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Residual disease predicts outcomes after definitive resection for incidental gallbladder cancer.

Publication ,  Journal Article
Butte, JM; Kingham, TP; Gönen, M; D'Angelica, MI; Allen, PJ; Fong, Y; DeMatteo, RP; Jarnagin, WR
Published in: J Am Coll Surg
September 2014

BACKGROUND: Residual disease (RD) at definitive resection of incidental gallbladder cancer (IGBCA) influences outcome, but its clinical relevance with respect to anatomic site is incompletely characterized. STUDY DESIGN: Consecutive patients with IGBCA undergoing re-exploration from 1998 to 2009 were identified; those submitted to a complete resection were analyzed. Demographics and tumor- and treatment-related variables were correlated with RD and survival. Cancer-specific survival was stratified by site of RD (local [gallbladder bed]; regional [bile duct, lymph nodes]; distant [discontiguous liver, port site, peritoneal]). RESULTS: Of the 135 patients submitted to re-exploration, RD was found in 82 (61%) overall and in 63 (54%) of 116 patients submitted to resection; the most common site was regional (n = 27, 43%). The T stage of the gallbladder specimen was the only independent predictor of RD (T1b = 35.7%, T2 = 48.3%, T3 = 70%, p = 0.015). The presence of RD at any site dramatically reduced median disease-free survival (DFS) (11.2 vs 93.4 months, p < 0.0001) and disease-specific survival (DSS) (25.2 months vs not reached, p < 0.0001) compared with no RD, respectively. Disease-specific survival did not differ according to RD location, with all anatomic sites being equally poor (p = 0.87). Residual disease at any site predicted DFS (hazard ratio [HR] 3.3, 95% CI 1.9 to 5.7, p = 0.0003) and DSS (HR 2.4, 95% CI 1.2 to 4.6, p = 0.01), independent of all other tumor-related variables. CONCLUSIONS: Survival in patients with RD at local or regional sites was not significantly different than that seen in stage IV disease, with neither subgroup clearly benefiting from reoperation. Outcomes were poor in all patients with RD, regardless of location.

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Published In

J Am Coll Surg

DOI

EISSN

1879-1190

Publication Date

September 2014

Volume

219

Issue

3

Start / End Page

416 / 429

Location

United States

Related Subject Headings

  • Surgery
  • Retrospective Studies
  • Prognosis
  • Neoplasm, Residual
  • Middle Aged
  • Male
  • Incidental Findings
  • Humans
  • Gallbladder Neoplasms
  • Female
 

Citation

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ICMJE
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Butte, J. M., Kingham, T. P., Gönen, M., D’Angelica, M. I., Allen, P. J., Fong, Y., … Jarnagin, W. R. (2014). Residual disease predicts outcomes after definitive resection for incidental gallbladder cancer. J Am Coll Surg, 219(3), 416–429. https://doi.org/10.1016/j.jamcollsurg.2014.01.069
Butte, Jean M., T Peter Kingham, Mithat Gönen, Michael I. D’Angelica, Peter J. Allen, Yuman Fong, Ronald P. DeMatteo, and William R. Jarnagin. “Residual disease predicts outcomes after definitive resection for incidental gallbladder cancer.J Am Coll Surg 219, no. 3 (September 2014): 416–29. https://doi.org/10.1016/j.jamcollsurg.2014.01.069.
Butte JM, Kingham TP, Gönen M, D’Angelica MI, Allen PJ, Fong Y, et al. Residual disease predicts outcomes after definitive resection for incidental gallbladder cancer. J Am Coll Surg. 2014 Sep;219(3):416–29.
Butte, Jean M., et al. “Residual disease predicts outcomes after definitive resection for incidental gallbladder cancer.J Am Coll Surg, vol. 219, no. 3, Sept. 2014, pp. 416–29. Pubmed, doi:10.1016/j.jamcollsurg.2014.01.069.
Butte JM, Kingham TP, Gönen M, D’Angelica MI, Allen PJ, Fong Y, DeMatteo RP, Jarnagin WR. Residual disease predicts outcomes after definitive resection for incidental gallbladder cancer. J Am Coll Surg. 2014 Sep;219(3):416–429.
Journal cover image

Published In

J Am Coll Surg

DOI

EISSN

1879-1190

Publication Date

September 2014

Volume

219

Issue

3

Start / End Page

416 / 429

Location

United States

Related Subject Headings

  • Surgery
  • Retrospective Studies
  • Prognosis
  • Neoplasm, Residual
  • Middle Aged
  • Male
  • Incidental Findings
  • Humans
  • Gallbladder Neoplasms
  • Female