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1.
Chest ; 160(5): e523-e526, 2021 11.
Article in English | MEDLINE | ID: mdl-34743857

ABSTRACT

CASE PRESENTATION: A 57-year-old man with history of stage IIIB right-sided malignant pleural mesothelioma was admitted from his oncologist's office for progressive dyspnea of two weeks duration. He had associated dyspnea at rest and a new dry cough. He denied sputum production, hemoptysis, or fevers, but he did endorse chills, fatigue, and weight loss. The patient was a veteran of the Navy and had extensive international travel in his 20s. He had never been incarcerated and denied any sick contacts or recent travels. He had received a diagnosis of mesothelioma 11 months earlier after presenting to his physician's office with complaints of shortness of breath on exertion. Initial imaging revealed a large right-sided pleural effusion with irregular pleural thickening. He underwent right-sided thoracoscopy, and the pleural biopsy result was consistent with epithelioid mesothelioma. Because of invasion of his seventh rib, he was not a candidate for surgery and underwent palliative radiation and chemotherapy with cisplatin, pemetrexed, and bevacizumab. He was undergoing his eighth cycle of chemotherapy at the time of presentation.


Subject(s)
Chemoradiotherapy/methods , Lung , Mesothelioma, Malignant , Multiple Pulmonary Nodules/diagnostic imaging , Neoplasm Metastasis/diagnostic imaging , Pleural Neoplasms , Biopsy/methods , Bronchoscopy/methods , Diagnosis, Differential , Disease Progression , Dyspnea/diagnosis , Dyspnea/etiology , Fatal Outcome , Humans , Lung/diagnostic imaging , Lung/pathology , Male , Mesothelioma, Malignant/pathology , Mesothelioma, Malignant/physiopathology , Mesothelioma, Malignant/therapy , Middle Aged , Neoplasm Staging , Pleural Neoplasms/pathology , Pleural Neoplasms/physiopathology , Pleural Neoplasms/therapy , Radiography, Thoracic/methods , Tomography, X-Ray Computed/methods
2.
Thorac Cancer ; 12(11): 1752-1756, 2021 06.
Article in English | MEDLINE | ID: mdl-33949775

ABSTRACT

BACKGROUND: Malignant pleural mesothelioma (MPM) is a rare, highly aggressive and deadly disease with a poor patient life expectancy. A few years ago, the main challenge was the histological diagnosis of this disease; at present, the search for the best therapeutic strategy is now a priority. However, an optimal therapeutic strategy is not yet clear, despite growing efforts in the treatment armamentarium and research, and at the era of tailored and individualized treatment, tools to predict patient survival are needed for therapeutic decision-making. Among them, the LENT scoring system was developed to predict prognosis in patients with malignant pleural effusion. The aim of this study was to assess the performance of the LENT score in predicting prognosis in patients with MPM. METHODS: A retrospective observational study was conducted by analyzing the prospective collected databases of patients undergoing medical thoracoscopy in a single center with a final diagnosis of MPM confirmed by the MESOPATH National Reference Center. RESULTS: A total of 41 patients with MPM were studied. All patients underwent platinum-based chemotherapy combined with pemetrexed ± bevacizumab. No high-risk category patients were found using the LENT scoring system in this cohort. The median (range) LENT score at the time of medical thoracoscopy was 0 (0-3) and the median survival was 15.5 (2-54) months for the entire cohort. The median survival of low-risk and moderate-risk category patients was 21.4 months (2-54, 32 patients) and 6.7 months (2-19, nine patients), respectively. A total of 27 patients with MPM of epithelial subgroup had a median LENT score of 1 (0-2) with a 26 (2-54) months median survival. The median LENT score and median survival of nonepithelial mesothelioma patients (biphasic MPM subgroup, eight patients; sarcomatoid MPM subgroup, six patients) were 0 (0-3) and 11 (2-52) months, respectively. CONCLUSIONS: Applied to a homogenous cohort of MPM patients, the LENT score underestimated prognosis and was not useful per se for the management of this disease, as evidenced in the epithelial mesothelioma subgroup of patients in our study.


