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Higher Radiation Dose to the Immune Cells Correlates with Worse Tumor Control and Overall Survival in Patients with Stage III NSCLC: A Secondary Analysis of RTOG0617.
Jin, Jian-Yue; Hu, Chen; Xiao, Ying; Zhang, Hong; Paulus, Rebecca; Ellsworth, Susannah G; Schild, Steven E; Bogart, Jeffrey A; Dobelbower, Michael Chris; Kavadi, Vivek S; Narayan, Samir; Iyengar, Puneeth; Robinson, Cliff; Greenberger, Joel S; Koprowski, Christopher; Machtay, Mitchell; Curran, Walter; Choy, Hak; Bradley, Jeffrey D; Kong, Feng-Ming Spring.
Afiliación
  • Jin JY; Department of Radiation Oncology, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, OH 44106, USA.
  • Hu C; NRG Oncology Statistics and Data Management Center, Philadelphia, PA 19103, USA.
  • Xiao Y; Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21218, USA.
  • Zhang H; Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA 19103, USA.
  • Paulus R; Department of Radiation Oncology, School of Medicine, University of Maryland, Maryland, MD 20742, USA.
  • Ellsworth SG; NRG Oncology Statistics and Data Management Center, Philadelphia, PA 19103, USA.
  • Schild SE; Department of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA 16251, USA.
  • Bogart JA; Department of Radiation Oncology, Mayo Clinic Hospital, Phoenix, AZ 85054, USA.
  • Dobelbower MC; Department of Radiation Oncology, State University of New York Upstate Medical University, Syracuse, NY 13210, USA.
  • Kavadi VS; Department of Radiation Oncology, University of Alabama at Birmingham Cancer Center, Birmingham, AL 35233, USA.
  • Narayan S; USON-Texas Oncology-Sugar Land, Sugar Land, TX 77479, USA.
  • Iyengar P; Michigan Cancer Research Consortium CCOP, Ann Arbor, MI 48106, USA.
  • Robinson C; Department of Radiation Oncology, University of Texas Southwestern Medical School, Dallas, TX 75235, USA.
  • Greenberger JS; Department of Radiation Oncology, Washington University in St. Louis, St. Louis, MO 63108, USA.
  • Koprowski C; Department of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA 16251, USA.
  • Machtay M; Christiana Care Health Services, Inc. CCOP, Newark, DE 19718, USA.
  • Curran W; Department of Radiation Oncology, Penn State University Cancer Institute, Hershey, PA 17033, USA.
  • Choy H; Department of Radiation Oncology, Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.
  • Bradley JD; Department of Radiation Oncology, University of Texas Southwestern Medical School, Dallas, TX 75235, USA.
  • Kong FS; Department of Radiation Oncology, Washington University in St. Louis, St. Louis, MO 63108, USA.
Cancers (Basel) ; 13(24)2021 Dec 08.
Article en En | MEDLINE | ID: mdl-34944813
ABSTRACT

Background:

We hypothesized that the Effective radiation Dose to the Immune Cells (EDIC) in circulating blood is a significant factor for the treatment outcome in patients with locally advanced non-small-cell lung cancer (NSCLC).

Methods:

This is a secondary study of a phase III trial, NRG/RTOG 0617, in patients with stage III NSCLC treated with radiation-based treatment. The EDIC was computed as equivalent uniform dose to the entire blood based on radiation doses to all blood-containing organs, with consideration of blood flow and fractionation effect. The primary endpoint was overall survival (OS), and the secondary endpoints were progression-free survival (PFS) and local progression-free survival (LPFS). The EDIC-survival relationship was analyzed with consideration of clinical significant factors.

Results:

A total of 456 patients were eligible. The median EDIC values were 5.6 Gy (range, 2.1-12.2 Gy) and 6.3 Gy (2.1-11.6 Gy) for the low- and high-dose groups, respectively. The EDIC was significantly associated with OS (hazard ratio [HR] = 1.12, p = 0.005) and LPFS (HR = 1.09, p = 0.02) but PFS (HR = 1.05, p = 0.17) after adjustment for tumor dose, gross tumor volume and other factors. OS decreased with an increasing EDIC in a non-linear pattern the two-year OS decreased first with a slope of 8%/Gy when the EDIC < 6 Gy, remained relatively unchanged when the EDIC was 6-8 Gy, and followed by a further reduction with a slope of 12%/Gy when the EDIC > 8 Gy.

Conclusions:

The EDIC is a significant independent risk factor for poor OS and LPFS in RTOG 0617 patients with stage III NSCLC, suggesting that radiation dose to circulating immune cells is critical for tumor control. Organ at risk for the immune system should be considered during RT plan.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Cancers (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Cancers (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos