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Comparison of efficacy and safety between simultaneous integrated boost intensity-modulated radiotherapy and standard-dose intensity-modulated radiotherapy in locally advanced esophageal squamous cell carcinoma: a retrospective study
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Abstract
Objective
This study aimed to evaluate the efficacy and safety of simultaneous integrated boost intensity-modulated radiotherapy (SIB-IMRT) versus standard-dose intensity-modulated radiotherapy (SD-IMRT) in the treatment of locally advanced esophageal squamous cell carcinoma.
Methods
From July 2003 to March 2014, 1748 patients in a single center who received definitive chemoradiotherapy were included in the analysis. A total of 109 patients who underwent SIB-IMRT and fulfilled all inclusion and exclusion criteria were identified as the study group. A total of 266 patients who underwent SD-IMRT (60 Gy/30 fractions, 2 Gy/fraction, 1 time/day, 5 times/week) during the same period were selected as the control group. Propensity score matching (PSM) was used to balance the baseline characteristics. Survival status, treatment failure mode, and the occurrence of adverse events were compared between the two groups.
Results
There were more women and more cervical and upper thoracic cancers (P = 0.038, < 0.001, respectively) in the SIB-IMRT group before case matching. The median progression-free survival (PFS) in the SD-IMRT and SIB-IMRT groups was 22 and 19 months, respectively, and the median overall survival duration was 24 and 22 months, respectively, with χ2 = 0.244 and P = 0.621. After PSM of 1:1, 138 patients entered the final analysis (69 cases from each group). The median PFS of the SD-IMRT group and the SIB-IMRT group was 13 and 18 months, respectively, with χ2 = 8.776 and P = 0.003. The 1‑, 3‑, and 5‑year overall survival rates were 66.7, 21.7, and 8.7% and 65.2, 36.2, and 27.3%, respectively, and the median overall survival duration was 16 and 22 months, respectively, with χ2 = 5.362 and P = 0.021. Treatment failure mode: 5‑year local regional recurrence rates of SD-IMRT and SIB-IMRT were 50.7 and 36.2%, respectively, with χ2 = 2.949 and P = 0.086. The 5‑year distant metastasis rates of the two groups were 36.2 and 24.6%, respectively, with χ2 = 2.190 and P = 0.139. Adverse events: 3 patients experienced grade 4–5 toxicity (2.2%), including one case of grade 4 radiation esophagitis and two cases of grade 5 radiation pneumonitis, all in the SD-IMRT group; 14 patients experienced grade 3 adverse events (10.1%), primarily including radiation esophagitis, radiation pneumonitis, and hematological toxicity.
Conclusion
The technique of SIB-IMRT was safe and reliable compared with SD-IMRT. In addition, SIB-IMRT had locoregional control advantages and potential survival benefits.
Springer Science and Business Media LLC
Title: Comparison of efficacy and safety between simultaneous integrated boost intensity-modulated radiotherapy and standard-dose intensity-modulated radiotherapy in locally advanced esophageal squamous cell carcinoma: a retrospective study
Description:
Abstract
Objective
This study aimed to evaluate the efficacy and safety of simultaneous integrated boost intensity-modulated radiotherapy (SIB-IMRT) versus standard-dose intensity-modulated radiotherapy (SD-IMRT) in the treatment of locally advanced esophageal squamous cell carcinoma.
Methods
From July 2003 to March 2014, 1748 patients in a single center who received definitive chemoradiotherapy were included in the analysis.
A total of 109 patients who underwent SIB-IMRT and fulfilled all inclusion and exclusion criteria were identified as the study group.
A total of 266 patients who underwent SD-IMRT (60 Gy/30 fractions, 2 Gy/fraction, 1 time/day, 5 times/week) during the same period were selected as the control group.
Propensity score matching (PSM) was used to balance the baseline characteristics.
Survival status, treatment failure mode, and the occurrence of adverse events were compared between the two groups.
Results
There were more women and more cervical and upper thoracic cancers (P = 0.
038, < 0.
001, respectively) in the SIB-IMRT group before case matching.
The median progression-free survival (PFS) in the SD-IMRT and SIB-IMRT groups was 22 and 19 months, respectively, and the median overall survival duration was 24 and 22 months, respectively, with χ2 = 0.
244 and P = 0.
621.
After PSM of 1:1, 138 patients entered the final analysis (69 cases from each group).
The median PFS of the SD-IMRT group and the SIB-IMRT group was 13 and 18 months, respectively, with χ2 = 8.
776 and P = 0.
003.
The 1‑, 3‑, and 5‑year overall survival rates were 66.
7, 21.
7, and 8.
7% and 65.
2, 36.
2, and 27.
3%, respectively, and the median overall survival duration was 16 and 22 months, respectively, with χ2 = 5.
362 and P = 0.
021.
Treatment failure mode: 5‑year local regional recurrence rates of SD-IMRT and SIB-IMRT were 50.
7 and 36.
2%, respectively, with χ2 = 2.
949 and P = 0.
086.
The 5‑year distant metastasis rates of the two groups were 36.
2 and 24.
6%, respectively, with χ2 = 2.
190 and P = 0.
139.
Adverse events: 3 patients experienced grade 4–5 toxicity (2.
2%), including one case of grade 4 radiation esophagitis and two cases of grade 5 radiation pneumonitis, all in the SD-IMRT group; 14 patients experienced grade 3 adverse events (10.
1%), primarily including radiation esophagitis, radiation pneumonitis, and hematological toxicity.
Conclusion
The technique of SIB-IMRT was safe and reliable compared with SD-IMRT.
In addition, SIB-IMRT had locoregional control advantages and potential survival benefits.
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