Evidence map›Paper›PMID 40738926›Full record

ArticleScientific reports2025

Impact of local therapy in metastatic renal cell carcinoma during medical treatment in a retrospective analysis.

Sena Hoffer, Hendrik Eggers, Tabea Fröhlich, Paula Kappler, Maria-Luisa Tiemann, Viktor Grünwald, Christoph Henkenberens, Mohamed Omar, Robert M Blach, Florian Heidel and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Sena Hoffer *Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, OE 6860, Carl-Neuberg Str. 1, Hannover, Germany. hoffer.sena@mh-hannover.de.
Hendrik Eggers *Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, OE 6860, Carl-Neuberg Str. 1, Hannover, Germany.
Tabea FröhlichDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, OE 6860, Carl-Neuberg Str. 1, Hannover, Germany.
Paula KapplerDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, OE 6860, Carl-Neuberg Str. 1, Hannover, Germany.
Maria-Luisa TiemannDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, OE 6860, Carl-Neuberg Str. 1, Hannover, Germany.
Viktor GrünwaldDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, OE 6860, Carl-Neuberg Str. 1, Hannover, Germany.
Christoph HenkenberensDepartment of Radiotherapy, Hannover Medical School, Hannover, Germany.
Mohamed OmarClaudia Von Schilling Comprehensive Cancer Center Lower Saxony, Hannover, Germany.
Robert M BlachClaudia Von Schilling Comprehensive Cancer Center Lower Saxony, Hannover, Germany.
Florian HeidelDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, OE 6860, Carl-Neuberg Str. 1, Hannover, Germany.
Philipp IvanyiDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, OE 6860, Carl-Neuberg Str. 1, Hannover, Germany. Ivanyi.philipp@mh-hannover.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current guidelines on treatment of metastatic renal cell carcinoma (mRCC) suggest an emerging role of local therapy (LT). Still there is a lack of data which patients may benefit from additional LT once medical treatment (MT) is initiated. We retrospectively aim to characterize LT in patients with mRCC who underwent LT while receiving MT. 315/401 mRCC patients were eligible, thereof 163 (51.7%) received LT during MT (LT( +)), while 152 (48.3%) received only MT (LT(-)). Radiotherapy (49.1%) and surgery (41.7%) were the most frequently administered LT modalities. Overall survival (OS) was not superior in LT( +) vs. LT(-) (35.9, (95%-CI [confidence interval]: 29.8-42.0) vs. 20.3, (95%-CI: 10.3-30.3) months, log-rank p = 0.117). However, in a subgroup analysis the duration of MT prior to initiation of LT (≤ 6 months 24.1 (95%-CI: 18.6-29.6) vs. > 6 months: 43.0 (95%-CI: 32.2-36.2) months, log-rank p = 0.005) and the type of progression (oligoprogression: 44.0 (95%-CI: 31.5-56.5) vs. systemic progression: 29.6 (95%-CI: 23.4-35.8) months, log-rank p = 0.03) were associated with improved OS. We present the largest analysis of LT during MT. Our study has enhanced our understanding of LT utilization in mRCC after MT is already initiated. Ultimately, the inclusion of LT could improve OS in selected patients receiving MT.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAdultAgedAged, 80 and overCombined Modality TherapyFemaleHumansMaleMiddle AgedNeoplasm MetastasisRetrospective StudiesTreatment OutcomeLocal therapyMultimodal treatmentPalliative treatmentRadiation therapyRenal cell carcinomaSurgery

Identifiers

PMID40738926
PMCPMC12310947

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Registered trials

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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.