GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Material
Language
Years
Subjects(RVK)
  • 1
    In: Tạp chí Y học Việt Nam, Vietnam Medical Journal, Vietnam Medical Association, Vol. 508, No. 1 ( 2022-01-05)
    Abstract: Mục tiêu: Nhận xét nồng độ AFP, AFP-L3, PIVKA II và đặc điểm siêu âm ổ bụng ở bệnh nhân viêm gan B tại Bệnh viện Bạch Mai. Đối tượng và phương pháp nghiên cứu: Nghiên cứu tiến cứu 311 bệnh nhân viêm gan B được làm xét nghiệm AFP, AFP-L3, PIVKA II và siêu âm ổ bụng từ tháng 10 năm 2019 đến tháng 3 năm 2021. Kết quả nghiên cứu: Nhóm tuổi thường gặp nhất từ 41-70 tuổi (68,5%). Tuổi trung bình 48,7±12,3 tuổi, bệnh gặp nhiều ở nam hơn nữ (gấp 2,5 lần). Triệu chứng lâm sàng thường gặp nhất gồm: chán ăn (25,7%), mệt mỏi (32,5%), đau bụng hạ sườn phải (16,7%), chướng bụng (16,7%), vàng da (17,4%). 77,5% bệnh nhân không có xơ gan, và 22,5% bệnh nhân có xơ gan. 2,3% bệnh nhân mắc cả viêm gan B và viêm gan C. Giá trị trung vị của AFP, AFP-L3, PIVKA ở nhóm tăng các chỉ số này lần lượt là 17,2 ng/mL; 9,4% và 24,0 mAU/mL tương ứng. Có  7,4% bệnh nhân có khối u gan trên siêu âm trong đó 78,3% u gan có kích thước dưới 3 cm. Các tổn thương u gan đều là tổn thương lành tính. Kết luận: Nồng độ AFP, AFP-L3, PIVKA ở bệnh nhân viêm gan B có kèm theo xơ gan hoặc không và ngưỡng tăng không cao. Với nhóm bệnh nhân này cần lưu ý để theo dõi định kỳ nhằm phát hiện sớm ung thư gan.
    Type of Medium: Online Resource
    ISSN: 1859-1868
    Language: Unknown
    Publisher: Vietnam Medical Journal, Vietnam Medical Association
    Publication Date: 2022
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    In: Tạp chí Y học Việt Nam, Vietnam Medical Journal, Vietnam Medical Association, Vol. 508, No. 1 ( 2022-01-05)
    Abstract: Mục tiêu: Mô tả một số đặc điểm lâm sàng và cận lâm sàng của nhóm bệnh nhân viêm gan C; đánh giá mối tương quan của bộ ba AFP, AFP – L3 với PIVKA-II với các đặc điểm bệnh nhân viêm gan C. Đối tượng và phương pháp: Nghiên cứu mô tả tiến cứu trên 33 đối tượng viêm gan C. Kết quả: Bệnh nhân nam giới chiếm đa số, tỷ lệ nam/nữ là 2/1, tuổi trung bình cả nam và nữ là 53,7 tuổi. Trong số các bệnh nhân viêm gan C, nghiện rượu là đặc điểm có tỷ lệ cao nhất 39,4%. Các triệu chứng lâm sàng thường gặp là chán ăn, mệt mỏi, chướng bụng. Các chỉ số cao hơn giá trị người bình thường là AST 173,5 ± 449 U/L, ALT  121,8 ± 258,4 U/L. Nhóm bệnh nhân có u, một trong ba chỉ số AFFP, AFP-L3, PIVKA-II vượt ngưỡng có tỷ lệ là 87,5%, trong nhóm bệnh nhân không có u, cả ba chỉ số dưới ngưỡng là 22,2%. Kết luận: Giá trị AFP, AFP-L3% và PIVKA-II tăng cao trong đa số bệnh nhân viêm gan C có xuất hiện khối u.