Subject(s)
Mesothelioma, Malignant/physiopathology , Pleural Neoplasms/physiopathology , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Prognosis , Retrospective Studies , Risk Factors
3.
Hum Exp Toxicol ; 40(11): 1817-1824, 2021 Nov.
Article in English | MEDLINE | ID: mdl-33998299

ABSTRACT

INTRODUCTION: Malignant pleural mesothelioma (MPM) is a malignant tumor that is associated mostly with asbestos exposure. The present study was to evaluates the diagnostic value of neopterin, periostin, YKL-40, Tenascin-C (TNC), and Indolamine 2,3-dioxygenase (IDO) as noninvasive markers of malign pleural mesothelioma. METHODS: Included in the study were 30 patients diagnosed with malign pleural mesothelioma, and 25 people as a control group. Biomarker levels were determined using an enzyme immunoassay . A Mann-Whitney U test and Spearman correlation methods were used for the statistical analysis. RESULTS: All evaluated biomarkers were found to be significantly higher in the MPM group than in the control group (p < 0.05). There was no effect of such variables as gender, age or MPMsubtype on the parameters (p > 0.05) in the patient group. All biomarkers were positively correlated with each other (p < 0.001). CONCLUSIONS: The current non-invasive biomarkers that can be used in the diagnosis of MPM yielded significant results and can make important contributions to the early diagnosis of MPM.


Subject(s)
Asbestos/toxicity , Cell Adhesion Molecules/blood , Chitinase-3-Like Protein 1/blood , Indoleamine-Pyrrole 2,3,-Dioxygenase/blood , Mesothelioma, Malignant/chemically induced , Mesothelioma, Malignant/diagnosis , Neopterin/blood , Tenascin/blood , Adult , Biomarkers, Tumor/blood , Cross-Sectional Studies , Female , Humans , Male , Mesothelioma, Malignant/blood , Mesothelioma, Malignant/physiopathology , Middle Aged , Pleural Neoplasms/chemically induced , Pleural Neoplasms/diagnosis , Pleural Neoplasms/physiopathology , Prospective Studies
4.
J Thorac Cardiovasc Surg ; 159(5): 2082-2091.e1, 2020 05.
Article in English | MEDLINE | ID: mdl-31866087

ABSTRACT

OBJECTIVE: Cytotoxic CD8+ tumor infiltrating lymphocytes (TILs) can contribute to the benefit of hypofractionated radiation, but programmed cell death pathways (programmed cell death 1 and programmed cell death ligand 1 [PD-1/PD-L1]) may provide a mechanism of tumor immune escape. We therefore reviewed the influence of PD-1/PD-L1 and CD8+ TILs on survival after accelerated hypofractionated hemithoracic radiation followed by extrapleural pneumonectomy for malignant pleural mesothelioma (MPM). METHODS: Sixty-nine consecutive patients undergoing the protocol of Surgery for Mesothelioma after Radiation Therapy (SMART) between November 2008 and February 2016 were analyzed for the presence of PD-L1 on tumor cells, PD-1 on inflammatory cells, and CD8+ TILs. Comparison was made with a cohort of patients undergoing extrapleural pneumonectomy after induction chemotherapy (n = 14) and no induction (n = 2) between March 2005 and October 2008. PD-L1 expression on tumor cells ≥1% was considered positive. CD8+ TILs and PD-1 expression were scored as a percentage of positive cells. RESULTS: PD-L1 was negative in 75% of MPM after completion of SMART. CD8+ TILs ranged between 0.24% and 8.47% (median 2%). CD8+ TILs ≥2% was associated with significantly better survival in epithelioid MPM (median survival 3.7 years vs 2.3 years in CD8+ TILs <2%; P = .02). PD-L1 positivity was associated with worse survival in biphasic MPM (median survival, 0.4 years vs 1.5 years in biphasic PD-L1 negative tumors; P = .07) after SMART. Multivariate analysis demonstrated that epithelioid MPM, nodal disease, and CD8+ TILs were independent predictors of survival after SMART. CONCLUSIONS: The influence of tumor microenvironment on survival differs between epithelioid and nonepithelioid MPM. CD8+ TILs is an independent factor associated with better survival in epithelioid MPM treated with SMART.


