Evidence map›Paper›PMID 40718633›Full record

ArticleMolecular and clinical oncology2025

Durvalumab consolidation after chemoradiotherapy for locoregional recurrent non-small cell lung cancer.

Keiichiro Suminaga, Hironori Yoshida, Yusuke Shima, Hiroshi Yoshida, Kentaro Hashimoto, Tatsuya Ogimoto, Kazutaka Hosoya, Tomoko Funazo, Hitomi Ajimizu, Takashi Nomizo and 4 more

Abstract read
In one paragraph

Article in Molecular and clinical oncology, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Keiichiro SuminagaDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Hironori YoshidaDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Yusuke ShimaDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Hiroshi YoshidaDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Kentaro HashimotoDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Tatsuya OgimotoDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Kazutaka HosoyaDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Tomoko FunazoDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Hitomi AjimizuDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Takashi NomizoDepartment of Therapeutic Oncology, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Masahiro YoneyamaDepartment of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Noriko KishiDepartment of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Hiroaki OzasaDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Toyohiro HiraiDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Locoregional recurrence is one of the main failure patterns following curative treatment for non-small cell lung cancer (NSCLC). Although an optimal treatment strategy for patients with locoregional recurrence has not yet been established, chemoradiotherapy (CRT) is widely used in clinical practice. Treatment with CRT followed by durvalumab, a programmed death ligand 1 inhibitor, has become the standard treatment for unresectable locally advanced NSCLC. However, the efficacy of durvalumab consolidation therapy for locoregional recurrent NSCLC remains unclear. Therefore, patients with NSCLC treated with CRT at the Kyoto University Hospital (Kyoto, Japan) between January 2010 and December 2022, were retrospectively analyzed. The efficacy and safety of durvalumab consolidation between patients with locoregionally recurrent and locally advanced NSCLC who received treatment and those who did not were compared. Among 198 patients with NSCLC treated with CRT, 43 had a locoregional recurrence and 12 received durvalumab consolidation. The median progression-free survival (PFS) was not reached in the durvalumab group and was 13.6 months in the non-durvalumab group [hazard ratio (HR), 0.69; 95% confidence interval, 0.28-1.71; P=0.42). The 12-, 18-, and 24-month PFS rates in the durvalumab group were 58.3, 58.3, and 50.0%, respectively. Pneumonitis was more frequent in the durvalumab group; however, no grade 3 or higher cases were observed. In conclusion, durvalumab consolidation after CRT for locoregional recurrent NSCLC demonstrated favorable efficacy and acceptable toxicity compared with treatment without durvalumab. Similar to patients with locally advanced NSCLC, those with locoregionally recurrent NSCLC may benefit from durvalumab consolidation therapy after CRT.

Indexed as

chemoradiotherapydurvalumablocoregional recurrenceNSCLCPFS

Identifiers

PMID40718633
PMCPMC12290361

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