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Effectiveness and safety of immunotherapy in advanced NSCLC with pericardial effusions: a global retrospective multicenter study

  • Talal El Zarif
  • , Sarah Abou Alaiwi
  • , Amin H. Nassar
  • , Eleonora Gariazzo
  • , Valentina Santo
  • , Edoardo Garbo
  • , Mihaela Aldea
  • , Francesco Paoloni
  • , Sagal Pannu
  • , Karl Semaan
  • , Omar Chehab
  • , Malak Hoballah
  • , Vishal Navani
  • , Yizhuo Gao
  • , Daniel Meyers
  • , Igor Stukalin
  • , Arjun Mittra
  • , Mingjia Li
  • , Nicholas Jones
  • , Shirly Grynberg
  • Ronnie Shapira, Alexi Vasbinder, Salim S. Hayek, Elias Bou Farhat, Marc Eid, Eddy Saad, Dory Freeman, Kaushal Parikh, Aakash Desai, Caleb Smith, Edward El-Am, Frank Aboubakar Nana, Simone Foderaro, Javier Baena, Mercedes Herrera, Alessio Cortellini, David J. Pinato, James Korolewicz, Chul Kim, Paul Sackstein, Ryan A. Denu, Walid Macaron, Noha Abdel-Wahab, Tomas G. Neilan, João A.C. Lima, Narjust Florez, Pasi Janne, Biagio Ricciuti, Federica Pecci, Toni K. Choueiri, Jennifer M. Kwan, Abdul Rafeh Naqash

Research output: Contribution to journal › Article › peer-review

Abstract

Background: There is limited data on immune checkpoint inhibitor (ICI) use in patients with non-small cell lung cancer (NSCLC) and known pericardial effusions. Methods: This international multi-center observational retrospective study included patients with advanced NSCLC with or without pericardial effusions receiving ICIs. Immune-related adverse events (irAEs) were graded per CTCAE v5.0. Overall survival (OS) and progression-free survival (PFS) were estimated by the Kaplan-Meier method. Cox proportional hazards multivariable models assessed the association between survival outcomes and clinicopathologic variables, and an inverse probability of treatment weighting (IPTW) model compared outcomes between the two groups. Results: A total of 1248 patients with advanced NSCLC treated with ICIs across 13 institutions were included. Of these, 85 patients (6.8%) had pre-existing pericardial effusions. Compared to controls, patients with pericardial effusions were younger (median age 63 vs 67 years, P = .007), diagnosed more frequently with PD-L1 positive tumors (96% vs 76%, P < .001), and had a higher median number of baseline metastatic sites (3 vs 1, P < .001). IrAEs were similar between both groups (42% vs 38%), and no cardiac irAEs occurred in patients with pericardial effusions. PFS (median 5.6 vs 4.6 months, P = .3) and OS (median 10.2 vs 14.7 months, P = .50) were not statistically different between patients with pericardial effusions and the controls, respectively. In both multivariable and IPTW models, pericardial effusions were not associated with PFS or OS. Conclusions: Among patients with NSCLC and pre-existing pericardial effusions, ICIs demonstrate meaningful clinical benefit similar to those without effusions, with no new cardiac or severe toxicities.

Original languageEnglish (US)
Article numberoyag277
JournalOncologist
Volume31
Issue number9
DOIs
StatePublished - Sep 2026
Externally publishedYes

Keywords

  • efficacy
  • immune checkpoint inhibitor
  • non-small cell lung cancer
  • pericardial effusion
  • safety

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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