Publication

Recent developments in the management of germ cell tumors

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Last modified
  • 05/22/2025
Type of Material
Authors
    Pavlos Msaouel, The University of Texas M.D. Anderson Cancer CenterMehmet Asim Bilen, Emory UniversityMiao Zhang, The University of Texas M.D. Anderson Cancer CenterMatthew Campbell, The University of Texas M.D. Anderson Cancer CenterJennfier Wang, The University of Texas M.D. Anderson Cancer CenterShi-Ming Tu, The University of Texas M.D. Anderson Cancer Center
Language
  • English
Date
  • 2017-05-01
Publisher
  • Lippincott, Williams & Wilkins
Publication Version
Copyright Statement
  • © 2017 Wolters Kluwer Health, Inc. All rights reserved.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1040-8746
Volume
  • 29
Issue
  • 3
Start Page
  • 172
End Page
  • 178
Grant/Funding Information
  • Pavlos Msaouel is supported by the National Institutes of Health T32 CA009666 grant.
  • This work was supported in part by the National Institutes of Health through MD Anderson’s Cancer Center Support Grant CA016672 (used the Clinical Trials Support Resource)
Abstract
  • Purpose of review In the present review, we summarize the recent developments in the management of germ cell tumors (GCTs). Recent findings Treatment-related acute and late-onset toxicity remains a key challenge in the management of GCTs. Recent data show that patients with large retroperitoneal lymph node metastases are at increased risk of venous thromboembolism and may benefit from prophylactic anticoagulation. Predictive models have been developed to identify patients with residual retroperitoneal lymph node masses who are more likely to benefit from surgical resection. However, their clinical use remains hampered by relatively low accuracy. There are currently multiple conventional-dose chemotherapy (CDCT) options for salvage therapy in patients with refractory or recurrent disease. In addition, more efficacious high-dose chemotherapy (HDCT) regimens continue to be developed. The role of salvage CDCT versus HDCT is currently being prospectively investigated. Finally, intratumoral heterogeneity is a common finding in cancer and an obvious observation in GCTs. Despite intratumoral heterogeneity, recent studies on nonseminomatous GCT have identified distinct histological subgroups and a potentially lethal clinical phenotype. Importantly, comprehensive molecular profiling so far has not elucidated the biologic basis or the clinical underpinnings of intratumoral heterogeneity in GCTs. Summary Remaining challenges to be addressed include minimizing therapeutic toxicity and improving outcomes in patients with refractory/recurrent GCTs or malignant transformation of teratomas.
Author Notes
  • Corresponding Author: Shi-Ming Tu, MD, Department of Genitourinary Medical Oncology, Unit 1374, The University of Texas MD Anderson Cancer Center, 1155 Pressler St, Houston, TX 77030-3721, Fax: 713-745-1625, stu@mdanderson.org
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, Medicine and Surgery

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