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Journal Thoracic Oncology

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Abstracts <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017<br />

PUB094 CORRELATION OF CLINICOPATHOLOGIC FEATURES AND<br />

LUNG SQUAMOUS CELL CARCINOMA SUBTYPES ACCORDING TO<br />

THE 2015 WHO CLASSIFICATION<br />

Yongfeng Yu, Shun Lu<br />

Shanghai Lung Cancer Center, Shanghai Chest Hospital, Shanghai/China<br />

Background: This study aimed to determine the relationship between<br />

clinicopathologic features and lung squamous cell carcinoma subtypes<br />

according to the 2015 WHO classification. Methods: We identified 368<br />

operable lung squamous cell carcinoma patients who had undergone a<br />

complete surgical resection at Shanghai Chest Hospital between April<br />

2015 and March 2016. Results: Among all patients, the percentages of lung<br />

squamous cell carcinoma subtypes were: 68.5%(252/368), 26.2%(97/368),<br />

and 5.1%(19/368) for keratinizing squamous cell carcinoma(KSCC),<br />

nonkeratinizing squamous cell carcinoma(NKSCC), and basaloid squamous<br />

cell carcinoma(BSCC), respectively.There were more smokers in patients<br />

with KSCC than in patients with other subtypes (p=0.004). There were<br />

no significant relationships between pathological subtypes and other<br />

clinicopathologic features, such as gender, age, location type, type of<br />

resection, stage, visceral pleural involvement, lymphovascular invasion, and<br />

lymph node involvement. The expressions of P40, CK5/6, TTF-1, Napsin A,<br />

and CK7 were also not significantly different in three subtypes.Conclusion:<br />

Our study revealed that there were no significant relationships between<br />

clinicopathologic features and lung squamous cell carcinoma subtypes.<br />

Keywords: Lung Squamous cell carcinoma, pathological subtype,<br />

clinicopathologic feature<br />

center of the lung by an air tube (bronchus). Large cell carcinomas can occur in<br />

any part of the lung. Liposomes were used as Effective encapsulation of both<br />

hydrophobic & hydrophilic molecules. Due to their ability to solubilize poorly<br />

water soluble drugs, facilitate their nebulization, minimizing clinical drug<br />

dose and reducing toxicity, prolonging and targeting release of therapeutic<br />

agents by modification of liposome surface. Methods: The failures of the<br />

present delivery systems are – Oral administration of etoposide at varying<br />

dosage for the treatment of lung cancer causes GI toxicity and disturbances<br />

of liver function. The parenteral administration of etoposide for lung<br />

cancer treatment has been reported to cause severe hepatic impairment<br />

and Hypotension. Moreover, intravenously injected ligands mediated<br />

liposomes have been limited due to - Leakage of their contents before they<br />

reach the target tissue, Rapid clearance from the blood stream, uptake by<br />

the macrophages of liver and spleen. Results: Liposomes were prepared by<br />

lipid cast film method, optimized and then coupled with Mannose. Drug<br />

loaded Liposomes were characterized in-vitro for shape, size, and stability<br />

in various body fluids. The Air-jet nebulizer system was used for aerosol and<br />

was characterized for Appearance, Leak Test, Internal Pressure, Amount<br />

discharge/ actuation, Spray Pattern area and Penetration Efficiency. The<br />

in-vivo study comprised of estimation of serum and tissue distribution of<br />

drug and fluorescence microscopy.Conclusion: Liposomes formed were<br />

multilamellar and were found to be stable in gastric and intestinal fluids.<br />

Fluorescence microscopy suggested that liposomes were taken up by the gut<br />

associated lymphoid tissues and therapeutic level of drug can be achieved<br />

at desired site. Thus, from the results obtained it can be concluded that<br />

the Aerosolized mannose liposomes can deliver drug to the cancerous cells<br />

in an effective way and hold great potential for lung targeting. Through<br />

mannosylated liposomes, therapeutic level of drug can be achieved at desired<br />

site. The system carried dual function, firstly retention of drug and secondly<br />

selective delivery of etoposide to lungs.<br />

Keywords: etoposide, Aerosols, liposomes<br />

PUB095 COMPUTED TOMOGRAPHY IMAGING OF SUPERIOR VENA<br />

CAVA INVOLVEMENT IN T4-CLASSED LUNG CANCER<br />

Henda Neji 1 , Salma Jebri 1 , Monia Attia 1 , Ines Baccouche 1 , Mahdi Afrit 2 , Houda<br />

Elbanna 1 , Soumaya Laabidi 2 , Saoussen Hantous 1 , Amel Mekkaoui 1 , Khaoula<br />

