A retrospective observational study on cutaneous adverse events induced by immune checkpoint inhibitors.


Journal

Italian journal of dermatology and venereology
ISSN: 2784-8450
Titre abrégé: Ital J Dermatol Venerol
Pays: Italy
ID NLM: 101778002

Informations de publication

Date de publication:
Dec 2023
Historique:
medline: 29 11 2023
pubmed: 28 11 2023
entrez: 28 11 2023
Statut: ppublish

Résumé

Cutaneous adverse events (CAEs) related to oncological therapies are a common scenario in daily clinical practice. This is a retrospective observational study collecting the data regarding CAEs of patients treated with immune checkpoints inhibitors (ICIs) in four different Italian centers. Of 323 patients included, 305 were evaluable for this analysis; 182 patients (59.7%) had metastatic cutaneous melanoma (CM), 99 (32.5%) non-small cell lung cancer (NSCLC) and 24 (7.8%) renal cell carcinoma (RCC). The most frequent CAEs that we found, considering all the 305 patients, were pruriginous maculopapular rash (10.2% of the patients), vitiligo-like areas (7.2% of the patients), psoriasiform rash (6.2% of the patients), asymptomatic maculopapular rash (4.6% of the patients), and lichenoid rash (4.3% of the patients). Vitiligo-like areas occurred more frequently in patients with CM, while a lichenoid rash was more frequently observed in patients with RCC. Treatment interruption was related to drug-induced CAEs in 15.4% of melanoma patients and 0.0% of lung and kidney patients. Patients developing a cutaneous adverse event had better overall response rate and higher progression free survival and overall survival than the patients without CAEs. Our study brings new information on the characteristics of CAEs related to ICIs treatment in three different types of cancers, CM, NSCLC and RCC.

Sections du résumé

BACKGROUND BACKGROUND
Cutaneous adverse events (CAEs) related to oncological therapies are a common scenario in daily clinical practice.
METHODS METHODS
This is a retrospective observational study collecting the data regarding CAEs of patients treated with immune checkpoints inhibitors (ICIs) in four different Italian centers.
RESULTS RESULTS
Of 323 patients included, 305 were evaluable for this analysis; 182 patients (59.7%) had metastatic cutaneous melanoma (CM), 99 (32.5%) non-small cell lung cancer (NSCLC) and 24 (7.8%) renal cell carcinoma (RCC). The most frequent CAEs that we found, considering all the 305 patients, were pruriginous maculopapular rash (10.2% of the patients), vitiligo-like areas (7.2% of the patients), psoriasiform rash (6.2% of the patients), asymptomatic maculopapular rash (4.6% of the patients), and lichenoid rash (4.3% of the patients). Vitiligo-like areas occurred more frequently in patients with CM, while a lichenoid rash was more frequently observed in patients with RCC. Treatment interruption was related to drug-induced CAEs in 15.4% of melanoma patients and 0.0% of lung and kidney patients. Patients developing a cutaneous adverse event had better overall response rate and higher progression free survival and overall survival than the patients without CAEs.
CONCLUSIONS CONCLUSIONS
Our study brings new information on the characteristics of CAEs related to ICIs treatment in three different types of cancers, CM, NSCLC and RCC.

Identifiants

pubmed: 38015482
pii: S2784-8671.23.07542-4
doi: 10.23736/S2784-8671.23.07542-4
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Observational Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

437-444

Investigateurs

Ignazio Stanganelli (I)
Daniela Massi (D)
Pietro Quaglino (P)
Corrado Caracò (C)
Virginia Ferraresi (V)
Antonio M Grimaldi (AM)
Roberto Patuzzo (R)
Giuseppe Palmieri (G)
Mario Mandalà (M)

Auteurs

Matelda Medri (M)

Unit of Skin Cancer, IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori, IRST, Meldola, Forlì-Cesena, Italy.

Francesco Savoia (F)

Unit of Skin Cancer, IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori, IRST, Meldola, Forlì-Cesena, Italy - francesco.savoia@irst.emr.it.

Flavia Foca (F)

Unit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori, IRST, Meldola, Forlì-Cesena, Italy.

Anna Miserocchi (A)

Unit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori, IRST, Meldola, Forlì-Cesena, Italy.

Pietro Quaglino (P)

Department of Medical Sciences, Dermatologic Clinic, University of Turin Medical School, Turin, Italy.

Marco Rubatto (M)

Department of Medical Sciences, Dermatologic Clinic, University of Turin Medical School, Turin, Italy.

Giulia Gullo (G)

Department of Medical Sciences, Dermatologic Clinic, University of Turin Medical School, Turin, Italy.

Chiara Nardini (C)

Department of Medical Sciences, Dermatologic Clinic, University of Turin Medical School, Turin, Italy.

Vincenzo Panasiti (V)

Unit of Plastic and Reconstructive Surgery, Campus Bio-Medico University, Rome, Italy.

Michele DE Tursi (M)

Department of Innovative Technologies in Medicine and Dentistry, University G. D'Annunzio of Chieti-Pescara, Chieti, Italy.

Pietro DI Marino (P)

Department of Innovative Technologies in Medicine and Dentistry, University G. D'Annunzio of Chieti-Pescara, Chieti, Italy.

Gabriella Brancaccio (G)

Unit of Dermatology, Luigi Vanvitelli University of Campania, Naples, Italy.

Emilio F Giunta (EF)

Unit of Oncology, Luigi Vanvitelli University of Campania, Naples, Italy.

Stefania Napolitano (S)

Unit of Oncology, Luigi Vanvitelli University of Campania, Naples, Italy.

Elisa Cinotti (E)

Unit of Dermatology, Department of Medical, Surgical and Neurological Sciences, University of Siena, Siena, Italy.

Marco Brusasco (M)

Unit of Dermatology, Department of Clinical and Experimental Medicine, University of Parma, Parma, Italy.

Ignazio Stanganelli (I)

Unit of Skin Cancer, IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori, IRST, Meldola, Forlì-Cesena, Italy.
Unit of Dermatology, Department of Clinical and Experimental Medicine, University of Parma, Parma, Italy.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH