Badgwell Brian, Ikoma Naruhiko, Murphy Mariela Blum, Li Jenny, Wang Xuemei, Minsky Bruce D, Estrella Jeannelyn, Mansfield Paul, Ajani Jaffer, Das Prajnan
Department of Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Department of Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Int J Radiat Oncol Biol Phys. 2025 Feb 1;121(2):423-431. doi: 10.1016/j.ijrobp.2024.08.042. Epub 2024 Sep 4.
The purpose of this phase 1 trial was to evaluate the safety and toxicity of preoperative short-course chemoradiotherapy (CRT) as part of total neoadjuvant therapy (TNT) for patients with potentially resectable gastric or gastroesophageal adenocarcinoma.
Patients were enrolled between March 2021 and December 2022 and received CRT (30 Gy radiation in 10 fractions with concurrent capecitabine or 5-fluorouracil), then received systemic therapy for 2 months, and then underwent surgery. The primary endpoint was CRT safety; secondary endpoints were pathologic complete response, perioperative complications, and overall survival (OS).
Of the 24 patients enrolled in the trial, 10 (42%) had bleeding, 3 (13%) had gastric outlet obstruction, and 2 (8%) had cirrhosis. Twelve patients (50%) had clinical nodal involvement. Twenty patients (83%) had poorly differentiated tumors, and 13 (54%) had signet ring cell histology. All patients completed CRT. CRT treatment-related toxic effects included grade 3 lymphopenia in 7 patients (29%), grade 4 lymphopenia in 1 (4%), and grade 3 anemia in 1 (4%). After CRT, 22 patients (92%) received chemotherapy, 1 patient (4%) with a microsatellite instability-high tumor received immunotherapy, and 1 patient (4%) underwent resection without systemic therapy. All patients underwent attempted resection, and gastrectomy was performed in 20 (83%). The R0 resection rate was 95%. Two patients had pathologic complete response, and an additional 5 had ≤1% viable tumor. Three patients had surgical complications [grade 1 in 1 patient (4%), grade 3b in 1 (4%), and grade 4a in 1 (4%)]; no patients died within 90 days. The median follow-up time was 28 months, and median OS was not reached. The 1- and 3-year OS rates were 96% and 85%, respectively.
Short-course CRT may be safely used as part of planned TNT for patients with potentially resectable gastric or gastroesophageal adenocarcinoma. The promising rates of treatment completion, pathologic response, and OS support further research of TNT for gastric cancer.
本1期试验的目的是评估术前短程放化疗(CRT)作为潜在可切除的胃或胃食管腺癌患者全新辅助治疗(TNT)一部分的安全性和毒性。
患者于2021年3月至2022年12月入组,接受CRT(10次分割给予30 Gy放疗,同时使用卡培他滨或5-氟尿嘧啶),然后接受2个月的全身治疗,随后接受手术。主要终点是CRT的安全性;次要终点是病理完全缓解、围手术期并发症和总生存期(OS)。
在试验入组的24例患者中,10例(42%)有出血,3例(13%)有胃出口梗阻,2例(8%)有肝硬化。12例患者(50%)有临床淋巴结受累。20例患者(83%)有低分化肿瘤,13例(54%)有印戒细胞组织学类型。所有患者均完成CRT。CRT治疗相关的毒性反应包括7例患者(29%)出现3级淋巴细胞减少,1例(4%)出现4级淋巴细胞减少,1例(4%)出现3级贫血。CRT后,22例患者(92%)接受了化疗,1例微卫星高度不稳定肿瘤患者(4%)接受了免疫治疗,1例患者(4%)未接受全身治疗即接受了手术切除。所有患者均尝试进行了切除,20例(83%)进行了胃切除术。R0切除率为95%。2例患者达到病理完全缓解,另外5例患者存活肿瘤≤1%。3例患者出现手术并发症[1例患者为1级(4%),1例为3b级(4%),1例为4a级(4%)];90天内无患者死亡。中位随访时间为28个月,中位OS未达到。1年和3年OS率分别为96%和85%。
短程CRT可安全地作为潜在可切除的胃或胃食管腺癌患者计划TNT的一部分使用。治疗完成率、病理缓解率和OS率令人鼓舞,支持对胃癌TNT进行进一步研究。