Journal Article10.3892/OR.12.3.557
Sequence-dependence of cisplatin and 5-fluorouracil in advanced and recurrent gastric cancer
Wasaburo Koizumi,Minoru Kurihara,K Hasegawa,Akimichi Chonan,Yasuhiko Kubo,Ryuichiro Maekawa,Ryozo Iwasaki,Sasai T,Yoshio Fukuyama,Kunitsugu Ishikawa,Kazuo Miyoshi,Koichi Yasutake,Makoto Hayakawa +12 more
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TL;DR: CDDP should be given before 5-FU in patients with gastric cancer when treated with a combination of CDDP and5-FU, according to the results of this controlled study.
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Abstract: This randomized controlled clinical trial was designed to compare the safety and effectiveness of different sequences of treatment with cisplatin (CDDP) and 5-fluorouracil (5-FU) in patients with unresectable advanced and post-operative recurrent gastric cancer. Patients with unresectable advanced or post-operative recurrent gastric cancer were randomly assigned by a registration center to group A or B. Group A received CDDP (80 mg/m(2)) as a continuous 2-h intravenous infusion on day 1 and 5-FU (700 mg/m(2)) as a continuous intravenous infusion on days 2-5. Group B was given 5-FU (700 mg/m(2)) as a continuous intravenous infusion on days 1-4, followed by CDDP (80 mg/m(2)) as a continuous 2-h intravenous infusion on day 5. Each course of chemotherapy was repeated every 28 days. A total of 74 patients were enrolled. One patient died accidentally, and 5 could not be evaluated. Response was assessable in 68 patients. The response rate was 31.3% (10/32) in group A as compared with 13.9% (5/36) in group B. Although the response rate was higher in Group A, the difference was not significant (p=0.085). The response rate in patients with diffuse type tumors was significantly lower in group B. There was no difference between the groups in response among patients with intestinal type tumors. The median overall survival was 239 and 174 days and time to progression was 175 and 140 days in group A and group B, respectively. Although there were trends toward longer survival and time to progression in group A, the differences between the groups were not statistically significant. There was also no difference in the type or incidence of adverse reactions. The results of this controlled study indicate that the overall response rate was slightly but not significantly higher in patients who received CDDP before 5-FU. Among patients with diffuse type tumors, the response rate was significantly lower when 5-FU was administered before CDDP. Our results suggest that CDDP should be given before 5-FU in patients with gastric cancer when treated with a combination of CDDP and 5-FU.
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Citations
MAVGAE: a multimodal framework for predicting asymmetric drug-drug interactions based on variational graph autoencoder.
Zengqian Deng,Jie Xu,Yinfei Feng,Liangcheng Dong,Yuanyuan Zhang +4 more
TL;DR: A framework based on multimodal data and a variational graph autoencoder named MAVGAE for predicting asymmetric drug interactions and Experimental validation on a large-scale drug dataset demonstrates the framework's high accuracy and reliability in predicting non-symmetrical drug interactions.
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Systemic therapy for advanced gastric cancer: a clinical practice guideline
TL;DR: To improve survival, a platinum agent should be included in any combination chemotherapy regimen, and oral capecitabine is preferred over intravenous 5-fluorouracil (5fu), which is, epirubicin-cisplatin-capecitABine is preferable over the prior standard regimen, epIRubic in-cISplatin -5fu (ecf).
OUP accepted manuscript
25 Apr 2022
TL;DR: Wang et al. as discussed by the authors designed a directed graph attention network (DGAT-DDI) to predict asymmetric drug-drug interactions (DDIs) in poly-drug treatments.
DRGATAN: Directed relation graph attention aware network for asymmetric drug-drug interaction prediction
TL;DR: This study proposes DRGATAN, a directed relation graph attention aware network, to predict asymmetric drug-drug interactions by leveraging multi-relational role embeddings and outperforming advanced methods in experimental results and case analysis.