    Type of Medium: Online Resource
    ISSN: 1859-1868
    Language: Unknown
    Publisher: Vietnam Medical Journal, Vietnam Medical Association
    Publication Date: 2022
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    In: VNU Journal of Science: Medical and Pharmaceutical Sciences, Vietnam National University Journal of Science, Vol. 38, No. 3 ( 2022-09-23)
    Abstract: Abstract: This paper aims to determine the rate of epidermal growth factor receptor (EGFR) gene mutations in advanced and metastatic squamous cell lung cancer in Vietnamese patients. EGFR mutation testing was performed on 559 formalin-fixed paraffin-embedded tissue samples from advanced and metastatic squamous cell lung cancer patients by real-time PCR. The results showed that EGFR mutations were found in 8.4%. Most of them were exon 19 deletions, approximately 51.1%. Multivariate analysis showed that EGFR mutations were more prevalent in gender (p 〈 0.0001). In conclusion, EGFR mutation testing should be performed in patients with squamous cell lung cancer. Keywords: Lung squamous cell carcinoma, EGFR gene.     
    Type of Medium: Online Resource
    ISSN: 2588-1132 , 2615-9309
    Language: Unknown
    Publisher: Vietnam National University Journal of Science
    Publication Date: 2022
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    In: Molecular and Clinical Oncology, Spandidos Publications, Vol. 19, No. 2 ( 2023-06-30)
    Type of Medium: Online Resource
    ISSN: 2049-9450 , 2049-9469
    Language: Unknown
    Publisher: Spandidos Publications
    Publication Date: 2023
    detail.hit.zdb_id: 2796865-0
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    In: Journal of Health and Development Studies, Hanoi University of Public Health, Vol. 07, No. 06 ( 2023-12-29), p. 113-122
    Abstract: Background: Determine the level of KIAA1199 gene copy in FFPE tissue samples of colorectal cancer (CR) patients and evaluate of the relationship between KIAA1199 gene copy level and some clinical and pathological symptoms of CRC patients at Duc Giang General Hospital in year 2022-2023. Methods: A cross-sectional descriptive study on 40 FFPE samples and 40 corresponding medical records of CRC patients diagnosted and treated at Duc Giang General Hospital in year 2022-2023. Result: 26/40 FFPE tissue samples (65.0%) were processed to meet the requirements for RNA extraction quality to evaluate the KIAA1199 gene copy level. Furthermore, 20/26 samples (76.9%) had a higher level of KIAA1199 gene copy in tumor tissue than in normal tissue. There was a statistically significant association between increased KIAA1199 gene copy levels and level of tumor differentiations and types in CR patients (p 〈 0.05); among them, CR patients with neoplasms have increased 11.3 times the KIAA1199 gen copy level higher than CR patients with other types of tumors (p 〈 0.05). However, it was not possible to evaluate the statistically significant relationship between the KIAA1199 gene copy level and some histopathological characteristics such as tumor location, tumor number, histopathological type, level of serosal invasion, lymph node metastasis, and stages classified according to TNM (p 〉 0.05). Conclusion: In this study, the KIAA1199 gene copy levels in tumor tissue increased more strongly than in normal tissue and a statistically significant relationship between the increased KIAA1199 gene copy levels and the tumor differentiations and types in CR patients (p 〈 0.05).
    Type of Medium: Online Resource
    ISSN: 2588-1442
    Uniform Title: Mối liên quan giữa mức độ sao chép gen KIAA1199 với một số đặc điểm lâm sàng, giải phẫu bệnh của người bệnh ung thư đại trực tràng tại Bệnh viện đa khoa Đức Giang năm 2022-2023
    Language: Unknown
    Publisher: Hanoi University of Public Health
    Publication Date: 2023
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Online Resource
    Online Resource
    Vietnam National University Journal of Science ; 2021
    In:  VNU Journal of Science: Medical and Pharmaceutical Sciences Vol. 37, No. 4 ( 2021-12-07)
    In: VNU Journal of Science: Medical and Pharmaceutical Sciences, Vietnam National University Journal of Science, Vol. 37, No. 4 ( 2021-12-07)
