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A retrospective analysis of the safety and efficacy of apatinib in treating advanced metastatic colorectal cancer 被引量:4
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作者 Li Wang Juan Lu +7 位作者 Yi Liu Yunfei Gao man kong Jiandong Yang Bin kong Xuebing Li Xifen Huang Wenzhong Pei 《Oncology and Translational Medicine》 2017年第5期210-216,共7页
Objective Colorectal cancer(CRC) is a heterogeneous disease in which both epigenetic alterations and gene mutations transform normal cells into cancer cells. Apart from a variety of standard treatments, there are few ... Objective Colorectal cancer(CRC) is a heterogeneous disease in which both epigenetic alterations and gene mutations transform normal cells into cancer cells. Apart from a variety of standard treatments, there are few options available to improve a CRC patient's overall survival(OS) and quality of a life. The objective of the present retrospective study was to analyze the response and toxicity associated with apatinib in patients with metastatic CRC(m CRC).Method Data on the use of apatinib as salvage therapy were collected from patients diagnosed with m CRC, Eastern Cooperative Oncology Group(ECOG) performance status ≤ 3, from the Luhe Hospital. A total of 17 patients with stage IV unresectable m CRC, who received at least one cycle of apatinib, between October 2015 and February 2017, were involved in this study. Our primary endpoints were the overall response rate(ORR) and disease control rate(DCR), and the secondary objectives were progression-free survival(PFS), OS and safety.Result Seventeen patients with a median age of 62 years(34–83 years) were enrolled. Twelve patients were male, and the location of the primary tumor was in the colon and the rectum in 9 and 8 patients, respectively. Liver metastasis was observed in 9 patients and lung metastasis in 5. The ECOG performance status was 0 to 2 in 13 patients. The ORR at the first evaluation was 17.6 %(3/17). The DCR was 82.4%(14/17). The median PFS was 3.0 months(95% confidence interval(CI): 1.924–4.076 months) and the median OS was 5.4 months(95% CI: 3.383–7.417 months). Grade 1–2 adverse events included hypertension(52.9%), fatigue(64.7%), anorexia(29.4%), hoarseness(23.5%), proteinuria(23.5%), and development of rashes(17.6%). Grade 3 adverse events included thrombocytopenia(5.9%) and proteinuria(5.9%). There were no Grade 4 adverse events in our analysis.Conclusions Apatinib was found to be both safe and effective in the treatment of advanced m CRC, and its associated toxicities were acceptable and manageable. However, further studies are required to validate these findings. 展开更多
关键词 COLORECTAL cancer targeted therapy apatinib VASCULAR ENDOTHELIAL growth factor receptor-2 (VEGFR-2) ANGIOGENESIS inhibitor
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Microbial Transformation of Taxoids and Synthesis of Taxoids with an Oxetane Ring 被引量:1
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作者 Shang Hut HU Xu Fang TIAN +3 位作者 Wen Yi HE man kong Di An SUN Qi Cheng FANG(Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050) 《Chinese Chemical Letters》 SCIE CAS CSCD 1998年第1期39-43,共5页
Microbial trdrisformation of taxoids was inveStigared: taxoid 2 was transformed into 1β and 14β hydroxylated derivahves 3 and 4, unnatural taxoid 6 was transformed into 1β-hydroxy derivative 7 and 11(15-1) abeotaxa... Microbial trdrisformation of taxoids was inveStigared: taxoid 2 was transformed into 1β and 14β hydroxylated derivahves 3 and 4, unnatural taxoid 6 was transformed into 1β-hydroxy derivative 7 and 11(15-1) abeotaxane 8. Taxoids with an oxetane ring, 11-13 were synthesized from 1 via chemical reachons. 展开更多
关键词 TAXOID abeotaxane oxetane ring chemoenzymatic method
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Intramolecular Oxidative Transformations of 1,4-Diary1-2, 3-Dimethy1-2, 3-Epoxybutane with DDQ
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作者 Jun Biao CHANG A.T.McPHAIL +1 位作者 man kong Jing Xi XIE(Institute of Materia Medica.Chinese Academy of Medical Sciences and Peking Union MedicalCollege. Beijing. 100050.China Department of Chemistry. P.M.Gross Chemical Laboratory.Duke University, Durham.NC 277 《Chinese Chemical Letters》 SCIE CAS CSCD 1996年第8期691-692,共2页
Treatment of 1.4-diary1 -2. 3 -dimethy1-2, 3-epoxide of butane(1) with 2. 3-dichloro-5.6 6dicyano-1.4-benzoquinone(DDQ) in trifluoroacetic acid (TFA)furnishes a new benzofuran typeIignan (2) The structure of (2) was e... Treatment of 1.4-diary1 -2. 3 -dimethy1-2, 3-epoxide of butane(1) with 2. 3-dichloro-5.6 6dicyano-1.4-benzoquinone(DDQ) in trifluoroacetic acid (TFA)furnishes a new benzofuran typeIignan (2) The structure of (2) was esbolished by MS,IR,UV and NMR spectra.and X-ravcrystallographic analysis. 展开更多
关键词 DDQ Epoxybutane INTRAMOLECULAR OXIDATIVE TRANSFORMATIONS Diary1 Dimethy1
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An Improved Differential Fault Analysis on Block Cipher KLEIN-64
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作者 Min Long man kong +1 位作者 Sai Long Xiang Zhang 《Computers, Materials & Continua》 SCIE EI 2020年第11期1425-1436,共12页
KLEIN-64 is a lightweight block cipher designed for resource-constrained environment,and it has advantages in software performance and hardware implementation.Recent investigation shows that KLEIN-64 is vulnerable to ... KLEIN-64 is a lightweight block cipher designed for resource-constrained environment,and it has advantages in software performance and hardware implementation.Recent investigation shows that KLEIN-64 is vulnerable to differential fault attack(DFA).In this paper,an improved DFA is performed to KLEIN-64.It is found that the differential propagation path and the distribution of the S-box can be fully utilized to distinguish the correct and wrong keys when a half-byte fault is injected in the 10th round.By analyzing the difference matrix before the last round of S-box,the location of fault injection can be limited to a small range.Thus,this improved analysis can greatly improve the attack efficiency.For the best case,the scale of brute-force attack is only 256.While for the worst case,the scale of brute-force attack is far less than 232 with another half byte fault injection,and the probability for this case is 1/64.Furthermore,the measures for KLEIN-64 in resisting the improved DFA are proposed. 展开更多
关键词 Block cipher KLEIN-64 differential fault analysis half-byte fault injection
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STEREOSTRUCTURAL DETERMINATION OF ADDITION PRODUCTS FROM ISOFURANOGERMACRENE AND MALEIMIDE BY NMR TECHNIQUES
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作者 Xiu Wen HAN man kong +5 位作者 Wen Yi HE Chang Fu XU Shi Zhen MAO Xiao Long XU Yan Wu YANG Guo Xi WANG 《Chinese Chemical Letters》 SCIE CAS CSCD 1992年第11期891-894,共4页
The stereostructures of the title compounds were shown to be represented by (A) and (B).
关键词 NMR STEREOSTRUCTURAL DETERMINATION OF ADDITION PRODUCTS FROM ISOFURANOGERMACRENE AND MALEIMIDE BY NMR TECHNIQUES NOE
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