1.XELOX plus bevacizumab as a ifrst-ine treatment for Chinese patients with metastatic colorectal cancer:a retrospective study
Jidong CAI ; Weijun LI ; Linhua LI
Chinese Journal of Biochemical Pharmaceutics 2014;(2):68-70,73
Objective To observe the efifcacy and safety of XELOX plus bevacizumab as a ifrst-ine treatment for Chinese patients with metastatic colorectal cancer. Methods In this study, we retrospectively reviewed cases in which XELOX plus bevacizumab were administered in order to evaluate its efifcacy and safety in clinical practice.In total, 40 patients with mCRC who presented at Fuchu Hospital received XELOX plus bevacizumab as a ifrst?line treatment from September, 2009 to April, 2012. Eligible patients had histologically conifrmed mCRC. XELOX consisted of a 2-h intravenous infusion of oxaliplatin 130 mg/m 2 on day 1 plus oral capecitabine 1,000 mg/m 2 twice daily for two weeks of athree?week cycle. Overall survival (OS) and survival benefit were analyzed when patients continued with XELOX plus bevacizumab beyond disease progression. Results The median progression?free survival (PFS) was 290 days [95%conif-dence interval (CI):222?409 days] and the median OS was 816 days (95%CI:490?842 days). The response rate (RR:complete plus partial response) was 67.5%, and the disease control rate (RR plus stable disease) was 90%. Conclusion XELOX plus bevacizumab may be considered a routine ifrst?line treatment option for patients with mCRC.
2.Influence of Porphyromonas gingivalis on vascular intima adhesion factors and metalloproteinases
Wei SUN ; Shanglang CAI ; Yu SONG ; Jidong ZHANG
Chinese Journal of cardiovascular Rehabilitation Medicine 2014;23(2):113-117
Objective: To observe influence of porphyromonas gingivalis (Pg, a main pathogenic bacterium of periodontal disease) on vascular intima adhesion factors and metalloproteinases. Methods: A total of 60 rats were randomly and equally divided into blank control group, Pg low dose group (Pg 2ml) and Pg high dose group (Pg 5ml) according to number table. The latter two groups respectively received intramuscular injection of corresponding dose Pg every three days without antibiotic intervention for 12 weeks. Then their venous blood was taken to measure levels of intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), matrix metalloproteinase (MMP)-3 and MMP-9 in three groups. Results: Compared with blank control group, there were significant increase in contents of ICAM-1 [(175.79±14.30)ng/ml vs.(182.62±15.07)ng/ml, (189.39±14.93)ng/ml]、VCAM-1 [(256.49±37.17)ng/ml vs.(271.58±32.85)ng/ml , (286.66±30.66)ng/ml] 、 MMP-3 [(3.23±0.69)ng/ml vs.(3.61±0.82)ng/ml, (3.97±0.83)ng/ml]及 MMP-9 [(1.30±0.39)mg/L vs.(1.48±0.39)mg/L, 1.67±0.45)mg/L ](P <0.05,or <0.01),Compared with Pg low dose group, there were significant increase in levels of above indexes in Pg high dose group (P<0.05). Conclusion: Porphyromonas gingivalis can significantly increase serum contents of vascular intima adhesion factors and metalloproteinases, aggravating pathological development of coronary heart disease.
3.Application of Circulating Tumor DNA in Precision Diagnosis and Treatment of Colorectal Cancer
Wentao YANG ; Minghan LI ; Jidong CAI ; Cong LI ; Wang SONG ; Ye XU
Cancer Research on Prevention and Treatment 2024;51(3):157-162
Colorectal cancer (CRC) is one of the most common malignant tumors recorded worldwide. This condition has high morbidity and mortality and seriously endangers people's health. Traditional diagnostic models fail to meet people's current needs for real-time monitoring of tumors. Compared with traditional detection methods, ctDNA detection is not only noninvasive but can also attain real-time detection of comprehensive genomic information of tumors. The advancement of detection technology has gradually highlighted the potential of ctDNA detection in the clinical treatment of CRC. This article reviews the advancements on the clinical application of ctDNA in early screening, minimal residual disease detection, and guidance on individualized treatment of CRC patients.