Use and outcomes of laparoscopic-assisted colectomy for cancer in the United States
- PMID: 18794419
- DOI: 10.1001/archsurg.143.9.832
Use and outcomes of laparoscopic-assisted colectomy for cancer in the United States
Abstract
Background: Laparoscopic-assisted colectomy (LAC) has gained acceptance for the treatment of colon cancer. However, long-term outcomes of LAC have not been examined at the national level outside of experienced centers.
Objective: To compare use and outcomes of LAC and open colectomy (OC).
Design: Retrospective cohort study.
Setting: National Cancer Data Base.
Patients: Patients who underwent LAC (n = 11 038) and OC (n = 231 381) for nonmetastatic colon cancer (1998-2002).
Main outcome measures: Regression methods were used to assess use and outcomes of LAC compared with OC.
Results: Laparoscopic-assisted colectomy use increased from 3.8% in 1998 to 5.2% in 2002 (P < .001). Patients were significantly more likely to undergo LAC if they were younger than 75 years, had private insurance, lived in higher-income areas, had stage I cancer, had descending and/or sigmoid cancers, or were treated at National Cancer Institute-designated hospitals. Compared with those undergoing OC, patents undergoing LAC had 12 or more nodes examined less frequently (P < .001), similar perioperative mortality and recurrence rates, and higher 5-year survival rates (64.1% vs 58.5%, P < .001). After adjusting for patient, tumor, treatment, and hospital factors, 5-year survival was significantly better after LAC compared with OC for stage I and II but not for stage III cancer. Highest-volume centers had comparable short- and long-term LAC outcomes compared with lowest-volume hospitals, except highest-volume centers had significantly higher lymph node counts (median, 12 vs 8 nodes; P < .001).
Conclusions: Laparoscopic-assisted colectomy and OC outcomes are generally comparable in the population. However, survival was better after an LAC than after an OC in select patients.
Comment in
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Is laparoscopic colectomy a good operation for colon cancer?Arch Surg. 2009 Mar;144(3):290-1; author reply 291. doi: 10.1001/archsurg.2008.566. Arch Surg. 2009. PMID: 19289674 No abstract available.
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