Subject(s)
Mesothelioma , Pleural Neoplasms , Tumor Microenvironment/physiology , Adult , Aged , Aged, 80 and over , B7-H1 Antigen/analysis , CD8-Positive T-Lymphocytes/cytology , Female , Humans , Male , Mesothelioma/diagnosis , Mesothelioma/mortality , Mesothelioma/physiopathology , Mesothelioma/therapy , Middle Aged , Neoplastic Stem Cells/cytology , Pleura/chemistry , Pleura/surgery , Pleural Neoplasms/diagnosis , Pleural Neoplasms/mortality , Pleural Neoplasms/physiopathology , Pleural Neoplasms/therapy , Prognosis , Radiation Dose Hypofractionation
5.
Medicine (Baltimore) ; 98(48): e18251, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31770288

ABSTRACT

RATIONALE: Small cell carcinoma (SCC) occurs mostly in the lung, and small cell lung cancer accounts for 13% of newly diagnosed lung cancers. Only 2.5% of SCC occurs in extrapulmonary sites, and SCC of pleural origin is especially very uncommon. PATIENT CONCERNS: An 85-year-old man presenting with progressive dyspnea for more than 7 days. DIAGNOSES: Computed tomography scan of the chest showed massive pleural effusion and diffuse nodular thickening of the pleura on the right chest. Sonography-guided needle biopsy of the pleural mass was performed and histologic and immunohistochemical findings revealed SCC. Since no parenchymal lung lesion was observed, the patient was finally diagnosed with SCC of the pleura (SCCP). INTERVENTIONS: Due to the patient's old age and poor performance status, chemotherapy was not performed and only drainage of pleural effusion was conducted for symptom relief. OUTCOMES: Dyspnea improved after pleural effusion drainage. The patient was discharged and transferred to a local medical center for hospice care. LESSONS: Although primary SCCP is extremely rare, SCCP should also be considered as well as mesothelioma in case of presence of a pleural-based mass with massive pleural effusion.


Subject(s)
Carcinoma, Small Cell , Dyspnea , Pleural Effusion, Malignant , Pleural Neoplasms , Thoracentesis/methods , Aged, 80 and over , Carcinoma, Small Cell/complications , Carcinoma, Small Cell/pathology , Carcinoma, Small Cell/physiopathology , Dyspnea/diagnosis , Dyspnea/etiology , Hospice Care , Humans , Image-Guided Biopsy/methods , Male , Pleura/diagnostic imaging , Pleura/pathology , Pleural Effusion, Malignant/diagnosis , Pleural Effusion, Malignant/etiology , Pleural Effusion, Malignant/physiopathology , Pleural Effusion, Malignant/therapy , Pleural Neoplasms/complications , Pleural Neoplasms/pathology , Pleural Neoplasms/physiopathology , Tomography, X-Ray Computed/methods , Ultrasonography, Interventional/methods
6.
Am J Ind Med ; 62(6): 503-510, 2019 06.
Article in English | MEDLINE | ID: mdl-31046142

ABSTRACT

OBJECTIVE: To evaluate the frequency and severity of pleuropulmonary alterations in anthophyllite-exposed former workers in Itapira, São Paulo, Brazil. The amphibole anthophyllite, a magnesium-iron silicate, had its mining, marketing, and use forbidden in Brazil in 1995. METHODS: Former workers were followed from 1999 to 2011. All completed chest X-ray interpreted using the International Labour Office (ILO) classification. High-resolution computed tomography was used at the final evaluation. Spirometry assessed forced vital capacity (FVC), forced expiratory volume in the first second (FEV1), and FEV1/FVC throughout the follow-up period. Samples from the mined ore were analyzed by X-ray diffraction (XRD) and scanning electron microscopy coupled to energy dispersive spectroscopy (SEM-EDS). RESULTS: XRD and SEM-EDS confirmed the presence in ore of anthophyllite at a concentration of 75%, in addition to tremolite and other amphiboles in lower concentrations. Twenty-eight subjects were evaluated. Median time of exposure was 3 years (minimum = 1; maximum = 18; interquartile interval = 1-4). Twenty cases of pleural abnormalities were diagnosed in 26 evaluated (77%). The average latency time was 25.6 ± 7.4 years. Two individuals (7.7%) showed progressive worsening of diffuse pleural thickening (DPT) and exhibited an annual FVC decrease of 85 mL and 150 mL, respectively. CONCLUSION: This small sample showed a very high index of nonmalignant pleural abnormalities in anthophyllite-exposed workers compared with workers exposed to other kinds of fibers. Rapidly progressive DPT, defined by the severity of pleural compromise, was possibly secondary to the presence of other amphibole types in the inhaled dust. No significant loss of FVC was found in the studied group as a whole. No cases of asbestosis, lung carcinoma, and mesothelioma were diagnosed in this cohort.


