A phase II trial of low dose administration of 5-fluorouracil and cisplatin in patients with advanced and recurrent gastric cancer.

Author(s):  
R Kim ◽  
S Murakami ◽  
Y Ohi ◽  
H Inoue ◽  
K Yoshida ◽  
...  
Oncology ◽  
2010 ◽  
Vol 79 (5-6) ◽  
pp. 337-342 ◽  
Author(s):  
Bunzo Nakata ◽  
Akihito Tsuji ◽  
Yasushi Mitachi ◽  
Naoyuki Taenaka ◽  
Toshiki Kamano ◽  
...  

2008 ◽  
Vol 40 (3) ◽  
pp. 106 ◽  
Author(s):  
Gun Hi Kang ◽  
Gwang Sil Kim ◽  
Hyo Rak Lee ◽  
Young Jin Yuh ◽  
Sung Rok Kim

2005 ◽  
Vol 35 (12) ◽  
pp. 720-726 ◽  
Author(s):  
Keun-Wook Lee ◽  
Seock-Ah Im ◽  
Tak Yun ◽  
Eun Kee Song ◽  
Im il Na ◽  
...  

2020 ◽  
Vol 38 (4_suppl) ◽  
pp. 350-350
Author(s):  
Masashi Hirota ◽  
Shigeyuki Tamura ◽  
Hirokazu Taniguchi ◽  
Atsushi Takeno ◽  
Hiroshi Imamura ◽  
...  

350 Background: Paclitaxel is a key drug in second-line chemotherapy for advanced or recurrent gastric cancer (AGC) and nanoparticle albumin-bound paclitaxel (nab-PTX) is also widely used in Japan. A previous phase II trial in Japan showed the effectiveness of nab-PTX (260 mg/m2) administered every 3 weeks (q3w) in patients with AGC with a response rate (RR) of 27.8%; however, toxicity was major concern with grade ≥3 neutropenia (49.1%) and peripheral neuropathy (23.6%). To solve this problem, we investigated the efficacy and safety of low-dose q3w nab-PTX regimen in AGC. Methods: Eligibility requirements included: aged ≥20 years, HER2-negative, histologically confirmed, unresectable or recurrent gastric adenocarcinoma, one or more prior chemotherapy containing fluoropyrimidine regimens, presence of measurable lesion(s) according to RECIST ver. 1.1, ECOG PS of 0–2, and adequate organ function. Nab-PTX was administered at a dose of 220 mg/m2 every 3 weeks. The primary endpoint was the RR. Secondary endpoints were overall survival (OS), progression-free survival (PFS), disease-control rate (DCR), incidence of adverse events, relative dose intensity and proportion of patients who received subsequent chemotherapy. Results: Thirty-three patients were enrolled from 10 institutions in Japan. Of the 32 patients treated with protocol therapy, RR (CR, PR) was 3.1% (95% CI, 0–16.2%), which was not reached the protocol-specified threshold (p = 0.966). DCR (CR, PR, SD) was 37.5% (95% CI, 21.1–56.3%), median OS and PFS were 6.3 months (95% CI, 4.4–14.2) and 2.2 months (95% CI, 1.8-3.1). Relative dose intensity was 97.8% (215 mg/m2). 62.5% of patients received subsequent chemotherapy. Most common grade ≥3 adverse events were neutropenia (38%), anemia (13%), fatigue (19%), anorexia (16%), and peripheral neuropathy (13%). Conclusions: Low-dose regimen of q3w nab-PTX was slightly less toxic, although it did not demonstrate the same effect as the original regimen in response rate. Therefore, it is not recommended for AGC in second or later line setting. Clinical trial information: UMIN 000012701.


2014 ◽  
Vol 105 (7) ◽  
pp. 812-817 ◽  
Author(s):  
Yasutsuna Sasaki ◽  
Tomohiro Nishina ◽  
Hirofumi Yasui ◽  
Masahiro Goto ◽  
Kei Muro ◽  
...  

2011 ◽  
Vol 29 (15_suppl) ◽  
pp. e14515-e14515
Author(s):  
Y. Rino ◽  
T. Oshima ◽  
N. Yukawa ◽  
R. Yamada ◽  
T. Sato ◽  
...  

1991 ◽  
Vol 9 (3) ◽  
pp. 464-467 ◽  
Author(s):  
L G Feun ◽  
R Gonzalez ◽  
N Savaraj ◽  
J Hanlon ◽  
M Collier ◽  
...  

A phase II trial of piritrexim (2,4-diamino-6[2,5-dimethoxybenzyl]-5-methyl pyrido-[2,3d] pyrimidine, 301U74; PTX) was conducted for patients with metastatic malignant melanoma using an intermittent, low-dose oral administration schedule. PTX was administered at a starting dose of 25 mg orally three times per day for 5 days weekly for 3 weeks followed by 1 week of rest. Thirty-one patients were entered onto the study. Among 31 patients assessable for response, there were two complete responses (CRs) and five partial responses (PRs) for a response rate (CR plus PR) of 23% (95% confidence limit, 10% to 42%). Five responses occurred in soft tissue lesions, and two responses occurred in lung lesions. The initial dose schedule was well tolerated. The dose-limiting toxicity was myelosuppression. PTX administered in this schedule appears to be active against malignant melanoma. Further clinical trials to confirm these results are underway.


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