Objective
To evaluate the oncologic outcomes and histologic concordance of postchemotherapy
residual liver mass resection with postchemotherapy retroperitoneal lymph node dissection
(PC-RPLND).
Methods
Retrospective review of our prospectively maintained germ cell tumor (GCT) surgical
database identified patients with nonseminomatous GCT who underwent both postchemotherapy
residual liver mass resection and PC-RPLND between 1990 and 2015.
Results
A total of 36 patients were identified, of whom 29 (81%) presented with a liver mass
at initial diagnosis and 17 (47%) received second-line chemotherapy before liver resection.
Teratoma was found in 8 (22%) and 5 (14%) of PC-RPLND and liver resection specimens,
respectively. Viable GCT was found in 5 (14%) and 4 (11%) of PC-RPLND and liver resection
specimens, respectively. Histologic discordance was observed in 4 of 19 patients (21%;
95% confidence interval [CI] 6.1%-46%); in all cases, liver resection specimens contained
teratoma or viable GCT while PC-RPLND revealed only fibrosis or necrosis. At 3 years
after surgical intervention, the Kaplan-Meier estimated probability of cancer-specific
survival was 75% (95% CI 55%-85%) and the probability of progression-free survival
was 75% (95% CI 56%-87%).
Conclusion
In this contemporary cohort, clinically significant discordance was observed between
the histology of metastatic liver masses and that of retroperitoneal lymph nodes.
The benefit of postchemotherapy liver mass resection for patients with advanced nonseminomatous
GCT is supported by favorable survival outcomes. Until more reliable predictors of
postchemotherapy histology exist, complete surgical resection of all sites of residual
disease should be performed whenever feasible.
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References
- Clinical outcome following post-chemotherapy retroperitoneal lymph node dissection in men with intermediate- and poor-risk nonseminomatous germ cell tumour.BJU Int. 2007; 99: 993-997
- The management of subcentimeter residual mass in NSGCT: pcRPLND vs. observation.Urol Oncol. 2011; 29: 842-847
- The role of lymphadenectomy for testicular cancer: indications, controversies, and complications.Urol Clin North Am. 2011; 38 (vi): 439-449
- Pathologic findings and clinical outcome of patients undergoing retroperitoneal lymph node dissection after multiple chemotherapy regimens for metastatic testicular germ cell tumors.Cancer. 2007; 109: 528-535
- Retroperitoneal lymph node dissection after chemotherapy.BJU Int. 2009; 104: 1404-1412
- Viable malignant cells after primary chemotherapy for disseminated nonseminomatous germ cell tumors: prognostic factors and role of postsurgery chemotherapy—results from an international study group.J Clin Oncol. 2001; 19: 2647-2657
- Outcomes in patients with clinical stage III NSGCT who achieve complete clinical response to chemotherapy at extraretroperitoneal disease site.Urology. 2012; 79: 1079-1084
- The total number of retroperitoneal lymph nodes resected impacts clinical outcome after chemotherapy for metastatic testicular cancer.Urology. 2010; 75: 1431-1435
- Long-term clinical outcome after postchemotherapy retroperitoneal lymph node dissection in men with residual teratoma.J Clin Oncol. 2007; 25: 1033-1037
- Prediction of residual retroperitoneal mass histology after chemotherapy for metastatic nonseminomatous germ cell tumor: multivariate analysis of individual patient data from six study groups.J Clin Oncol. 1995; 13: 1177-1187
- Clinical impact of residual extraretroperitoneal masses in patients with advanced nonseminomatous germ cell testicular cancer.Urology. 2012; 79: 156-159
- Management of post-chemotherapy extra-retroperitoneal residual masses.World J Urol. 2009; 27: 489-492
- Comparison of histological results from the resection of residual masses at different sites after chemotherapy for metastatic non-seminomatous germ cell tumours.Eur J Cancer. 1997; 33: 843-847
- International Germ Cell Consensus Classification: a prognostic factor-based staging system for metastatic germ cell cancers.J Clin Oncol. 1997; 15: 594-603
- Is retroperitoneal histology predictive of liver histology at concurrent post-chemotherapy retroperitoneal lymph node dissection and hepatic resection?.J Urol. 2010; 184: 949-953
- Surgical therapy for testicular cancer metastatic to the liver.HPB (Oxford). 2007; 9: 199-200
- Hepatic metastasectomy for testicular germ cell tumors: is it worth it?.J Gastrointest Surg. 2009; 13: 595-601
- Role of postchemotherapy surgery in the management of patients with liver metastases from germ cell tumors.Ann Surg. 2005; 242: 260-266
- Multimodality treatment of patients with liver metastases from germ cell tumors: the role of surgery.Cancer. 2001; 92: 578-587
- Residual masses after chemotherapy for metastatic testicular cancer: the clinical implications of the association between retroperitoneal and pulmonary histology. Re-analysis of Histology in Testicular Cancer (ReHiT) Study Group.J Urol. 1997; 158: 474-478
- Clinical outcome and predictors of survival in late relapse of germ cell tumor.J Clin Oncol. 2008; 26: 5524-5529
- Risks of the uncontrolled retroperitoneum.Ann Surg Oncol. 2003; 10: 100-101
Article info
Publication history
Published online: April 25, 2018
Accepted:
April 10,
2018
Received:
January 19,
2018
Footnotes
Financial Disclosure: The authors declare that they have no relevant financial interests.
Identification
Copyright
© 2018 Elsevier Inc. All rights reserved.