Nationwide Patterns of Care for Stage II Nonseminomatous Germ Cell Tumor of the Testicle

被引:13
作者
Ghandour, Rashed [1 ]
Ashbrook, Caleb [1 ]
Freifeld, Yuval [1 ]
Singla, Nirmish [1 ]
El-Asmar, Jose M. [2 ]
Lotan, Yair [1 ]
Margulis, Vitaly [1 ]
Eggener, Scott [3 ]
Woldu, Solomon [1 ]
Bagrodia, Aditya [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Urol, 2001 Inwood Rd,West Campus Bldg 3,Floor 4, Dallas, TX 75390 USA
[2] Amer Univ Beirut, Dept Surg, Div Urol, Med Ctr, Beirut, Lebanon
[3] Univ Chicago, Dept Surg, Sect Urol, 5841 S Maryland Ave, Chicago, IL 60637 USA
来源
EUROPEAN UROLOGY ONCOLOGY | 2020年 / 3卷 / 02期
关键词
Nonseminomatous germ cell tumors; Retroperitoneal disease; Stage II; Chemotherapy; Retroperitoneal lymph node dissection; Testis cancer; Testicular cancer; LYMPH-NODE DISSECTION; PROSPECTIVE MULTICENTER TRIAL; PRIMARY CHEMOTHERAPY; CANCER; MANAGEMENT; CISPLATIN; SURVIVAL; MEN;
D O I
10.1016/j.euo.2019.06.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Management strategies for advanced testicular cancer published from a few, high-volume clinical centers may not be generalizable. Objective: To discern treatment patterns for stage II nonseminomatous germ cell tumor (NSGCT) in a nationwide cancer registry. Design, setting, and participants: The National Cancer Database was queried for patients with a stage II NSGCT from 2004 to 2014. Patients were stratified by clinical nodal status: cN1/stage IIA, cN2/stage IIB, and cN3/stage IIIC. Outcomes measurements and statistical analysis: Logistic regression was performed to determine factors independently associated with primary retroperitoneal lymph node dissection (RPLND), primary chemotherapy, and postchemotherapy RPLND (PC-RPLND). Results and limitations: A total of 2203 patients (stages IIA, n = 1060; IIB, n = 869; and IIC, n = 274) met the inclusion criteria. Overall, 83% of patients underwent primary chemotherapy, while 17% underwent primary RPLND. Stratified by stage, use of primary chemotherapy was 78%, 88%, and 86% for stages IIA, IIB, and IIC, respectively. Overall, 24% of patients underwent PC-RPLND. Factors independently associated with a lower likelihood of undergoing primary RPLND were a more recent diagnosis and a higher clinical nodal stage. Conversely, patients treated at high-volume facilities were more likely to receive primary RPLND. Factors associatedwith ahigherlikelihood of undergoing PC-RPLND includedahigher clinical nodal stage, treatment at a high-volume center, and a greater distance of patient travel. Associations based on serum tumor markers could not be assessed. Conclusions: For clinical stage II NSGCT, nationwide utilization of primary chemotherapy is increasing compared with RPLND and is the preferred therapy for more advanced nodal disease. Primary RPLND may be underutilized in stage IIA disease. Utilization of PC-RPLND is driven by nodal stage as well as accessibility of a high-volume center. Patient summary: The use of primary retroperitoneal lymph node dissection (RPLND) in early nodal disease is declining, while upfront chemotherapy is increasingly utilized. Primary RPLND may identify patients who are actually pN0 and would not benefit from systemic chemotherapy. Primary RPLND and postchemotherapy RPLND are performed more frequently at centers of excellence. (C) 2019 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:198 / 206
页数:9
相关论文
共 34 条
  • [1] PROGNOSTIC FACTORS IN UNSELECTED PATIENTS WITH NONSEMINOMATOUS METASTATIC TESTICULAR CANCER - A MULTICENTER EXPERIENCE
    AASS, N
    KLEPP, O
    CAVALLINSTAHL, E
    DAHL, O
    WICKLUND, H
    UNSGAARD, B
    BALDETORP, L
    AHLSTROM, S
    FOSSA, SD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (05) : 818 - 826
  • [2] Cancer-Specific Outcomes Among Young Adults Without Health Insurance
    Aizer, Ayal A.
    Falit, Benjamin
    Mendu, Mallika L.
    Chen, Ming-Hui
    Choueiri, Toni K.
    Hoffman, Karen E.
    Hu, Jim C.
    Martin, Neil E.
    Quoc-Dien Trinh
    Alexander, Brian M.
    Nguyen, Paul L.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (19) : 2025 - U62
  • [3] Prediction of necrosis after chemotherapy of advanced germ cell tumors: Results of a prospective multicenter trial of the German Testicular Cancer Study Group
    Albers, P
    Weissbach, L
    Krege, S
    Kliesch, S
    Hartmann, M
    Heidenreich, A
    Walz, P
    Kuczyk, M
    Fimmers, R
    [J]. JOURNAL OF UROLOGY, 2004, 171 (05) : 1835 - 1838
  • [4] [Anonymous], [No title captured]
  • [5] [Anonymous], [No title captured]
  • [6] [Anonymous], [No title captured]
  • [7] Long-term toxicity of cisplatin in germ-cell tumor survivors
    Chovanec, M.
    Abu Zaid, M.
    Hanna, N.
    El-Kouri, N.
    Einhorn, L. H.
    Albany, C.
    [J]. ANNALS OF ONCOLOGY, 2017, 28 (11) : 2670 - 2679
  • [8] Cohen RA., 2017, HLTH INSURANCE COVER
  • [9] Evaluation of primary standard cisplatin-based chemotherapy for clinical stage II non-seminomatous germ cell tumours of the testis
    Culine, S
    Theodore, C
    Court, BH
    Perrin, JL
    Droz, JP
    [J]. BRITISH JOURNAL OF UROLOGY, 1997, 79 (02): : 258 - 262
  • [10] CLINICAL STAGE-B NONSEMINOMATOUS GERM-CELL TESTIS CANCER - THE INDIANA-UNIVERSITY EXPERIENCE (1965-1989) USING ROUTINE PRIMARY RETROPERITONEAL LYMPH-NODE DISSECTION
    DONOHUE, JP
    THORNHILL, JA
    FOSTER, RS
    ROWLAND, RG
    BIHRLE, R
    [J]. EUROPEAN JOURNAL OF CANCER, 1995, 31A (10) : 1599 - 1604