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Featured researches published by Ling Dai.


Journal of Crystal Growth | 1996

Experiment on the thermocapillary convection of a mercury liquid bridge in a floating half zone

Jian Han; Zheng Sun; Ling Dai; Jianling Xie; W.R. Hu

A liquid bridge of a floating half zone consisting of liquid mercury sealed in a glass tube with nitrogen atmosphere was used for the experiment of thermocapillary convection with a low Prandtl number liquid. A non-contacted diagnostic method was developed to monitor the surface flow and the surface oscillation. A growing surface film (or skin) is a crucial source to suppress thermocapillary convection, and is discussed in this paper. For the case of a mercury Liquid bridge, the critical Marangoni number was obtained as 900, and the oscillatory frequency was around 5 Hz.


Thoracic Cancer | 2015

Circulating PD-L1 in NSCLC patients and the correlation between the level of PD-L1 expression and the clinical characteristics

Jie Zhang; Jing Gao; Yanyan Li; Jun Nie; Ling Dai; Weiheng Hu; Xiaoling Chen; Jindi Han; Xiangjuan Ma; Guangming Tian; Di Wu; Lin Shen; Jian Fang

The programmed cell death‐1/programmed cell death‐1 ligand (PD‐1/PD‐L1) pathway plays a crucial role in tumor evasion. This study evaluated the association between circulating PD‐L1 expression and clinical characteristics in patients with advanced non‐small cell lung cancer (NSCLC).


Cancer Chemotherapy and Pharmacology | 2014

Addition of aprepitant improves protection against cisplatin-induced emesis when a conventional anti-emetic regimen fails

Weiheng Hu; Jian Fang; Jun Nie; Ling Dai; Xiaoling Chen; Jie Zhang; Xiangjuan Ma; Guangming Tian; Jindi Han

ObjectiveWe investigated whether aprepitant, a neurokinin-1 antagonist, could decrease chemotherapy-induced nausea and vomiting (CINV) following cisplatin, when a conventional anti-emetic regimen had failed.MethodsThis was a prospective study (April 2011–April 2012) of patients with lung cancer, treated with cisplatin at the Beijing Cancer Hospital, and initially receiving granisetron, dexamethasone, and metoclopramide as anti-emetics. If patients experienced vomiting of grade ≥2 and required rescue anti-emetic medications during the first cycle, oral aprepitant was added in subsequent cycles (day 1: 125xa0mg; days 2–3: 80xa0mg once daily). Acute (day 1) and delayed (days 2–5) nausea and vomiting, use of rescue medications, and occurrence of adverse reactions were monitored after the start of chemotherapy.ResultsTwenty-five of 132 patients (18.9xa0%) were administered aprepitant for secondary prophylaxis against emesis during the second cycle of chemotherapy. The incidences of acute and delayed nausea were 52 and 100xa0% in the first cycle, but 8 and 72xa0% in the second cycle. The incidences of acute and delayed vomiting were 20 and 100xa0% in the first cycle, but 0 and 36xa0% in the second cycle. No patients required rescue medications or intravenous rehydration during the second cycle. Aprepitant was not associated with additional adverse events.ConclusionsIn patients with lung cancer receiving cisplatin-based chemotherapy, the addition of aprepitant to a 5-HT3 antagonist, dexamethasone, and metoclopramide improves protection against CINV when the conventional anti-emetic regimen fails.


Medicine | 2016

Efficacy and safety of extended use of platinum-based doublet chemotherapy plus endostatin in patients with advanced nonsmall cell lung cancer

Weiheng Hu; Jian Fang; Jun Nie; Ling Dai; Jie Zhang; Xiaoling Chen; Xiangjuan Ma; Guangming Tian; Di Wu; Sen Han; Jindi Han; Yang Wang; Jieran Long

