Modified retroperitoneal lymph node dissection for post‐chemotherapy residual tumour: a long‐term update

Objective To update previously reported outcomes of modified‐template post‐chemotherapy retroperitoneal lymph node dissection (PC‐RPLND) in appropriately selected patients with metastatic non‐seminomatous germ cell tumour (NSGCT), as our previous report was criticised for short follow‐up and so we n...

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Published inBJU international Vol. 120; no. 1; pp. 104 - 108
Main Authors Cho, Jane S., Kaimakliotis, Hristos Z., Cary, Clint, Masterson, Timothy A., Beck, Stephen, Foster, Richard
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.07.2017
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ISSN1464-4096
1464-410X
1464-410X
DOI10.1111/bju.13844

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Abstract Objective To update previously reported outcomes of modified‐template post‐chemotherapy retroperitoneal lymph node dissection (PC‐RPLND) in appropriately selected patients with metastatic non‐seminomatous germ cell tumour (NSGCT), as our previous report was criticised for short follow‐up and so we now provide a long‐term update on this cohort. Patients and Methods In all, 100 patients with normal serum markers after cisplatin‐based chemotherapy and residual retroperitoneal tumour underwent modified PC‐RPLND between 1991 and 2004. Using a prospectively managed institutional testicular cancer database, long‐term follow‐up was obtained. Results As previously reported, 43 patients underwent a right‐modified template, 18 patients underwent a full‐left‐modified template, and 39 patients underwent a left‐modified template. The updated long‐term median follow‐up for the entire cohort is 125 months. Seven patients developed recurrent disease with a median (range) time to recurrence of 11 (6–102) months, and one patient died from recurrent disease in the chest 4 years after surgery. All recurrences were outside the boundaries of a full‐bilateral template RPLND, with the most common location of recurrence being the chest. The 5‐ and 10‐year recurrence‐free survival rates were 93% and 92%, respectively. The overall survival at 10 years was 99%. Conclusions In appropriately selected patients with low‐volume disease before and after chemotherapy, a modified template has durable long‐term efficacy without risk of in‐field recurrences at a median follow‐up of 125 months.
AbstractList To update previously reported outcomes of modified-template post-chemotherapy retroperitoneal lymph node dissection (PC-RPLND) in appropriately selected patients with metastatic non-seminomatous germ cell tumour (NSGCT), as our previous report was criticised for short follow-up and so we now provide a long-term update on this cohort. In all, 100 patients with normal serum markers after cisplatin-based chemotherapy and residual retroperitoneal tumour underwent modified PC-RPLND between 1991 and 2004. Using a prospectively managed institutional testicular cancer database, long-term follow-up was obtained. As previously reported, 43 patients underwent a right-modified template, 18 patients underwent a full-left-modified template, and 39 patients underwent a left-modified template. The updated long-term median follow-up for the entire cohort is 125 months. Seven patients developed recurrent disease with a median (range) time to recurrence of 11 (6-102) months, and one patient died from recurrent disease in the chest 4 years after surgery. All recurrences were outside the boundaries of a full-bilateral template RPLND, with the most common location of recurrence being the chest. The 5- and 10-year recurrence-free survival rates were 93% and 92%, respectively. The overall survival at 10 years was 99%. In appropriately selected patients with low-volume disease before and after chemotherapy, a modified template has durable long-term efficacy without risk of in-field recurrences at a median follow-up of 125 months.
Objective To update previously reported outcomes of modified-template post-chemotherapy retroperitoneal lymph node dissection (PC-RPLND) in appropriately selected patients with metastatic non-seminomatous germ cell tumour (NSGCT), as our previous report was criticised for short follow-up and so we now provide a long-term update on this cohort. Patients and Methods In all, 100 patients with normal serum markers after cisplatin-based chemotherapy and residual retroperitoneal tumour underwent modified PC-RPLND between 1991 and 2004. Using a prospectively managed institutional testicular cancer database, long-term follow-up was obtained. Results As previously reported, 43 patients underwent a right-modified template, 18 patients underwent a full-left-modified template, and 39 patients underwent a left-modified template. The updated long-term median follow-up for the entire cohort is 125 months. Seven patients developed recurrent disease with a median (range) time to recurrence of 11 (6-102) months, and one patient died from recurrent disease in the chest 4 years after surgery. All recurrences were outside the boundaries of a full-bilateral template RPLND, with the most common location of recurrence being the chest. The 5- and 10-year recurrence-free survival rates were 93% and 92%, respectively. The overall survival at 10 years was 99%. Conclusions In appropriately selected patients with low-volume disease before and after chemotherapy, a modified template has durable long-term efficacy without risk of in-field recurrences at a median follow-up of 125 months.
