Evidence map›Paper›PMID 39856583›Full record

ArticleBMC cancer2025

Radiotherapy(R) Integration(I) Strategy for Small(S)-Cell Lung Cancer in Extensive(E) Stage (RISE) with up to 10 metastases- a study protocol of a randomized phase II trial.

Łukasz Kuncman, Jacek Fijuth, Damian Tworek, Ewa Sierko, Paweł Cisek, Michał Masłowski, Maja Lisik-Habib, Magdalena Orzechowska, Katarzyna Galwas-Kliber, Adam Antczak and 7 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06529081 (Assessment of Radiotherapy Strategies for Use in Combined Treatment of Small-cell Lung Cancer at the Stage of Extensive Disease - a Research Experiment), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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.

NCT06529081 narecruitingnot on this map

Assessment of Radiotherapy Strategies for Use in Combined Treatment of Small-cell Lung Cancer at the Stage of Extensive Disease - a Research Experiment

TypeinterventionalSponsorCopernicus Memorial HospitalRan2024 to 2029Enrolled165ConditionsSmall Cell Lung CarcinomaArmsPalliative Radiotherapy, Radical/Ablative Radiotherapy
3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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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

17 authors.

Łukasz KuncmanDepartment of Radiotherapy, Medical University of Łódź, Łódź, Poland.
Jacek FijuthDepartment of Radiotherapy, Medical University of Łódź, Łódź, Poland.
Damian TworekDepartment of General and Oncological Pulmonology, Medical University of Łódź, Łódź, Poland.
Ewa SierkoDepartment of Radiotherapy, Maria-Sklodowska-Curie Oncology Center, Bialystok, Poland.
Paweł CisekDepartment of Brachytherapy, Saint John's Cancer Center, Lublin, Poland.
Michał MasłowskiDepartment of External Beam Radiotherapy, Copernicus Memorial Hospital in Lodz Comprehensive Cancer Center and Traumatology, Łódź, Poland.
Maja Lisik-HabibDepartment of Proliferative Diseases, Copernicus Memorial Hospital in Lodz Comprehensive Cancer Center and Traumatology, Łódź, Poland.
Magdalena OrzechowskaDepartment of Molecular Carcinogenesis, Medical University of Łódź, Łódź, Poland.
Katarzyna Galwas-KliberIInd Radiotherapy and Chemotherapy Clinic and Teaching Hospital, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice, 44-100, Poland.
Adam AntczakDepartment of General and Oncological Pulmonology, Medical University of Łódź, Łódź, Poland.
Izabela ChmielewskaDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Barbara ZiółkowskaIInd Radiotherapy and Chemotherapy Clinic and Teaching Hospital, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice, 44-100, Poland.
Marta Kurczewska-MichalakDepartment of Clinical Oncology, Copernicus Memorial Hospital in Lodz Comprehensive Cancer Center and Traumatology, Łódź, Poland.
Wojciech KuźnickiDepartment of Radiotherapy, Medical University of Łódź, Łódź, Poland.
Nina JędrzejczakDepartment of External Beam Radiotherapy, Copernicus Memorial Hospital in Lodz Comprehensive Cancer Center and Traumatology, Łódź, Poland.
Kinga RanoszekDepartment of External Beam Radiotherapy, Copernicus Memorial Hospital in Lodz Comprehensive Cancer Center and Traumatology, Łódź, Poland.
Mateusz BilskiDepartment of Brachytherapy, Saint John's Cancer Center, Lublin, Poland. bilskimat@gmail.com.

Funding

Medical Research Agency 2023/ABM/01/00040
6 · The paper itself

Abstract

backgroundThe current standard of care (SoC) for patients with extensive-disease small-cell lung cancer (ED-SCLC) is chemo-immunotherapy. The efficacy of radiotherapy (RT) for chest consolidation has been established for patients with ED-SCLC who have responded to chemotherapy. There is a lack of data on incorporating RT as chest consolidation and metastasis-directed therapy for ED-SCLC. The RISE (Radiotherapy for Extensive-Stage Small-Cell Lung Cancer) study aims to evaluate the effectiveness of different RT strategies for residual lesions for patients with ED-SCLC who receive chemo-immunotherapy.

methodsA total of 165 patients with ED-SCLC will be recruited, with 55 patients assigned to each of the three study arms. Patients with stabilization or partial regression, according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, during chemo-immunotherapy will be included. • Arm I will serve as the control group, comprising patients who continue SoC of programmed death-ligand 1 (PD-L1)/programmed death-1 (PD-1) immunotherapy (durvalumab or atezolizumab) following platinum-based chemo-immunotherapy. • Arm II will receive the SoC with consolidative RT to the chest area and potentially, according to palliative indications to metastatic lesions, delivered in 30 Gy in 3-Gy fractions. • Arm III will receive SoC with RT of 45 Gy in 3-Gy fractions to the chest area and stereotactic body radiotherapy (SBRT) with 24 Gy in 8-Gy fractions to the metastatic lesions. Blood samples for circulating tumor DNA (ctDNA) will be collected before RT, during each week of treatment, and at the time of disease progression. The primary endpoint is progression-free survival (PFS) based on RECIST 1.1 or patient death. 1. Secondary endpoints are OS, treatment toxicity (frequency of G3 toxicity according to CTCAE v.5.0), area of progression (primary tumor localization/new lesions), Overall response rate (ORR), and the response rate in non-irradiated lesions. DISCUSSION: The study population of patients with ED-SCLC has a poor prognosis. Dose-escalated chest RT and SBRT (for up to 10 metastases) administered with modern techniques offer the possibility to improve OS and PFS.

trial registrationClinicaltrials.gov NCT06529081 (Registered 26th Jul 2024).

Indexed as

Lung NeoplasmsSmall Cell Lung CarcinomaAdultAgedClinical Trials, Phase II as TopicFemaleHumansMaleMiddle AgedNeoplasm MetastasisNeoplasm StagingRandomized Controlled Trials as TopicChemotherapyImmunotherapyLung cancerOligometastatic diseaseRadiotherapy

Identifiers

PMID39856583
PMCPMC11760097

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Registered trials

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.