Fatal pneumonitis associated with intensity-modulated radiation therapy for mesothelioma
Fatal pneumonitis associated with intensity-modulated radiation therapy for mesothelioma
Allen AM, Czerminska M, Janne PA, Sugarbaker DJ, Bueno R, Harris JR, Court L, Baldini EH.
Department of Radiation Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, MA, USA.
PURPOSE: To describe the initial experience at Dana-Farber
Cancer Institute/Brigham and Women's Hospital with intensity-modulated
radiation therapy (IMRT) as adjuvant therapy after extrapleural
pneumonectomy (EPP) and adjuvant chemotherapy.
METHODS AND MATERIALS: The medical records of patients
treated with IMRT after EPP and adjuvant chemotherapy were
retrospectively reviewed. IMRT was given to a dose of 54 Gy to the
clinical target volume in 1.8 Gy daily fractions. Treatment was
delivered with a dynamic multileaf collimator using a sliding window
technique. Eleven of 13 patients received heated intraoperative
cisplatin chemotherapy (225 mg/m(2)). Two patients received neoadjuvant
intravenous cisplatin/pemetrexed, and 10 patients received adjuvant
cisplatin/pemetrexed chemotherapy after EPP but before radiation
therapy. All patients received at least 2 cycles of intravenous
chemotherapy. The contralateral lung was limited to a V20 (volume of
lung receiving 20 Gy or more) of 20% and a mean lung dose (MLD) of 15
Gy. All patients underwent fluorodeoxyglucose positron emission
tomography (FDG-PET) for staging, and any FDG-avid areas in the
hemithorax were given a simultaneous boost of radiotherapy to 60 Gy.
Statistical comparisons were done using two-sided t test.
RESULTS: Thirteen patients were treated with IMRT from
December 2004 to September 2005. Six patients developed fatal
pneumonitis after treatment. The median time from completion of IMRT to
the onset of radiation pneumonitis was 30 days (range 5-57 days). Thirty
percent of patients (4 of 13) developed acute Grade 3 nausea and
vomiting. One patient developed acute Grade 3 thrombocytopenia. The
median V20, MLD, and V5 (volume of lung receiving 5 Gy or more) for the
patients who developed pneumonitis was 17.6% (range, 15.3-22.3%), 15.2
Gy (range, 13.3-17 Gy), and 98.6% (range, 81-100%), respectively, as
compared with 10.9% (range, 5.5-24.7%) (p = 0.08), 12.9 Gy (range,
8.7-16.9 Gy) (p = 0.07), and 90% (range, 66-98.3%) (p = 0.20),
respectively, for the patients who did not develop pneumonitis.
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