Evidence map›Paper›PMID 42445410›Full record

ArticleTranslational cancer research2026

Low-dose radiotherapy combined with immune checkpoint inhibitors in advanced malignancies: a real-world exploratory study.

Kai Xin, Liping Deng, Meiqing Ding, Mengmeng Feng, Xiahui Wu, Lijing Zhu

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Article in Translational cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Kai XinDepartment of Oncology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Liping DengDepartment of Oncology, Nanjing Drum Tower Hospital, The Clinical College of Nanjing Medical University, Nanjing, China.
Meiqing DingDepartment of Oncology, Nanjing Drum Tower Hospital, The Clinical College of Nanjing Medical University, Nanjing, China.
Mengmeng FengDepartment of Oncology, Taikang Xianlin Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Xiahui WuDepartment of Oncology, Taikang Xianlin Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Lijing ZhuDepartment of Oncology, Nanjing Drum Tower Hospital, The Clinical College of Nanjing Medical University, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patients with advanced malignancies often have limited treatment options after failure of systemic therapy, and the prognosis remains poor. Low-dose radiotherapy (LDRT) has been proposed to enhance antitumor immunity and may improve the efficacy of immune checkpoint inhibitors (ICIs). We aimed to evaluate the clinical activity and safety of LDRT combined with ICIs in patients with advanced malignancies in a real-world clinical setting. Methods: This single-center retrospective real-world study included patients with advanced malignancies treated at Taikang Xianlin Drum Tower Hospital who received LDRT (2 Gy × 3 fractions, total dose 6 Gy) directed to progressive lesions in combination with programmed cell death protein 1/programmed death-ligand 1 (PD-1/PD-L1) inhibitors. Clinical characteristics, treatment details, tumor response, follow-up data, and treatment-related adverse events were retrospectively collected and analyzed. The primary endpoints were objective response rate (ORR) and progression-free survival (PFS), while the secondary endpoint was disease control rate (DCR). Safety was assessed according to the incidence of treatment-related adverse events. Results: Thirteen patients with various advanced malignancies were included in the analysis. The ORR was 38.5% and the DCR was 76.9%. The median PFS was 6.7 months. Notably, all documented disease progression occurred outside the irradiated fields, whereas the irradiated lesions remained locally controlled during follow-up. Treatment-related adverse events were mainly chemotherapy-related hematologic toxicities. No clinically significant immune-related adverse events, radiotherapy-related toxicities, or treatment-related deaths were observed. Conclusions: LDRT combined with ICIs showed preliminary clinical activity with acceptable tolerability in this small real-world cohort of patients with advanced malignancies. Although limited by the small sample size, this approach may represent a feasible treatment option for selected patients and should be further evaluated in prospective studies.

Indexed as

advanced malignanciesimmune checkpoint inhibitors (ICIs)immunotherapyLow-dose radiotherapy (LDRT)real-world study

Identifiers

PMID42445410
PMCPMC13357330

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.