Stereotactic Body Radiotherapy for Lymph Node Oligometastases: Real-World Evidence From 90 Consecutive Patients.

local therapy lymph node metastases oligometastases radiotherapy stereotactic body radiotherapy

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2020
Historique:
received: 12 10 2020
accepted: 24 12 2020
entrez: 22 2 2021
pubmed: 23 2 2021
medline: 23 2 2021
Statut: epublish

Résumé

To evaluate the efficacy and toxicity of extracranial stereotactic body radiotherapy (SBRT) in the treatment of oligometastatic lymph node involvement in the mediastinum, retroperitoneum, or pelvis, in a consecutive group of patients from real clinical practice outside clinical trials. A retrospective analysis of 90 patients with a maximum of four oligometastases and various primary tumors (the most common being colorectal cancers). The endpoints were local control of treated metastases (LC), freedom from widespread dissemination (FFWD), progression-free survival (PFS), overall survival (OS), and freedom from systemic treatment (FFST). Acute and delayed toxicities were also evaluated. The median follow-up after SBRT was 34.9 months. The LC rate at three and five years was 68.4 and 56.3%, respectively. The observed median FFWD was 14.6 months, with a five-year FFWD rate of 33.7%. The median PFS was 9.4 months; the three-year PFS rate was 19.8%. The median FFST was 14.0 months; the five-year FFST rate was 23.5%. The OS rate at three and five years was 61.8 and 39.3%, respectively. Median OS was 53.1 months. The initial dissemination significantly shortened the time to relapse, death, or activation of systemic treatment-LC (HR 4.8, p < 0.001), FFWD (HR 2.8, p = 0.001), PFS (HR 2.1, p = 0.011), FFST (HR 2.4, p = 0.005), OS (HR 2.2, p = 0.034). Patients classified as having radioresistant tumors noticed significantly higher risk in terms of LC (HR 13.8, p = 0.010), FFWD (HR 3.1, p = 0.006), PFS (HR 3.5, p < 0.001), FFST (HR 3.2, p = 0.003). The multivariable analysis detected statistically significantly worse survival outcomes for initially disseminated patients as well as separately in groups divided according to radiosensitivity. No grade III or IV toxicity was reported. Our study shows that targeted SBRT is a very effective and low toxic treatment for oligometastatic lymph node involvement. It can delay the indication of cytotoxic chemotherapy and thus improve and maintain patient quality of life. The aim of further studies should focus on identifying patients who benefit most from SBRT, as well as the correct timing and dosage of SBRT in treatment strategy.

Identifiants

pubmed: 33614499
doi: 10.3389/fonc.2020.616494
pmc: PMC7892582
doi:

Types de publication

Journal Article

Langues

eng

Pagination

616494

Informations de copyright

Copyright © 2021 Burkon, Selingerova, Slavik, Pospisil, Bobek, Kominek, Osmera, Prochazka, Vrzal, Kazda and Slampa.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Petr Burkon (P)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.
Department of Radiation Oncology, Faculty of Medicine, Masaryk University, Brno, Czechia.

Iveta Selingerova (I)

Research Center for Applied Molecular Oncology (RECAMO), Masaryk Memorial Cancer Institute, Brno, Czechia.

Marek Slavik (M)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.
Department of Radiation Oncology, Faculty of Medicine, Masaryk University, Brno, Czechia.

Petr Pospisil (P)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.
Department of Radiation Oncology, Faculty of Medicine, Masaryk University, Brno, Czechia.

Lukas Bobek (L)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.

Libor Kominek (L)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.

Pavel Osmera (P)

Department of Nuclear Medicine and PET Center, Masaryk Memorial Cancer Institute, Brno, Czechia.

Tomas Prochazka (T)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.
Department of Radiation Oncology, Faculty of Medicine, Masaryk University, Brno, Czechia.

Miroslav Vrzal (M)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.

Tomas Kazda (T)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.
Department of Radiation Oncology, Faculty of Medicine, Masaryk University, Brno, Czechia.
Central European Institute of Technology, Masaryk University, Brno, Czechia.

Pavel Slampa (P)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czechia.
Department of Radiation Oncology, Faculty of Medicine, Masaryk University, Brno, Czechia.

Classifications MeSH