1.Epidemiological characteristics and strategies for prevention and elimination of malaria in Qingdao, Shandong Province, China from 1949 to 2021
Shi, L.M. ; Liu, S.Z. ; Dou, X.J. ; Liu, X.Y. ; Feng, E.Q. ; Liang, J.W. ; Kong, X.L. ; Ji, F.Y.
Tropical Biomedicine 2024;41(No.2):134-141
Malaria is an insect-borne disease transmitted by Anopheles mosquitoes or the importation of
Plasmodium-infected blood, posing a serious threat to human health and life safety. This study aims
to analyze the incidence of malaria in Qingdao at various stages from 1949 to 2021, to collate the
control measures taken at different epidemic stages to assess the effectiveness of malaria control, and
to identify a set of malaria control strategies suitable for Qingdao, while providing Chinese experience
for other countries or cities in their malaria elimination efforts. A retrospective survey was used to
collect information on malaria cases, control measures and prevention and control effects in Qingdao
from 1949 to 2021, and to evaluate malaria control strategies and measures in Qingdao. 704 155 cases
have been reported from 1949 to 2021, with three epidemic peaks: the incidence rate was 1715.9/100
000 in 1961, 1409.7/100 000 in 1965, and the most severe case occurred in 1972, with an incidence
rate of 1635.6/100 000 and a case count exceeding 90 000. Throughout the various stages of malaria
epidemics, Qingdao has effectively eliminated indigenous malaria by implementing diverse preventive
and control measures. Since the last indigenous case of Plasmodium vivax was reported in 2002, all
locally reported cases have been imported, mainly by returning migrant workers from Africa. This study
examines a range of malaria prevention and control strategies and interventions that are appropriate
for Qingdao. These measures have enabled Qingdao to successfully eliminate malaria and maintain
malaria-free status for more than 20 years. These measures can also serve as a reference for similarly
situated cities in Africa and Southeast Asia.
2.The Clinical Outcomes of Different First-Line EGFR-TKIs Plus Bevacizumab in Advanced EGFR-Mutant Lung Adenocarcinoma
Yen-Hsiang HUANG ; Kuo-Hsuan HSU ; Chun-Shih CHIN ; Jeng-Sen TSENG ; Tsung-Ying YANG ; Kun-Chieh CHEN ; Kang-Yi SU ; Sung-Liang YU ; Jeremy J.W. CHEN ; Gee-Chen CHANG
Cancer Research and Treatment 2022;54(2):434-444
Purpose:
The aim of this study was to investigate the efficacy of various epidermal growth factor receptor (EGFR)–tyrosine kinase inhibitors (TKIs) plus bevacizumab in advanced EGFR-mutant lung adenocarcinoma patients.
Materials and Methods:
From August 2016 to October 2020, we enrolled advanced lung adenocarcinoma patients harboring exon 19 deletion or L858R receiving gefitinib, erlotinib and afatinib plus bevacizumab as the first-line treatment for the purposes of analysis.
Results:
A total of 36 patients were included in the final analysis. Three patients received gefitinib, 17 received erlotinib, and 16 received afatinib combined with bevacizumab as the first-line treatment. The objective response rate was 77.8%, and disease control rate was 94.4%. The overall median progression-free survival (PFS) was 16.4 months, while the median PFS was 17.1 months in patients with exon 19 deletion, and 16.2 months in patients with L858R mutation (p=0.311). Regarding the use of different EGFR-TKIs, the median PFS was 17.1 months in the erlotinib group and 21.6 months in the afatinib group (p=0.617). In patients with brain metastasis at baseline, the median PFS was 18.9 months in the erlotinib group and 16.4 months in the afatinib group (p=0.747). Amongst patients harboring exon 19 deletion, the median PFS was 16.2 months in the erlotinib group and not-reached in the afatinib group (p=0.141). In patients with L858R mutation, the median PFS was 18.9 months in the erlotinib group and 16.2 months in the afatinib group (p=0.481).
Conclusion
Our research demonstrates that not only erlotinib combined with bevacizumab, but also afatinib plus bevacizumab as first-line treatment, provides solid clinical efficacy in advanced EGFR-mutant lung adenocarcinoma patients.


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