scholarly journals Updated analysis of a phase II study of SOX plus trastuzumab for the patients with HER2 positive advanced or recurrent gastric cancer: KSCC/HGCSG/CCOG/PerSeUS1501B

2018 ◽  
Vol 29 ◽  
pp. viii225
Author(s):  
S. Yuki ◽  
K. Shinozaki ◽  
T. Kashiwada ◽  
T. Kusumoto ◽  
M. Iwatsuki ◽  
...  
2014 ◽  
Vol 32 (3_suppl) ◽  
pp. 79-79 ◽  
Author(s):  
Tsunehiro Takahashi ◽  
Kazuhiro Nishikawa ◽  
Akira Miki ◽  
Hirokazu Noshiro ◽  
Takaki Yoshikawa ◽  
...  

79 Background: The global, randomized, phase III ToGA study showed that the first-line treatment of trastuzumab (T-mab) combined with capecitabine and cisplatin a survival (OS) benefit for patients (pts) with HER2 positive advanced or recurrent gastric cancer. However, there is no report concerning about the efficacy and safety of T-mab containing second-line treatment for T-mab naïve pts with HER2 positive advanced or recurrent gastric cancer. Therefore, we planned a phase II study of paclitaxel plus T-mab in this setting. Methods: JFMC45-1102 is multicentre phase II study. Pts with HER2 positive (IHC3+ or IHC2+/FISH+), histologically confirmed gastric adenocarcinoma, age ≥ 20, received one or more prior chemotherapy but no prior therapy with T-mab, normal left ventricular ejection fraction (LVEF ≥ 50%) were eligible. Pts received paclitaxel (80 mg/m2 on days 1, 8, and, 15 q4w) plus T-mab (8 mg/kg for the initial dose, followed by 6 mg/kg q3w) until disease progression, unacceptable toxicity or patient’s refusal. The primary endpoint was overall response rate (ORR), and the secondary endpoints include progression free survival (PFS), time to treatment failure (TTF), OS and safety. Results: A total of 47 pts were enrolled from September 2011 to March 2012.The primary endpoint ORR was 37.0% (95%CI, 23 to 52).Complete response was observed in 1 case (2.2%).The PFS data was matured, and the median PFS was 5.09 months (95%CI, 3.79 to 6.49), TTF 5.09 months (95%CI, 3.72 to 6.49), OS 16.81 months (95%CI, 13.54 to 18.65). One patient died of lung pulmonary fibrosis during therapy. The most common grade 3-4 adverse events were leucopenia (17.4%), neutropenia (32.6%), anemia (15.2%). Conclusions: Combination chemotherapy of paclitaxel plus T-mab is generally well tolerated and showed promising activity for T-mab naïve patients with HER2 positive previously treated advanced or recurrent gastric cancer. Clinical trial information: UMIN000006223.


2018 ◽  
Vol 29 ◽  
pp. viii224-viii225
Author(s):  
K. Chin ◽  
A. Takashima ◽  
K. Minashi ◽  
S. Kadowaki ◽  
T. Nishina ◽  
...  

2019 ◽  
Vol 84 (6) ◽  
pp. 1365-1365
Author(s):  
Fernando Rivera ◽  
C. Romero ◽  
P. Jimenez-Fonseca ◽  
M. Izquierdo-Manuel ◽  
A. Salud ◽  
...  

Phase II study to evaluate the efficacy of Trastuzumab in combination with Capecitabine.


2009 ◽  
Vol 12 (4) ◽  
pp. 212-218 ◽  
Author(s):  
Takaki Yoshikawa ◽  
Akira Tsuburaya ◽  
Ken Shimada ◽  
Atsushi Sato ◽  
Makoto Takahashi ◽  
...  

2007 ◽  
Vol 25 (18_suppl) ◽  
pp. 15025-15025
Author(s):  
H. Takiuchi ◽  
H. Imamura ◽  
M. Imano ◽  
Y. Kimura ◽  
H. Ishida ◽  
...  

15025 Background: We report here results of phase II study for a combination therapy with paclitaxel/doxifluridine to treat advanced/recurrent gastric cancer showing resistance to S-1. S-1 is an oral fluoropyrimidine drug that combines tegafur, CDHP, and oxonic acid (Oxo), which has been most frequently used in Japan. Methods: Subject registration was started to employ 35 patients with advanced/recurrent gastric cancer, who were selected among those with measurable lesions fitting to RECIST, and with resistant to S-1 treatment (PS, 0–2; and patient’s ages ranged from over 20 to under 75 years). We employed dosages that Hyodo et. al. used in phase I study and recommended as a standard regimen including paclitaxel, 80 mg/m2, i.v. on days 1 and 8; and doxifluridine, 600 mg/m2, p.o. on days 1–14.. These were repeated every 3 weeks. Primary endpoint of present phase II study was: RR; and secondary endpoints were OS, PFS, and onset rate of adverse events. Results: From September, 2003 to March, 2005, 35 patients were registered: including 28 men; 7 women; median age of 66 years (range, 49–75 years); and PS levels were, zero with 21 and one with 14 patients. In 33 eligible patients, except 2, clinical usefulness was evaluated resulting in response rate of 18.2% (PR, 6; SD, 15; PD, 10; and NE, 2 patients). OS was 321 days, and PFS was 119 days. Severe adverse events were found in 3 patients to discontinue the present treatment though; other adverse events were relatively mild without no death due to the present therapy. Conclusions: Patients in the present study with advanced/recurrent gastric cancer were those resistant to S-1 treatment. Response rate was 18.2% increasing to 63.6% when SD was added. OS resulted in relatively long period of 321 days, while OS from initial time starting S-1 treatment was 619 days. This suggests that the present treatment is useful as the sequential therapy. Adverse events were controllable suggesting a high reliability of the present therapy. In conclusion, the present therapy with paclitaxel/doxifluridine could be a treatment of choice as an useful second line chemotherapy for patients undergone S-1 treatment. No significant financial relationships to disclose.


2010 ◽  
Vol 33 (1) ◽  
pp. 56-60 ◽  
Author(s):  
Chong Kun Im ◽  
Sun Young Rha ◽  
Hei-Cheul Jeung ◽  
Joong Bae Ahn ◽  
Sang Joon Shin ◽  
...  

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