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40 岁及以上复发转移性生殖细胞肿瘤患者接受大剂量化疗和外周血造血干细胞移植的生存结局和毒性。

Survival outcomes and toxicity in patients 40 years old or older with relapsed metastatic germ cell tumors treated with high-dose chemotherapy and peripheral blood stem cell transplantation.

机构信息

Division of Hematology-Oncology, Indiana University Simon Comprehensive Cancer Center, Indianapolis, Indiana.

Department of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana.

出版信息

Cancer. 2021 Oct 15;127(20):3751-3760. doi: 10.1002/cncr.33771. Epub 2021 Jul 14.

Abstract

BACKGROUND

High-dose chemotherapy (HDCT) plus peripheral blood stem cell transplantation (PBSCT) is effective salvage therapy for relapsed metastatic germ cell tumors (GCTs) but has potential toxicity. Historically, an age of ≥40 years has been associated with greater toxicity and worse outcomes.

METHODS

This is a retrospective analysis of 445 consecutive patients with relapsed GCT treated with HDCT and PBSCT with tandem cycles at Indiana University from between 2004-2017 per our institutional regimen. Kaplan-Meier methods and log-rank tests were used for progression-free survival (PFS) and overall survival (OS) analysis.

RESULTS

A total of 329 patients were <40 years of age, whereas 116 patients were ≥40 years of age; HDCT was used as second-line therapy in 85% and 79%, respectively. Median follow-up time was 42.5 months (range, 0.3-173.4 months). Grade ≥3 toxicities were similar between either group, except for greater pulmonary (P = .02) and renal toxicity (P = .01) in the ≥40-years-of-age group. Treatment-related mortality was similar between both age groups: 10 patients (3%) in the <40-years-of-age group and 4 patients (3.5%) in ≥40-years-of-age group died from complications of HDCT. Two-year PFS for <40 years of age versus ≥40 years of age was 58.7% versus 59.6% (P = .76) and 2-year OS was 63.9% versus 61.5% (P = .93). Factors predicting worse PFS included Eastern Cooperative Oncology Group performance status ≥1, platinum refractory disease, nonseminoma histology, and not completing 2 cycles of HDCT. Age was not an independent predictor of worse outcomes.

CONCLUSIONS

HDCT plus PBSCT is effective salvage therapy in patients ≥40 years of age with relapsed metastatic GCT. Patients ≥40 years of age experience similar rates of toxicity and treatment-related mortality as those <40 years of age.

摘要

背景

高剂量化疗(HDCT)加外周血干细胞移植(PBSCT)是治疗复发性转移性生殖细胞瘤(GCT)的有效挽救疗法,但具有潜在毒性。从历史上看,年龄≥40 岁与更大的毒性和更差的结果相关。

方法

这是印第安纳大学 2004-2017 年期间按照机构方案用 HDCT 和 PBSCT 进行串联周期治疗的 445 例复发性 GCT 连续患者的回顾性分析。使用 Kaplan-Meier 方法和对数秩检验进行无进展生存(PFS)和总生存(OS)分析。

结果

共有 329 名患者年龄<40 岁,116 名患者年龄≥40 岁;HDCT 分别作为二线治疗在 85%和 79%的患者中使用。中位随访时间为 42.5 个月(范围,0.3-173.4 个月)。两组之间的≥3 级毒性相似,但≥40 岁组的肺部毒性(P=0.02)和肾脏毒性(P=0.01)更高。两组的治疗相关死亡率相似:<40 岁组有 10 例(3%)患者和≥40 岁组有 4 例(3.5%)患者死于 HDCT 并发症。<40 岁组与≥40 岁组的 2 年 PFS 分别为 58.7%和 59.6%(P=0.76),2 年 OS 分别为 63.9%和 61.5%(P=0.93)。预测 PFS 较差的因素包括东部肿瘤协作组表现状态≥1、铂耐药疾病、非精原细胞瘤组织学和未完成 2 个周期的 HDCT。年龄不是预后不良的独立预测因素。

结论

HDCT 加 PBSCT 是治疗复发性转移性 GCT 患者≥40 岁的有效挽救疗法。年龄≥40 岁的患者与<40 岁的患者具有相似的毒性和治疗相关死亡率发生率。

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