To update previously reported outcomes of modified-template post-chemotherapy retroperitoneal lymph node dissection (PC-RPLND) in appropriately selected patients with metastatic non-seminomatous germ cell tumour (NSGCT), as our previous report was criticised for short follow-up and so we now provide a long-term update on this cohort.OBJECTIVETo update previously reported outcomes of modified-template post-chemotherapy retroperitoneal lymph node dissection (PC-RPLND) in appropriately selected patients with metastatic non-seminomatous germ cell tumour (NSGCT), as our previous report was criticised for short follow-up and so we now provide a long-term update on this cohort.In all, 100 patients with normal serum markers after cisplatin-based chemotherapy and residual retroperitoneal tumour underwent modified PC-RPLND between 1991 and 2004. Using a prospectively managed institutional testicular cancer database, long-term follow-up was obtained.PATIENTS AND METHODSIn all, 100 patients with normal serum markers after cisplatin-based chemotherapy and residual retroperitoneal tumour underwent modified PC-RPLND between 1991 and 2004. Using a prospectively managed institutional testicular cancer database, long-term follow-up was obtained.As previously reported, 43 patients underwent a right-modified template, 18 patients underwent a full-left-modified template, and 39 patients underwent a left-modified template. The updated long-term median follow-up for the entire cohort is 125 months. Seven patients developed recurrent disease with a median (range) time to recurrence of 11 (6-102) months, and one patient died from recurrent disease in the chest 4 years after surgery. All recurrences were outside the boundaries of a full-bilateral template RPLND, with the most common location of recurrence being the chest. The 5- and 10-year recurrence-free survival rates were 93% and 92%, respectively. The overall survival at 10 years was 99%.RESULTSAs previously reported, 43 patients underwent a right-modified template, 18 patients underwent a full-left-modified template, and 39 patients underwent a left-modified template. The updated long-term median follow-up for the entire cohort is 125 months. Seven patients developed recurrent disease with a median (range) time to recurrence of 11 (6-102) months, and one patient died from recurrent disease in the chest 4 years after surgery. All recurrences were outside the boundaries of a full-bilateral template RPLND, with the most common location of recurrence being the chest. The 5- and 10-year recurrence-free survival rates were 93% and 92%, respectively. The overall survival at 10 years was 99%.In appropriately selected patients with low-volume disease before and after chemotherapy, a modified template has durable long-term efficacy without risk of in-field recurrences at a median follow-up of 125 months.CONCLUSIONSIn appropriately selected patients with low-volume disease before and after chemotherapy, a modified template has durable long-term efficacy without risk of in-field recurrences at a median follow-up of 125 months.
Objective To update previously reported outcomes of modified‐template post‐chemotherapy retroperitoneal lymph node dissection (PC‐RPLND) in appropriately selected patients with metastatic non‐seminomatous germ cell tumour (NSGCT), as our previous report was criticised for short follow‐up and so we now provide a long‐term update on this cohort. Patients and Methods In all, 100 patients with normal serum markers after cisplatin‐based chemotherapy and residual retroperitoneal tumour underwent modified PC‐RPLND between 1991 and 2004. Using a prospectively managed institutional testicular cancer database, long‐term follow‐up was obtained. Results As previously reported, 43 patients underwent a right‐modified template, 18 patients underwent a full‐left‐modified template, and 39 patients underwent a left‐modified template. The updated long‐term median follow‐up for the entire cohort is 125 months. Seven patients developed recurrent disease with a median (range) time to recurrence of 11 (6–102) months, and one patient died from recurrent disease in the chest 4 years after surgery. All recurrences were outside the boundaries of a full‐bilateral template RPLND, with the most common location of recurrence being the chest. The 5‐ and 10‐year recurrence‐free survival rates were 93% and 92%, respectively. The overall survival at 10 years was 99%. Conclusions In appropriately selected patients with low‐volume disease before and after chemotherapy, a modified template has durable long‐term efficacy without risk of in‐field recurrences at a median follow‐up of 125 months.
Author Kaimakliotis, Hristos Z.
Cho, Jane S.
Masterson, Timothy A.
Beck, Stephen
Cary, Clint
Foster, Richard
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Keywords testes cancer
modified template
retroperitoneal lymph node dissection
post-chemotherapy
Language English
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Snippet Objective To update previously reported outcomes of modified‐template post‐chemotherapy retroperitoneal lymph node dissection (PC‐RPLND) in appropriately...
To update previously reported outcomes of modified-template post-chemotherapy retroperitoneal lymph node dissection (PC-RPLND) in appropriately selected...
Objective To update previously reported outcomes of modified-template post-chemotherapy retroperitoneal lymph node dissection (PC-RPLND) in appropriately...
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StartPage 104
SubjectTerms Adult
Antineoplastic Combined Chemotherapy Protocols
Biopsy
Cancer
Chemotherapy
Chest
Cisplatin
Female
Follow-Up Studies
Humans
Lymph
Lymph Node Excision
Lymph nodes
Lymphatic system
Male
Metastases
modified template
Neoplasm, Residual - mortality
Neoplasm, Residual - pathology
Neoplasms, Germ Cell and Embryonal - mortality
Neoplasms, Germ Cell and Embryonal - pathology
Neoplasms, Germ Cell and Embryonal - therapy
post‐chemotherapy
retroperitoneal lymph node dissection
Retroperitoneal Neoplasms - mortality
Retroperitoneal Neoplasms - pathology
Retroperitoneal Neoplasms - therapy
Retroperitoneal Space - pathology
Retrospective Studies
Surgery
Survival
testes cancer
Testicular cancer
Testicular Neoplasms - mortality
Testicular Neoplasms - pathology
Testicular Neoplasms - therapy
Treatment Outcome
Tumors
Young Adult
Title Modified retroperitoneal lymph node dissection for post‐chemotherapy residual tumour: a long‐term update
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fbju.13844
https://www.ncbi.nlm.nih.gov/pubmed/28296054
https://www.proquest.com/docview/1910162010
https://www.proquest.com/docview/1877856498
Volume 120
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