BACKGROUND: There is limited information on risk factors for treatment-related pneumonitis in esophageal cancer patients. AIM OF THE STUDY: To determine factors associated with treatment-related pneumonitis in esophageal cancer patients treated with definitive chemoradiotherapy. MATERIALS AND METHODS: We retrospectively reviewed clinical data from esophageal cancer patients treated with definitive chemoradiotherapy from 2000 to 2003. Demographic, clinical, and treatment-related data were collected for all patients. The time to occurrence of grade > or =2 pneumonitis was calculated from the end of radiotherapy. Univariate analyses were performed to determine the existence of any association between patient demographic, clinical, or treatment characteristics and pneumonitis. RESULTS: In total, 96 patients were included in the study with a median follow-up of 8 months (range, <1-48 months). Among them, 23 patients also received an average of two cycles of systemic chemotherapy before the initiation of concurrent chemoradiation. The incidence of grade > or =2 pneumonitis was 22% at 1 year. Systemic chemotherapy before concurrent chemoradiation was significantly associated with an increased risk of grade > or =2 pneumonitis (p = 0.003), with the 1-year incidence of grade > or =2 pneumonitis for patients with and without systemic chemotherapy being 49 and 14%, respectively. No other clinical or dosimetric factors investigated were associated with the risk of grade > or =2 pneumonitis. CONCLUSIONS: Systemic chemotherapy before concurrent chemoradiation was significantly associated with an increased risk of grade > or =2 pneumonitis, suggesting that induction chemotherapy may have sensitized the lung tissue to radiation damage in esophageal cancer patients.
BACKGROUND: There is limited information on risk factors for treatment-related pneumonitis in esophageal cancerpatients. AIM OF THE STUDY: To determine factors associated with treatment-related pneumonitis in esophageal cancerpatients treated with definitive chemoradiotherapy. MATERIALS AND METHODS: We retrospectively reviewed clinical data from esophageal cancerpatients treated with definitive chemoradiotherapy from 2000 to 2003. Demographic, clinical, and treatment-related data were collected for all patients. The time to occurrence of grade > or =2 pneumonitis was calculated from the end of radiotherapy. Univariate analyses were performed to determine the existence of any association between patient demographic, clinical, or treatment characteristics and pneumonitis. RESULTS: In total, 96 patients were included in the study with a median follow-up of 8 months (range, <1-48 months). Among them, 23 patients also received an average of two cycles of systemic chemotherapy before the initiation of concurrent chemoradiation. The incidence of grade > or =2 pneumonitis was 22% at 1 year. Systemic chemotherapy before concurrent chemoradiation was significantly associated with an increased risk of grade > or =2 pneumonitis (p = 0.003), with the 1-year incidence of grade > or =2 pneumonitis for patients with and without systemic chemotherapy being 49 and 14%, respectively. No other clinical or dosimetric factors investigated were associated with the risk of grade > or =2 pneumonitis. CONCLUSIONS: Systemic chemotherapy before concurrent chemoradiation was significantly associated with an increased risk of grade > or =2 pneumonitis, suggesting that induction chemotherapy may have sensitized the lung tissue to radiation damage in esophageal cancerpatients.
Authors: Hekun Jin; Susan L Tucker; Hui Helen Liu; Xiong Wei; Sue Sun Yom; Shulian Wang; Ritsuko Komaki; Yuhchyau Chen; Mary K Martel; Radhe Mohan; James D Cox; Zhongxing Liao Journal: Radiother Oncol Date: 2008-10-18 Impact factor: 6.280
Authors: Samual R Francis; Christopher J Anker; Brian Wang; Greg V Williams; Kristen Cox; Douglas G Adler; Dennis C Shrieve; Bill J Salter Journal: J Appl Clin Med Phys Date: 2013-07-08 Impact factor: 2.102
Authors: F Klevebro; J A Elliott; A Slaman; B D Vermeulen; S Kamiya; C Rosman; S S Gisbertz; P R Boshier; J V Reynolds; I Rouvelas; G B Hanna; M I van Berge Henegouwen; S R Markar Journal: Ann Surg Oncol Date: 2019-06-10 Impact factor: 5.344