Radiotherapy and High-Dose Interleukin-2: Clinical and Immunological Results of a Proof of Principle Study in Metastatic Melanoma and Renal Cell Carcinoma.
Adult
Aged
Antineoplastic Agents
/ administration & dosage
Carcinoma, Renal Cell
/ immunology
Chemoradiotherapy
/ adverse effects
Dose Fractionation, Radiation
Female
Humans
Infusions, Intravenous
Interleukin-2
/ administration & dosage
Italy
Kidney Neoplasms
/ immunology
Male
Melanoma
/ immunology
Middle Aged
Proof of Concept Study
Prospective Studies
Radiation Dosage
Recombinant Proteins
/ administration & dosage
Skin Neoplasms
/ immunology
Time Factors
Treatment Outcome
IFN-γ ELISPOT assay
clinical immunomonitoring
high dose IL-2
metastatic melanoma
radiotherapy
renal cell carcinoma
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
16
09
2021
accepted:
13
10
2021
entrez:
15
11
2021
pubmed:
16
11
2021
medline:
17
2
2022
Statut:
epublish
Résumé
High-dose interleukin-2 (HD IL-2) has curative potential in metastatic melanoma (MM) and renal cell carcinoma (RCC). Radiotherapy (RT) kills cancer cells and induces immunomodulatory effects. Prospective trials exploring clinical and immunological properties of combined RT/HD IL-2 are still needed. We designed a phase II, single-arm clinical trial for patients with MM and RCC. The treatment schedule consisted of 3 daily doses of 6-12 Gy of RT to 1-5 non-index metastatic fields, before IL-2 at the first and third treatment cycle. HD IL-2 was administered by continuous infusion for 72 hours and repeated every 3 weeks for up to 4 cycles, thereafter every 4 weeks for a maximum of 2 cycles. The primary endpoint was the immunological efficacy of the combined RT/HD IL-2 treatment (assessed by IFN-γ ELISPOT). Nineteen out of 22 patients were evaluable for immunological and clinical response. Partial response occurred in 3 (15.7%) patients and stable disease was observed in 7 (36.8%). The disease control rate was 52.6% after a median follow up of 39.2 months. According to Common Terminology Criteria for Adverse Events 4.0 (CTCAE 4.0), the majority of toxicities were grade 1-2. Immunological responses were frequent and detected in 16 (84.2%) patients. Increased levels of IL-8 and IL-10 in melanoma, circulating effector memory CD4+ and intratumoral CD8+ T cells in both tumor types were detected after therapy. Overall the treatment was well tolerated and immunologically active. Immunomonitoring and correlative data on tumor and peripheral blood cell subsets suggest that this combination treatment could be a promising strategy for patients progressing after standard treatments.
Identifiants
pubmed: 34777395
doi: 10.3389/fimmu.2021.778459
pmc: PMC8578837
doi:
Substances chimiques
Antineoplastic Agents
0
Interleukin-2
0
Recombinant Proteins
0
aldesleukin
M89N0Q7EQR
Types de publication
Clinical Trial, Phase II
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
778459Informations de copyright
Copyright © 2021 Bulgarelli, Piccinini, Petracci, Pancisi, Granato, de Rosa, Guidoboni, Petrini, Ancarani, Foschi, Romeo, Tontini, De Giorgi, Lolli, Gentili, Valmorri, Rossi, Ferroni, Casadei, Cortesi, Crudi and Ridolfi.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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