Objective
To determine the pathologic findings and clinical outcome of patients with pure embryonal
carcinoma (EC) of the testis who were diagnosed with testis cancer from January 1989
to January 2013 who underwent an orchiectomy, cisplatin-based chemotherapy and a postchemotherapy
retroperitoneal lymph node dissection (PC-RPLND).
Methods
We compared those patients with 100% EC with those with mixed nonseminomatous germ
cell tumor pathology who underwent a PC-RPLND.
Results
Of 1105 patients who underwent a PC-RPLND, 145 had pure EC. Twenty-six percent of
patients presented with metastatic disease outside the retroperitoneum. Patients with
mixed histologies tended to have worse International Germ Cell Cancer Collaborative
Group risk compared to those with EC at orchiectomy (P = .037). Histology at PC-RPLND revealed fibrosis or necrosis in 76%, mature teratoma
in 19% and viable cancer in 4%. Over one-third of the patients had a residual mass
of <1 cm prior to RPLND; of whom 15% harbored mature teratoma in PC-RPLND histology.
The Kaplan–Meier estimated probability of recurrence at 5 years of follow-up was 3.1%
(95% CI 1.2%, 8.0%) for EC histology, 7.3% lower than mixed histology. For cancer-specific
mortality, the Kaplan–Meier estimated probability at 5 years was 4.6% (95% CI 3.3%,
6.3%) and 1.7% (95% CI 0.4%, 6.8%) for mixed and pure EC histologies, respectively.
Conclusion
Approximately 20% of patients with pure EC had teratoma at PC-RPLND. We have shown
that those with a maximum node size of <1 cm should not be precluded from RPLND.
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Article info
Publication history
Published online: February 02, 2018
Accepted:
January 10,
2018
Received:
November 14,
2017
Footnotes
Financial Disclosure: The authors declare that they have no relevant financial interests.
Funding Support: This work was supported by: National Cancer Institute [P50-CA92629 and P30-CA008748], the Sidney Kimmel Center for Prostate and Urologic Cancers, and David H. Koch through the Prostate Cancer Foundation, the Richard Capri Foundation.
Identification
Copyright
© 2018 Elsevier Inc. All rights reserved.