scholarly journals Efficacy and Safety of Apatinib for Elderly Patients with Advanced or Metastatic Gastric Cancer After Failure of at Least First-Line Chemotherapy: A Multi-Center, Single-Arm, Phase II Study

2021 ◽  
Vol Volume 14 ◽  
pp. 4499-4508
Author(s):  
Dengfeng Ren ◽  
Guoxiu Wang ◽  
Yu Zhang ◽  
Jie Kan ◽  
Qiuxia Dong ◽  
...  
2012 ◽  
Vol 16 (3) ◽  
pp. 411-419 ◽  
Author(s):  
Vincenzo Catalano ◽  
Renato Bisonni ◽  
Francesco Graziano ◽  
Paolo Giordani ◽  
Paolo Alessandroni ◽  
...  

Chemotherapy ◽  
2012 ◽  
Vol 58 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Xiao Jun Xiang ◽  
Ling Zhang ◽  
Feng Qiu ◽  
Feng Yu ◽  
Zheng Yu Zhan ◽  
...  

2009 ◽  
Vol 20 (4) ◽  
pp. 281-286 ◽  
Author(s):  
Jian Guo Zhao ◽  
Feng Qiu ◽  
Jian Ping Xiong ◽  
Ling Zhang ◽  
Xiao Jun Xiang ◽  
...  

2011 ◽  
Vol 35 (12) ◽  
pp. 823-830 ◽  
Author(s):  
Marianne Fonck ◽  
Réné Brunet ◽  
Yves Becouarn ◽  
Jean-Louis Legoux ◽  
Jérôme Dauba ◽  
...  

2007 ◽  
Vol 46 (3) ◽  
pp. 324-329 ◽  
Author(s):  
Efraim Idelevich ◽  
Natalie Karminsky ◽  
Michael Dinerman ◽  
Rivka L. Katsenelson ◽  
Nana Ben Zvi ◽  
...  

2006 ◽  
Vol 24 (18_suppl) ◽  
pp. 4076-4076
Author(s):  
J. Lee ◽  
W. Kang ◽  
S. Lee ◽  
J. Kwon ◽  
H. Kim ◽  
...  

4076 Background: Previous phase II study showed a high efficacy and safety of FOLFOXIRI (irinotecan, oxaliplatin, 5-fluorouracil, leucovorin) combination chemotherapy in metastatic colorectal cancer. This non-randomized open label phase II study evaluated the efficacy and safety of FOLFOXIRI in metastatic or recurrent gastric cancer patients. Methods: Patients with: histologically proven, bidimensionally measurable, metastatic gastric adenocarcinoma, age 18 - 70 years, with a performance status 0 - 2, no prior chemotherapy or at least 12 months after adjuvant therapy, life expectancy > 3 months, signed written informed consent were eligible. Treatment consisted of irinotecan 150 mg/m2 day 1, oxaliplatin 85 mg/m2 day 1, leucovorin 100 mg/m2 day and 5-fluorouracil 2000 mg/m2 as a 48-h continuous infusion starting on day 1, repeated every 2 weeks until unacceptable toxicity, patients’ refusal, or up to 12 cycles. The planned sample size was 48 and the primary endpoint was response rate. Results: From August 2004 to August 2005, 48 patients were prospectively enrolled. The median age was 54 years (24 - 69) and male:female ratio was 1.3:1. In total, 379 cycles were administered with a median of 9 cycles per patient (range, 1–12) and 45/48 patients were evaluable for treatment response. Three patients were not assessable for response due patients’ refusal for further chemotherapy following the first cycle. By per-protocol analysis, the objective response rate was 73.3 % (95% CI, 60.8–85.8) with 2 CRs and 31 PRs. Four patients (9%) had stable disease and 8 patients (18%) had progressive disease. The estimated median survival of all patients was 14.0 months (95% CI, 11.8 - 16.2 ) and the estimated median time-to-progression was 8.9 months (95% CI, 6.7–11.0). In total of 379 cycles administered, most common grade 3/4 toxicities were neutropenia (11% of all cycles) and emesis (12%). Grade 2 peripheral neuropathy occurred in 5 patients. One (2%) patient had severe tumor bleeding and 5 (10%) patients experienced grade 3 diarrhea. Conclusions: FOLFOXIRI combination chemotherapy showed a very promising preliminary anti-tumor activity and was generally well tolerated as a first-line treatment for patients with metastatic gastric cancer. No significant financial relationships to disclose.


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