Evidence map›Paper›PMID 40821396›Full record

ArticleClinical and translational radiation oncology2025

Efficacy of radiotherapy and radiotherapy with hyperthermia to delay change of systemic therapy in patients with metastatic melanoma.

Paulina Chmiel, Mateusz Jacek Spałek, Hanna Koseła-Paterczyk, Piotr Łukasz Rutkowski, Paulina Jagodzińska-Mucha, Paweł Rogala, Katarzyna Kozak, Maria Telejko, Aneta Maria Borkowska

Abstract read
In one paragraph

Article in Clinical and translational radiation oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

9 authors.

Paulina ChmielDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Mateusz Jacek SpałekDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Hanna Koseła-PaterczykDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Piotr Łukasz RutkowskiDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Paulina Jagodzińska-MuchaDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Paweł RogalaDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Katarzyna KozakDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Maria TelejkoDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Aneta Maria BorkowskaDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The use of radiotherapy (RT) and RT with hyperthermia (HT) as a local treatment for oligoprogression in many tumors is becoming increasingly prevalent. However, there is currently limited data regarding RT efficacy in prolonging systemic therapy in melanoma. To address this lack of evidence, we conducted a single-institution study to establish the role of RT and RT + HT in delaying the time to systemic treatment switch in metastatic melanoma (MM). Methods: Patients with MM who received RT or RT + HT for oligoprogressive lesions at the referral center between 2018 and 2023 were identified. Oligoprogression was defined as up to five progressive metastases. Systemic treatment included immunotherapy and BRAF/MEK inhibitors. All patients who received radiotherapy to the brain and lungs were excluded. The primary endpoint was time to the next systemic therapy (TTNST) after RT/RT + HT. The secondary endpoints included overall survival (OS) and progression-free survival (PFS). Factors influencing TTNST were analyzed. Results: 156 patients were included, 82 patients had RT + HT while 74 had RT only. The median follow-up was 23 months (15.2-34). Immunotherapy was used in 82.7 % and BRAF/MEK inhibitors in 17.3 % of patients. The median TTNST for the overall cohort was 26 months (95 % CI: 14.5- NA), the mTTNST for patients treated with RT + HT was 14 months (95 % CI: 11.4-NA), and for patients treated with RT as sole treatment, it was 28 months (95 % CI: 18.3-NA) (p = 0.6). The median PFS from local treatment was 8 months (95 % CI: 5.1-16) for patients who received RT and 10 months (95 % CI: 5.6-12.6) for patients who received RT + HT (p = 0.9). The median OS from RT was 50 months (95 % CI: 40- NA) for patients who received RT and was not reached for patients who received RT + HT (p = 0.031). None of the analyzed factors influenced median TTNST. Conclusion: Both RT and RT + HT have been demonstrated to extend the duration of systemic treatment in patients with metastatic melanoma. The combination of RT + HT is suggested to be more efficacious than RT alone in the therapy of oligoprogressive disease during systemic treatment of patients, especially for OS.

Indexed as

BRAF/MEK, radiotherapyHyperthermia, HTICIsImmune checkpoint inhibitorsMelanomaRT

Identifiers

PMID40821396
PMCPMC12351170

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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.