Evidence map›Paper›PMID 42137989›Full record

ArticleMultidisciplinary respiratory medicine2026

Diagnosis and management of interstitial lung disease with concomitant lung cancer in Italy: Results from the ICARO clinician survey.

Giulia Maria Stella, Valerio Maria Carrozzo, Sara Lettieri, Giulia Alaimo, Enrica Capelletto, Paolo Cameli, Laura Carrozzi, Fabrizio Luppi, Fabio Perrotta

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Article in Multidisciplinary respiratory medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Giulia Maria StellaUniversity of Pavia.
Valerio Maria CarrozzoUniversità della Campania.
Sara LettieriIRCCS Policlinico San Matteo.
Giulia AlaimoUniversità della Campania.
Enrica CapellettoSan Luigi University Hospital, Orbassano.
Paolo CameliUniversità di Siena.
Laura CarrozziUniversità di Pisa.
Fabrizio LuppiUniversità Milano Bicocca.
Fabio PerrottaUniversità della Campania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoexistence of interstitial lung disease (ILD), particularly idiopathic pulmonary fibrosis (IPF), and lung cancer poses major diagnostic and therapeutic challenges, yet clinical management remains heterogeneous. The project aims to describe current Italian practices for integrated management of ILD with concomitant lung cancer.  Methods: ICARO (Interstiziopatia e Cancro del polmone: AppRoccio al management clinico integratO) is a national cross-sectional clinician survey conducted in Italy on behalf of the Italian Respiratory Society from  November 2024 to March 2025. A 12-item multiple-choice questionnaire assessed diagnostic strategies, treatment preferences, and perceived toxicity risks. Invitations were sent to X physicians, among which 38 ansewered (35 specialists and senior 3 registrars (age range: 28-68 years).  Results: An ILD multidisciplinary team was available in 26/38 (71.1%) centres. Diagnostic procedures for lung cancer in ILD patients were reported as performed "always/often" by 14/38 (36.8%), with the main concern being ILD progression after procedures (31/38 - 81.6%). Most respondents continued antifibrotic therapy during systemic cancer treatment (28/38- 73.7%). Combined chemotherapy plus immune checkpoint inhibitors was perceived as the highest-risk regimen by 19/38 physicians (50%), and 20/38 (52.6%) were hesitant to offer neoadjuvant immunotherapy in stage II-IIIa NSCLC. Severe toxicity from radiotherapy was reported as frequent by 8/38 (21.1%).  Conclusions: Italian clinicians report substantial variability in diagnostic and therapeutic strategies for lung cancer in ILDs, driven mainly by concern for ILD progression and treatment-related pulmonary toxicity. Although limited, this study unveils an urgent need for further prospective studies to better define the safety and efficacy of combined therapeutic approaches and to establish evidence-based guidelines to support clinical decision-making.

Indexed as

diagnosisidiopathic pulmonary fibrosis, IPF, treatment, therapy, future perspectiveslung cancerPersonalised medicine

Identifiers

PMID42137989
PMCPMC13313607

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.