    Abstract: This paper aims to evaluate the GALAD score in diagnosing hepatocellular carcinoma. The paper conducted a retrospective study of 86 Hepatocellular Carcinoma patients who underwent AFP, AFP-L3, and PIVKA II. The results show that the average age of the patients was 57.7 ± 11.14, the ratio of male/female was 11.34/1. The median values of AFP, AFP-L3, and PIVKA-II before treatment were 196 ng/mL, 16.2%, and 3154.5 mAU/mL, respectively. The sensitivity of AFP, AFP-L3, and PIVKA-II was 80.2%; 58.1%; and 88.4%, respectively. The combination of the three markers also showed a high sensitivity of 94.2%. The mean value of GALAD in the patients was 5.83 ± 5.3. The liver cancer probability index was 0.8485 ± 0.276. Overall, the paper results suggest that using the BALAD score is both easy to practice and economical, which is highly useful for the early detection of hepatocellular carcinoma. Keywords: Hepatocellular carcinoma, PIVKA-II, GALAD score. References [1] H. Sung, J. Ferlay, M. E. Rebecca, L. Siegel et al., Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries, CA: aA Cancer Journal For Clinicians, 2021.[2] M. Makuuchi et al., Development of Evidence‐based Clinical Guidelines for the Diagnosis and Treatment of Hepatocellular Carcinoma in Japan Hepatology Research, Vol. 38, No. 1, 2008, pp. 37-51. 7[3] M. Makuuchi, Clinical Practice Guidelines for Hepatocellular Carcinoma-the Japan Society of Hepatology 2009 update, Hepatol Res, Vol. 40, No. 1, 2010, pp. 2-144. [4] G. M. N. O. Wongjarupong, N. R. Chaiteerakij et al., Model Combining Pre-transplant Tumor Biomarkers and Tumor Size Shows More Utility Iin Predicting Hepatocellular Carcinoma Recurrence and Survival than the BALAD Models, World Journal of Gastroenterology, Vol. 24, No. 12, 2018, pp. 1321-1331. [5] L. R. Roberts, Current Status of the GALAD and BALAD Biomarker Models for Hepatocellular Carcinoma, Gastroenterology & Hepatology, Vol. 15, No. 12, 2019, pp. 672-675. [6] L.N. Khue, M.T. Khoa at el 2020, Guideline about Diagnosis and Treatment some type of Cancer, Ministry of Health, 2020, pp. 900-935. [7] National Comprehensive Cancer Network, Hepatocellular Carcinoma, 2020. [8] J. D. Yang, B. D. Addissie, K. C. Mara et al., GALAD Score for Hepatocellular Carcinoma Detection in Comparison with Liver Ultrasound and Proposal of GALADUS Score, Cancer Epidemiol Biomarkers Prev, Vol. 28, No. 3, 2019, pp. 531-538. [9] T. T. Ngoc, Studying the Role of Alpha-fetoprotein, Alpha-fetoprotein-L3 and Des-gamma-carboxy Prothrombin in Diagnosis and Treatment Of Hepatocellular Carcinoma, Thesis of PhD, Hanoi Medical University, 2020. [10] G. P. Caviglia, M. L. Abate, E. Petrini et al., Highly Sensitive Alpha-fetoprotein, Lens Culinaris Agglutinin-reactive Fraction of Alpha-fetoprotein and Des-gamma-carboxyprothrombin for Hepatocellular Carcinoma Detection, Hepatol Res, Vol. 46, No. 3, 2016, pp. E130-E135. [11] S. Berhane, H. Toyoda, T. Tada et al., Role of the GALAD and BALAD-2 Serologic Models in Diagnosis of Hepatocellular Carcinoma and Prediction of Survival in Patients, Vol. 14, No. 6, 2016, pp. 875-886. e6. [12] J. Best, L. P. Bechmann, J. P. Sowa et al., GALAD Score Detects Early Hepatocellular Carcinoma in an International Cohort of Patients with Nonalcoholic Steatohepatitis, Clin Gastroenterol Hepatol, Vol. 18, No. 3, 2020, pp. 728-735.e4.
    Type of Medium: Online Resource
    ISSN: 2588-1132 , 2615-9309
    Language: Unknown
    Publisher: Vietnam National University Journal of Science
    Publication Date: 2021
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    Online Resource
    Online Resource
    Universidad Tecnica de Manabi ; 2023
    In:  International journal of health sciences Vol. 7, No. S1 ( 2023-04-14), p. 93-103
    In: International journal of health sciences, Universidad Tecnica de Manabi, Vol. 7, No. S1 ( 2023-04-14), p. 93-103
    Abstract: Background: Mutations of KRAS gene are common in cancers; they are detected at a very high rate in colon cancer (CC) and considered the negative factor of the disease. CC is among deadliest cancers in Vietnam, and KRAS status for non-polyp colon cancer (NPCC) was rarely reported from the country. We, in this study, aim to determine KRAS mutations and associations of mutation status with clinicopathological features in Vietnamese NPCC patients. Methods: Patients with NPCC (stages II or III) and without historical or current polyp appearance were included. Genomic DNA samples were prepared from dissected tumors and specific sequences of KRAS gene were amplified by PCR. The mutations at codons 12, 13, 59, 60, 61, 117 and 146 of the gene were determined by using a commercial kit. Possible associations of the KRAS mutation with clinicopathological properties were analyzed by using SPSS and GraphPad Prism. Key findings: KRAS mutation rate was 47.9% in NPCC patients; mutations in exon 2 accounted for 91.4% of all detected mutations. Moreover, the KRAS mutation rate was higher in females (57.1%) than in males (39.8%).
