The HILUS-Trial-a Prospective Nordic Multicenter Phase 2 Study of Ultracentral Lung Tumors Treated With Stereotactic Body Radiotherapy.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
07 2021
Historique:
received: 17 11 2020
revised: 15 03 2021
accepted: 18 03 2021
pubmed: 7 4 2021
medline: 10 8 2021
entrez: 6 4 2021
Statut: ppublish

Résumé

Stereotactic body radiation therapy of thoracic tumors close to the central airways implies risk of severe toxicity. We report a prospective multicenter phase 2 trial for tumors located less than or equal to 1 cm from the proximal bronchial tree with primary end point of local control and secondary end point of toxicity. Stereotactic body radiation therapy with 7 Gy × 8 was prescribed to the 67% isodose encompassing the planning target volume. The patients were stratified to group A (tumors ≤ 1 cm from the main bronchi and trachea) or group B (all other tumors). Risk factors for treatment-related death were tested in univariate analysis, and a logistic regression model was developed for fatal bronchopulmonary bleeding versus dose to the main bronchi and trachea. A total of 65 patients (group A/group B, n = 39/26) were evaluated. The median distance between the tumor and the proximal bronchial tree was 0 mm (0-10 mm). The 2-year local control was 83%. Grade 3 to 5 toxicity was noted in 22 patients, including 10 cases of treatment-related death (bronchopulmonary hemorrhage, n = 8; pneumonitis, n = 1; fistula, n = 1). Dose to the combined structure main bronchi and trachea and tumor distance to the main bronchi were important risk factors. Dose modeling revealed minimum dose to the "hottest" 0.2 cc to the structure main bronchi and trachea as the strongest predictor for lethal bronchopulmonary hemorrhage. On the basis of the presented data, 7 Gy × 8, prescribed to the planning target volume-encompassing isodose, should not be used for tumors located within 1 cm from the main bronchi and trachea. Group B-type tumors may be considered for the treatment on the basis of an individual risk-benefit assessment and a maximum dose to the main bronchi and trachea in the order of 70 to 80 Gy (equivalent dose in 2 Gy fractions).

Identifiants

pubmed: 33823286
pii: S1556-0864(21)02074-8
doi: 10.1016/j.jtho.2021.03.019
pii:
doi:

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1200-1210

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2021 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

Karin Lindberg (K)

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Theme Cancer, Section of Head, Neck, Lung and Skin Tumours, Karolinska University Hospital, Stockholm, Sweden. Electronic address: karin.lindberg@ki.se.

Vitali Grozman (V)

Section of Thoracic Radiology, Department of Imaging and Physiology, Karolinska University Hospital, Stockholm, Sweden; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Kristin Karlsson (K)

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Section of Radiotherapy Physics and Engineering, Department of Medical Radiation Physics and Nuclear Medicine, Karolinska University Hospital, Stockholm, Sweden.

Sara Lindberg (S)

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Theme Cancer, Section of Head, Neck, Lung and Skin Tumours, Karolinska University Hospital, Stockholm, Sweden.

Ingmar Lax (I)

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Section of Radiotherapy Physics and Engineering, Department of Medical Radiation Physics and Nuclear Medicine, Karolinska University Hospital, Stockholm, Sweden.

Peter Wersäll (P)

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Section of Radiotherapy, Department of Cancer, Karolinska University Hospital, Stockholm, Sweden.

Gitte Fredberg Persson (GF)

Section of Radiotherapy, Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark; Department of Oncology, Herlev-Gentofte Hospital, University of Copenhagen, Herlev, Denmark; Department of Clinical Medicine, Faculty of Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Mirjana Josipovic (M)

Section of Radiotherapy, Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Azza Ahmed Khalil (AA)

Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.

Ditte Sloth Moeller (DS)

Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.

Jan Nyman (J)

Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Ninni Drugge (N)

Department of Therapeutic Radiation Physics, Sahlgrenska University Hospital, Gothenburg, Sweden.

Per Bergström (P)

Department of Oncology, Northern Sweden University Hospital, Umeå, Sweden.

Jörgen Olofsson (J)

Department of Oncology, Northern Sweden University Hospital, Umeå, Sweden.

Lotte Victoria Rogg (LV)

Department of Oncology, Oslo University Hospital, Oslo, Norway.

Christina Ramberg (C)

Department of Medical Physics, Oslo University Hospital, Oslo, Norway.

Charlotte Kristiansen (C)

Department of Oncology, Vejle Hospital, University Hospital of Southern Denmark, Vejle, Denmark.

Stefan Starup Jeppesen (SS)

Department of Oncology, Odense University Hospital, Odense C, Denmark; Institute of Clinical Research, University of Southern Denmark, Odense C, Denmark.

Tine Bjørn Nielsen (TB)

Laboratory of Radiation Physics, Odense University Hospital, Odense C, Denmark.

Britta Lödén (B)

Oncology department, Central Hospital in Karlstad, Karlstad, Sweden.

Hans-Olov Rosenbrand (HO)

Oncology department, Central Hospital in Karlstad, Karlstad, Sweden.

Silke Engelholm (S)

Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund, Sweden.

André Haraldsson (A)

Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund, Sweden.

Charlotte Billiet (C)

Department of Radiation Oncology, Iridium Kankernetwerk, Wilrijk (Antwerp), Belgium; Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk-Antwerp, Belgium.

Rolf Lewensohn (R)

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Theme Cancer, Section of Head, Neck, Lung and Skin Tumours, Karolinska University Hospital, Stockholm, Sweden.

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Classifications MeSH