0.03). In contrast, treatment with paclitaxel and carboplatin showed a significant correlation with DFI >12 months (p = 0.04). The median post-relapse overall survival (RS) was 23.9 months. In multivariate analysis, CA125 ≥ 100 U/mL prior to relapse (p < 0.01), distant metastasis (p < 0.01), DFI ≤ 12 months (p = 0.02), and not performing para-aortic lymphadenectomy (p = 0.01) were independently related to poor RS. Conclusions: Relapse of endometrial cancer following adjuvant chemotherapy often occurs by 1 year after treatment, with common relapse sites of the abdominal cavity and regional lymph nodes. Among treatment-related factors, RS was correlated with DFI and para-aortic lymphadenectomy.
AB - Objective: This study was to analyze patterns and risk factors of relapse after postoperative adjuvant chemotherapy for endometrial cancer. Methods: Among patients enrolled in a randomized phase III trial (JGOG2043) investigating the efficacy of adjuvant chemotherapy for endometrial cancer at a high risk of progression, the recurrent patients were studied. Clinical information were collected, and correlation between relapse-related factors and clinicopathological factors were analyzed. Results: Among 193 patients analyzed, 50% had local relapse and 63% had distant relapse. Local relapse involved regional lymph nodes in 30%, while distant relapse involved the abdominal cavity in 42%. Imaging was used to confirm relapse in 83%, and the median disease-free interval (DFI) was 11.5 months. Factors showing a significant correlation with DFI ≤12 months were residual tumor at surgery (p < 0.01), Grade 3 histology (p < 0.01), and lymph node metastasis (p = 0.03). In contrast, treatment with paclitaxel and carboplatin showed a significant correlation with DFI >12 months (p = 0.04). The median post-relapse overall survival (RS) was 23.9 months. In multivariate analysis, CA125 ≥ 100 U/mL prior to relapse (p < 0.01), distant metastasis (p < 0.01), DFI ≤ 12 months (p = 0.02), and not performing para-aortic lymphadenectomy (p = 0.01) were independently related to poor RS. Conclusions: Relapse of endometrial cancer following adjuvant chemotherapy often occurs by 1 year after treatment, with common relapse sites of the abdominal cavity and regional lymph nodes. Among treatment-related factors, RS was correlated with DFI and para-aortic lymphadenectomy.
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U2 - 10.1016/j.ygyno.2019.09.023
DO - 10.1016/j.ygyno.2019.09.023
M3 - Article
C2 - 31601493
AN - SCOPUS:85073034828
SN - 0090-8258
VL - 155
SP - 413
EP - 419
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 3
ER -