    Type of Medium: Online Resource
    ISSN: 2550-696X , 2550-6978
    URL: Issue
    Language: Unknown
    Publisher: Universidad Tecnica de Manabi
    Publication Date: 2023
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Online Resource
    Online Resource
    Vietnam National University Journal of Science ; 2022
    In:  VNU Journal of Science: Medical and Pharmaceutical Sciences Vol. 38, No. 1 ( 2022-03-24)
    In: VNU Journal of Science: Medical and Pharmaceutical Sciences, Vietnam National University Journal of Science, Vol. 38, No. 1 ( 2022-03-24)
    Abstract: This study aims to describe EGFR mutation status detected in plasma samples and analyze some related factors in non-small cell lung cancer patients after treatment with the generation I and II Tyrosine Kinase inhibitors at Bach Mai Hospital. Patients and methods: A retrospective descriptive study on 75 patients with non-small cell lung cancer tested for EGFR mutations in plasma after treatment with 1st or 2nd EGFR-TKIs in 2019-2020. Results: EGFR mutations were detected in 97.3% plasma samples;  the T790M mutation accounted for  37.3% and is accompanied by a sensitive mutation TKI; The T790M mutations ratio after treatment was higher than before treatment with TKIs (p 〈 0.001); the median total duration of EGFR-TKI treatment was significantly longer in patients with T790M mutation than in those without (16.8 months vs 12.5 months, p = 0.005); the T790M mutation ratio was higher in patients with a deletion on exon 19 than in L858R mutation on exon 21 (p=0.028), in Erlotinib treatment group higher than in Gefitinib and Afatinib treatment group (51.4% vs. with 20.0% and 33.3%, p=0.039). Conclusions: EGFR mutation plasma test helps to monitor disease progression and detect resistance mutations T790M in NSCLC patients after TKI generation I and II. Keywords: non-small cell lung cancer, EGFR mutations, T790M mutations, TKIs.. References [1] H. Sung et al., Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers In 185 Countries, CA: A Cancer Journal for Clinicians. Vol. 71, No. 3, 2021, pp. 209-249, https://doi.org/10.3322/caac.21660.[2] N. V. Hieu, Oncology, Medical Publisher, 2015.[3] P. N. Ding et al., Plasma Pre-treatment T790M Relative Allelic Frequency in Patients with Advanced EGFR-mutated Non-small Cell Lung Cancer Predicts Treatment Response to Subsequent-Line Osimertinib, Translational Lung Cancer Research, Vol. 10, No. 4, 2021, pp. 1623-1634, https://doi.org/10.1186/s40169-020-0269-y.[4] N. Yamamoto et al., Erlotinib Plus Bevacizumab Vs Erlotinib Monotherapy as First-line Treatment for Advanced EGFR Mutation-positive Non-squamous Non-small-cell Lung Cancer: Survival Follow-up Results of the Randomized JO25567 Study, Lung Cancer, Vol. 151, 2021, pp.20-24, https://doi.org/10.1016/j.lungcan.2020.11.020.[5] D. S. Ettinger et al., NCCN Guidelines Insights: Non–Small Cell Lung Cancer, Version 2, 2021: Featured Updates to the NCCN Guidelines", Journal of the National Comprehensive Cancer Network, Vol. 19, No. 3, 2021, pp. 254-266, https://doi.org/10.6004/jnccn.2021.0013.[6] K. Usui et al., Plasma ctDNA Monitoring During Epidermal Growth Factor Receptor (EGFR)-Tyrosine Kinase Inhibitor Treatment in Patients With EGFR-mutant Non-small Cell Lung Cancer (JP-CLEAR trial), Japanese Journal of Clinical Oncology, Vol. 49, No. 6, 2021, pp. 554-558, https://doi.org/10.1093/jjco/hyz023.[7] M. Nagasaka et al., Liquid Biopsy for Therapy Monitoring in Early-stage Non-small Cell Lung Cancer, Molecular Cancer, Vol. 20, No. 1, 2021, pp. 82, https://doi.org/10.1186/s12943-021-01371-1.[8] M. D. Re et al., Incidence of T790M in Patients with NSCLC Progressed to Gefitinib, Erlotinib, and Afatinib: A Study on Circulating Cell-free DNA, Clinical Lung Cancer, Vol. 21, No. 3, 2020, pp. 232-237, https://doi.org/10.1016/j.cllc.2019.10.003.