211P - Early tumor shrinkage (ETS) and depth of response (DpR) in patients with advanced gastric cancer (AGC) receiving S1 plus cisplatin (SP) or capecita...

Date 19 December 2015
Event ESMO Asia 2015 Congress
Session Poster presentation 1
Topics Anti-Cancer Agents & Biologic Therapy
Gastric Cancer
Presenter NAOTOSHI Sugimoto
Citation Annals of Oncology (2015) 26 (suppl_9): 42-70. 10.1093/annonc/mdv523
Authors N. Sugimoto1, T. Yoshinami1, S. Yamamoto1, T. Yagi2, F. Imamura1
  • 1Clinical Oncology, Osaka Medical Center for Cancer and Cardiovascular Dideases, 537-8511 - Osaka/JP
  • 2Clinical Oncology, Osaka Medical Center for Cancer and Cardiovascular Dideases, Osaka/JP

Abstract

Aim/Background

In the Japanese Gastric Cancer Treatment Guideline (4th edition), S1 plus cisplatin (SP) is mentioned the standard (recommendation 1) and capecitabine plus cisplatin (XP) is considered as recommendation 2 for AGC in first-line setting. But few reports were existed about the comparison between XP and SP. Moreover, no report was found about the comparison of Early tumor shrinkage (ETS) and depth of response (DpR) between them.

Methods

The selection criteria were pathologically proven AGC (HER2 negative or unknown); no previous chemotherapy; performance status 0-2; able to oral intake; and adequate organ functions. The patients in XP group, capecitabine 1,000mg/m2 was given orally twice daily for 14days followed by a 7-day rest; cisplatin 80mg/m2 on day1 was given by intravenous infusion. In SP group, S1 40mg/m2 was given orally twice daily for 21 days followed by a 14-day rest and cisplatin 60mg/m2 intravenous infusion on day8.

Results

The analysis covered 115 patients over the period from May 2008 to June

2014. The median age was 64 years (range 22-81); 76 males and 39 females; PS 0/1/2 score 85/29/1; 31 patients were treated XP and 84 patients were treated SP. Progression-free survival and overall survival were 6.6 and 16.4 months with XP and 6.1 and 13.3 months with SP (no significant difference). The response rates were XP/SP 61%/50%. The ETS (over 20% tumor shrinkage in 6-8weeks) rate were 83% in XP and 61% in SP (p = 0.09). DpR were 47.1% in XP and 40.5% in SP (p = 0.31). The rate of grade 3-4 toxicity in XP/SP were; neutropenia 23%/15%, anemia 16%/20%, nausea 0%/3%, anorexia 3%/ 8%, fatigue 0%/ 4%, hyponatremia 3%/0%. There was no treatment death in both groups.

Conclusions

It is suggested that XP can give AGC patients high ETS rate and DpR with safety. So we are recruiting the prospective study for AGC patients with multiple lymph node metastases in neoadjuvant setting (OGSG 1401, UMIN 000014071).

Clinical trial identification

Disclosure

N. Sugimoto: Chugai, Taiho, Yakult, Eli Lilly, Merckserono, Takeda. All other authors have declared no conflicts of interest.