Prognostic impact of the number and total tumor burden of secondary cerebral lesions in patients with resected brain metastases of non-small cell lung cancers.

brain metastases non–small cell lung cancer oncology surgical resection survival total tumor burden

Journal

Journal of neurosurgery
ISSN: 1933-0693
Titre abrégé: J Neurosurg
Pays: United States
ID NLM: 0253357

Informations de publication

Date de publication:
19 Jan 2024
Historique:
received: 22 08 2023
accepted: 13 11 2023
medline: 19 1 2024
pubmed: 19 1 2024
entrez: 19 1 2024
Statut: aheadofprint

Résumé

Systemic therapeutic advancements have improved the prognosis of cancer patients, leading to surgery more frequently being carried out for patients with multiple brain metastases (BM). The underlying evidence for the strategy is currently lacking. This study aimed to evaluate the prognostic significance of the number of BM and total tumor burden (TTB) on the overall survival (OS) of patients with resected BM of non-small cell lung cancer (NSCLC) in a modern series. In this monocentric retrospective series, patients who underwent resection of BM of NSCLC between 2015 and 2021 were included. Demographic, clinical, and histological parameters were collected, and formal radiological volumetric analyses were performed. Prognostic biomarkers for cerebral progression-free survival (C-PFS) and OS were analyzed with univariate and multivariate Cox proportional hazards analysis. One hundred eighty-four patients were included in the study. Among these, 108 patients (58.7%) presented with a single brain metastasis, 36 patients (19.6%) with 2 BM, 22 patients (11.9%) with 3 BM, and 18 patients (9.8%) with more than 3 BM (maximum 15 BM). The mean ± SD (range) preoperative tumor burden was 23.1 ± 25.3 (1.1-145.3) cm3. The mean residual tumor burden after surgery was 0.3 ± 0.8 (0.0-6.3) cm3. By the time of the analysis, 128 patients (69.6%) had died. The median follow-up duration was 49.0 months (95% CI 39.6-63.6). The median OS was 19.2 months (95% CI 13.2-24.0), and the survival rates at 6 months, 1 year, and 2 years were 76% (95% CI 69%-82%), 61% (95% CI 53%-67%), and 43% (95% CI 35%-50%), respectively. The median C-PFS was 8.4 months (95% CI 7.2-12.0). In the Cox multivariate regression model, younger age (< 65 years), single brain metastasis, adjuvant brain radiation therapy, adjuvant use of targeted therapy, and TTB < 7 cm3 were all independent predictors of longer OS. In this era of modern systemic treatments for cancer, the number of BM and total cerebral tumor burden remain significant prognostic factors of OS. However, resection should be considered as an option even in those patients with multiple BM in order to enhance patient clinical status, enable further local and systemic treatment delivery, and improve their survival and quality of life.

Identifiants

pubmed: 38241682
doi: 10.3171/2023.11.JNS231923
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-11

Auteurs

Sidonie Sauvageot (S)

1Department of Neurosurgery, Gui de Chauliac University Hospital, Montpellier, France.

Caroline Mollevi (C)

2Desbrest Institute of Epidemiology and Public Health, INSERM, Montpellier, France.

Quentin D Thomas (QD)

3Department of Medical Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.
4Oncogenic Pathways in Lung Cancer, Montpellier Cancer Research Institute (IRCM), INSERM U1194, Montpellier, France.

Marie Charissoux (M)

5Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.

Amélie Darlix (A)

3Department of Medical Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.
6Institute of Functional Genomics, Montpellier University CNRS, INSERM U1191, Montpellier, France.

Valérie Rigau (V)

6Institute of Functional Genomics, Montpellier University CNRS, INSERM U1191, Montpellier, France.
7Department of Pathology and Onco-biology, Gui de Chauliac University Hospital, Montpellier, France.

Luc Bauchet (L)

1Department of Neurosurgery, Gui de Chauliac University Hospital, Montpellier, France.
6Institute of Functional Genomics, Montpellier University CNRS, INSERM U1191, Montpellier, France.

Xavier Quantin (X)

8Department of Thoracic Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.

Jean Louis Pujol (JL)

9Thoracic Oncology Unit, University Hospital of Montpellier, Montpellier, France; and.
10Cancerology Research Institute of Montpellier (IRCM), National Institute for Health and Medical Research (INSERM) Unit-U1194, Montpellier, France.

Benoit Roch (B)

9Thoracic Oncology Unit, University Hospital of Montpellier, Montpellier, France; and.
10Cancerology Research Institute of Montpellier (IRCM), National Institute for Health and Medical Research (INSERM) Unit-U1194, Montpellier, France.

Julien Boetto (J)

1Department of Neurosurgery, Gui de Chauliac University Hospital, Montpellier, France.
6Institute of Functional Genomics, Montpellier University CNRS, INSERM U1191, Montpellier, France.

Classifications MeSH