Literature DB >> 31283034

Prognostic role of pathologic response and cytoreductive status at interval debulking surgery after neoadjuvant chemotherapy for advanced epithelial ovarian cancer.

Margaret I Liang1,2,3, Emily N Prendergast1,2,3, Jeanine N Staples1, Christine H Holschneider3, Joshua G Cohen2, Ilana Cass1.   

Abstract

BACKGROUND: We sought to determine if complete pathologic response (cPR) and cytoreductive status at interval debulking surgery (IDS) after neoadjuvant chemotherapy (NACT) are associated with improved clinical outcomes in ovarian cancer.
METHODS: We evaluated 91 patients with advanced ovarian cancer who underwent NACT and IDS. Pathologic response, cytoreductive status, and outcomes were determined. Descriptive statistics, bivariate analysis, and Kaplan-Meier survival probabilities were calculated.
RESULTS: cPR occurred in 9 (10%), microscopic pathologic response (microPR) in 18 (20%), and macroscopic pathologic response (macroPR) in 64 (70%) patients. Median progression-free survival (PFS) for patients with cPR was significantly improved compared with patients with any pathologic residual disease (microPR/macroPR; undefined vs 10.9 months, P = .01); whereas, microPR was not associated with significantly improved PFS compared with macroPR (16.3 months vs 10 months, P = .08). Cytoreduction to no gross residual disease was associated with improved PFS (undefined vs 7.5 months vs 5.5 months, P < .01) and overall survival (undefined vs 38.7 months vs 12 months, P < .01) compared with visible residual disease less than or equal to 1 cm or suboptimal.
CONCLUSIONS: cPR is uncommon (10%) after NACT for advanced ovarian cancer. Better pathologic response and cytoreductive status are associated with improved PFS, emphasizing the importance of both chemotherapy response and surgical effort.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  complete pathologic response; cytoreduction surgical procedures; neoadjuvant therapy; ovarian epithelial cancer

Mesh:

Year:  2019        PMID: 31283034     DOI: 10.1002/jso.25612

Source DB:  PubMed          Journal:  J Surg Oncol        ISSN: 0022-4790            Impact factor:   3.454


  5 in total

1.  Clinical analysis of pathologic complete responders in advanced-stage ovarian cancer.

Authors:  Christopher J LaFargue; Katelyn F Handley; Nicole D Fleming; Alpa M Nick; Anca Chelariu-Raicu; Bryan Fellman; Tara Castellano; Aiko Ogasawara; Marianne Hom-Tedla; Erin A Blake; Alexandre A B A da Costa; Aleia K Crim; Alejandro Rauh-Hain; Shannon N Westin; Robert L Coleman; Koji Matsuo; Glauco Baiocchi; Kosei Hasegawa; Kathleen Moore; Anil K Sood
Journal:  Gynecol Oncol       Date:  2022-02-23       Impact factor: 5.482

2.  Application of J-Plasma in the excision of diaphragmatic lesions as part of complete cytoreduction in patients with advanced ovarian cancer.

Authors:  Vasilios Theodoulidis; Anastasia Prodromidou; Emmanouil Stamatakis; Nicholas Alexakis; Alexandros Rodolakis; Dimitrios Haidopoulos
Journal:  Mol Clin Oncol       Date:  2022-05-18

3.  Timing of surgery in patients with partial response or stable disease after neoadjuvant chemotherapy for advanced ovarian cancer.

Authors:  Roni Nitecki; Nicole D Fleming; Bryan M Fellman; Larissa A Meyer; Anil K Sood; Karen H Lu; J Alejandro Rauh-Hain
Journal:  Gynecol Oncol       Date:  2021-04-16       Impact factor: 5.304

4.  Microscopic diseases remain in initial disseminated sites after neoadjuvant chemotherapy for stage III/IV ovarian, tubal, and primary peritoneal cancer.

Authors:  Shinichi Tate; Kyoko Nishikimi; Kazuyoshi Kato; Ayumu Matsuoka; Michiyo Kambe; Takako Kiyokawa; Makio Shozu
Journal:  J Gynecol Oncol       Date:  2019-12-09       Impact factor: 4.401

5.  Elevated microRNA-7 inhibits proliferation and tumor angiogenesis and promotes apoptosis of gastric cancer cells via repression of Raf-1.

Authors:  Jing Lin; Zewa Liu; Shasha Liao; E Li; Xiaohua Wu; Wanting Zeng
Journal:  Cell Cycle       Date:  2020-09-15       Impact factor: 4.534

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.