Subject(s)
Asbestos, Amphibole/adverse effects , Asbestosis/epidemiology , Lung Neoplasms/diagnosis , Mesothelioma/diagnosis , Occupational Exposure/adverse effects , Pleural Neoplasms/epidemiology , Aged , Asbestos, Amphibole/analysis , Asbestosis/etiology , Brazil/epidemiology , Cohort Studies , Databases, Factual , Environmental Monitoring/methods , Female , Humans , Incidence , Lung Neoplasms/chemically induced , Lung Neoplasms/epidemiology , Male , Maximum Allowable Concentration , Mesothelioma/chemically induced , Mesothelioma/epidemiology , Mesothelioma, Malignant , Middle Aged , Mining , Occupational Health , Pleural Neoplasms/chemically induced , Pleural Neoplasms/physiopathology , Retrospective Studies , Risk Assessment , Spirometry/methods , Time Factors , Vital Capacity
7.
Am J Ind Med ; 62(6): 471-477, 2019 06.
Article in English | MEDLINE | ID: mdl-31087402

ABSTRACT

BACKGROUND: While asbestos has long been known to cause mesothelioma, quantitative exposure-response data on the relation of mesothelioma risk and exposure to chrysotile asbestos are sparse. METHODS: Quantitative relationships of mortality from mesothelioma and pleural cancer were investigated in an established cohort of 5397 asbestos textile manufacturing workers in North Carolina, USA. Eligible workers were those employed between 1950 and 1973 with mortality follow-up through 2003. Individual exposure to chrysotile fibres was estimated on the basis of 3420 air samples covering the entire study period linked to work history records. Exposure coefficients adjusted for age, race, and time-related covariates were estimated by Poisson regression. RESULTS: Positive, statistically significant associations were observed between mortality from all pleural cancer (including mesothelioma) and time since first exposure (TSFE) to asbestos (rate ratio [RR], 1.19; 95% confidence interval [CI], 1.06-1.34 per year), duration of exposure, and cumulative asbestos fibre exposure (RR, 1.15; 95% CI, 1.04-1.28 per 100 f-years/mL; 10-year lag). Analyses of the shape of exposure-response functions suggested a linear relationship with TSFE and a less-than-linear relationship with cumulative exposure. Restricting the analysis to years when mesothelioma was coded as a unique cause of death yielded stronger but less precise associations. CONCLUSIONS: These observations support with quantitative data the conclusion that chrysotile causes mesothelioma and encourage exposure-response analyses of mesothelioma in other cohorts exposed to chrysotile.


Subject(s)
Asbestos, Serpentine/adverse effects , Lung Neoplasms/chemically induced , Lung Neoplasms/mortality , Mesothelioma/chemically induced , Mesothelioma/mortality , Occupational Exposure/adverse effects , Pleural Neoplasms/chemically induced , Pleural Neoplasms/mortality , Adult , Age Factors , Asbestos, Serpentine/analysis , Cohort Studies , Confidence Intervals , Environmental Monitoring/methods , Evaluation Studies as Topic , Female , Humans , Lung Neoplasms/physiopathology , Male , Maximum Allowable Concentration , Mesothelioma/physiopathology , Mesothelioma, Malignant , Middle Aged , North Carolina/epidemiology , Occupational Diseases/etiology , Occupational Diseases/mortality , Occupational Exposure/analysis , Pleural Neoplasms/physiopathology , Retrospective Studies , Risk Assessment , Sex Factors , Survival Analysis , Textile Industry
8.
Eur J Clin Nutr ; 73(10): 1412-1421, 2019 10.
Article in English | MEDLINE | ID: mdl-30886321

ABSTRACT

BACKGROUND/OBJECTIVES: Malignant pleural mesothelioma (MPM) is an incurable cancer and optimizing daily physical activity and quality of life are key goals of patient management. Little is known about the prevalence of pre-sarcopenia and malnutrition in MPM or their associations with patient outcomes. This study aimed to determine the prevalence of pre-sarcopenia and malnutrition in MPM and investigate if activity levels and quality of life differed according to body composition and nutritional status. SUBJECTS/METHODS: Patients with a diagnosis of MPM were recruited. Pre-sarcopenia was defined as low appendicular skeletal muscle mass (≤ 7.26 kg/m2 for men and ≤ 5.45 kg/m2 for women), measured by dual energy X-ray absorptiometry. Malnutrition was defined as a rating of B or C on the Patient-Generated Subjective Global Assessment. Outcome measures included objective activity levels (Actigraph GT3X) and health-related quality of life (HRQoL; Functional Assessment of Cancer Therapy General). RESULTS: Sixty-one people participated (79% male, median age 69 [IQR 62-74] years and median BMI 25.8 [IQR 24.3-28.4] kg/m2). Fifty-four percent were pre-sarcopenic and 38% were malnourished. Percent of time spent in light activity/day was lower in participants with pre-sarcopenia compared with non-sarcopenic participants (median 25.4 [IQR 19.8-32.1]% vs. 32.3 [27.1-35.6]%; p = 0.008). Participants with malnutrition had poorer HRQoL than well-nourished participants (mean 69.0 (16.3) vs. 84.4 (13.3); p < 0.001). CONCLUSION: Participants with MPM had high rates of pre-sarcopenia and malnutrition. Pre-sarcopenia was associated with poorer activity levels, whilst malnutrition was associated with poorer quality of life. Interventions that aim to address reduced muscle mass and weight loss, should be tested in MPM to assess their impact on patient outcomes.


