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2009年NCCN肺癌指南关于放疗的部分原文如下:
Modern 3-dimensional conformal RT techniques with CT or CT/positron emission tomography (PET)--based treatment planning should be used on all patients.The dose volume histogram (DVH) for the lungs,esophagus, heart, liver, kidney, and spinal cord should be used to minimize normal tissue toxicity (see NSCL-C ). Whenever feasible,respiratory management techniques (such as 4-dimensional CT and respiratory gating) should be incorporated in the radiation set up and delivery. Treatment planning should be on CT scans obtained in the treatment position. IV contrast for diagnostic or simulation CT should be used for better target and normal tissue delineation whenever possible. PET/CT is preferable for treatment plans rather than CT alone for the gross tumor volume (GTV) delineation in cases with substantial atelectasis.
In general, photon beam energy between 4-10 MV is recommended for most patients. If a large tumor is involving the mediastinum or the primary tumor is a large and proximal lesion with patient’s separation more than 20 cm, 15 MV or 18 MV photon energy can also be used. If the tumor is fixed to the vertebral body, located at the superior sulcus, or involves the bilateral mediastinum, intensity-modulated radiotherapy (IMRT) should be considered to avoid overdose to normal tissues. Involved field radiation to high dose without elective nodal treatment has been shown to have less toxicity, superior survival, and low risk of isolated nodal relapse.In patients receiving radiation therapy or chemoradiation with curative intent, treatment interruptions or dose reductions for manageable acute toxicities (that is, grade 3 esophagitis, pneumonitis, hematologic toxicities) should be avoided by following the recommended dose-volume constraints (see NSCL-C ). 98-100 In the preoperative chemoradiation setting, a total dose of 45-50 Gy in 1.8-2 Gy fractions should be used to treat all volumes of gross disease (see NSCL-5 and NSCL-C ).101 Doses greater than 50 Gy in the preoperative setting have been reported to be safe at select institutions; however, this is still considered experimental.To avoid postoperative pulmonary toxicity, preoperative chemoradiotherapy should be avoided if pneumonectomy is required.Surgery in a field that has had 60 Gy is difficult, because the landmarks disappear with high doses of radiation. Thus, surgeons are often wary of resection in areas that have previously received RT doses of more than 45 Gy, especially patients who have received RT doses of more than 60 Gy (ie, patients who have received definitive concurrent chemoradiation). Therefore, the radiation dose should be carefully considered if patients might be eligible for surgery. Radiation therapy should continue to definitive dose without interruption if the patient is not a surgical candidate. Postoperative radiation should include the bronchial stump and mediastinum. A total dose of 50 Gy should be delivered in 1.8 to 2 Gy fractions for negative margins. For extranodal extension or microscopic positive margins, a total dose of 54-60 Gy (in 1.8 to 2 Gy fractions) should be used (see NSCL-C ). For gross residual tumor, a total dose up to 70 Gy should be used. Because of the higher risk of local failure, concurrent adjuvant chemoradiation can be used if recommended in the guidelines and if the patient can tolerate it.
In the definitive concurrent chemoradiation setting, a total radiation dose up to 74 Gy in 2 Gy fractions should be used to treat all volumes of gross disease.Three-dimensional treatment planning is imperative with dose volume histogram assessments of lung function to estimate the risk of pneumonitis (see NSCL-C ). 110,111 Elective nodal radiation is not mandated.Studies suggest that stereotactic body radiotherapy (SBRT) and radiofrequency ablation (RFA) may be options for node-negative patients who either refuse surgery or cannot tolerate surgery because of poor PS, significant cardiovascular risk, poor pulmonary function, and/or comorbidities. When stereotactic radiosurgery was used in 245 patients (T1-2), local control was 85% at 2 years and 5 years.Radiation Therapy Oncology Group (RTOG) 0236 trial is currently assessing SBRT. Optimal candidates for SBRT include patients with node negative peripheral tumors less than 5 cm.Optimal candidates for RFA include patients with an isolated peripheral lesion less than 3 cm; RFA can be used for previously irradiated tissue and for palliation.119 A recent study with RFA in 33 patients with NSCLC yielded overall survival of 70% (95% CI, 51%–83%) at 1 year and 48% (30%-65%) at 2 years. Patients with stage I NSCLC (n=13) had a 2-year overall survival of 75% (45–92%). RT with (or without) chemotherapy should be offered as potentially curative treatment to patients with stage I and II NSCLC who are medically inoperable but of reasonable PS and life expectancy (see NSCL-B and NSCL-C ). However, a study in 4,357 patients with stage I or II NSCLC who did not have surgical resection found that median survival was improved (by 5-7 months) in patients treated with RT, although 5-year survival was not significantly different when compared with patients not receiving RT.
[ 本帖最后由 围棋 于 2009-5-13 17:12 编辑 ] |
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