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

Chemotherapy Nonseminomatous germ cell tumors Retroperitoneal disease Retroperitoneal lymph node dissection Stage II Testicular cancer Testis cancer

Journal

European urology oncology
ISSN: 2588-9311
Titre abrégé: Eur Urol Oncol
Pays: Netherlands
ID NLM: 101724904

Informations de publication

Date de publication:
04 2020
Historique:
received: 11 04 2019
revised: 20 05 2019
accepted: 11 06 2019
pubmed: 6 7 2019
medline: 15 12 2020
entrez: 6 7 2019
Statut: ppublish

Résumé

Management strategies for advanced testicular cancer published from a few, high-volume clinical centers may not be generalizable. To discern treatment patterns for stage II nonseminomatous germ cell tumor (NSGCT) in a nationwide cancer registry. 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. Logistic regression was performed to determine factors independently associated with primary retroperitoneal lymph node dissection (RPLND), primary chemotherapy, and postchemotherapy RPLND (PC-RPLND). 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 associated with a higher likelihood of undergoing PC-RPLND included a higher 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. 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. 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.

Sections du résumé

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 associated with a higher likelihood of undergoing PC-RPLND included a higher 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.

Identifiants

pubmed: 31272940
pii: S2588-9311(19)30082-3
doi: 10.1016/j.euo.2019.06.007
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

198-206

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Rashed Ghandour (R)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Caleb Ashbrook (C)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Yuval Freifeld (Y)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Nirmish Singla (N)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Jose M El-Asmar (JM)

Division of Urology, Department of Surgery, American University of Beirut Medical Center, Beirut, Lebanon.

Yair Lotan (Y)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Vitaly Margulis (V)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Scott Eggener (S)

Section of Urology, Department of Surgery, University of Chicago, Chicago, IL, USA.

Solomon Woldu (S)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Aditya Bagrodia (A)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Electronic address: aditya.bagrodia@utsouthwestern.edu.

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