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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 />

Conclusion: The present analysis shows that additional intracavitary cisplatinfibrin<br />

after eP/D and previous i.v. induction chemotherapy with cisplatin/<br />

pemetrexed can lead to electrolyte disorders and drop in hemoglobin<br />

concentration. However, none of the mentioned laboratory findings had a<br />

clinically significant impact on the patients’ postoperative course.<br />

Keywords: Mesothelioma, chemotherapy, pleurectomy / decortication,<br />

toxicity<br />

POSTER SESSION 3 – P3.03: MESOTHELIOMA/THYMIC MALIGNANCIES/ESOPHAGEAL<br />

CANCER/OTHER THORACIC<br />

MESOTHELIOMA CLINICAL –<br />

WEDNESDAY, DECEMBER 7, 2016<br />

P3.03-045 TREATMENT OF MALIGNANT PLEURAL MESOTHELIOMA<br />

BEYOND FIRST-LINE AMONG HISPANICS (MESO-CLICAP)<br />

Luis Corrales 1 , Andrés Cardona 2 , Oscar Arrieta 3 , George Oblitas 4 , Leonardo<br />

Rojas 5 , Ludwing Bacon 6 , Claudio Martin 7 , Beatriz Wills 8 , Mauricio Cuello 9 , Luis<br />

Alberto Mas Lopez 10 , Carlos Vargas 2 , Hernan Carranza 2 , Jorge Otero 2 , Maria<br />

Perez 11 , Lisde González 4 , Luis Chirinos 12 , Pilar Archila 13 , Rafael Rosell 14<br />

1 Clinical <strong>Oncology</strong> Department, Hospital San Juan de Dios (San José, Costa Rica),<br />

San Jose/Costa Rica, 2 Medical <strong>Oncology</strong>, Clinical and Traslational <strong>Oncology</strong><br />

Group, Institute of <strong>Oncology</strong>, Clínica Del Country, Bogota/Colombia, 3 <strong>Thoracic</strong><br />

<strong>Oncology</strong> Unit and Laboratory of Personalized Medicine, Instituto Nacional de<br />

Cancerologia, Mexico City/Mexico, 4 Hospital Oncológico Luis Razetti, Caracas,<br />

Venezuela, Caracas/Venezuela, 5 Centro Javeriano de Oncología, Hospital<br />

Universitario San Ignacio, Bogotá/Colombia, 6 <strong>Oncology</strong> Department, Hospital<br />

Roberto Calderón, Managua, Nicaragua, Managua/Nicaragua, 7 Department of<br />

Clinical <strong>Oncology</strong>, Instituto Alexander Fleming, Buenos Aires/Argentina, 8 Internal<br />

Medicine Department, Johns Hopkins Hospital, Baltimore, Maryland/United<br />

States of America, 9 Medical <strong>Oncology</strong> Department, Udelar (Montevideo, Uruguay),<br />

Montevideo/Uruguay, 10 Medical <strong>Oncology</strong>, Instituto Nacional de Enfermedades<br />

Neoplásicas, Lima/Peru, 11 Medical <strong>Oncology</strong>, Arsuve, Caracas, Venezuela, Caracas/<br />

Venezuela, 12 Clínica de Prevención Del Cáncer, Caracas, Venezuela, Caracas/<br />

Venezuela, 13 Pathology, Foundation for Clinical and Applied Cancer Research –<br />

Ficmac, Bogota/Colombia, 14 Imppc (Cancer Biology & Precision Medicine Program),<br />

Catalan Institute of <strong>Oncology</strong>, Badalona, Barcelona/Spain<br />

Background: Platinum/Pemetrexed chemotherapy is standard of care<br />

in first-line (FL) treatment of malignant pleural mesothelioma (MPM).<br />

Different second and third lines regimens are also considered, but the optimal<br />

treatment has not yet been defined. Methods: The aim of this study was to<br />

evaluate clinical outcomes of second (SL) and third line (TL) therapies in a<br />

series of MPMs included in a retrospective multinational database (MeSO-<br />

CLICaP). Clinical records of MPM-patients who received treatment beyond FL<br />

from 2008 to 2016 were reviewed. Study endpoints were response, overallsurvival<br />

(OS), and progression-free-survival (PFS) for SL and TL, stratified<br />

for patient characteristics, FL-outcomes, and type of regimen. Out of 124<br />

patients, 79 received SL/TL and had sufficient clinical data. Results: Of the<br />

124 patients included in the MeSO-CLICaP registry, 79 (64%) received some<br />

treatment after first line. Median age was 59 years (range 33-81), 42 (53%)<br />

were men, 74% were current or former smokers and 77% had a baseline ECOG<br />

0-1. After FL, 57 patients (76%) achieved disease-control (PR 24/32% and SD<br />

33/44%) and 18 had a time-to-progression ≥8 months. Median PFS and OS to<br />

SL were 6.2 (95%CI 4.9-7.4) and 16.1 (95%CI 14.5-17.6) months, respectively.<br />

According to a multivariate analysis, disease control after SL-therapy was<br />

significantly related to pemetrexed-based treatment (OR 2.46; p=0.017) and<br />

FL-TTP≥12 months (OR 3.50; p=0.006). Improved PFS to SL was related to<br />

younger age (

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