CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Treatment of Non-Hodgkin Lymphoma Involving Head and Neck Sites with a 1.5 T MR-Linac: Preliminary Results from a Prospective Observational Study.
Treatment of Non-Hodgkin Lymphoma Involving Head and Neck Sites with a 1.5 T MR-Linac: Preliminary Results from a Prospective Observational Study.
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淋巴瘤通常对放疗敏感,因此治疗期间病灶体积往往缩小。MRI直线加速器具有优异软组织分辨能力,并可每日重新勾画大体肿瘤体积和临床靶体积,因此可能有益于淋巴瘤治疗;但目前关于MR-linac用于该适应证的文献不足。
开展前瞻性观察研究,纳入接受Elekta Unity MR-linac治疗的头颈部非霍奇金淋巴瘤(NHL)患者,收集前8例患者的临床及剂量学数据并结合相关病历资料。
7例为B细胞淋巴瘤(弥漫性大B细胞淋巴瘤3例、MALT淋巴瘤2例、滤泡性淋巴瘤1例、套细胞淋巴瘤1例),1例为T细胞/NK细胞淋巴瘤。4例接受根治性放疗,3例接受挽救治疗,1例接受CAR-T 桥接治疗。2例病变累及眼眶,6例累及颈部淋巴结。大体肿瘤体积中位数为5.74 cc,临床靶体积为127.01 cc,计划靶体积为210.37 cc。7例处方剂量为24–50 Gy、每次2 Gy;1例为24 Gy、每次3 Gy。所有患者均发生急性毒性;放疗结束时5例最高为1级,3例为2级。放疗后1个月,7例仍有1级毒性,未报告2级毒性。所有患者首次影像学评估均在中位101.5天后完成,且均达到完全缓解。中位随访330天时,无患者发生局部进展,1例发生远处进展。
采用1.5 T MR-linac治疗头颈部NHL可行,毒性不超过2级,且缓解率和疾病控制效果良好。
Purpose : Lymphomas are generally radiosensitive; therefore, disease volume tends to shrink during radiotherapy courses. As MRI-linac provides excellent soft tissue definition and allows daily re-contouring of gross tumor volume and clinical target volume, its adoption could be beneficial for the treatment of lymphomas. Nonetheless, at this time there is a lack of literature regarding the use of MR-linac in this context. Methods : A prospective observational study was conducted on patients affected by non-Hodgkin lymphoma (NHL) involving head and neck (H&N) sites and treated with Elekta Unity MR-Linac. The clinical and dosimetric data of the first eight patients were collected and integrated with relevant data from medical records. Results : Seven patients had B-cell lymphoma (three DLBCL, two MALT, one follicular, and one mantle-cell) and one T-cell/NK lymphoma. The intent of RT was radical for four patients, salvage treatment for three, and CAR-T bridging for one.
Two patients presented orbital localizations and six cervical lymphonodal sites. Median GTV was 5. 74 cc, median CTV 127. 01 cc, and median PTV 210. 37 cc. The prescribed dose was 24-50 Gy in 2 Gy fractions for seven patients and 24 Gy in 3 Gy fractions for one patient. All the patients experienced acute toxicity, the maximum grade was G1 for five patients and G2 for three at the end of RT. One month after radiotherapy seven patients still experienced G1 toxicity, but no toxicity grade 2 was reported.
First radiological assessment was performed for all the patients after a median of 101. 5 days, reporting complete response in all the cases. After a median follow up of 330 days, no patient experienced local disease progression, while one patient developed distant progression. Conclusions : radiotherapy for NHL with H&N localization using a 1. 5 T MR-linac was feasible, with no >G2 toxicity and optimal response rate and disease control.
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