Recognition of and treatment recommendations for oligometastatic disease in multidisciplinary tumor boards.

Local therapy Multidisciplinary tumor board Oligometastasis

Journal

Clinical and translational radiation oncology
ISSN: 2405-6308
Titre abrégé: Clin Transl Radiat Oncol
Pays: Ireland
ID NLM: 101713416

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 03 10 2022
revised: 08 11 2022
accepted: 10 11 2022
entrez: 24 11 2022
pubmed: 25 11 2022
medline: 25 11 2022
Statut: epublish

Résumé

Growing evidence supports a combined modality treatment strategy for patients with oligometastatic disease. However, lack of phase III trial data and uncertainties around patient selection highlight the importance of multidisciplinary tumor boards (MDT) in therapeutic decision-making. This study aimed to analyze the recognition of and treatment recommendations for oligometastatic patients by MDTs at a large comprehensive cancer center in order to better understand current treatment patterns of oligometastasis. For this retrospective single-center cross-sectional study, oligometastatic patients were identified by screening oncological PET and concurrent brain MRI scans conducted at our center in 2020. MDT discussions and recommendations within four weeks of the imaging diagnosis of oligometastasis were analyzed. Logistic regression analysis was used to identify predictors for the addition of local therapy to standard-of-care. A total of 787 oligometastatic cases were identified. Lung cancer and mesothelioma, skin cancer, and prostate cancer were the most common histologies with 231 (29 %), 160 (20 %), and 84 (11 %) cases, respectively. Almost half of the cases (46 %) had one distant metastasis on imaging only. More than half (56 %) of all oligometastatic cases were discussed at an MDT. In 47 % of cases, for which a therapeutic recommendation was reached in an MDT, local therapy was part of the therapeutic strategy. On logistic regression analysis, oligometastatic skin cancer was significantly associated with a recommendation for local therapy (p < 0.05), whereas the number of oligometastases was not (p = 0.202). More than half of oligometastatic cases were discussed in MDTs, of which more than every second received a recommendation including the addition of local therapy. This frequency of MDT use underscores the importance of multidisciplinary decision-making, yet efforts should be increased to standardize reporting and use standard nomenclature on oligometastasis in MDTs to better frame multidisciplinary discussion.

Sections du résumé

Background and introduction UNASSIGNED
Growing evidence supports a combined modality treatment strategy for patients with oligometastatic disease. However, lack of phase III trial data and uncertainties around patient selection highlight the importance of multidisciplinary tumor boards (MDT) in therapeutic decision-making. This study aimed to analyze the recognition of and treatment recommendations for oligometastatic patients by MDTs at a large comprehensive cancer center in order to better understand current treatment patterns of oligometastasis.
Materials and methods UNASSIGNED
For this retrospective single-center cross-sectional study, oligometastatic patients were identified by screening oncological PET and concurrent brain MRI scans conducted at our center in 2020. MDT discussions and recommendations within four weeks of the imaging diagnosis of oligometastasis were analyzed. Logistic regression analysis was used to identify predictors for the addition of local therapy to standard-of-care.
Results UNASSIGNED
A total of 787 oligometastatic cases were identified. Lung cancer and mesothelioma, skin cancer, and prostate cancer were the most common histologies with 231 (29 %), 160 (20 %), and 84 (11 %) cases, respectively. Almost half of the cases (46 %) had one distant metastasis on imaging only. More than half (56 %) of all oligometastatic cases were discussed at an MDT. In 47 % of cases, for which a therapeutic recommendation was reached in an MDT, local therapy was part of the therapeutic strategy. On logistic regression analysis, oligometastatic skin cancer was significantly associated with a recommendation for local therapy (p < 0.05), whereas the number of oligometastases was not (p = 0.202).
Conclusion UNASSIGNED
More than half of oligometastatic cases were discussed in MDTs, of which more than every second received a recommendation including the addition of local therapy. This frequency of MDT use underscores the importance of multidisciplinary decision-making, yet efforts should be increased to standardize reporting and use standard nomenclature on oligometastasis in MDTs to better frame multidisciplinary discussion.

Identifiants

pubmed: 36420098
doi: 10.1016/j.ctro.2022.11.008
pii: S2405-6308(22)00107-0
pmc: PMC9676209
doi:

Types de publication

Journal Article

Langues

eng

Pagination

123-129

Informations de copyright

© 2022 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. PB cited research grants to the institution from ViewRay Inc. (Mountain View, CA, USA). NA has received grants from ViewRay Inc. and BrainLab and personal fees from AstraZeneca, Debiopharm, ViewRay and BrainLab, and non-financial support from ViewRay, all outside of the submitted work. MH has received research support from GE Healthcare, a fund by the Alfred and Annemarie von Sick legacy for translational and clinical cardiac and oncological research, and a grant by the Clinical Research Priority Program (CRRP) “Artificial Intelligence in oncological Imaging” of the University Zurich, all outside of the submitted work.

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Auteurs

Sebastian M Christ (SM)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Philip Heesen (P)

Faculty of Medicine, University of Zurich, Zurich, Switzerland.

Urs J Muehlematter (UJ)

Department of Nuclear Medicine, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Kaspar Pohl (K)

Faculty of Medicine, University of Zurich, Zurich, Switzerland.

Gabriel William Thiel (G)

Faculty of Medicine, University of Zurich, Zurich, Switzerland.

Jonas Willmann (J)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Maiwand Ahmadsei (M)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Tiuri E Kroese (TE)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Michael Mayinger (M)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Panagiotis Balermpas (P)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Andreas Wicki (A)

Department of Medical Oncology and Hematology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Nicolaus Andratschke (N)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Martin Huellner (M)

Department of Nuclear Medicine, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Matthias Guckenberger (M)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Classifications MeSH