Subject(s)
Body Composition , Exercise/physiology , Lung Neoplasms/physiopathology , Mesothelioma/physiopathology , Nutritional Status , Pleural Neoplasms/physiopathology , Quality of Life , Aged , Australia/epidemiology , Cross-Sectional Studies , Diet , Female , Humans , Male , Malnutrition/epidemiology , Mesothelioma, Malignant , Middle Aged , Prospective Studies , Sarcopenia/epidemiology
10.
Ann Surg Oncol ; 25(6): 1572-1579, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29616420

ABSTRACT

INTRODUCTION: The change in TNM classification of malignant pleural mesothelioma (MPM) between the seventh and eighth edition classifications has resulted in the downstaging of many advanced-stage patients into pathological stage IB. Many mesotheliomas without lymph node metastasis have been classified as stage IB in the eighth edition classification. Stage IB mesotheliomas comprised a heterogeneous group with different prognosis. It is necessary to clarify the prognostic factors in this group. METHODS: Between September 2009 and August 2016, a total of 89 patients with MPM underwent curative intent surgery [pleurectomy decortication n = 57 (64.1%), extrapleural pneumonectomy n = 32 (35.9%)] at our institution. Of these, 40 were reclassified as stage IB according to the eighth edition TNM classification. Independent unfavorable prognostic factors were identified by univariate analyses using the log-rank test and Cox proportional hazards regression models. RESULTS: Three independent significant factors were identified that indicated an unfavorable prognosis: a nonepithelioid subtype, lymphovascular invasion, and preoperative forced expiratory volume in 1 s (FEV1) < 2000 ml. Patients with no, one, and two of these risk factors showed 3-year overall survival probabilities of 94.7, 62.5, and 0%, respectively. The 3-year survival of patients with one factor did not differ significantly from that of patients with stage III MPM, whereas that of patients with two factors was significantly shorter (p = 0.015). CONCLUSIONS: Independent poor prognostic factors for patients with stage IB MPM patients, allowing subgroups with poorer and more favorable prognoses to be identified. This should help personalize decisions on adjuvant chemotherapy.


Subject(s)
Mesothelioma/pathology , Mesothelioma/therapy , Pleural Neoplasms/pathology , Pleural Neoplasms/therapy , Aged , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Blood Vessels/pathology , Chemotherapy, Adjuvant , Cisplatin/administration & dosage , Female , Forced Expiratory Volume , Humans , Lymphatic Vessels/pathology , Male , Mesothelioma/physiopathology , Neoadjuvant Therapy , Neoplasm Invasiveness , Neoplasm Staging , Pemetrexed/administration & dosage , Pleural Neoplasms/physiopathology , Pneumonectomy , Preoperative Period , Prognosis , Proportional Hazards Models , Risk Factors , Survival Rate
12.
BMC Cancer ; 18(1): 178, 2018 02 13.
Article in English | MEDLINE | ID: mdl-29433474

