Promising novel therapies for relapsed and refractory testicular germ cell tumors

被引:3
|
作者
Kozakova, Kristyna [1 ,2 ]
Mego, Michal [2 ,3 ,4 ]
Cheng, Liang [3 ,5 ,6 ]
Chovanec, Michal [2 ,3 ,4 ]
机构
[1] Natl Canc Inst, Dept Anesthesiol & Intens Care Med, Bratislava, Slovakia
[2] Comenius Univ, Fac Med, Dept Oncol 2, Bratislava, Slovakia
[3] Natl Canc Inst, Bratislava, Slovakia
[4] Indiana Univ, Simon Canc Ctr, Div Hematol Oncol, Indianapolis, IN 46204 USA
[5] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[6] Indiana Univ Sch Med, Dept Urol, Indianapolis, IN 46202 USA
关键词
Germ cell tumor; refractory germ cell tumor; cisplatin resistance; salvage treatment; high-dose chemotherapy; targeted therapy; epigenetics; HIGH-DOSE CHEMOTHERAPY; LYMPH-NODE DISSECTION; PHASE-II TRIAL; CISPLATIN-INDUCED OTOTOXICITY; IMMUNE-INFLAMMATION INDEX; INITIAL SALVAGE THERAPY; TERM-FOLLOW-UP; LONG-TERM; COMBINATION CHEMOTHERAPY; CARDIOVASCULAR TOXICITY;
D O I
10.1080/14737140.2021.1838279
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Germ cell tumors (GCTs) are the most common solid malignancies in young men. The overall cure rate of GCT patients in metastatic stage is excellent, however; patients with relapsed or refractory disease have poor prognosis. Attempts to treat refractory disease with novel effective treatment to improve prognosis have been historically dismal and the ability to predict prognosis and treatment response in GCTs did not sufficiently improve in the last three decades. Areas covered We performed a comprehensive literature search of PubMed/MEDLINE to identify original and review articles (years 1964-2020) reporting on current improvement salvage treatment in GCTs and novel treatment options including molecularly targeted therapy and epigenetic approach. Review articles were further searched for additional original articles. Expert opinion Despite multimodal treatment approaches the treatment of relapsed or platinum-refractory GCTs remains a challenge. High-dose chemotherapy (HDCT) regimens with autologous stem-cell transplant (ASCT) from peripheral blood showed promising results in larger retrospective studies. Promising results from in vitro studies raised high expectations in molecular targets. So far, the lacking efficacy in small and unselected trials do not shed a light on targeted therapy. Currently, wide inclusion of patients into clinical trials is highly advised.
引用
收藏
页码:53 / 69
页数:17
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