Abstract The aim of this study was to investigate the efficacy and safety of the extended use of platinum-based doublet chemotherapy (PT-DC) plus endostatin in patients with advanced nonsmall cell lung cancer (NSCLC). We performed a retrospective analysis of 200 newly diagnosed advanced NSCLC patients who had received at least 1 cycle of endostatin plus PT-DC between September 2009 and November 2014. Of these patients, 155 received 4 or more cycles of therapy (the extended therapy group), while 45 received less than 4 cycles of therapy (the control group). Clinical tumor responses, progression-free survival (PFS), overall survival (OS), and toxicity profiles were recorded and retrospectively analyzed. In the extended therapy group, 67 patients (43.2%) achieved a best overall response rate of partial response (PR), while in the control group, 13 patients (28.9%) had a best overall response rate of PR. After a median follow-up of 15.9 months, the median PFS and OS were 8.0 and 23.1 months in the extended arm and 5.8 and 14.0 months in the control arm, respectively. There were statistically significant differences in median PFS and OS between these 2 arms. Hematologic and gastrointestinal toxicities occurred more frequently in the extended therapy group, but no statistically significant difference was detected in grade 3 to 4 toxicities overall between these 2 groups. In conclusion, extended treatment using endostatin combined with PT-DC can provide additional survival benefits and satisfactory toxicity profiles in previously untreated patients with NSCLC, which merits further evaluation in a larger prospective study.


Chinese Journal of Lung Cancer | 2010

Analysis of prognostic factors of 80 advanced NSCLC patients treated with gefitinib for more than 6 months

Ling Dai; Jian Fang; Jun Nie; Weiheng Hu; Xiaoling Chen; Jindi Han; Guangming Tian; Sen Han; Xuyi Liu

BACKGROUNDnSome clinical predictors can be used to evaluate the efficacy of epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) therapy for non-small cell lung cancer (NSCLC), including female, East-Asian, non-smoker, adenocarcinoma, skin rash, etc. The aim of this study is to explore the prognosis of advanced NSCLC patients treated with gefitinib for more than 6 months.nnnMETHODSnEighty advanced NSCLC patients treated with gefitinib for more than 6 months were collected from January, 2005 to March, 2010. The association of their clinical characteristics with median progression-free survival time (PFS) was analysed.nnnRESULTSnSignificantly longer median PFS were found in patients with > 70 years old, earlier clinical stage (IIIb), non-bone metastasis (27 months vs 12 months; 32 months vs 12 months; 16 months vs 10 months, P < 0.05). There was no significant difference in median PFS between ECOG performance status 0-1 group and 2-4 group, between more than 4 cycles of chemotherapy and 1-4 cycles, between PFS of chemotherapy > 6 months group and ≤6 months group, however, ECOG 0-1 group and more than 4 cycles of chemotherapy or PFS of chemotherapy > 6 months group seemed to have longer median PFS (15 months vs 10 months; 16 months vs 12 months; 14 months vs 12 months). Compared with no skin rash and grade 0-I rash group, the patients with rash or grade ≥II rash had longer median PFS (16 months vs 13 months, P=0.171; 19 months vs 11 months, P=0.085). The median PFS was not related with sex, smoking index, pathological types, metastatic sites except bone, treatment strategy, etc (P > 0.05).nnnCONCLUSIONSnFor gefitinib treatment, longer median PFS is likely to be obtained in patients with > 70 years old, earlier clinical stage (IIIb), non-bone metastasis.


Asia-pacific Journal of Clinical Oncology | 2018

Efficacy, safety and predictive indicators of apatinib after multilines treatment in advanced nonsquamous nonsmall cell lung cancer: Apatinib treatment in nonsquamous NSCLC

Di Wu; Li Liang; Ligong Nie; Jun Nie; Ling Dai; Weiheng Hu; Jie Zhang; Xiaoling Chen; Jindi Han; Xiangjuan Ma; Guangming Tian; Sen Han; Jieran Long; Yang Wang; Ziran Zhang; Tao Xin; Jian Fang

Patients with advanced nonsquamous nonsmall cell lung cancer (NSCLC) who experienced progression with two or more lines chemotherapy have no treatment options that clearly confer a survival benefit. As a novel vascular endothelial growth factor receptor‐2 tyrosine kinase inhibitor, apatinib has a certain antitumor effect for various solid tumors. The present study evaluated the efficacy and safety of apatinib in advanced nonsquamous NSCLC as salvage treatment in Chinese real‐world practice.


