z-logo
Premium
Efficacy of trastuzumab emtansine in Japanese patients with previously treated HER2‐positive locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma: A subgroup analysis of the GATSBY study
Author(s) -
Shitara Kohei,
Honma Yoshitaka,
Omuro Yasushi,
Yamaguchi Kensei,
Chin Keisho,
Muro Kei,
Nakagawa Shintaro,
Kawakami Satoe,
Hironaka Shuichi,
Nishina Tomohiro
Publication year - 2020
Publication title -
asia‐pacific journal of clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 29
eISSN - 1743-7563
pISSN - 1743-7555
DOI - 10.1111/ajco.13243
Subject(s) - taxane , medicine , trastuzumab emtansine , hazard ratio , trastuzumab , clinical endpoint , docetaxel , oncology , adverse effect , confidence interval , cancer , gastroenterology , randomized controlled trial , breast cancer
Aim The phase II/III GATSBY study (NCT01641939) showed that trastuzumab emtansine did not have an efficacy benefit over taxane in patients with previously treated, human epidermal growth factor receptor 2 (HER2)‐positive advanced or metastatic gastric or gastroesophageal junction cancer. We evaluated patients from Japanese centers within GATSBY. Methods In stage one, patients (randomized 2:2:1) received trastuzumab emtansine 3.6 mg/kg every 3 weeks, trastuzumab emtansine 2.4 mg/kg weekly, or physician's choice of taxane (docetaxel 75 mg/m² every 3 weeks or paclitaxel 80 mg/m² weekly). In stage two, patients (randomized 2:1) received trastuzumab emtansine 2.4 mg/kg weekly or taxane. Eligible patients had centrally assessed HER2‐positive disease and progression during or after first‐line therapy. Primary endpoint was overall survival. We present the 2.4 mg/kg weekly data. Results Eighty‐two patients were randomized (intention‐to‐treat: 48 to trastuzumab emtansine 2.4 mg/kg weekly, 23 to taxane; September 2012‐August 2014) at 19 sites. Median overall survival was 11.8 months (95% confidence interval [CI], 9.3‐16.3) with trastuzumab emtansine 2.4 mg/kg weekly and 10.0 months (95% CI, 7.1‐18.2) with taxane (unstratified hazard ratio = 0.94, 95% CI, 0.52‐1.72). Trastuzumab emtansine 2.4 mg/kg weekly, versus taxane, was associated with fewer grade ≥3 adverse events (AEs; 52.1% vs 68.2%) and serious AEs (14.6% vs 18.2%). There were no fatal AEs. Conclusions Efficacy in Japanese patients within GATSBY was consistent with the overall population; overall survival was not prolonged with trastuzumab emtansine 2.4 mg/kg weekly versus taxane. The safety profile of trastuzumab emtansine was similar to the overall population.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here