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Pleural Mesothelioma by Surgery

Mesothelioma Empowerment

Treatment of Malignant Pleural Mesothelioma by Surgery

Robert B. Cameron, MD

Introduction. Malignant pleural mesothelioma is a diffuse tumor of the pleural lining that,unlike many solid tumors, does not easily lend itself to complete surgical resection. The tumor abuts all 12 ribs and intercostal muscles, aorta, esophagus, vertebral bodies, diaphragm, pericardium, great vessels, thymus, and the entire visceral lung surface (figure 1). Removal of all these structures with true pathological clear margins (R0 resection) is not possible. Therefore, the use of surgery in this disease requires significant compromise of normal surgical oncology principles and a strategic plan to remediate the inherent deficiencies in an incomplete resection.

Mesothelioma Characteristics Favoring Surgery. Surgical resection of diffuse pleural disease from solid tumor epithelial malignancies, including lung, colon, esophageal, pancreatic, and breast cancer almost never can be achieved due to their physically invasive nature; however, specific mesothelioma characteristics make surgery not only feasible—but even potentially therapeutically beneficial. Due to the mesodermal origin of the mesothelium, mesothelioma behaves less like most other common solid tumors with endodermal origins and more like other “mesenchymal” tumors, such as sarcomas. Importantly, both mesotheliomas and sarcomas grow with “pushing” rather than “infiltrative” borders and have a pseudocapsule. This physical property allows surgeons to “pull” the tumor off all of the pleural-covered surfaces (like removing a sarcoma through its pseudocapsule), making operations for mesothelioma even possible. Further, the metastatic spread of the epithelioid subtype of mesothelioma (vs biphasic and sarcomatoid) is primarily locoregional with distant metastatic disease occurring late. Specifically, lymph node metastases occur in 50.4%-57.6% of epithelioid (1,2), 32%-41.7% of biphasic (1,3), and only in a few nodes in < 28% of sarcomatoid tumors (1). Interestingly, this is similar to the characteristics of epithelioid sarcomas. which commonly develop lymph node metastases in 22%-45% (4-7) while the incidence of lymph node involvement in more classical “spindle” sarcomas is low--only 3-4%.(8,9) However, it is the relatively low rate of distant hematogenous metastases with epithelioid tumors (vs biphasic and sarcomatoid tumors) that favors the use of locoregional therapies, such as surgery and radiation.

Mesothelioma Characteristics Against Surgery. Like virtually all mesenchymal tumors including the sarcomas, mesothelioma has a high incidence of wound seeding following invasive procedures (needle tracks and surgical incisions). The tendency for surgical site seeding does not particularly favor surgery and has two important implications. First, surgical biopsies should be minimized to avoid unnecessary areas of chest wall invasion and should be limited to an subsequently easily re-resectable area, such as the low lateral chest wall but never the visceral pleura to avoid invasion into the lung, mediastinal pleura, or pericardium. Secondly, “extended” surgical resections remove natural barriers to the spread of mesothelioma (ie., pericardium and diaphragm). This can unwittingly spread the tumor to new previously uninvolved body cavities, such as the pericardial space and peritoneum with marked treatment consequences.

Surgical Rationale. As noted above, surgical resection of pleural mesothelioma, no matter how radical, cannot provide a better oncologic result than an R1 resection--resection with microscopic residual disease. Such surgical results are almost never accepted with other solid tumors. The question is why do surgeons persist in “debulking” pleural mesothelioma? There are no randomized controlled trials to provide a rationale for this practice; however, there are several observations that seemingly support the use of surgery in this disease. First, surgery can remove all visible disease (R1 resection) in a high percentage of patients—116/121 (95.9%) in our UCLA experience(1)—equivalent to an otherwise rare complete response to systemic drug therapy. Secondly, the microscopic residual disease that remains following surgery is likely to be controlled more easily by adjuvant therapy than gross disease. Thirdly, the majority of mesothelioma patients still succumb to local rather than distant metastatic disease, supporting the use of more aggressive local therapies to prolong overall survival. Fourthly, most locally advanced solid tumors require multimodality therapy for any chance at cure. Fifth surgery provides a unique access to the entire locoregional tumor “bed.” Thus, surgery can provide physical access for intraoperative adjuvant therapies, such as photodynamic therapy; betadine lavage; hyperthermic chemotherapy; and gene, cytokine/chemokine, and stem cell therapies, which albeit remain unproven, are currently under investigation. Finally, multimodality therapy utilizing aggressive surgical resection at specialized centers like ours at UCLA, almost uniformly report long-term survival (5-15 years or more) in surgical patients. (1,10). Similar long-term survival following any other therapy combination is exceedingly rare, if it exists at all.

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