ABSTRACT

BACKGROUND: Patients with advanced lung cancer (LC) or malignant pleural mesothelioma (MPM) exhibit limitation of exercise capacities and alteration of quality of life (QoL) induced by cancer and its treatment. Few studies assessed pulmonary rehabilitation (PR) in these chemotherapy-treated patients, and none evaluated a home-based PR program. METHODS: In this prospective uncontrolled observational pilot study, patients treated by chemotherapy for LC or MPM were screened for a home-based PR program combining exercise training with global cares including therapeutic education and psychosocial management. Feasibility and safety were evaluated by attendance and adherence to PR program. Various exercise tolerance tests, including 6-min walk test (6MWT) and 6-min stepper test (6MST), were performed before and after PR associated with, QoL and psychological assessment (VSRQ and HAD, respectively). RESULTS: 243 patients were considered eligible but only 71 (60.6 ± 8.8 years) started a PR and 47 completed the program. Refusals to participate were mostly related to lack of motivation whereas withdrawals to PR were related to cancer-related medical issues. No adverse event related to PR was observed. Baseline 6MWT distance was associated with performance status (r = - 0.45, p = 0.001) and mMRC dyspnea scale (r = - 0.49, p < 0.001) but not with lung cancer stage. Post-PR reassessment showed 6MWT stability and 6MST improvement in patients who completed the program. Daily physical activity (p = 0.007) and anxiety (p = 0.02) scores were significantly improved. CONCLUSIONS: Home-based PR was feasible and safe in patients with advanced LC or MPM. Exercise capacities stability in patients who completed the PR program suggests that PR might be beneficial. Further studies are warranted to confirm and to improve the potential value of PR in these patients.


Subject(s)
Exercise Therapy/methods , Home Care Services , Lung Neoplasms/rehabilitation , Mesothelioma/rehabilitation , Pleural Neoplasms/rehabilitation , Aged , Combined Modality Therapy , Feasibility Studies , Female , Humans , Lung Neoplasms/drug therapy , Lung Neoplasms/physiopathology , Male , Mesothelioma/drug therapy , Mesothelioma/physiopathology , Middle Aged , Pilot Projects , Pleural Neoplasms/drug therapy , Pleural Neoplasms/physiopathology , Prospective Studies , Quality of Life , Treatment Outcome
15.
Rev Med Inst Mex Seguro Soc ; 54(6): 770-776, 2016.
Article in Spanish | MEDLINE | ID: mdl-27819788

ABSTRACT

Malignant pleural mesothelioma is an occupational tumor caused by asbestos exposure. In Mexico, as asbestos usage is not prohibited, an increase in the number of cases is expected. Asbestos exposure is ubiquitous due to the great amount of products in which it is present. Its carcinogenicity is caused as the inhaled asbestos fibers cannot be eliminated by macrophages and, thus, they travel to the pleura through lymphatic pathways, producing a persistent inflammatory response. Diagnosis approach includes occupational history, along with clinical signs and symptoms, and paraclinical studies, such as pleural fluid cytology, chest x-rays, computed tomography, magnetic resonance imaging, and biopsy with immunohistochemistry. The main differential diagnosis is lung adenocarcinoma. Regarding the treatment of this tumor, it mainly comprises palliative care, even though chemotherapy, radiotherapy, and, in selected cases, surgical treatments have been used. There is an urgent need for general physicians and specialists to identify asbestos exposure, in order to make a timely diagnosis. Research is necessary to develop screening and prompt diagnostic tools, along with an epidemiological surveillance program for the workers and the general population exposed to asbestos.


El mesotelioma maligno pleural es un tumor ocupacional ocasionado por la exposición a cualquier tipo de fibra de asbesto. Y dado que en México el uso del asbesto no está prohibido, se espera que la incidencia de este tumor siga aumentando. La exposición al asbesto es ubicua, debido a la gran diversidad de productos en los que se encuentra. Su carcinogenicidad está dada porque las fibras de asbesto inhaladas no pueden ser eliminadas por los macrófagos y viajan hacia la pleura por vía linfática, donde producen una reacción inflamatoria persistente. Para su diagnóstico se precisa de una historia clínica laboral, además de que hay que orientarse con base en el cuadro clínico y los estudios paraclínicos, como la citología de líquido pleural, radiografía de tórax, tomografía axial computarizada, resonancia magnética y biopsia con inmunohistoquímica. El principal diagnóstico diferencial es el adenocarcinoma de pulmón. El tratamiento es principalmente paliativo, aunque se ha utilizado quimioterapia, radioterapia y, en seleccionados casos, cirugía. Para lograr un diagnóstico oportuno y certero es de vital importancia identificar las exposiciones al asbesto. Por otra parte, es necesaria la investigación para desarrollar pruebas de diagnóstico temprano y tamizaje, además de un programa de vigilancia epidemiológica para los trabajadores y la población general expuesta al asbesto.


