Evidence map›Paper›PMID 27789196›Full record

Trial reportThe Lancet. Oncology2016

Local consolidative therapy versus maintenance therapy or observation for patients with oligometastatic non-small-cell lung cancer without progression after first-line systemic therapy: a multicentre, randomised, controlled, phase 2 study.

Daniel R Gomez, George R Blumenschein, J Jack Lee, Mike Hernandez, Rong Ye, D Ross Camidge, Robert C Doebele, Ferdinandos Skoulidis, Laurie E Gaspar, Don L Gibbons and 14 more

12 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase IIComparative StudyMulticenter Study
In one paragraph

Trial report in The Lancet. Oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 12 registered trials, which are not on this map. Cited by 553 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
553citing papers in PubMed, 6 pooled it
85.6field-weighted citation impact, top 1% of its field
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.

NCT01725165 phase2completednot on this map

A Randomized Phase II Study Assessing the Efficacy of Local Consolidative Therapy for Non-Small Cell Lung Cancer Patients With Induced Oligometastatic Disease

TypeinterventionalSponsorM.D. Anderson Cancer CenterRan2012 to 2024Enrolled85ConditionsRecurrent Lung Non-Small Cell Carcinoma, Stage IV Non-Small Cell Lung Cancer AJCC v7ArmsClinical Observation, External Beam Radiation Therapy, Laboratory Biomarker Analysis, Quality-of-Life Assessment, Standard Follow-Up Care
NCT03135652 phase2withdrawnnot on this mapstarted 2017, after this paper: background citation

Consolidative Radiotherapy for Colorectal Cancer Liver Metastases Receiving Surgery or Radiofrequency Ablation

TypeinterventionalSponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and TechnologyRan2017 to 2023Enrolled0ConditionsRadiotherapy, Colorectal Cancer, Liver MetastasesArmsadjuvant SBRT, Chemotherapy
NCT03142282 phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

Maintenance Chemotherapy Versus Consolidative Radiotherapy Plus Maintenance Chemotherapy for Unresectable Metastatic Colorectal Cancer: A Randomized Phase II Trial

TypeinterventionalSponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and TechnologyRan2019 to 2024Enrolled200ConditionsMetastatic Colorectal Cancer, RadiotherapyArmsmaintenance chemotherapy, Consolidative Radiotherapy
NCT03489616 naunknown statusnot on this mapstarted 2018, after this paper: background citation

Chemotherapy Combination With Local Radiotherapy and rhGM-CSF for Oligometastatic Stage IV NSCLC Patients Without Progression After First-line Chemotherapy: a Prospective Randomized Controlled Study

TypeinterventionalSponsorShandong Cancer Hospital and InstituteRan2018 to 2019Enrolled45ConditionsCarcinoma, Non-Small-Cell LungArmsrhGM-CSF, Pemetrexed, Local Radiotherapy, Single agent
NCT03595644 phase2completednot on this mapstarted 2017, after this paper: background citation

Maintenance Targeted Therapy With or Without Stereotactic Body Radiation Therapy for Stage IV Non-small Cell Lung Cancer: a Prospective, Multicenter, Randomized Controlled Clinical Trial.

TypeinterventionalSponsorTongji HospitalRan2017 to 2020Enrolled74ConditionsStage IV Non-small Cell Lung CancerArmsSBRT+TKI, TKI
NCT03610711 phase1 / phase2active not recruitingnot on this mapstarted 2019, after this paper: background citation

REACTION (Radiation Enhanced Assessment of Combination Therapies in Immuno-ONcology) - Nivolumab or Nivolumab in Combination With Other Immuno-oncology (IO) Agents After Targeted Systemic Radiation in Patients With Advanced Esophagogastric Cancer

TypeinterventionalSponsorSidney Kimmel Comprehensive Cancer Center at Johns HopkinsRan2019 to 2027Enrolled21ConditionsGastroesophageal Cancer, Immune Checkpoint InhibitionArmsNivolumab, Relatlimab
NCT03827577 phase3unknown statusnot on this mapstarted 2019, after this paper: background citation

