Mesothelioma : a clinical review Bradley J. Phillips, M.D. Burn-Trauma-ICU Adults & Pediatrics.

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Mesothelioma : a clinical review Bradley J. Phillips, M.D. Burn-Trauma-ICU Adults & Pediatrics

Mesothelioma the term was first used in 1921 by Eastwood & Martin to describe primary tumors of the pleura at that time, the diagnosis was extremely controversial (required autopsy examination) today, the diagnosis is still problematic –15 % of cases can not be differentiated from adenocarcinoma

Mesothelioma: 1960 Wagner, South African miners [Br J Ind Med] –first evidence implicating asbestos in the pathogenesis –landmark paper, began widespread investigation Incidence has reached “Epidemic” –European Experience:Expected Peak, (2, ,000 deaths/yr.) –U.S. Experience:Peaked in the 1970’s & since 1980 the incidence has been decreasing

Incidence (1) the increase in general incidence has been attributed to the widespread use of asbestos in the post-World War II period [McDonald 1987] Precautions were first taken in the U.S. Europe was “slow” to respond Effect on third-world countries

Incidence (2) Industrialized Countries –2 per million in females – per million in males regional differences are due to the level of industrial activity Areas with shipyards are at the highest risk Type is also a Factor: Crocidolite & Amosite > Chrysotile

Incidence (3) The occurrence of mesothelioma is related to an Occupational Exposure to Asbestos Non-occupational environmental exposure leading to it’s development is uncommon Only 7.2 % of asbestos workers, will develop the disease Up to 50 % of patients, do not have any history of exposure

Incidence (4) cases due to exposure in buildings with asbestos insulation are extremely rare ! [Hughes et al. 1986: “quantitative risk”] [Lilienfield 1991: “four cases in school teachers”] there has never been prospective evidence to support the widespread removal of asbestos insulation...

3 Main Groups (1) Benign Localized Mesothelioma –“pleural fibroma” –Unassociated with asbestos exposure –Paraneoplastic syndromes occur in 1/3 –Arise from the visceral pleura –Unless incomplete, surgical resection is curative

Paraneoplastic Syndromes Seen mostly in the Benign Localized Form –Migrating Thrombitis –Thrombocytosis –Hemolytic Anemia –Hypoglycemia –Hypercalcemia –Pulmonary Hypertrophic Osteoarthropathy [Boutin 1998]

3 Main Groups (2) Malignant Localized Mesothelioma –20 % of all primary malignant pleural tumors are localized –Present as Symptomatic Masses –Difficult to differentiate from Chest Wall Neoplasms –Treatment Wide enbloc excision of all involved tissue Lung, Chest Wall, Soft Tissues, & Skin With incomplete excision, the prognosis approaches MDM External beam radiation is of little benefit

3 Main Groups (3) Malignant Diffuse Mesothelioma –Classical form –Related to exposure –Latent Period of 20 years –Smoking is an associated factor not for mesothelioma, but for overall survival rate typical scenario middle-aged man with pleuritic chest pain, shortness of breath, & a clear history of asbestos exposure

Malignant Mesothelioma 3 Cell Types –Epithelial Type:50 % of cases most often confused with adenocarcinoma –Mesenchymal Type:16 % of cases –Mixed Type:34 % of cases

Pathogenecity Benign pleural plaques are the most common manifestation of asbestos exposure usually develop on the parietal or diaphragmatic pleura malignant mesothelioma is thought to originate from the parietal pleura high concentrations of asbestos fibers in the lung are associated with bronchial carcinoma [Antilla 1993]

Clinical Points (1) Mean Age of Patients:60 –has been reported in children (unrelated to asbestos) [Fraire 1988] Clinical signs/symptoms depend on the stage –TNM Classification –Early-Stage Disease:Symptoms are Rare –Late-Stage Disease:Pain, Dyspnea, Moderate Effusion

Clinical Points (2) the initial chest radiograph leading to a diagnosis of mesothelioma reveals a pleural effusion 92 % of the time 7 % of the time, a Multinodular Pleural Tumor was found 0.5 % of the time, an Empyema 0.5 % of the time, a Spontaneous Pneumothorax [Boutin 1993]

Clinical Points (3) On thoracentesis, the pleural fluid is an Exudate with little evidence of inflammation & a high number of mesothelial cells Cytology of the fluid is 30 % sensitive ! [Renshaw 1997] Removal of the pleural fluid improves the possibility of establishing the diagnosis

Clinical Points (4) “Diagnostic Work-Up” CXR (with thoracentesis) Chest C.T. irregular, nodular pleural thickening spread into the diaphragm, pericardium, chest wall, or mediastinal lymph nodes is difficult to assess [Masilta 1991] Thoracoscopy with Biopsy MRI

Staging (1) Stage I: tumor isolated to ipsilateral pleura or lung Stage II: tumor invades chest wall, mediastinum, pericardium, or contralateral pleura Stage III: tumor involves both thorax & abdomen Stage IV: distant blood-borne metastases

Staging (2) Expected Survival –Stage I:16 months –Stage II:9 months –Stage III:5 months [Cohen 1995]

