Graabak Gustav, Grønberg Bjørn Henning, Killingberg Kristin Toftaker, Halvorsen Tarje Onsøien
Department of Clinical and Molecular Medicine, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Oncology, St Olav's Hospital, Trondheim University Hospital, Trondheim, Norway.
JTO Clin Res Rep. 2024 May 16;5(9):100688. doi: 10.1016/j.jtocrr.2024.100688. eCollection 2024 Sep.
F-fluorodeoxyglucose positron emission tomography-computed tomography (PET-CT) is recommended for staging and defining target volume in limited-stage SCLC, though the impact on outcomes compared with CT staging and elective nodal irradiation (ENI) is not well documented. We analyzed patients receiving 45 Gy/30 fractions in two randomized trials of thoracic radiotherapy (TRT) in limited-stage SCLC (HAST and THORA trials) to evaluate whether PET-CT for staging and radiotherapy planning reduces radiotoxicity and improves survival.
Patients in HAST were staged with CT of the thorax and upper abdomen and brain magnetic resonance imaging of the brain. Patients in THORA were staged with PET-CT in addition. All patients were to receive four courses of platinum/etoposide chemotherapy and concurrent TRT starting three to four weeks after the first chemotherapy course. In HAST, target volumes included pathological lesions on CT plus ENI of lymph node stations 4-7 (bilateral). In THORA, target volumes were limited to PET-CT-positive lesions (selective nodal irradiation [SNI]).
A total of 149 patients were included (PET-CT/SNI: n = 76, CT/ENI: n=73); the median age was 64 years, 56% were women, 85% had PS 0 to 1, and 81% had stage III disease. The PET-CT/SNI group experienced less grade 3-4 esophagitis (18% versus 33%, = 0.043), less grade >=1 pneumonitis (5% versus 16%, = 0.028), and less dysphagia after TRT (mean scores on European Organisation for Research and Treatment of Cancer 13-item lung cancer module: 45 versus 72). There was no difference in median overall survival (24 versus 25 mo, = 0.59) or progression-free survival (11 versus 11 mo, = 0.23).
Using PET-CT for staging and target volume definition of TRT reduces acute radiotoxicity but does not improve overall or progression-free survival in limited-stage SCLC.
氟脱氧葡萄糖正电子发射断层扫描-计算机断层扫描(PET-CT)被推荐用于局限期小细胞肺癌(SCLC)的分期及确定靶区体积,不过与CT分期及选择性淋巴结照射(ENI)相比,其对治疗结果的影响尚无充分文献记载。我们分析了在两项局限期SCLC胸部放疗(TRT)随机试验(HAST和THORA试验)中接受45 Gy/30分次放疗的患者,以评估PET-CT用于分期及放疗计划是否能降低放射性毒性并提高生存率。
HAST试验中的患者接受胸部和上腹部CT检查及脑部磁共振成像检查进行分期。THORA试验中的患者除上述检查外还接受PET-CT检查。所有患者均接受四个疗程的铂类/依托泊苷化疗,并在首个化疗疗程后三至四周开始同步TRT。在HAST试验中,靶区体积包括CT上的病理性病变以及4-7组淋巴结(双侧)的ENI。在THORA试验中,靶区体积仅限于PET-CT阳性病变(选择性淋巴结照射[SNI])。
共纳入149例患者(PET-CT/SNI组:n = 76,CT/ENI组:n = 73);中位年龄为64岁,56%为女性,85%的患者体能状态(PS)为0至1,8..1%为Ⅲ期疾病。PET-CT/SNI组3-4级食管炎发生率较低(18%对33%,P = 0.043),≥1级肺炎发生率较低(5%对16%,P = 0.028),TRT后吞咽困难发生率较低(欧洲癌症研究与治疗组织肺癌13项模块的平均得分:45对72)。中位总生存期(24个月对25个月,P = 0.59)或无进展生存期(11个月对11个月,P = 0.23)无差异。
使用PET-CT进行TRT的分期及靶区体积定义可降低急性放射性毒性,但不能提高局限期SCLC患者的总生存期或无进展生存期。