OMEGA, A Randomized Trial of Local Ablative Therapy Vs. Conventional Treatment in Oligometastatic NSCLC

TypeinterventionalSponsorAzienda Ospedaliera Universitaria Integrata VeronaRan2019 to 2022Enrolled195ConditionsCarcinoma, Non-Small-Cell LungArmsSurgical removal of primary and/or of all oligometastases, Non-surgical LAT, Standard medical therapy
NCT03862911 naactive not recruitingnot on this mapstarted 2019, after this paper: background citation

Phase III Randomized Controlled Trial and Economic Evaluation of Stereotactic Ablative Radiotherapy for Comprehensive Treatment of Oligometastatic (1-3 Metastases) Cancer (SABR-COMET-3)

TypeinterventionalSponsorBritish Columbia Cancer AgencyRan2019 to 2030Enrolled330ConditionsMetastatic TumorsArmspalliative radiotherapy, Stereotactic ablative radiotherapy
NCT03905317 phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

A Single-Armed Phase II Study of Radiation and Bevacizumab Maintenance Therapy for Oligometastasis of Lung Adenocarcinoma With Negative Driver Gene

TypeinterventionalSponsorSun Yat-sen UniversityRan2019 to 2022Enrolled66ConditionsLung AdenocarcinomaArmsBevacizumab Injection, chest radiation, concurrent chemotherapy
NCT04905550 phase2unknown statusnot on this mapstarted 2021, after this paper: background citation

An Exploratory Clinical Study of Almonertinib in Combination With Craniocerebral Radiotherapy in First-line Treatment of EGFR Positive Non-Small Cell Lung Cancer(NSCLC) With Brain Metastases

TypeinterventionalSponsorChongqing University Cancer HospitalRan2021 to 2024Enrolled50ConditionsNon-Small Cell Lung Cancer (NSCLC)ArmsAlmonertinib, Stereotactic Radiotherapy(SRT) or Stereotactic Radiosurgery(SRS) or Whole-Brain Radiotherapy(WBRT)
NCT05987826 phase2recruitingnot on this mapstarted 2023, after this paper: background citation

Furmonertinib Mesylate Neoadjuvant Treatment of Resectable Stage Ⅱ-ⅢB Non-small Cell Lung Cancer Patients With Epidermal Growth Factor Receptor(EGFR)Sensitive Mutation:a Prospective,Muliticenter,Open Label,Phase Ⅱ Single-arm Study

TypeinterventionalSponsorShanghai Zhongshan HospitalRan2023 to 2029Enrolled40ConditionsNon-Small Cell Lung CancerArmsFurmonertinib
NCT05998993 nanot yet recruitingnot on this mapstarted 2023, after this paper: background citation

Phase II Study to Evaluate the Efficacy and Safety of SBRT as an Adjunctive Intervention for Oligoresidual Disease in EGFR Mutant NSCLC With First-Line Osimertinib Treatment

TypeinterventionalSponsorCentro de Tratamiento e Investigación sobre Cáncer, Luis Carlos Sarmiento AnguloRan2023 to 2028Enrolled35ConditionsEGF-R Positive Non-Small Cell Lung Cancer, Non Small Cell Lung Cancer, EGFR Exon 19 Deletion, EGFR Exon 21 MutationArmsStereotactic Body Radiation Therapy SBRT
3 · Its place in the literature

Who cites it

553 citing papers in PubMed, 6 syntheses or guidelines pooled it, 1,066 citations in OpenAlex.

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493 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 3 institutions in 2 countries.

Daniel R GomezDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Electronic address: dgomez@mdanderson.org.
George R BlumenscheinDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
J Jack LeeDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Mike HernandezDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Rong YeDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
D Ross CamidgeDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO, USA.
Robert C DoebeleDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO, USA.
Ferdinandos SkoulidisDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Laurie E GasparDepartment of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO, USA.
Don L GibbonsDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jose A KaramDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Brian D KavanaghDepartment of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO, USA.
Chad TangDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ritsuko KomakiDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Alexander V LouieDepartment of Medical Oncology, London Health Sciences Center, London, ON, Canada.
David A PalmaDepartment of Radiation Oncology, London Health Sciences Center, London, ON, Canada.
Anne S TsaoDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Boris SepesiDepartment of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
William N WilliamDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jianjun ZhangDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Qiuling ShiDepartment of Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Xin Shelley WangDepartment of Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Stephen G SwisherDepartment of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
John V HeymachDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · USUniversity of Colorado Denver · USLondon Health Sciences Centre · CA

