Patrick Cheung1, Sergio Faria2, Shahida Ahmed2, Pierre Chabot2, Jonathan Greenland2, Elizabeth Kurien2, Islam Mohamed2, James R Wright2, Helmut Hollenhorst2, Catherine de Metz2, Holly Campbell2, Thi Toni Vu2, Anand Karvat2, Elaine S Wai2, Yee C Ung2, Glenwood Goss2, Frances A Shepherd2, Patti O'Brien2, Keyue Ding2, Chris O'Callaghan2. 1. Sunnybrook Odette Cancer Centre, University of Toronto, Toronto, Ontario, Canada (PC, YCU); Montreal General Hospital, McGill University, Montreal, Quebec, Canada (SF); CancerCare Manitoba, Winnipeg, Manitoba, Canada (SA); Hopital Maisonneuve-Rosemont, Montreal, Quebec, Canada (PC); Dr. H. Bliss Murphy Cancer Centre, St John's, Newfoundland, Canada (JG); Tom Baker Cancer Centre, Calgary, Alberta, Canada (EK); BC Cancer Agency-Cancer Centre for the Southern Interior, Kelowna, British Columbia, Canada (IM); Juravinski Cancer Centre, McMaster University, Hamilton, Ontario, Canada (JRW); QEII Centre for Clinical Research Trials, Halifax, Nova Scotia, Canada (HH); Cancer Centre of Southeastern Ontario, Queen's University, Kingston, Ontario, Canada (CdM); Atlantic Health Sciences Corporation, Saint John Regional Hospital, Saint John, New Brunswick, Canada (HC); CHUM - Hopital Notre-Dame, Montreal, Quebec, Canada (TTV); BC Cancer Agency-Fraser Valley Centre, Surrey, British Columbia, Canada (AK); BC Cancer Agency-Vancouver Island Cancer Centre, Victoria, British Columbia, Canada (ESW); Ottawa Health Research Institute-General Division, Ottawa, Ontario, Canada (GG); University Health Network-OCI/Princess Margaret Hospital, University of Toronto, Toronto, Ontario, Canada (FAS); NCIC Clinical Trials Group, Queen's University, Kingston, Ontario, Canada (PO, KD, CO). patrick.cheung@sunnybrook.ca. 2. Sunnybrook Odette Cancer Centre, University of Toronto, Toronto, Ontario, Canada (PC, YCU); Montreal General Hospital, McGill University, Montreal, Quebec, Canada (SF); CancerCare Manitoba, Winnipeg, Manitoba, Canada (SA); Hopital Maisonneuve-Rosemont, Montreal, Quebec, Canada (PC); Dr. H. Bliss Murphy Cancer Centre, St John's, Newfoundland, Canada (JG); Tom Baker Cancer Centre, Calgary, Alberta, Canada (EK); BC Cancer Agency-Cancer Centre for the Southern Interior, Kelowna, British Columbia, Canada (IM); Juravinski Cancer Centre, McMaster University, Hamilton, Ontario, Canada (JRW); QEII Centre for Clinical Research Trials, Halifax, Nova Scotia, Canada (HH); Cancer Centre of Southeastern Ontario, Queen's University, Kingston, Ontario, Canada (CdM); Atlantic Health Sciences Corporation, Saint John Regional Hospital, Saint John, New Brunswick, Canada (HC); CHUM - Hopital Notre-Dame, Montreal, Quebec, Canada (TTV); BC Cancer Agency-Fraser Valley Centre, Surrey, British Columbia, Canada (AK); BC Cancer Agency-Vancouver Island Cancer Centre, Victoria, British Columbia, Canada (ESW); Ottawa Health Research Institute-General Division, Ottawa, Ontario, Canada (GG); University Health Network-OCI/Princess Margaret Hospital, University of Toronto, Toronto, Ontario, Canada (FAS); NCIC Clinical Trials Group, Queen's University, Kingston, Ontario, Canada (PO, KD, CO).