Ben Miled-M’Rad 1<br />

1 Abderrahmen Mami Hospital, Ariana/Tunisia, 2 <strong>Oncology</strong>, Abderrahmen Mami<br />

Hospital, Ariana/Tunisia<br />

Background: Superior vena cava (SVC) can be involved in many ways in<br />

patients with lung cancer. This latter is considered to be the most frequent<br />

cause of SVC syndrome which is a medical emergency requiring prompt<br />

evaluation and treatment. The SVC syndrome can reveal the disease or can be<br />

discovered on computed tomography (CT) of the chest. The objectives of our<br />

study are to specify CT characteristics of SVC involvement in T4-classed lung<br />

cancer and to estimate the frequency of its total obstruction in this patients<br />

category. Methods: Retrospective review of CT scans of 177 consecutive<br />

patients with T4-classed lung cancer, newly and fully diagnosed in our<br />

institution during the year 2015. All CT examinations were performed after<br />

contrast agent administration. Only patients with mediastinal involvement<br />

were retained. Every aspect of SVC involvement was noticed separately.<br />

Results: Among the 177 patients, mediastinal invasion was observed in 132<br />

cases (74.5%). SVC was involved in 32 cases (24%). Lung cancer was located<br />

on the right side in 91% of cases. The involvement included: - A contact with<br />

the tumor with loss of the fat layer (n= 7) - An inclusion of the vessel in the<br />

tumoral mass with narrowing of the lumen (n=17) - An intraluminal tumoral<br />

bud (n=8) - A complete obliteration (n= 6) Collateral venous circulation was<br />

observed in 8 cases. Adenocarcinoma and small cell lung cancer were the most<br />

frequent histological types responsible for SVC involvement Clinical signs of<br />

SVC syndrome were obvious in only 6 patientsConclusion: Superior vena cava<br />

involvement is quite frequent in advanced stage of lung cancer. However,<br />

the total tumoral obstruction of this vessel is rare. CT helps defining the<br />

mechanism and the severity of the SVC involvement.<br />

Keywords: superior vena vava, lung cancer, Advanced stage<br />

PUB097 CARBON NANOTUBES FOR EFFICIENT MITOCHONDRIAL<br />

TUMOR TARGETING<br />

Gomed Agarwal 1 , Saurabh Bhargava 2 , Vishal Bhargava 1<br />

1 Guru Teg Bahadur Hospital, Kanpur/India, 2 Manav Bharti University, Kanpur/India<br />

Background: Cancer is uncontrollable growth of cells which are devoid of<br />

apoptosis. We developed a novel strategy ie Ligand mediated tumor targeting<br />

via carrier systems. Multiwalled Carbon nanotubes (MWCNTs) were used as it<br />

directly enters into the cell without passing through endo-lysosomes, large<br />

inner volume, distinct inner and outer surfaces & have ability to enter the cell<br />

by spontaneous mechanism. Thus, proposed work envisages Rhodamine-123<br />

conjugated Paclitaxel loaded functionalized-CNTs to provide enhanced cell<br />

permeation in order to enhance mitochondrial availability of Paclitaxel.<br />

Methods: The raw MWCNT were procured and purified, oxidized & then<br />

conjugated with rhodamine-123 by carbodimide method. The MWCNT’s were<br />

characterized in-vitro for shape & size by Scanning(SEM) & Transmission<br />

Electron Microscopy(TEM), FTIR analysis, X-ray diffraction and zeta potential<br />

determined. Stability studies were performed at exaggerated conditions<br />

along with Hemolytic Toxicity Study. The Cell Cytotoxicity Study-MTT Assay<br />

was done using Hela cell lines. Mitochondrial localization was determined<br />

by CLSM study. The in-vivo part of the study comprised of determining the<br />

distribution of drug in various organs by fluorescence microscopy. Results:<br />

The Rhodamine-123 conjugated MWCNTs were prepared and characterized.<br />

The CNTs showed high paclitaxel loading, sustained release, and excellent<br />

biocompatibility as evident by in-vitro drug release and low hemolytic<br />

toxicity. MTT assay against HeLa cell lines suggested the potential anticancer<br />

activity of the developed system. CLSM study suggested that mitochondrial<br />

specific localization of Rhodamine-123 conjugated MWCNTs in HeLa cells.<br />

Conclusion: Thus, Rhodamine-123 conjugated Paclitaxel loaded f-CNTs system<br />

have potential to provide an enhanced cell permeation and mitochondrial<br />

localization for effective tumour chemotherapy.<br />

Keywords: paclitaxel, CNT<br />

PUB096 ENHANCED DELIVERY OF ANTICANCER DRUG TO THE<br />

LUNGS VIA LIPOSOMAL AEROSOLS<br />

Mani Agarwal 1 , Mani Bhargava 2 , Saurabh Bhargava 3<br />

1 Manav Bharti University, Kanpur/India, 2 Icfai University, Kanpur/India, 3 Guru Teg<br />

Bahadur Hospital, Kanpur/India<br />

Background: Lung cancer tends to spread very early, and is a very life<br />

threatening cancer and one of the most difficult cancers to treat. Non-small<br />

cell lung cancer (NSCLC) usually grows and spreads more slowly than small cell<br />

lung cancer. There are three forms of NSCLC: Adenocarcinomas are found in<br />

an outer area of the lung. Squamous cell carcinomas are usually found in the<br />

PUB098 PANIC DISORDER AND DYSPNOEA IN PATIENTS WITH<br />

LUNG CANCER IN A NIGERIAN DE,-ADDICTION UNIT<br />

Victor Lasebikan<br />

Psychiatry, College of Medicine, University of Ibadan, Ibadan/Nigeria<br />

Background: The objectives of this study were to determine the prevalence<br />

and dyspnoea and panic disorder in patients with lung cancer in a teaching<br />

hospital and also do determine the association between them. Methods:<br />

S792 <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017

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