BACKGROUND: Resection of the inferior vena cava (IVC) is occasionally performed for patients with advanced malignancy in the retroperitoneum.
In the current study, we assessed the oncological effectiveness of IVC resection combined with tumor resection. We also addressed peri- and postoperative complications associated with resection and reconstruction of the IVC.
METHODS: Between 1984 and 2011, a total of 23 patients underwent caval resection concurrently with retroperitoneal tumor excision. Primary tumor histology was renal cell carcinoma in 19 patients, metastatic germ cell tumor in 2, and leiomyosarcoma, and adrenal cancer in 1 patient each. Clinicopathological data from these patients were retrospectively reviewed.
RESULTS: IVC reconstruction was performed by direct suture in 11 patients, patch repair in 8 and graft replacement in 3 patients. Interruption of the IVC was performed in one patient. There was no lethal complication or pulmonary embolism. Intracaval thrombosis, although patent, was observed in four patients after surgery. All patients underwent infrarenal IVC reconstruction. The median follow-up was 12 months (range 1-121 months). Of the 20 patients without distant metastasis at the time of surgery, complete resection was achieved in 14, whereas 6 patients had positive margins. Although nine patients developed distant metastases postoperatively, there was no local recurrence. The overall survival, progression-free survival and cause-specific survival in those RCC patients without distant metastasis at the time of surgery were 56.1, 47.0 and 60.4 %, respectively, at 5 years.
CONCLUSIONS: For advanced malignancies involving the IVC, resection is a safe and feasible procedure for selected patients.
Written by:
Kato S, Tanaka T, Kitamura H, Masumori N, Ito T, Kawaharada N, Tsukamoto T. Are you the author?
Department of Urology, Sapporo Medical University School of Medicine, S-1, W-16, Chuo-ku, Sapporo, 060-8543, Japan.
Reference: Int J Clin Oncol. 2012 Sep 6. Epub ahead of print.
doi: 10.1007/s10147-012-0473-x
PubMed Abstract
PMID: 22956175
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