Evidence map›Paper›PMID 39419904›Full record

SynthesisStrahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]2025

Neoadjuvant chemoradiotherapy in combination with deep regional hyperthermia followed by surgery for rectal cancer: a systematic review and meta-analysis.

Adela Ademaj, Sonja Stieb, Cihan Gani, Oliver J Ott, Dietmar Marder, Roger A Hälg, Susanne Rogers, Pirus Ghadjar, Rainer Fietkau, Hans Crezee and 1 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Observational
  3. Article
  4. Review
  5. Article
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.

Adela AdemajCentre for Radiation Oncology, Cantonal Hospital Aarau, 5001, Aarau, Switzerland. adela.ademaj@ksa.ch.
Sonja StiebCentre for Radiation Oncology, Cantonal Hospital Aarau, 5001, Aarau, Switzerland.
Cihan GaniDepartment of Radiation Oncology, Universitätsklinikum Tübingen, 72076, Tübingen, Germany.
Oliver J OttDepartment of Radiation Oncology, Universitätsklinikum Erlangen, 91054, Erlangen, Germany.
Dietmar MarderCentre for Radiation Oncology, Cantonal Hospital Aarau, 5001, Aarau, Switzerland.
Roger A HälgCentre for Radiation Oncology, Cantonal Hospital Aarau, 5001, Aarau, Switzerland.
Susanne RogersCentre for Radiation Oncology, Cantonal Hospital Aarau, 5001, Aarau, Switzerland.
Pirus GhadjarDepartment of Radiation Oncology, Charité-Universitätsmedizin Berlin, Freie Universität Berlin, Berlin Institute of Health, Humboldt-Universität zu Berlin, Berlin, Germany.
Rainer FietkauDepartment of Radiation Oncology, Universitätsklinikum Erlangen, 91054, Erlangen, Germany.
Hans CrezeeDepartment of Radiation Oncology, Amsterdam UMC, Cancer Center Amsterdam, University of Amsterdam, 1105 AZ, Amsterdam, The Netherlands.
Oliver RiestererCentre for Radiation Oncology, Cantonal Hospital Aarau, 5001, Aarau, Switzerland.

Funding

H2020 Marie Skłodowska-Curie Actions 955625
6 · The paper itself

Abstract

background and purposeCombining chemoradiotherapy (CRT) with deep regional hyperthermia (HT) shows promise for enhancing clinical outcomes in selected rectal cancer patients. This study aimed to integrate the evidence and evaluate the efficacy of this combined treatment approach. MATERIALS AND

methodsA systematic search of the PubMed, Scopus, and Mendeley databases was performed. This review was conducted according to the PRISMA guidelines. The quality of studies was evaluated using the Newcastle-Ottawa scale (NOS). Random-effects meta-analyses (DerSimonian and Laird) were performed. The primary outcome was pathological complete response (pCR), and secondary endpoints were overall survival (OS), disease-free survival (DFS), local recurrence-free survival (LRFS), and toxicity.

resultsIn total, 12 studies were included, mostly of moderate quality. Patients with locally advanced rectal cancer (LARC; n = 760) and locally recurrent rectal cancer (LRRC; n = 22) were eligible. The pooled pCR rate was 19% (95% confidence interval [CI]: 16-22%) among all 782 patients and 19% (95%CI:16-23%) among 760 LARC patients. Due to significant study heterogeneity, survival outcomes were pooled by excluding LRRC patients. The pooled 5‑year OS rate among 433 LARC patients was 87% (95%CI: 83-90%). The pooled 5‑year DFS and LRFS in LARC patients were 75% (95%CI: 70-80%) and 95% (95%CI: 92-97%), respectively. There was a lack of consistent reporting of HT treatment parameters and toxicity symptoms among the studies.

conclusionThe collective clinical evidence showed that neoadjuvant CRT combined with HT in rectal cancer patients is feasible, with a 19% pCR rate and excellent survival outcomes in long term follow-up.

Indexed as

Chemoradiotherapy, AdjuvantHyperthermia, InducedNeoadjuvant TherapyRectal NeoplasmsDisease-Free SurvivalFeasibility StudiesHumansNeoplasm Recurrence, LocalPathologic Complete ResponseSurvival RateTreatment OutcomeChemoradiotherapyDeep regional hyperthermiaLocally advanced rectal cancerLocally recurrent rectal cancer

Identifiers

PMID39419904
PMCPMC11754347

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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.