4.6 Article

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

期刊

GYNECOLOGIC ONCOLOGY
卷 165, 期 1, 页码 82-89

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ygyno.2022.02.006

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资金

  1. MD Anderson Ovarian Cancer Moon Shot
  2. National Institutes of Health [CA016672, CA217685, CA209904]
  3. American Cancer Society
  4. Ovarian Cancer Research Alliance
  5. Gordon Fund
  6. Dunwoody Fund
  7. Gulf Coast Consortia, through the Computational Cancer Biology Training Program (CPRIT Grant) [RP170593]
  8. GOG Scholar Investigator Award
  9. National Institutes of Health National Cancer Institute [K08 CA234333]
  10. Frank McGraw Memorial Chair in Cancer Research

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The study aimed to determine the clinical characteristics of patients who achieved pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) and to identify predictive or prognostic factors associated with pCR. The results showed that women with pCR after NACT had significantly longer recurrence-free survival (RFS) compared to those with residual viable tumor at the time of interval tumor-reductive surgery, and CA125 may serve as a biomarker for identifying these extreme responders preoperatively.
Objective. To determine the clinical characteristics of patients who attained pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) and to identify specific predictive or prognostic factors associated with pCR. Methods. Two distinct populations of patients who underwent NACT followed by interval tumor reductive surgery (TRS) were used in this retrospective study. The first contained 472 patients from a single institution. The second contained only pCR patients (67); those identified from population one, plus 44 obtained through collaborative institutions. Cox analysis and log-rank tests were performed to assess associations between clinical characteristics and pCR outcome, recurrence-free survival (RFS), and overall survival (OS). Results. The median RFS and OS in our pCR-only population was 24.2 and 80.8 months, respectively, with a median follow-up time of 32.4 months. In our single institution population, 23 patients attained pCR (4.9%) and had longer RFS compared to non-pCR patients with viable microscopic, optimal, or suboptimal residual disease (24.3 vs. 12.1 vs. 11.6 vs. 9.6months, p = 0.025, 0.012, 0.008, respectively), and longer OS compared to those with optimal or suboptimal residual disease (54.5 vs. 29.4 vs. 25.7 months, p = 0.027, 0.007, respectively). Patients were more than three-fold likely to attain pCR if their CA125 value was normal at the time of surgery (OR 3.54, 95% CI: 1.14-11.05, p = 0.029). Conclusions. Women with pCR after NACT have significantly longer RFS compared to those with residual viable tumor at the time of interval tumor-reductive surgery, and CA125 is plausible biomarker for identifying these extreme responders preoperatively. (C) 2022 Elsevier Inc. All rights reserved.

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