Evidence map›Paper›PMID 42057823›Full record

ArticleFrontiers in oncology2026

Salvage definitive or hypofractionated radiotherapy for oligometastatic recurrence after durvalumab consolidation in limited-stage small-cell lung cancer: a two-case report.

Jiahui Shan, Jiayi Yu, Dan Yang, Xiao Chang, Leilei Jiang, Liuhua Long, Yue Teng, Xin Dong, Rong Yu, Huiming Yu and 1 more

Abstract readCase Reports
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Jiahui Shan *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Jiayi Yu *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Dan YangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Xiao ChangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Leilei JiangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Liuhua LongKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Yue TengKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Xin DongKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Rong YuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Huiming YuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Anhui ShiKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ADRIATIC trial demonstrated that consolidation durvalumab after concurrent chemoradiotherapy (cCRT) improves progression-free survival (PFS) and overall survival (OS) in limited-stage small cell lung cancer (LS-SCLC), establishing a new standard of care. However, a proportion of patients still develop distant relapse, and optimal salvage strategies after immunotherapy remain unclear. While metastasis-directed radiotherapy, including stereotactic radiotherapy and hypofractionated radiotherapy, has shown benefit in selected oligometastatic non-small cell lung cancer (NSCLC), evidence in SCLC is limited. Here, we describe two LS-SCLC patients who developed limited metastatic relapse after cCRT followed by durvalumab consolidation: one with a solitary adrenal metastasis and the other with two brain metastases. Both patients received salvage radiotherapy (adrenal hypofractionated radiotherapy: 54 Gy in 15 fractions to GTV and 45 Gy in 15 fractions to PTV; brain lesions treated with whole-brain radiotherapy with simultaneous integrated boost [WBRT-SIB]: 40 Gy in 10 fractions to metastatic foci and 30 Gy in 10 fractions to the whole brain). Both patients experienced durable disease control exceeding four years without additional systemic therapy during follow-up. These two cases provide hypothesis-generating clinical observations suggesting that, in carefully selected LS-SCLC patients with limited metastatic relapse, curative-intent local radiotherapy may be feasible and warrants prospective evaluation.

Indexed as

case reportdurvalumabhypofractionated radiotherapyimmunotherapy failurelimited-stage small cell lung canceroligometastasisWBRT-SIB

Identifiers

PMID42057823
PMCPMC13120957

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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.