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Tissue Bank and Biomarkers CoreP50CA058187 · NCI · UNIVERSITY OF COLORADO DENVER · PI NEMENOFF, RAPHAEL A. · 1992 to 2018
$43.8M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA058187
6 · The paper itself

Abstract

backgroundEvidence from retrospective studies suggests that disease progression after first-line chemotherapy for metastatic non-small-cell lung cancer (NSCLC) occurs most often at sites of disease known to exist at baseline. However, the potential effect of aggressive local consolidative therapy for patients with oligometastatic NSCLC is unknown. We aimed to assess the effect of local consolidative therapy on progression-free survival.

methodsIn this multicentre, randomised, controlled, phase 2 study, eligible patients from three hospitals had histological confirmation of stage IV NSCLC, three or fewer metastatic disease lesions after first-line systemic therapy, an Eastern Cooperative Oncology Group performance status score of 2 or less, had received standard first-line systemic therapy, and had no disease progression before randomisation. First-line therapy was four or more cycles of platinum doublet therapy or 3 or more months of EGFR or ALK inhibitors for patients with EGFR mutations or ALK rearrangements, respectively. Patients were randomly assigned (1:1) to either local consolidative therapy ([chemo]radiotherapy or resection of all lesions) with or without subsequent maintenance treatment or to maintenance treatment alone, which could be observation only. Maintenance treatment was recommended based on a list of approved regimens, and observation was defined as close surveillance without cytotoxic treatment. Randomisation was not masked and was balanced dynamically on five factors: number of metastases, response to initial therapy, CNS metastases, intrathoracic nodal status, and EGFR and ALK status. The primary endpoint was progression-free survival analysed in all patients who were treated and had at least one post-baseline imaging assessment. The study is ongoing but not recruiting participants. This study is registered with ClinicalTrials.gov, number NCT01725165.

findingsBetween Nov 28, 2012, and Jan 19, 2016, 74 patients were enrolled either during or at the completion of first-line systemic therapy. The study was terminated early after randomisation of 49 patients (25 in the local consolidative therapy group and 24 in the maintenance treatment group) as part of the annual analyses done by the Data Safety Monitoring Committee of all randomised trials at MD Anderson Cancer Center, and before a planned interim analysis of 44 events. At a median follow-up time for all randomised patients of 12·39 months (IQR 5·52-20·30), the median progression-free survival in the local consolidative therapy group was 11·9 months (90% CI 5·7-20·9) versus 3·9 months (2·3-6·6) in the maintenance treatment group (hazard ratio 0·35 [90% CI 0·18-0·66], log-rank p=0·0054). Adverse events were similar between groups, with no grade 4 adverse events or deaths due to treatment. Grade 3 adverse events in the maintenance therapy group were fatigue (n=1) and anaemia (n=1) and in the local consolidative therapy group were oesophagitis (n=2), anaemia (n=1), pneumothorax (n=1), and abdominal pain (n=1, unlikely related).

interpretationLocal consolidative therapy with or without maintenance therapy for patients with three or fewer metastases from NSCLC that did not progress after initial systemic therapy improved progression-free survival compared with maintenance therapy alone. These findings suggest that aggressive local therapy should be further explored in phase 3 trials as a standard treatment option in this clinical scenario.

fundingMD Anderson Lung Cancer Priority Fund, MD Anderson Cancer Center Moon Shot Initiative, and Cancer Center Support (Core), National Cancer Institute, National Institutes of Health.

Indexed as

AdultAgedAged, 80 and overCarcinoma, Non-Small-Cell LungFemaleHumansLung NeoplasmsMaleMiddle AgedNeoplasm Metastasis

Identifiers

PMID27789196
PMCPMC5143183
OpenAlexW2536769127

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

and 6 more above

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.