J Cancer 2021; 12(3):946-953. doi:10.7150/jca.52711 This issue Cite

Research Paper

The added value of CA125 normalization before interval debulking surgery to the chemotherapy response score for the prognostication of ovarian cancer patients receiving neoadjuvant chemotherapy for advanced disease

Wei-feng Liang1,2*, Li-juan Wang2*, Hui Li2, Chang-hao Liu2, Miao-fang Wu2✉, Jing Li2✉

1. Department of Gynecology and Obstetrics, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, 266035, People's Republic of China.
2. Department of Gynecologic Oncology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, People's Republic of China.
*These authors contributed equally to this work.

Citation:
Liang Wf, Wang Lj, Li H, Liu Ch, Wu Mf, Li J. The added value of CA125 normalization before interval debulking surgery to the chemotherapy response score for the prognostication of ovarian cancer patients receiving neoadjuvant chemotherapy for advanced disease. J Cancer 2021; 12(3):946-953. doi:10.7150/jca.52711. https://www.jcancer.org/v12p0946.htm
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Abstract

Objective: To investigate whether CA125 normalization following neoadjuvant chemotherapy (NACT) can complement the chemotherapy response system (CRS) in the prognostication of patients with tubo-ovarian high-grade serous carcinoma (HGSC).

Methods: In total, 118 HGSC patients who received NACT followed by interval debulking surgery (IDS) for FIGO stage IIIC-IV disease were included, and their clinical data were retrospectively reviewed. The primary endpoint was progression-free survival (PFS). Cox regression analysis was performed to identify predictors of PFS.

Results: Following NACT, CRS3 was noted in 35 patients (29.7%), and CA125 normalization (≤ 35 U/ml) was noted in 54 patients (45.8%). Both CRS3 and CA125 normalization were identified as independent prognosticators of PFS. Combining these two factors, we stratified the 106 patients into three groups with different risks of recurrence: low-risk group (CRS3 + post-NACT CA125≤ 35 U/ml; n = 17, 14.4%), intermediate-risk group (CRS3 + post-NACT CA125 > 35 U/ml; n = 19, 16.1%) and high-risk group (CRS1-2; n= 82, 69.5%). The differences in PFS between the three groups were significant (log-rank test, P < 0.0001). In Cox regression analyses, the new stratification method was found to have an independent prognostic effect.

Conclusion: Both the CRS system and the normalization of CA125 following NACT could reliably predict the risk of recurrence following primary treatment. The combination of the two factors refined the prognostic stratification of HGSC patients who were treated with NACT and IDS.

Keywords: biomarkers, chemotherapy, gynecologic oncology, prognosis


Citation styles

APA
Liang, W.f., Wang, L.j., Li, H., Liu, C.h., Wu, M.f., Li, J. (2021). The added value of CA125 normalization before interval debulking surgery to the chemotherapy response score for the prognostication of ovarian cancer patients receiving neoadjuvant chemotherapy for advanced disease. Journal of Cancer, 12(3), 946-953. https://doi.org/10.7150/jca.52711.

ACS
Liang, W.f.; Wang, L.j.; Li, H.; Liu, C.h.; Wu, M.f.; Li, J. The added value of CA125 normalization before interval debulking surgery to the chemotherapy response score for the prognostication of ovarian cancer patients receiving neoadjuvant chemotherapy for advanced disease. J. Cancer 2021, 12 (3), 946-953. DOI: 10.7150/jca.52711.

NLM
Liang Wf, Wang Lj, Li H, Liu Ch, Wu Mf, Li J. The added value of CA125 normalization before interval debulking surgery to the chemotherapy response score for the prognostication of ovarian cancer patients receiving neoadjuvant chemotherapy for advanced disease. J Cancer 2021; 12(3):946-953. doi:10.7150/jca.52711. https://www.jcancer.org/v12p0946.htm

CSE
Liang Wf, Wang Lj, Li H, Liu Ch, Wu Mf, Li J. 2021. The added value of CA125 normalization before interval debulking surgery to the chemotherapy response score for the prognostication of ovarian cancer patients receiving neoadjuvant chemotherapy for advanced disease. J Cancer. 12(3):946-953.

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