Role of CTLA-4 blockade and dacarbazine therapy following anti-PD-1 resistance in melanoma

Many patients with advanced melanoma eventually stop responding to PD-1 immunotherapy, and effective treatments are limited. Recent studies suggest that older chemotherapy drugs such as dacarbazine and temozolomide may work better after prior PD-1 therapy and can stimulate the immune system when combined with CTLA-4 blockade (ipilimumab). This review summarises clinical evidence and biological mechanisms supporting these combinations, including how chemotherapy-induced DNA damage can release tumour antigens, activate interferon pathways, and reawaken exhausted T cells. Because these regimens are relatively safe, inexpensive, and widely available, they may provide a realistic treatment option for patients in health systems where modern cell-based therapies are not accessible. Further clinical trials with integrated biomarker research are needed to identify which patients benefit most from this approach.

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Publication Details

Journal
Discover Oncology
Published
2026-03-16
DOI
https://doi.org/10.1007/s12672-026-04816-5
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
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article

Role of CTLA-4 blockade and dacarbazine therapy following anti-PD-1 resistance in melanoma

Vincas Urbonas, Audrius Dulskas
Discover Oncology
Cancer Immunotherapy and Biomarkers
article

Role of CTLA-4 blockade and dacarbazine therapy following anti-PD-1 resistance in melanoma

Vincas Urbonas, Audrius Dulskas
article en

Abstract

Many patients with advanced melanoma eventually stop responding to PD-1 immunotherapy, and effective treatments are limited. Recent studies suggest that older chemotherapy drugs such as dacarbazine and temozolomide may work better after prior PD-1 therapy and can stimulate the immune system when combined with CTLA-4 blockade (ipilimumab). This review summarises clinical evidence and biological mechanisms supporting these combinations, including how chemotherapy-induced DNA damage can release tumour antigens, activate interferon pathways, and reawaken exhausted T cells. Because these regimens are relatively safe, inexpensive, and widely available, they may provide a realistic treatment option for patients in health systems where modern cell-based therapies are not accessible. Further clinical trials with integrated biomarker research are needed to identify which patients benefit most from this approach.

Discover Oncology
National Cancer Institute (LT)
Good health and well-being
Openalex Percentile: Top 20%
Cancer Immunotherapy and Biomarkers
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