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Immune checkpoint inhibitors and Carbon iON radiotherapy In solid Cancers with stable disease (ICONIC)

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-517378-22-00
Acronym
CNAO 44 2021C
Enrollment
27
Registered
2024-11-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Locally advanced or metastatic non-small cell lung cancer (NSCLC), Locally advanced or metastatic urothelial carcinoma, Unresectable or metastatic melanoma, Untreated recurrent/metastatic head & neck sqamous cell carcinoma (HNSCC)

Brief summary

Objective response rate (ORR) according to RECIST, assessed at least 8 weeks after CIRT, Toxicity according to CTCAE version 5.0

Detailed description

progression-free survival (PFS), overall survival (OS), objective response rate (ORR) according to irRECIST, percentage of patients with disease progression as best response, objective response of the metastatic lesion treated with CIRT, disease control rate (DCR) according to RECIST, defined as ORR+SD

Interventions

DRUGPEMBROLIZUMAB
DRUGATEZOLIZUMAB
DRUGNIVOLUMAB
DRUGCEMIPLIMAB

Sponsors

Fondazione Centro Nazionale Di Adroterapia Oncologica
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Objective response rate (ORR) according to RECIST, assessed at least 8 weeks after CIRT, Toxicity according to CTCAE version 5.0

Secondary

MeasureTime frame
progression-free survival (PFS), overall survival (OS), objective response rate (ORR) according to irRECIST, percentage of patients with disease progression as best response, objective response of the metastatic lesion treated with CIRT, disease control rate (DCR) according to RECIST, defined as ORR+SD

Countries

Italy

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026