JASPAC 01: Randomized phase III trial of adjuvant chemotherapy with gemcitabine versus S-1 for patients with resected pancreatic cancer.

Author:

Fukutomi Akira1,Uesaka Katsuhiko1,Boku Narikazu2,Kanemoto Hideyuki1,Konishi Masaru3,Matsumoto Ippei4,Kaneoka Yuji5,Shimizu Yasuhiro6,Nakamori Shoji7,Sakamoto Hirohiko8,Morinaga Soichiro9,Kainuma Osamu10,Imai Koji11,Sata Naohiro12,Hishinuma Shoichi13,Nakamura Takayuki14,Kanai Michio15,Hirano Satoshi16,Yoshikawa Yukinobu17,Ohashi Yasuo18

Affiliation:

1. Shizuoka Cancer Center, Shizuoka, Japan

2. St. Marianna University School of Medicine, Kawasaki, Japan

3. National Cancer Center Hospital East, Kashiwa, Japan

4. Kobe University Graduate School of Medicine, Kobe, Japan

5. Ogaki Municipal Hospital, Ogaki, Japan

6. Aichi Cancer Center Hospital, Nagoya, Japan

7. Osaka National Hospital, Osaka, Japan

8. Saitama Medical University International Medical Center, Saitama, Japan

9. Kanagawa Cancer Center, Yokohama, Japan

10. Chiba Cancer Center, Chiba, Japan

11. Asahikawa Medical University, Asahikawa, Japan

12. Jichi Medical University, Shimotsuke, Japan

13. Tochigi Cancer Center, Utsunomiya, Japan

14. Gunma Prefectural Cancer Center, Gunma, Japan

15. Kasugai Municipal Hospital, Kasugai, Japan

16. Hokkaido University Graduate School of Medicine, Sapporo, Japan

17. National Hospital Organization Kure Medical Center, Kure, Japan

18. The University of Tokyo, Tokyo, Japan

Abstract

4008 Background: Adjuvant chemotherapy with gemcitabine (G) has been standard treatment for resected pancreatic cancer (PC). In the GEST study, S-1 (S) had shown non-inferiority to G in overall survival (OS) for unresectable PC. The aim of this phase III study is to investigate non-inferiority of S to G on OS as adjuvant chemotherapy for resected PC. Methods: Patients (pts) after macroscopically curative resection of PC with an ECOG PS of 0-1 and adequate organ functions were randomly assigned to G (1000 mg/m2, iv, d1, 8 and 15, q4w, for 6 courses) or S (80/100/120 mg/day based on BSA, po, d1-28, q6w, for 4 courses) with balancing by surgical margins (R), nodal status (N) and institution. Primary endpoint was OS. With 180 pts per arm, the study had 80% power to prove non-inferiority with a margin of hazard ratio (HR) 1.25 on the basis of expected HR 0.87, with 0.05 two-sided alpha. Secondary endpoints were relapse-free survival (RFS), safety, and quality of life (EQ-5D). One interim analysis was planned after 180 deaths. Results: From 4/2007 to 6/2010, 385 pts were enrolled from 33 hospitals in Japan. 378 pts (G/S: 191/187) were included in the full analysis set. Pts characteristics (G/S) were well balanced (PS0: 67%/70%, R0: 86%/88%, N0: 38%/36%). Based on the interim analysis with 205 OS events, IDMC recommended to publish the results. OS at 2-years were 53% for G and 70% for S. HR for S to G was 0.56 (95% CI, 0.42-0.74, p<0.0001 for non-inferiority, p<0.0001 for superiority). On subgroup analysis, HRs for R0/R1, N0/N1 pts were 0.57 (95% CI, 0.42-0.78)/0.53 (0.27-1.05), 0.48 (0.28-0.83)/0.58 (0.41-0.80), respectively. RFS at 2-years were 29% for G and 49% for S. HR of relapse for S to G was 0.56 (95% CI, 0.43-0.71, log-rank p<0.0001). Incidences of grade 3/4 toxicities in G/S were leukopenia 39%/9%, hemoglobin decrease 17%/13%, thrombocytopenia 9%/4%, elevated AST 5%/1%, fatigue 5%/5%, and anorexia 6%/8%. Relative dose intensity of G/S was 84%/97%. EQ-5D QOL score in S was significantly better than that in G (p<0.0001). Conclusions: S-1 adjuvant chemotherapy is shown non-inferior, and furthermore, even superior to GEM. S-1 is considered as the new standard treatment for resected PC pts. Clinical trial information: UMIN000000655.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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