TY - JOUR
T1 - Final analysis of overall survival (OS) in the IPASS, an international multicenter phase III study on gefitinib and carboplatin/paclitaxel for treatment-naïve NSCLC patients
AU - Satouchi, Miyako
AU - Ichinose, Yukito
AU - Nishiwaki, Yutaka
AU - Ohe, Yuichiro
AU - Yamamoto, Nobuyuki
AU - Katakami, Nobuyuki
AU - Nakagawa, Kazuhiko
AU - Kiura, Katsuyuki
AU - Jiang, Haiyi
AU - Mok, Tony
AU - Saijo, Nagahiro
AU - Fukuoka, Masahiro
PY - 2012/4
Y1 - 2012/4
N2 - IPASS (Iressa Pan-Asia Study) is a phase III study conducted in East Asia that compared gefit-inib and carboplatin-paclitaxel among nonsmokers or former light smokers with pulmonary adenocarcinoma previously untreated with chemotherapy. It has already been reported that the primary endpoint progression-free survival (PFS), was significantly longer in the gefitinib group. Subset analysis via biomarkers has also been reported, whereby the gefitinib group in the epidermal growth factor receptor (EGFR) gene mutation subgroup showed a significantly greater extension in PFS and the gefitinib group in the mutation negative subgroup, a significantly shorter PFS. The final report on overall survival (OS) was reported at European Society for Medical Oncology (ESMO) congress in 2010, with the same content reported at a symposium in the Japan Lung Cancer Society Annual Meeting. The overall analysis showed an OS of 18.8 months in the gefitinib group and 17.4 months, chemotherapy group (HR = 0.90), indicating no difference between the two groups. Subset analysis respectively showed the median survival in the gefitinib and chemotherapy groups in the EGFR mutation positive subset to be 21.6 and 21.9 months, while the respective median survival in the negative cases was 11.2 and 12.7 months. These results indicate longer survival in any group among the EGFR mutation positive cases, but no difference in OS by treatment regardless of EGFR mutation status.
AB - IPASS (Iressa Pan-Asia Study) is a phase III study conducted in East Asia that compared gefit-inib and carboplatin-paclitaxel among nonsmokers or former light smokers with pulmonary adenocarcinoma previously untreated with chemotherapy. It has already been reported that the primary endpoint progression-free survival (PFS), was significantly longer in the gefitinib group. Subset analysis via biomarkers has also been reported, whereby the gefitinib group in the epidermal growth factor receptor (EGFR) gene mutation subgroup showed a significantly greater extension in PFS and the gefitinib group in the mutation negative subgroup, a significantly shorter PFS. The final report on overall survival (OS) was reported at European Society for Medical Oncology (ESMO) congress in 2010, with the same content reported at a symposium in the Japan Lung Cancer Society Annual Meeting. The overall analysis showed an OS of 18.8 months in the gefitinib group and 17.4 months, chemotherapy group (HR = 0.90), indicating no difference between the two groups. Subset analysis respectively showed the median survival in the gefitinib and chemotherapy groups in the EGFR mutation positive subset to be 21.6 and 21.9 months, while the respective median survival in the negative cases was 11.2 and 12.7 months. These results indicate longer survival in any group among the EGFR mutation positive cases, but no difference in OS by treatment regardless of EGFR mutation status.
KW - Epidermal growth factor receptor mutation
KW - Gefitinib (Iressa®)
KW - Iressa Pan-Asia Study (IPASS)
UR - http://www.scopus.com/inward/record.url?scp=84862528693&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84862528693&partnerID=8YFLogxK
U2 - 10.2482/haigan.52.153
DO - 10.2482/haigan.52.153
M3 - Review article
AN - SCOPUS:84862528693
SN - 0386-9628
VL - 52
SP - 153
EP - 160
JO - Japanese Journal of Lung Cancer
JF - Japanese Journal of Lung Cancer
IS - 2
ER -