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Details

Autor(en) / Beteiligte
Titel
Stereotactic Body Radiotherapy for Medically Inoperable Lung Cancer: Prospective, Single-Center Study of 108 Consecutive Patients
Ist Teil von
  • International journal of radiation oncology, biology, physics, 2012-02, Vol.82 (2), p.967-973
Ort / Verlag
New York, NY: Elsevier Inc
Erscheinungsjahr
2012
Quelle
MEDLINE
Beschreibungen/Notizen
  • Purpose To present the results of stereotactic body radiotherapy (SBRT) for medically inoperable patients with Stage I non–small-cell lung cancer (NSCLC) and contrast outcomes in patients with and without a pathologic diagnosis. Methods and Materials Between December 2004 and October 2008, 108 patients (114 tumors) underwent treatment according to the prospective research ethics board-approved SBRT protocols at our cancer center. Of the 108 patients, 88 (81.5%) had undergone pretreatment whole-body [18F]-fluorodeoxyglucose positron emission tomography/computed tomography. A pathologic diagnosis was unavailable for 33 (28.9%) of the 114 lesions. The SBRT schedules included 48 Gy in 4 fractions or 54–60 Gy in 3 fractions for peripheral lesions and 50–60 Gy in 8–10 fractions for central lesions. Toxicity and radiologic response were assessed at the 3–6-month follow-up visits using conventional criteria. Results The mean tumor diameter was 2.4-cm (range, 0.9–5.7). The median follow-up was 19.1 months (range, 1–55.7). The estimated local control rate at 1 and 4 years was 92% (95% confidence interval [CI], 86–97%) and 89% (95% CI, 81–96%). The cause-specific survival rate at 1 and 4 years was 92% (95% CI, 87–98%) and 77% (95% CI, 64–89%), respectively. No statistically significant difference was found in the local, regional, and distant control between patients with and without pathologically confirmed NSCLC. The most common acute toxicity was Grade 1 or 2 fatigue (53 of 108 patients). No toxicities of Grade 4 or greater were identified. Conclusions Lung SBRT for early-stage NSCLC resulted in excellent local control and cause-specific survival with minimal toxicity. The disease-specific outcomes were comparable for patients with and without a pathologic diagnosis. SBRT can be considered an option for selected patients with proven or presumed early-stage NSCLC.

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