Establishing the Diagnosis (1) thoracoscopy is indicated in any patient without a precise histopathological diagnosis in whom clinical & laboratory findings raise the suspicion of mesothelioma

Establishing the Diagnosis (2) Cardinal Characteristics –Age between –Previous occupational exposure to asbestos –Pleural Effusion –C.T. / MRI (with nodular lesions of the parietal pleura) [Boutin 1998]

V.A.T.S. (1) Mesothelioma takes on a “grape-like” appearance –patches of closely-spaced, smooth, translucid, poorly-vascularized nodules with a clear to yellowish color not unique to mesothelioma also seen with metastatic cancer of the pleura unlike benign inflammation (pleurisy), the pleura becomes hard & non-elastic - with biopsy, the cut edges do not bleed

V.A.T.S. (2) % of cases, the observed lesions are nonspecific –path report: “benign pleural inflammation” The more unimpressive the picture, the more biopsies should be taken (up to 20) Look for involvement of the Lung or Visceral Pleura

V.A.T.S. (3) 98 % sensitive in establishing the diagnosis Mortality is 1:8000 Complications are minimal –Subcutaneous Emphysema –Localized Infection –Minor Bleeding (< 100 cc) [Viallat 1991]

V.A.T.S. (4) 1 Problem:Seeding of the Trocar Path –unknown incidence but can occur –has been documented after thoracentesis & blind pleural biopsy can be prevented by performing Prophylactic Radiotherapy after healing to the point of entry [Rey 1995]

Natural History (1) Median Survival: months 5-year Survival:< 5 % Mesothelioma is a Local Disease –Invasion usually first involves the Lung & Diaphragm Progressive Retraction of the hemithorax leading to a “trapped lung” Peritoneal Infiltration - through the diaphragm or it’s posterior openings with secondary ascites

Natural History (2) Spread to the Endothoracic Fascia (T 2 ) or Intercostal Spaces (T 3 ) is common –Found in % of patients at the time of biopsy [Chahinian 1983] –Parietal involvement can be “massive” –UNCOMMON: Clinically-detectable lesions in bone, tissue, or brain Involvement of the contralateral lung

Natural History (3) however, at the time of autopsy, 50 % of patients will have metastatic spread [Antman 1981]

Natural History (4) Death is usually due to progressive dyspnea & respiratory insuffiency with extensive weight loss & muscle wasting

Treatment There is no single treatment which has proven effective... Surgery Radiation Chemotherapy Immunotherapy Gene Therapy

Treatment: Surgery (1) To ensure that surgery will be as curative as possible, resection must include: –the Pleura: Stage Ia –the Lung : Stages Ib, II, and III many cases will require resection of the diaphragm, pericardium, & chest wall

Treatment: Surgery (2) but does surgery improve survival ? Worn 1974, 248 Patients –62 Patients with Radical Pneumonectomy 2-yr. Survival, 37 % 5-yr. Survival, 10 % –Conservative Treatment 2-yr. Survival, 12.5 % 5-yr. Survival, 0 %

Treatment: Surgery (3) Probst 1990, 111 cases –Median survival was longer after pneumonectomy than any other method (1.4 months) operative mortality for radical pneumonectomy, across the board, is 25 %

Treatment: Surgery (4) A current review of all surgical series suggests that treatment protocols including surgery do extend survival... –Pleurectomy (2-yr. Survival) : % –Radical Pneumonectomy: % [Boutin 1998]

Treatment: Surgery (5) Aisner 1995 –The only prospective study –Pneumonectomy, w/o post-operative treatment 2-yr. Survival: 33 % Median Survival:10 months a prospective, randomized, phase III trial is required to find the appropriate role of surgery

Treatment: Radiation despite in-vivo success against mesothelial cells, this mode has not been proven successful in the clinical setting –Problem: size of the target area –Post-radiation fibrosis can further aggravate pain via compression of the chest wall & intercostal nerves –Is effective to prevent “seeding”

Treatment: Chemotherapy Responses seen in % of patients, but without improvement in overall mortality Doxorubicin Cisplatin Methotrexate Combined Protocols : % response

Treatment: Immunotherapy Intrapleural delivery of cytokines are currently being tested –Interferon-Gamma –Interleukin-2 Studies began in 1987 (150 patients) –Response Rates: % –Effect on Survival is unknown at present [Dreisen 1992]

Treatment: Gene Therapy trials have begun to evaluate the genetic transfer of thymidine kinase (from herpes virus to adenovirus) too early to judge effect or outcome… [Smythe 1995]

Conclusions (1) Mesothelioma kills - slowly & effectively… Early-stage disease: most important predictor of outcome To find “early-stage disease”, remember the risk factors –Age between –Previous occupational exposure to asbestos –Pleural Effusion –C.T. / MRI (with nodular lesions of the parietal pleura)

Conclusions (2) Diagnosis is best established by V.A.T.S. –Following invasive procedures, “seeding” will occur & should be treated by radiotherapy Treatment: “it is currently, the clinician’s choice” –Multimodal approach including radical surgery –“Limited-Role for Limited-Surgery” Palliative Relief of symptoms

mesothelioma …kills south african miners - european industrialists - american manufacturers - slowly but effectively...

questions ? Critical Care MedicineSBH-UTMB