MD Anderson Cancer Center
Gynecologic Oncology and Reproductive Medicine

Moderator of 2 Sessions

Session Type
Debate
Date
09/29/2022
Session Time
10:40 AM - 11:25 AM
Room
Hall 501
Session Icon
Live
Session Description
During the session, different approaches (surgery via laparotomy, surgery via laparoscopy, or no surgery) to patients with complete response after the treatment of neoadjuvant chemotherapy in advanced epithelial ovarian carcinoma will be discussed. The results of randomized trials will be presented in order to determine the most appropriate approach/approaches for this group of patients.
Session Type
Debate
Date
10/01/2022
Session Time
09:15 AM - 10:00 AM
Room
Hall 501
Session Icon
Live
Session Description
This session will focus on recent paradigm changes in treatment landscape of endometrial cancer with a focus on treatment of low grade endometrial cancer. Different approaches to treatment including chemotherapy, checkpoint inhibitor therapy, and combination therapy with pembrolizumab and lenvatanib will be discussed. The role of hormonal therapies (i.e.megesterol acetate, letrozole, etc) and hormonal combination therapies in the treatment of low grade endometrial cancer will be highlighted.

Presenter of 1 Presentation

COMBINATION THERAPY WITH TOPOTECAN, PACLITAXEL, AND BEVACIZUMAB IMPROVES PROGRESSION-FREE SURVIVAL IN PATIENTS WITH RECURRENT HIGH-GRADE NEUROENDOCRINE CARCINOMA OF THE CERVIX: A NECTUR STUDY

Session Type
Plenary Session
Date
09/29/2022
Session Time
04:55 PM - 05:55 PM
Room
Hall 501
Session Icon
Live
Lecture Time
05:27 PM - 05:35 PM
Onsite or Pre-Recorded
Onsite

Abstract

Objectives

The objective of this study was to evaluate the efficacy of the three-drug regimen topotecan, paclitaxel, and bevacizumab (TPB) in women with recurrent high-grade neuroendocrine cervical cancer (HGNECC).

Methods

This retrospective cohort study used data from the Neuroendocrine Cervical Tumor Registry (NeCTuR). The study compared women with recurrent HGNECC who received TPB as first- or second-line therapy for recurrence and women with recurrent HGNECC who received chemotherapy but not TPB. Progression-free survival from the start of treatment for recurrence to the next recurrence or death, overall survival from first recurrence, and response rates were evaluated.

Results

The study included 57 patients who received TPB as first- or second-line treatment for recurrence and 48 patients who received chemotherapy but not TPB for recurrence. Median progression-free survival was 8.2 months in the TPBgroup compared to 3.1 months in the non-TPBgroup, with a hazard ratio for progression of 0.23 (95% CI 0.14-0.40; P < 0.0001). In the TPB group, 16% had stable disease, 38% had a partial response, and 16% had a complete response. Significantly more patients in the TPB group than in the non-TPB group remained on treatment at 6 months (67% vs. 25%, P = 0.0002) and 1 year (24% vs. 6%, P = 0.03). Median overall survival was 16.9 months in the TPBgroup compared to 14.0 months in the non-TPB group, with a hazard ratio for death of 0.89 (95% CI 0.55-1.45).

Conclusions

TPB is an active regimen in women with recurrent HGNECC and improves progression-free survival while decreasing the hazard ratio for progression.

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