Evidence map›Paper›PMID 34638265›Full record

ArticleCancers2021

Continued versus Interrupted Targeted Therapy during Metastasis-Directed Stereotactic Radiotherapy: A Retrospective Multi-Center Safety and Efficacy Analysis.

Stephanie G C Kroeze, Corinna Fritz, Jana Schaule, Oliver Blanck, Klaus Henning Kahl, David Kaul, Shankar Siva, Sabine Gerum, An Claes, Nora Sundahl and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 15% 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.

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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Targeting ClassicalCancers · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Review
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

21 authors at 18 institutions in 6 countries.

Stephanie G C KroezeRadiation Oncology, University Hospital Zürich, 8011 Zurich, Switzerland.ORCID 0000-0002-1342-5310
Corinna FritzRadiation Oncology, University Hospital Zürich, 8011 Zurich, Switzerland.
Jana SchauleRadiation Oncology, University Hospital Zürich, 8011 Zurich, Switzerland.
Oliver BlanckRadiation Oncology, University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Klaus Henning KahlRadiation Oncology, University Hospital Augsburg, 86156 Augsburg, Germany.ORCID 0000-0002-0545-1367
David KaulRadiation Oncology, Charité-University Hospital Berlin, 12200 Berlin, Germany.ORCID 0000-0002-7906-5629
Shankar SivaRadiation Oncology, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne 3010, Australia.ORCID 0000-0003-2840-0658
Sabine GerumRadiation Oncology, University Hospital Munich, 80336 Munich, Germany.
An ClaesRadiation Oncology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.
Nora SundahlRadiation Oncology, University Hospital Ghent, 9000 Ghent, Belgium.
Sonja AdebahrDepartment of Radiation Oncology, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
Susanne SteraRadiation Oncology, University Hospital Frankfurt, 60318 Frankfurt, Germany.
Markus M SchymallaRadiation Oncology, Philipps-University Marburg, 35043 Marburg, Germany.
Nasrin Abbasi-SengerRadiation Oncology, University Hospital Jena, 07743 Jena, Germany.
Daniel BuergyRadiation Oncology, Universitätsmedizin Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.ORCID 0000-0001-5913-3332
Michael GeierRadiation Oncology, Ordensklinikum Linz, 4020 Linz, Austria.
Marcella SzuecsRadiation Oncology, University Hospital Rostock, 18059 Rostock, Germany.
Fabian LohausRadiation Oncology, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0003-4043-7066
Guido HenkeRadiation Oncology, Kantonsspital St. Gallen, 9007 St. Gallen, Switzerland.ORCID 0000-0002-9921-445X
Stephanie E CombsRadiation Oncology, Technical University Munich, 81675 Munich, Germany.
Matthias GuckenbergerRadiation Oncology, University Hospital Zürich, 8011 Zurich, Switzerland.
University Hospital of Zurich · CHCharité - Universitätsmedizin Berlin · DEGhent University Hospital · BEGoethe University Frankfurt · DEHeidelberg University · DEJena University Hospital · DEKantonsspital St. Gallen · CHKepler Universitätsklinikum · ATMünchen Klinik · DEPhilipps University of Marburg · DETechnical University of Munich · DEThe University of Melbourne · AUUniversity Children's Hospital Tübingen · DEUniversity Hospital Augsburg · DEUniversity Hospital Schleswig-Holstein · DEUniversity Medical Center Utrecht · NLUniversity of Freiburg · DEUniversity of Rostock · DE

Funding

Varian Medical Systems UZ-19/263
6 · The paper itself

Abstract

The increasing use of targeted therapy (TT) has resulted in prolonged disease control and survival in many metastatic cancers. In parallel, stereotactic radiotherapy (SRT) is increasingly performed in patients receiving TT to obtain a durable control of resistant metastases, and thereby to prolong the time to disseminated disease progression and switch of systemic therapy. The aims of this study were to analyze the safety and efficacy of SRT combined with TT in metastatic cancer patients and to assess the influence of continuous vs. interrupted TT during metastasis-directed SRT. The data of 454 SRTs in 158 patients from the international multicenter database (TOaSTT) on metastatic cancer patients treated with SRT and concurrent TT (within 30 days) were analyzed using Kaplan-Meier and log rank testing. Toxicity was defined by the CTCAE v4.03 criteria. The median FU was 19.9 mo (range 1-102 mo); 1y OS, PFS and LC were 59%, 24% and 84%, respectively. Median TTS was 25.5 mo (95% CI 11-40). TT was started before SRT in 77% of patients. TT was interrupted during SRT in 44% of patients, with a median interruption of 7 (range 1-42) days. There was no significant difference in OS or PFS whether TT was temporarily interrupted during SRT or not. Any-grade acute and late SRT-related toxicity occurred in 63 (40%) and 52 (33%) patients, respectively. The highest toxicity rates were observed for the combination of SRT and EGFRi or BRAF/MEKi, and any-grade toxicity was significantly increased when EGFRi (

Indexed as

BRAF inhibitorsconcurrentmetastasis-directed radiotherapystereotactictargeted therapytyrosine kinase inhibitors

Identifiers

PMID34638265
PMCPMC8507709
OpenAlexW3203213035

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.