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. 2012 Dec 27:7:222.
doi: 10.1186/1748-717X-7-222.

Hypofractionated radiotherapy for primary or secondary oligometastatic lung cancer using Tomotherapy

Affiliations

Hypofractionated radiotherapy for primary or secondary oligometastatic lung cancer using Tomotherapy

Heng-Jui Chang et al. Radiat Oncol. .

Abstract

Background: To retrospectively review the outcome of patients with primary or secondary oligometastatic lung cancer, treated with hypofractionated Tomotherapy.

Methods: Between April 2007 and June 2011, a total of 33 patients with oligometastatic intrapulmonary lesions underwent hypofractionated radiotherapy by Tomotherapy along with appropriate systemic therapy. There were 24 primary, and 9 secondary lung cancer cases. The radiation doses ranged from 4.5 to 7.0 Gy per fraction, multiplied by 8-16 fractions. The median dose per fraction was 4.5 Gy (range, 4.5-7.0 Gy), and the median total dose was 49.5 Gy (range, 45-72 Gy). The median estimated biological effective dose at 10 Gy (BED10) was 71.8 Gy (range, 65.3-119.0 Gy), and that at 3 Gy (BED3) was 123.8 Gy (range, 112.5-233.3 Gy). The mean lung dose (MLD) was constrained mainly under 1200 cGy. The median gross tumor volume (GTV) was 27.9 cm3 (range: 2.5-178.1 cm3).

Results: The median follow-up period was 25.8 months (range, 3.0-60.7 months). The median overall survival (OS) time was 32.1 months for the 24 primary lung cancer patients, and >40 months for the 9 metastatic lung patients. The median survival time of the patients with extra-pulmonary disease (EPD) was 11.2 months versus >50 months (not reached) in the patients without EPD (p < 0.001). Those patients with smaller GTV (≦27.9 cm3) had a better survival than those with larger GTV (>27.9 cm3): >40 months versus 12.85 months (p = 0.047). The patients with ≦2 lesions had a median survival >40 months, whereas those with ≧3 lesions had 26 months (p = 0.065). The 2-year local control (LC) rate was 94.7%. Only 2 patients (6.1%) developed ≧grade 3 radiation pneumonitis.

Conclusion: Using Tomotherapy in hypofractionation may be effective for selected primary or secondary lung oligometastatic diseases, without causing significant toxicities. Pulmonary oligometastasis patients without EPD had better survival outcomes than those with EPD. Moreover, GTV is more significant than lesion number in predicting survival.

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Figures

Figure 1
Figure 1
(A) Overall survival in oligometastatic primary lung cancer patients (n = 24). The median survival was 32.1 months. (B) Overall survival in secondary lung cancer patients (n = 9). Median survival was not reached.
Figure 2
Figure 2
Relationship between EPD status and overall survival rate. The EPD (−) group did not achieve median overall survival, while the overall survival in the EPD (+) group was only 11.2 months (p < 0.001).
Figure 3
Figure 3
Overall survival difference of 2 and 3 total oligometastatic lesions in all 33 patients. Median survival were undefined and 26 months separately (p = 0.065).
Figure 4
Figure 4
(A) EPD status in primary lung cancer also leads survival difference. EPD(+) vs EPD(−): 9.7 months vs not reached (p = 0.011). (B) EPD status in secondary lung cancer. EPD(+) vs EPD(−): 26 months vs not reached (p = 0.150).
Figure 5
Figure 5
MLD vs GTV.
Figure 6
Figure 6
Use GTV volume to predict survival.
Figure 7
Figure 7
MLD vs RP.

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