原发性中枢神经系统淋巴瘤治疗失败的模式。

IF 1.6 4区 医学 Q4 ONCOLOGY
James R Janopaul-Naylor, Jimmy S Patel, Manali Rupji, David C Qian, Kimberly B Hoang, Neal S McCall, Ashley J Schlafstein, Madison L Shoaf, Shawn Kothari, Jeffrey J Olson, Hui-Kuo Shu, Jim Zhong, Stewart G Neill, Bree Eaton
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引用次数: 0

摘要

目的:PCNSL 的进展仍然是挽救性疗法面临的挑战,包括大量发病和死亡的风险。我们报告了首次肿瘤进展的模式,以提供改进的机会:这是一项机构回顾性研究,从 2002 年到 2021 年连续对 95 例病理确诊的 PCNSL 患者进行了研究,其中 29 例患者的病情出现进展。采用Kaplan-Meier法、log-rank检验和Cox比例危险模型来描述患者、肿瘤和治疗变量与LC、PFS和首次失败模式之间的关系:大多数患者年龄在65岁以下(62%),KPS>70(64%),CSF细胞学检查阴性(70%)。在70名接受磁共振成像检查的患者中,中位肿瘤体积为12.6毫升(范围:0.5至67.8毫升)。中位随访11个月后,1年生存率为48%,1年生存率为80%。在 29 位病情恶化的患者中,24% 仅为远处转移,17% 为远处和局部转移,59% 仅为局部转移。在MVA中,LC与年龄(HR:1.08/y,P=0.02)、KPS(HR:0.10,P=0.02)、完成>6个周期的HD-MTX(HR:0.10,P14毫升肿瘤(OR:5.06,P=0.08))相关,1年LC为83%(14毫升)。LC与WBRT(P=0.37)、利妥昔单抗(P=0.12)或尝试全切(P=0.72)无明显关联:我们的研究结果再次证明了全身和鞘内治疗对 PCNSL 局部控制的重要性。结论:我们的研究结果再次证明了全身治疗和鞘内治疗对局部控制 PCNSL 的重要性,但大块肿瘤有局部治疗失败的趋势,因此需要进一步研究局部治疗或加强全身治疗的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patterns of Treatment Failure in Primary Central Nervous System Lymphoma.

Objectives: Progression of PCNSL remains a challenge with salvage therapies, including the risk of substantial morbidity and mortality. We report patterns of first tumor progression to inform opportunities for improvement.

Methods: This is an institutional retrospective review from 2002 to 2021 of 95 consecutive patients with pathologically confirmed PCNSL, of whom 29 experienced progressive disease. Kaplan-Meier method, log-rank test, and Cox proportional hazard models are used to characterize associations of patient, tumor, and treatment variables with LC, PFS, and patterns of first failure.

Results: Most patients were below 65 years old (62%) with KPS >70 (64%) and negative CSF cytology (70%). In 70 patients with MRIs, the median tumor volume was 12.6 mL (range: 0.5 to 67.8 mL). After a median follow-up of 11 months, 1-year PFS was 48% and 1-year LC was 80%. Of the 29 patients with progression, 24% were distant only, 17% were distant and local, and 59% were local only. On MVA, LC was associated with age (HR: 1.08/y, P =0.02), KPS (HR: 0.10, P =0.02), completion of >6 cycles of HD-MTX (HR: 0.10, P <0.01), and use of intrathecal chemotherapy (HR: 0.03, P <0.01). On UVA, local only first failure trended to be increased with >14 mL tumors (OR: 5.06, P =0.08) with 1-year LC 83% (<14 mL) versus 64% (>14mL). There were no significant associations with LC and WBRT ( P =0.37), Rituximab ( P =0.12), or attempted gross total resection ( P =0.72).

Conclusions: Our findings reaffirm the importance of systemic and intrathecal therapies for local control in PCNSL. However, bulky tumors trend to fail locally, warranting further investigation about the role of local therapies or systemic therapy intensification.

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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
130
审稿时长
4-8 weeks
期刊介绍: ​​​​​​​American Journal of Clinical Oncology is a multidisciplinary journal for cancer surgeons, radiation oncologists, medical oncologists, GYN oncologists, and pediatric oncologists. The emphasis of AJCO is on combined modality multidisciplinary loco-regional management of cancer. The journal also gives emphasis to translational research, outcome studies, and cost utility analyses, and includes opinion pieces and review articles. The editorial board includes a large number of distinguished surgeons, radiation oncologists, medical oncologists, GYN oncologists, pediatric oncologists, and others who are internationally recognized for expertise in their fields.
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