Future Oncology | 2016

Clinical characteristics associated with non-small-cell lung cancer harboring ALK rearrangements in Chinese patients

Guangming Tian; Xinliang Zhao; Jun Nie; Ling Dai; Weiheng Hu; Jie Zhang; Xiaoling Chen; Jindi Han; Xiangjuan Ma; Di Wu; Sen Han; Jieran Long; Yang Wang; Jian Fang

AIMnThe ALK inhibitor, crizotinib, has demonstrated effectiveness in patients with non-small-cell lung cancer harboring ALK rearrangements. As few studies of the clinical characteristics of Chinese patients with ALK rearrangements have been reported, we conduct this study to gain more understanding in such area among Chinese patients.nnnPATIENTS & METHODSnWe undertook a retrospective study of 288 non-small-cell lung cancer patients admitted to our institution over a period of 4.5 years.nnnRESULTSnFollowing testing, 14.9% of the patients (43/288) were found to be ALK fusion gene positive. Patient data including gender, age, smoking status, EGFR mutation status and medical imaging data were collected and analyzed.nnnCONCLUSIONnThe findings suggested that patients with ALK rearrangements are more likely to be young, have EGFR wild-type, and more likely to exhibit mucus secretion, solid tumor growth, lymph node metastasis and pleural metastasis.


Thoracic Cancer | 2014

Retrospective study of surgery versus non-surgical management in limited-disease small cell lung cancer

Jie Zhang; Xiaoling Chen; Jindi Han; Jun Nie; Ling Dai; Weiheng Hu; Guangming Tian; Xiangjuan Ma; Sen Han; Di Wu; Qingfeng Zheng; Yue Yang; Jian Fang

The role of surgery in limited small cell lung cancer (SCLC) is still controversial. To assess the role of surgery in SCLC we performed a retrospective analysis of survival in a group of limited stage patients, who were managed with trimodal therapy including surgery, or with chemotherapy and radiotherapy.


Chinese Journal of Lung Cancer | 2014

Multivariate Analysis of Prognostic Factors in the Eldly Patients with Small Cell Lung Cancer: A Study of 160 Patients

Xiaoling Chen; Jian Fang; Jun Nie; Ling Dai; Jie Zhang; Weiheng Hu; Jindi Han; Xiangjuan Ma; Guangming Tian; Sen Han; Di Wu; Jieran Long; Yang Wang

BACKGROUND AND OBJECTIVEnLung cancer is currently the leading cause of cancer death, two thirds of patients are over the age of 65. Small cell lung cancer (SCLC) accounts for about 15%-20% of all lung cancer. The objective of this study is to evaluate the survival of patients older than 65 with SCLC and analyze the independent prognostic factors in this group of patients.nnnMETHODSnA retrospective study has enrolled 160 cases of lung cancer aged over 65. The prognostic factors were analyzed by Kaplan-Meier and Cox multivariate proportional hazards model.nnnRESULTSn① The median follow-up time was 12 (2-109) months. 1-, 3-, and 5-year survival rate was 47.1%, 13.0%, 9.6% respectively, and 74.4%, 25.0%, 19.7% for limited-stage (LD), and 36.8%, 8.7%, 5.8% for extensive-stage (ED). Median survival time (MST) of all the patients was 12 months, 24 months for LD and 11 months for ED, respectively. ② Multivariate analysis suggested that performance status (PS) pre-treatment, the change of PS after treatment, stage, liver metastases and thoracic radiotherapy were the independent prognostic factors in all patients. ③ For LD-SCLC patients, PS pre-treatment, thoracic radiotherapy were the independent prognostic factors. The model of thoracic radiotherapy (concurrent chemoradiation vs sequential chemoradiation, early concurrent chemoradiation vs late concurrent chemoradiation) and prophylactic cranial irradiation (PCI) did not show significant difference. ④ For ED-SCLC patients, sex, the change of PS after treatment, chemotherapy, liver metastases, thoracic radiotherapy, PCI were the independent prognostic factors.nnnCONCLUSIONSnThe survival time is related to PS and thoracic radiotherapy in eldly patients. Besides, it is also related to sex, chemotherapy, liver metastases and PCI for ED-SCLC.


Chinese Journal of Lung Cancer | 2015

Effects of Local Radiation Combined with Chemotherapy in the treatment of Patients with Extensive-stage Small Cell Lung Cancer

Di Wu; Jian Fang; Jun Nie; Ling Dai; Xiaoling Chen; Jie Zhang; Weiheng Hu; Jindi Han; Xiangjuan Ma; Guangming Tian; Sen Han; Jieran Long; Yang Wang

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