Safety and efficacy of combined radiotherapy, immunotherapy and targeted agents in elderly patients: A literature review.


Journal

Critical reviews in oncology/hematology
ISSN: 1879-0461
Titre abrégé: Crit Rev Oncol Hematol
Pays: Netherlands
ID NLM: 8916049

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 25 05 2018
revised: 11 09 2018
accepted: 23 11 2018
entrez: 22 1 2019
pubmed: 22 1 2019
medline: 20 2 2019
Statut: ppublish

Résumé

Aim of the present review is to assess present data about the use of the association of Radiotherapy (RT) and targeted therapy/immunotherapy (TT/IT) in elderly people. PubMed database was searched for English literature published up to December 2017 using the keywords "radiotherapy" combined with "bevacizumab", "cetuximab", "trastuzumab", "erlotinib", "gefitinib", "sorafenib", "sunitinib", "vismodegib", "sonidegib", "ipilimumab", "pembrolizumab", "nivolumab". Studies performing RT and TT/IT in people aged >65-years were evaluated focusing on safety, toxicity and efficacy. Studies eligible for inclusion were: case reports, retrospective/prospective studies in which RT and new drugs were used concomitantly or sequentially, focusing on elderly sub-group. The systematic search identified 626 records. After exclusion of duplicates, full-text review, cross-referencing and paper that did not respect the inclusion criteria, 81 studies were included in this review. In elderly patients the combination of RT with cetuximab or bevacizumab seems feasible but with higher reported side effects. Patients' age should not limit the association of trastuzumab and RT in HER2 positive breast cancer. The concurrent administration of TKIs and RT appears to be feasible and effective. Regarding the Immune Check Point inhibitors and RT, tolerance seems similar among older and younger people but definitive data are lacking. Instead, the association of RT and vismodegib/sonidegib remains investigational. TT/IT in association of RT seems to be safe, but in elderly patients data concerning safety and toxicity are limited. Specific clinical trials on this population are encouraged.

Identifiants

pubmed: 30661652
pii: S1040-8428(18)30241-5
doi: 10.1016/j.critrevonc.2018.11.009
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

163-170

Informations de copyright

Copyright © 2018 Elsevier B.V. All rights reserved.

Auteurs

Liliana Belgioia (L)

Health Science Department (DISSAL) - University of Genoa and Radiation Oncology Department, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Isacco Desideri (I)

Department of Biomedical, Experimental and Clinical Sciences "Mario Serio", Section of Radiation Oncology, University of Florence, Italy.

Angelo Errico (A)

Radiation Oncology Department, Mons. R. Dimiccoli Hospital - ASL BT, Barletta, Italy.

Ciro Franzese (C)

Department of Radiotherapy and Radiosurgery Istituto Clinico Humanitas "Humanitas Cancer Center", Rozzano, Italy.

Antonino Daidone (A)

U.O Radioterapia Oncologica, Ospedale A. Ajello, Mazara del Vallo, Trapani - Radioterapia Oncologica, Centro di Medicina Nucleare, San Gaetano, Bagheria, Palermo, Italy.

Lorenza Marino (L)

Rem Radioterapia Viagrande Catania, Italy.

Michele Fiore (M)

Radiation Oncology, Campus Bio-Medico University, Rome, Italy.

Paolo Borghetti (P)

Radiation Oncology Department University and Spedali Civili, Brescia, Italy.

Daniela Greto (D)

Department of Biomedical, Experimental and Clinical Sciences "Mario Serio", Section of Radiation Oncology, University of Florence, Italy.

Alba Fiorentino (A)

Radiation Oncology Department, General Regional Hospital "F. Miulli", Acquaviva delle fonti, BA, Italy. Electronic address: a.fiorentino@miulli.it.

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Classifications MeSH