Abstract
BACKGROUND: A multi-institutional phase II trial was performed to assess a hypofractionated accelerated radiotherapy regimen for early stage non-small cell lung cancer (NSCLC) in an era when stereotactic body radiotherapy was not widely available. METHODS: Eighty patients with biopsy-proven, peripherally located, T1-3 N0 M0 NSCLC were enrolled. Eligible patients received 60 Gy in 15 fractions using a three-dimensional conformal technique without inhomogeneity correction. The gross tumour volume (GTV) was the primary tumor only, and the planning target volume (PTV) margin was 1.0 to 1.5cm. The primary endpoint was the 2-year primary tumor control rate. Toxicities were measured using the Common Terminology Criteria for Adverse Events version 3.0. RESULTS: The median follow-up of patients was 49 months (range = 21-63 months). The median age of patients was 75.9 years. The actuarial rate of primary tumor control was 87.4% (95% confidence interval [CI] = 76.2% to 93.5%) at 2 years. Overall survival was 68.7% (95% CI = 57.2% to 77.6%) at 2 years. The actuarial rates of developing regional and distant relapse at 2 years were 8.8% (95% CI = 4.1% to 18.7%) and 21.6% (95% CI = 13.5% to 33.5%), respectively. Tumor size greater than 3cm was associated with an increased risk of developing distant relapse (hazard ratio = 3.11; 95% CI = 1.30 to 7.42; two-sided log-rank test P = .007). The most common grade 3+ toxicities were fatigue (6.3%), cough (7.5%), dyspnea (13.8%), and pneumonitis (10.0%) CONCLUSIONS: Conformal radiotherapy to a dose of 60 Gy in 15 fractions resulted in favorable primary tumor control and overall survival rates in patients with T1-3 N0 M0 NSCLC. Severe toxicities were uncommon with this relatively simple treatment technique.
BACKGROUND: A multi-institutional phase II trial was performed to assess a hypofractionated accelerated radiotherapy regimen for early stage non-small cell lung cancer (NSCLC) in an era when stereotactic body radiotherapy was not widely available. METHODS: Eighty patients with biopsy-proven, peripherally located, T1-3 N0 M0 NSCLC were enrolled. Eligible patients received 60 Gy in 15 fractions using a three-dimensional conformal technique without inhomogeneity correction. The gross tumour volume (GTV) was the primary tumor only, and the planning target volume (PTV) margin was 1.0 to 1.5cm. The primary endpoint was the 2-year primary tumor control rate. Toxicities were measured using the Common Terminology Criteria for Adverse Events version 3.0. RESULTS: The median follow-up of patients was 49 months (range = 21-63 months). The median age of patients was 75.9 years. The actuarial rate of primary tumor control was 87.4% (95% confidence interval [CI] = 76.2% to 93.5%) at 2 years. Overall survival was 68.7% (95% CI = 57.2% to 77.6%) at 2 years. The actuarial rates of developing regional and distant relapse at 2 years were 8.8% (95% CI = 4.1% to 18.7%) and 21.6% (95% CI = 13.5% to 33.5%), respectively. Tumor size greater than 3cm was associated with an increased risk of developing distant relapse (hazard ratio = 3.11; 95% CI = 1.30 to 7.42; two-sided log-rank test P = .007). The most common grade 3+ toxicities were fatigue (6.3%), cough (7.5%), dyspnea (13.8%), and pneumonitis (10.0%) CONCLUSIONS: Conformal radiotherapy to a dose of 60 Gy in 15 fractions resulted in favorable primary tumor control and overall survival rates in patients with T1-3 N0 M0 NSCLC. Severe toxicities were uncommon with this relatively simple treatment technique.
Authors: Michelle Iocolano; Aaron T Wild; Margaret Hannum; Zhigang Zhang; Charles B Simone; Daphna Gelblum; Abraham J Wu; Andreas Rimner; Annemarie F Shepherd Journal: Acta Oncol Date: 2019-10-12 Impact factor: 4.089
Authors: N Rodríguez de Dios; X Sanz; P Foro; I Membrive; A Reig; A Ortiz; R Jiménez; M Algara Journal: Clin Transl Oncol Date: 2016-08-23 Impact factor: 3.405
Authors: Cole R Steber; Ryan T Hughes; Michael H Soike; Travis Jacobson; Corbin A Helis; Joshua C Farris; Michael K Farris Journal: Clin Lung Cancer Date: 2020-09-18 Impact factor: 4.785