Subject(s)
Mesothelioma , Occupational Diseases , Pleural Neoplasms , Combined Modality Therapy , Humans , Mesothelioma/diagnosis , Mesothelioma/epidemiology , Mesothelioma/physiopathology , Mesothelioma/therapy , Mexico/epidemiology , Occupational Diseases/diagnosis , Occupational Diseases/epidemiology , Occupational Diseases/physiopathology , Occupational Diseases/therapy , Palliative Care , Pleural Neoplasms/diagnosis , Pleural Neoplasms/epidemiology , Pleural Neoplasms/physiopathology , Pleural Neoplasms/therapy
16.
Chest ; 149(6): e157-60, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27287590

ABSTRACT

Myiasis refers to a parasitic infestation of vertebrate mammals by dipterous larvae (maggots) of higher flies. Infections in humans typically occur in tropical and subtropical regions, regions with limited medical access, and areas with poor hygiene and living conditions. Infestations in humans have been described in subcutaneous, nasal, ocular, oropharyngeal, and orotracheal cases; however, reports of pulmonary myiasis in humans in the United States and other developed countries are extremely rare. We describe a patient with recently diagnosed primary pleural angiosarcoma who presented to our clinic for the management of a thoracostomy tube and was diagnosed with pleural myiasis.


Subject(s)
Hemangiosarcoma , Myiasis , Paclitaxel/administration & dosage , Pleural Neoplasms , Thoracic Surgery, Video-Assisted/methods , Thoracostomy/methods , Aged , Anti-Bacterial Agents/administration & dosage , Antineoplastic Agents, Phytogenic/administration & dosage , Disease Management , Empyema, Pleural/etiology , Empyema, Pleural/microbiology , Empyema, Pleural/parasitology , Empyema, Pleural/therapy , Hemangiosarcoma/complications , Hemangiosarcoma/pathology , Hemangiosarcoma/physiopathology , Hemangiosarcoma/therapy , Humans , Hydropneumothorax/etiology , Hydropneumothorax/surgery , Male , Myiasis/complications , Myiasis/diagnosis , Myiasis/physiopathology , Myiasis/therapy , Pleural Cavity/parasitology , Pleural Cavity/pathology , Pleural Neoplasms/complications , Pleural Neoplasms/pathology , Pleural Neoplasms/physiopathology , Pleural Neoplasms/therapy
18.
Expert Rev Respir Med ; 9(5): 633-54, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26308799

ABSTRACT

Malignant mesothelioma is an aggressive cancer whose pathogenesis is causally linked to occupational exposure to asbestos. Familial clusters of mesotheliomas have been observed in settings of genetic predisposition. Mesothelioma incidence is anticipated to increase worldwide in the next two decades. Novel treatments are needed, as current treatment modalities may improve the quality of life, but have shown modest effects in improving overall survival. Increasing knowledge on the molecular characteristics of mesothelioma has led to the development of novel potential therapeutic strategies, including: molecular targeted approaches, that is the inhibition of vascular endothelial growth factor with bevacizumab; immunotherapy with chimeric monoclonal antibody, immunotoxin, antibody drug conjugate, vaccine and viruses; inhibition of asbestos-induced inflammation, that is aspirin inhibition of HMGB1 activity may decrease or delay mesothelioma onset and/or growth. We elaborate on the rationale behind new therapeutic strategies, and summarize available preclinical and clinical results, as well as efforts still ongoing.


Subject(s)
Lung Neoplasms/genetics , Lung Neoplasms/therapy , Mesothelioma/genetics , Mesothelioma/therapy , Molecular Targeted Therapy , Pleural Neoplasms/genetics , Pleural Neoplasms/therapy , Humans , Immunotherapy/methods , Lung Neoplasms/etiology , Lung Neoplasms/physiopathology , Mesothelioma/etiology , Mesothelioma/physiopathology , Mesothelioma, Malignant , Molecular Targeted Therapy/methods , Peritoneal Neoplasms/etiology , Peritoneal Neoplasms/genetics , Peritoneal Neoplasms/physiopathology , Peritoneal Neoplasms/therapy , Pleural Neoplasms/etiology , Pleural Neoplasms/physiopathology
19.
Cancer Res ; 75(19): 4188-97, 2015 Oct 01.
Article in English | MEDLINE | ID: mdl-26294214