[9] S. Jenkins et al., Plasma ctDNA Analysis for Detection of the EGFR T790M Mutation in Patients with Advanced Non–small Cell Lung Cancer", Journal of Thoracic Oncology, Vol. 12, No. 7, 2017, pp. 1061-1070, https://doi.org/10.1016/j.jtho.2017.04.003.[10] R. Ko et al., Frequency of EGFR T790M Mutation and Multimutational Profiles of Rebiopsy Samples from Non-small Cell Lung Cancer Developing Acquired Resistance to EGFR Tyrosine Kinase Inhibitors in Japanese Patients, BMC Cancer, Vol. 16, No. 1, 2016, pp. 864, https://doi.org/10.1186/s12885-016-2902-0.[11] N. Matsuo et al., Association of EGFR Exon 19 Deletion and EGFR-TKI Treatment Duration with Frequency of T790M Mutation in EGFR-Mutant Lung Cancer Patients, Scientific Reports, Vol. 6, No. 1, 2016, pp. 36458 , https://doi.org/10.1038/srep36458.[12] W. Fanget al., EGFR Exon 20 Insertion Mutations and Response to Osimertinib in Non-small-cell Lung Cancer, BMC Cancer, Vol. 19, No. 1, 2019, pp. 1-9, https://doi.org/10.1186/s12885-019-5820-0.[13] D. T. Hien, P. C. Phuong, Analysis of EGFR Mutations in Paraffin-covered Tissue Samples and some Related Factors from Non-small Cell Lung Cancer Patients Over 60 Years Old, Science and Technology Vietnam, Vol. 62, No. 7, 2020, pp. 1-5[14] S. Hong et al., Concomitant Genetic Alterations with Response to Treatment and Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Patients with EGFR-Mutant Advanced Non–small Cell Lung Cancer, JAMA Oncology, Vol. 4, No. 5, 2018, pp. 739-742, https://doi.org/10.1001/jamaoncol.2018.0049.
    Type of Medium: Online Resource
    ISSN: 2588-1132 , 2615-9309
    Language: Unknown
    Publisher: Vietnam National University Journal of Science
    Publication Date: 2022
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    Online Resource
    Online Resource
    Asian Medical Press Limited ; 2023
    In:  Asia-Pacific Journal of Oncology
    In: Asia-Pacific Journal of Oncology, Asian Medical Press Limited
    Abstract: Background Mutations of the KRAS gene are common in cancers; they are detected at a very high rate in colon cancer (CC) and are considered a negative disease factor. CC is among the deadliest cancers in Vietnam, and KRAS status for non-polyp colon cancer (NPCC) was rarely reported from the country. In this study, we aim to determine KRAS mutations and the associations of mutation status with clinicopathological features in Vietnamese NPCC patients. Methods Patients with NPCC (stages II or III) and without historical or current polyp appearance were included. Genomic DNA samples were prepared from dissected tumors, and specific sequences of the KRAS gene were amplified by PCR. The mutations at codons 12, 13, 59, 60, 61, 117, and 146 of the gene were determined by using a commercial kit. Possible associations of the KRAS mutation with clinicopathological properties were analyzed using SPSS and GraphPad Prism. Results The KRAS mutation rate was 47.9% in NPCC patients; mutations in exon 2 accounted for 91.4% of all detected mutations. Moreover, the KRAS mutation rate was higher in females (57.1%) than in males (39.8%). The association of KRAS mutation with female NPCC patients was further confirmed by multivariate regression data with OR=2.144 and p = 0.012. Conclusion The KRAS mutation rate was also higher in patients with right colon cancers. The mutated-KRAS-carrying patients potentially experienced anemia. The data provide important scientific background for the treatment and management of the disease.
    Type of Medium: Online Resource
    ISSN: 2708-7999 , 2708-7980
    Language: English
    Publisher: Asian Medical Press Limited
    Publication Date: 2023
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    In: Biomass and Bioenergy, Elsevier BV, Vol. 181 ( 2024-02), p. 107058-
    Type of Medium: Online Resource
    ISSN: 0961-9534
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2024
    detail.hit.zdb_id: 1496404-1
    SSG: 12
    SSG: 23
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...