不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Prognostic and Treatment Values of Baseline Metabolic Tumor Volume in Early-stage Extranodal NK/T-cell Lymphoma in the Modern Treatment Era.
Prognostic and Treatment Values of Baseline Metabolic Tumor Volume in Early-stage Extranodal NK/T-cell Lymphoma in the Modern Treatment Era.
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MTV 是一个独立的代谢生存预测因子,可能识别出在早期 ENKTCL 中更可能从 CMT 获益的患者。需要进一步前瞻性验证。
探讨最大标准化摄取值(SUVmax)和代谢肿瘤体积(MTV)在早期结外鼻型自然杀伤/T细胞淋巴瘤(ENKTCL)中的预后和治疗价值。
测量了122例早期ENKTCL患者原发肿瘤的MTV和SUVmax。评估了MTV和SUVmax的预后能力及其对治疗选择的指导意义。通过对16例患者肿瘤的转录组分析,探讨了MTV和SUVmax的潜在机制。
高SUVmax或大MTV的患者更可能具有不良临床因素。单因素分析中,SUVmax和MTV均与总生存期(OS)相关(分别为P = 0.029和0.001)。MTV与OS独立相关(P = 0.027),中介分析提示远处转移在统计学上解释了这一关联的98.2%。在中危和高危早期亚组中,MTV < 50 mL的患者OS和无进展生存期(PFS)显著优于MTV ≥ 50 mL的患者(两者P = 0.002),但生存结局与低危早期患者相当。此外,在MTV < 50 mL的患者中,放疗和综合治疗(CMT)产生了相当的PFS(P = 0.268)和OS(P = 0.570)。相反,对于MTV ≥ 50 mL的患者,与单纯RT相比,CMT带来了更好的PFS和OS(两者P < 0.001)。
To investigate the prognostic and treatment values of maximum standardized uptake value (SUVmax) and metabolic tumor volume (MTV) in early-stage extranodal nasal-type natural killer/T-cell lymphoma (ENKTCL).
MTV and SUVmax of the primary tumor in 122 patients with early-stage ENKTCL were measured. The prognostic capacity of MTV and SUVmax and their implications for treatment selection were evaluated. Potential mechanisms of MTV and SUVmax were evaluated through transcriptome analysis of tumors in 16 patients.
Patients with high-SUVmax or large-MTV were more likely to have adverse clinical factors. Both SUVmax and MTV were associated with overall survival (OS) in univariate analysis (P = 0.029 and 0.001, respectively). MTV was independently associated with OS (P = 0.027), and mediation analysis suggested that distant metastasis statistically accounted for 98.2% of this association. In the intermediate- and high-risk early-stage subgroup, patients with MTV < 50 mL had significantly better OS and progression-free survival (PFS) (both P = 0.002) than those with MTV ≥ 50 mL, but showed survival outcomes comparable to low-risk early-stage patients. Furthermore, radiotherapy and combined-modality therapy (CMT) yielded comparable PFS (P = 0.268) and OS (P = 0.570) in patients with MTV < 50 mL. In contrast, for patients with MTV ≥ 50 mL, CMT resulted in better PFS and OS (both P < 0.001) compared to RT alone.
MTV is an independent metabolic predictor of survival and may identify patients who are more likely to benefit from CMT in early-stage ENKTCL. Further prospective validation is warranted.
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