ABSTRACT

Diffuse malignant mesothelioma (DMM) is a tumor of serosal membranes with propensity for progressive local disease. Because current treatment options are largely ineffective, novel therapeutic strategies based on molecular mechanisms and the disease characteristics are needed to improve the outcomes of patients with this disease. Akt kinase interacting protein 1 (Aki1; Freud-1/CC2D1A) is a scaffold protein for the PI3K-PDK1-Akt signaling module that helps determine receptor signal selectivity for EGFR. Aki1 has been suggested as a therapeutic target, but its potential has yet to be evaluated in a tumor setting. Here, we report evidence supporting its definition as a therapeutic target in DMM. In cell-based assays, Aki1 silencing decreased cell viability and caused cell-cycle arrest of multiple DMM cell lines via effects on the PKA-CREB1 signaling pathway. Blocking CREB activity phenocopied Aki1 silencing. Clinically, Aki1 was expressed in most human DMM specimens where its expression correlated with phosphorylated CREB1. Notably, Aki1 siRNA potently blocked tumor growth in an orthotopic implantation model of DMM when administered directly into the pleural cavity of tumor-bearing mice. Our findings suggest an important role for the Aki1-CREB axis in DMM pathogenesis and provide a preclinical rationale to target Aki1 by intrathoracic therapy in locally advanced tumors.


Subject(s)
Cyclic AMP Response Element-Binding Protein/physiology , DNA-Binding Proteins/physiology , Lung Neoplasms/metabolism , Mesothelioma/metabolism , Neoplasm Proteins/physiology , Animals , Cell Cycle , Cell Line, Tumor , Cell Survival , Cyclic AMP Response Element-Binding Protein/antagonists & inhibitors , Cyclic AMP-Dependent Protein Kinases/metabolism , Gene Expression Regulation, Neoplastic , Humans , Lung Neoplasms/pathology , Mesothelioma/pathology , Mesothelioma, Malignant , Mice , Mice, SCID , Neoplasm Transplantation , Phosphorylation , Pleural Neoplasms/physiopathology , Protein Processing, Post-Translational , RNA Interference , RNA, Small Interfering/pharmacology , Signal Transduction , Transcription, Genetic
20.
Ann Thorac Surg ; 99(5): 1775-80, 2015 May.
Article in English | MEDLINE | ID: mdl-25827675

ABSTRACT

BACKGROUND: Maximal cytoreductive surgeries--extrapleural pneumonectomy and extended pleurectomy and decortication (EPD)--are effective surgical treatments in selected patients with malignant pleural mesothelioma. Extended pleurectomy and decortication results in equivalent survival yet better health-related quality of life (HRQoL). METHODS: Patients with malignant pleural mesothelioma were studied for the effects of EPD on HRQoL and pulmonary function. The European Organization for Research and Treatment of Cancer Core Quality of Life Questionaire-C30 was used to evaluate HRQoL before operation, and at 4 to 5 and 7 to 8 months postoperatively. Pulmonary function tests were measured immediately before and 5 to 7 months after the operation. Patients were compared according to World Health Organization baseline performance status (PS). RESULTS: Of the 36 patients enrolled, 17 were PS 0 and 19 were PS 1 or PS 2 at baseline. Patients in groups PS 1 and PS 2 had significantly worse global health, functional, and symptoms scores. After EPD, PS 0 patients had no change in global health or function and symptoms scores except for emotional function, whereas PS 1 or PS 2 patients showed improvements at 4 to 5 months with further improvements at 7 to 8 months. The PS 0 patients demonstrated a significant decrease in forced vital capacity (p = 0.001), forced expiratory volume in 1 second (p = 0.002), total lung capacity (p = 0.0006) and diffusing capacity of the lung for carbon monoxide (p = 0.003) after EPD, whereas no change was observed in PS 1 and PS 2 patients. CONCLUSIONS: Extended pleurectomy and decortication did not improve overall HRQoL and had a negative impact in pulmonary function in minimally symptomatic patients. In symptomatic patients, a significant improvement in HRQoL was observed after EPD, which continued at late follow-up, although the pulmonary function was not affected. As changes in HRQoL are multidimensional, the preservation of the pulmonary function may have contributed to the net benefit observed in PS 1 and PS 2 patients.


Subject(s)
Lung Neoplasms/surgery , Mesothelioma/surgery , Pleural Neoplasms/surgery , Pneumonectomy/methods , Quality of Life , Aged , Aged, 80 and over , Female , Follow-Up Studies , Health Status , Humans , Lung Neoplasms/physiopathology , Lung Neoplasms/psychology , Male , Mesothelioma/physiopathology , Mesothelioma/psychology , Mesothelioma, Malignant , Middle Aged , Pleural Neoplasms/physiopathology , Pleural Neoplasms/psychology , Recovery of Function , Social Behavior , Total Lung Capacity/physiology , Treatment Outcome
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