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CHIMERA: a phase II study of neoadjuvant pembrolizumab in combination with cisplatin or carboplatin and pemetrexed followed by surgery and adjuvant pembrolizumab in resectable pleural mesothelioma

delete2026-05-27
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G
Giulia Pasello *
D
Daniela Scattolin
E
Eleonora Faccioli
P
Paolo Andrea Zucali
G
Giuseppe Marulli
F
Federica Grosso
G
Giovanni Luca Ceresoli
M
Marcello Tiseo
A
Alessandra Bearz
F
Fabiana Letizia Cecere
L
Luana Calabrò
F
Francesco Callegarin
P
Paola Del Bianco
G
Gian Luca De Salvo
F
Federica Pezzuto
F
Fiorella Calabrese
V
Valentina Guarneri
A
Andrea Dell’Amore
F
Federico Rea
DOI:10.1016/j.cllc.2026.05.004delete
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Abstract

Abstract

En 中文
Pleural mesothelioma (PM) is a rare asbestos-related malignancy characterized by complex diagnosis and poor prognosis, with survival strongly influenced by histological subtype and eligibility for a multimodality approach, reserved for highly selected patients. While platinum–pemetrexed chemotherapy or the combination of ipilimumab plus nivolumab represent standard first-line options for unresectable disease, pembrolizumab combined with platinum–pemetrexed has demonstrated improved survival in advanced PM (IND227/Keynote483 trial). In resectable PM, multimodality treatment including surgery and chemotherapy remains preferred, yet pathological complete response (pCR) rates remain low at approximately 5%, and the role of perioperative immunotherapy is still poorly defined. CHIMERA is a prospective, open-label, multicenter phase II single-arm trial evaluating neoadjuvant pembrolizumab combined with platinum–pemetrexed chemotherapy followed by surgery and adjuvant pembrolizumab in patients with treatment-naïve, resectable stage I–IIIA epithelioid or biphasic PM. Patients receive three cycles of neoadjuvant pembrolizumab plus cisplatin or carboplatin and pemetrexed every three weeks, followed by centralized pleurectomy/decortication or extended pleurectomy/decortication in two high-volume referral centers, and subsequently 14 cycles of adjuvant pembrolizumab. The primary endpoint is pCR, with secondary endpoints including major pathological response, objective response rate, event-free survival, overall survival, treatment feasibility, and safety; translational tissue- and blood-based biomarker analyses are planned. The study is powered to detect an increase in pCR from 5% to 18%, requiring 40 patients to account for potential dropouts. By focusing on pathological efficacy within a standardized multimodality framework, CHIMERA aims to clarify the role of perioperative chemo-immunotherapy and to improve outcomes for patients with resectable PM.
Keywords:
pleural mesothelioma
neoadjuvant therapy
pembrolizumab
chemotherapy
pathological complete response
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Clinical Lung Cancer cover
Clinical Lung Cancer
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3.3
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