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Biomarker Expression and Clinical Outcomes in International Study of Chemoradiation and Magnetic Resonance Imaging-Based Image-Guided Brachytherapy for Locally Advanced Cervical Cancer: BIOEMBRACE.
Chopra, Supriya; Bosse, Tjalling; Horeweg, Nanda; Deodhar, Kedar; Menon, Santosh; Rafael, Tynisha; Pai, Venkatesh; Rijstenberg, Lucia; van Kemenade, Folkert; Kannan, Sadhana; Mahantshetty, Umesh; Segedin, Barbara; Huang, Fleur; Bruheim, Kjersti; Perez, Margarita; Rai, Bhavana; Tan, Li Tee; Giannakopoulos, Nadia; Schmid, Maximilian; Tanderup, Kari; Pötter, Richard; Nout, Remi A.
Afiliação
  • Chopra S; Department of Radiation Oncology and Medical Physics, Advanced Centre for Treatment Research and Education in Cancer, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India. Electronic address: schopra@actrec.gov.in.
  • Bosse T; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Horeweg N; Department of Radiation Oncology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Deodhar K; Department of Pathology, Tata Memorial Hospital, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Menon S; Department of Pathology, Tata Memorial Hospital, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Rafael T; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Pai V; Department of Radiation Oncology and Medical Physics, Advanced Centre for Treatment Research and Education in Cancer, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Rijstenberg L; Department of Pathology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
  • van Kemenade F; Department of Pathology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
  • Kannan S; Epidemiology and Clinical Trials Unit, Advanced Centre for Treatment Research and Education in Cancer, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Mahantshetty U; Department of Radiation Oncology and Medical Physics, Tata Memorial Hospital, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Segedin B; Department of Radiation Oncology, Institute of Oncology, Ljubljana, Slovenia.
  • Huang F; Department of Radiation Oncology, Cross Cancer Institute and University of Alberta, Edmonton, Alberta, Canada.
  • Bruheim K; Department of Radiation Oncology, Oslo University Hospital, Oslo, Norway.
  • Perez M; Department of Radiation Oncology, Navarra Investigacion Biomedical, Pampalona, Spain.
  • Rai B; Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Tan LT; Department of Clinical Oncology, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, United Kingdom.
  • Giannakopoulos N; Department of Pathology, Cross Cancer Institute and University of Alberta, Edmonton, Alberta, Canada.
  • Schmid M; Department of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
  • Tanderup K; Danish Cancer Particle Therapy, Aarhus University Hospital, Aarhus, Denmark; Institute of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Pötter R; Department of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
  • Nout RA; Department of Radiation Oncology, Leiden University Medical Centre, Leiden, The Netherlands; Department of Radiation Oncology, Erasmus University Medical Centre, Rotterdam, The Netherlands. Electronic address: r.nout@erasmusmc.nl.
Article em En | MEDLINE | ID: mdl-39067486
ABSTRACT

PURPOSE:

BIOEMBRACE was designed to study the impact of biomarkers in addition to clinicopathological factors on disease outcomes in patients treated with chemoradiation and magnetic resonance imaging (MRI)-guided brachytherapy (BT) for locally advanced cervical cancer in the EMBRACE study. METHODS AND MATERIALS Between 2018 and 2021, 8 EMBRACE-I sites contributed tumor tissue for the immunohistochemistry of p16, PD-L1, and L1CAM. These biomarkers and clinicopathological factors (International Federation of Gynecology and Obstetrics 2009 stage, nodal status, histology, and necrosis on MRI) were analyzed to predict poor response at BT (high-risk clinical target volume [HR-CTV] ≥ 40 cc) at BT) and 5-year local control, pelvic control, and disease-free survival. Interaction between p16, PD-L1, radiation therapy dose (HR-CTV D90), and disease outcomes was investigated. Univariable and multivariable analyses were performed.

RESULTS:

Two hundred sixty-four patients were included. The median HR-CTV D90 was 89 Gy (86-95). P-16 positive status, PD-L1 > 1%, and L1CAM ≥ 10% was noted in 86.6%, 20.1%, and 17.8% of patients, respectively. P16 negative status (odds ratio, 2.0; 95% CI, 1.0-5.7; P = .04) and necrosis on MRI (odds ratio, 2.1; 95% CI, 1.1-4.3; P < .02) independently predicted for HR-CTV ≥ 40 cc, as did the International Federation of Gynecology and Obstetrics stage and tumor width >5 cm. PD-L1 > 1% was associated with reduced local (82% vs 94%; P = .02) and pelvic control (79% vs 89%; P = .02). HR-CTV D90 < 85 Gy was associated with inferior 5-year local control in p16-positive patients, especially if PD-L1 was coexpressed. On multivariable analysis, PD-L1 > 1% was the only independent factor for 5-year local control (hazard ratio, 3.3; P = .04) and L1CAM ≥ 50% for pelvic control (hazard ratio, 5.5; 95% CI, 1.3-23.3; P = .02).

CONCLUSIONS:

P16 negative status and tumor necrosis on MRI are independently associated with poor response to chemoradiation, whereas PD-L1 > 1% and L1CAM ≥ 50% have an independent impact on local and pelvic control, suggesting an impact of biomarker expression on outcomes. Further validation is needed.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Radiat Oncol Biol Phys Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Radiat Oncol Biol Phys Ano de publicação: 2024 Tipo de documento: Article