Literature DB >> 34504308

Testicular Germ-Cell Tumors with Spermatic Cord Involvement: A Retrospective International Multi-Institutional Experience.

Maria Del Carmen Rodriguez Pena1, Sofia Canete-Portillo1, Ali Amin2, Manju Aron3, Piergiuseppe Colombo4, Roni Cox5, Dilek Ertoy Baydar6, Ivan Gallegos7, Francesca Khani8, Květoslava Michalova9, Roberta Lucianò10, Hiroshi Miyamoto11, Adeboye O Osunkoya12, Maria Rosaria Raspollini13, Diego F Sánchez14, Federico Scarfo10, Jeffrey S So15, Debra L Zynger16, Shi Wei1, George J Netto1, Cristina Magi-Galluzzi17.   

Abstract

The 8th Edition of the American Joint Committee on Cancer (AJCC) Staging Manual designates discontinuous involvement of spermatic cord soft tissue by testicular germ cell tumors as a metastatic deposit. We conducted a retrospective international multi-institutional study to validate the current recommendations. Thirty-three (72%) nonseminomatous and 13 (28%) seminomatous testicular germ cell tumors were collected from 15 institutions in America, Europe, and Asia. Testicular tumor size ranged from 1.3 to 18.0 cm (mean: 6.1). Cases were classified as discontinuous involvement of spermatic cord soft tissue (n = 26), continuous cord involvement (n = 17), or cord lymphovascular invasion (n = 3). The mean follow-up was 39 months. Clinical stage for discontinuous involvement of spermatic cord soft-tissue patients was I (local disease) in 2/24 (8%), II (regional disease) in 6/24 (25%), and III (distant disease) in 16/24 (67%) cases; 16 (67%) patients presented with distant metastasis. Clinical stage for continuous cord involvement patients was I in 9/17 (53%), II in 4/17 (23%), and III in 4/17 (23%); 4 (23%) patients presented with distant metastasis. Disease progression was seen in 4 patients with discontinuous involvement of spermatic cord soft tissue and 5 with continuous cord-involvement (p = 0.699). When comparing discontinuous and continuous cord involvement, a significant difference was found in cord margin status (p = 0.044), spermatic cord tumor size (p = 0.016), lymph-node involvement (p = 0.037), distant metastasis (p = 0.010), individual clinical stage (p = 0.003), and nonadvanced vs. advanced disease (p = 0.003) at presentation. In multivariate analysis, after adjusting for age, histology, testicular tumor size, percent of embryonal carcinoma, lymphovascular invasion, and cord margin status, discontinuous involvement of spermatic cord soft tissue was significantly associated (p = 0.011) with advanced clinical stage at presentation. Our findings support the designation of metastatic disease for discontinuous involvement of spermatic cord soft tissue, as introduced by the 8th edition of the AJCC staging.
© 2021. The Author(s), under exclusive licence to United States & Canadian Academy of Pathology.

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Year:  2021        PMID: 34504308     DOI: 10.1038/s41379-021-00912-9

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  3 in total

Review 1.  Testicular Cancer: Diagnosis and Treatment.

Authors:  Drew C Baird; Garrett J Meyers; Jocelyn S Hu
Journal:  Am Fam Physician       Date:  2018-02-15       Impact factor: 3.292

2.  Compliance and outcome of patients with stage 1 non-seminomatous germ cell tumors (NSGCT) managed with surveillance programs in seven Canadian centres.

Authors:  D Scott Ernst; Penny Brasher; Peter M Venner; Piotr Czaykowski; Malcolm J Moore; Leonard Reyno; Eric Winquist; Roanne Segal; Desiree Hao
Journal:  Can J Urol       Date:  2005-04       Impact factor: 1.344

3.  Spermatic cord contamination in testicular cancer.

Authors:  T Nazeer; J Y Ro; K H Kee; A G Ayala
Journal:  Mod Pathol       Date:  1996-07       Impact factor: 7.842

  3 in total

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