Your browser doesn't support javascript.
loading
The HILUS-Trial-a Prospective Nordic Multicenter Phase 2 Study of Ultracentral Lung Tumors Treated With Stereotactic Body Radiotherapy.
Lindberg, Karin; Grozman, Vitali; Karlsson, Kristin; Lindberg, Sara; Lax, Ingmar; Wersäll, Peter; Persson, Gitte Fredberg; Josipovic, Mirjana; Khalil, Azza Ahmed; Moeller, Ditte Sloth; Nyman, Jan; Drugge, Ninni; Bergström, Per; Olofsson, Jörgen; Rogg, Lotte Victoria; Ramberg, Christina; Kristiansen, Charlotte; Jeppesen, Stefan Starup; Nielsen, Tine Bjørn; Lödén, Britta; Rosenbrand, Hans-Olov; Engelholm, Silke; Haraldsson, André; Billiet, Charlotte; Lewensohn, Rolf.
Afiliação
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • Wersäll P; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Section of Radiotherapy, Department of Cancer, Karolinska University Hospital, Stockholm, Sweden.
  • 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, Copenha
  • Josipovic M; Section of Radiotherapy, Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Khalil AA; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  • Moeller DS; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  • Nyman J; Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Drugge N; Department of Therapeutic Radiation Physics, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Bergström P; Department of Oncology, Northern Sweden University Hospital, Umeå, Sweden.
  • Olofsson J; Department of Oncology, Northern Sweden University Hospital, Umeå, Sweden.
  • Rogg LV; Department of Oncology, Oslo University Hospital, Oslo, Norway.
  • Ramberg C; Department of Medical Physics, Oslo University Hospital, Oslo, Norway.
  • Kristiansen C; Department of Oncology, Vejle Hospital, University Hospital of Southern Denmark, Vejle, Denmark.
  • Jeppesen SS; Department of Oncology, Odense University Hospital, Odense C, Denmark; Institute of Clinical Research, University of Southern Denmark, Odense C, Denmark.
  • Nielsen TB; Laboratory of Radiation Physics, Odense University Hospital, Odense C, Denmark.
  • Lödén B; Oncology department, Central Hospital in Karlstad, Karlstad, Sweden.
  • Rosenbrand HO; Oncology department, Central Hospital in Karlstad, Karlstad, Sweden.
  • Engelholm S; Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund, Sweden.
  • Haraldsson A; Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund, Sweden.
  • Billiet C; Department of Radiation Oncology, Iridium Kankernetwerk, Wilrijk (Antwerp), Belgium; Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk-Antwerp, Belgium.
  • 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.
J Thorac Oncol ; 16(7): 1200-1210, 2021 07.
Article em En | MEDLINE | ID: mdl-33823286
ABSTRACT

INTRODUCTION:

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.

METHODS:

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.

RESULTS:

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.

CONCLUSIONS:

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).
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Radiocirurgia / Neoplasias Pulmonares Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Radiocirurgia / Neoplasias Pulmonares Idioma: En Ano de publicação: 2021 Tipo de documento: Article