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Association details:
Evidence:
Evidence Level:
Sensitive: A2 - Guideline
New
Source:
Excerpt:
Preferred Regimens: Carboplatin/Paclitaxel/trastuzumab (for HER2-positive uterine serous carcinoma)
Secondary therapy:
carboplatin + paclitaxel
Evidence Level:
Sensitive: C3 – Early Trials
New
Title:

Randomized Phase II Trial of Carboplatin-Paclitaxel Versus Carboplatin-Paclitaxel-Trastuzumab in Uterine Serous Carcinomas That Overexpress Human Epidermal Growth Factor Receptor 2/neu

Excerpt:
Among all patients, median progression free survival was 8.0 months (control) versus 12.6 months (experimental; P = .005; hazard ratio [HR], 0.44; 90% CI, 0.26 to 0.76). Similarly, median progression-free survival was 9.3 (control) versus 17.9 (experimental) months among 41 patients with stage III or IV disease undergoing primary treatment (P = .013; HR, 0.40; 90% CI, 0.20 to 0.80) and 6.0 (control) versus 9.2 months (experimental), respectively, among 17 patients with recurrent disease (P = .003; HR, 0.14; 90% CI, 0.04 to 0.53)....Addition of trastuzumab to carboplatin-paclitaxel was well tolerated and increased progression free survival. These encouraging results deserve further investigation to determine their impact on overall survival in patients with advanced or recurrent uterine serous carcinoma who overexpress HER2/neu.
Secondary therapy:
carboplatin + paclitaxel
DOI:
10.1200/JCO.2017.76.5966
Trial ID: