Literature DB >> 19557478

Complete soft tissue sarcoma resection is a viable treatment option for select elderly patients.

G Lahat1, A R Dhuka, S Lahat, A J Lazar, V O Lewis, P P Lin, B Feig, J N Cormier, K K Hunt, P W T Pisters, R E Pollock, D Lev.   

Abstract

BACKGROUND: Decreased performance status, comorbidities, and disease natural history may erode enthusiasm for soft tissue sarcoma (STS) resection in elderly patients. Consequently, we evaluated the outcome of elderly patients amenable to complete surgical resection treated at a single institution.
METHODS: Prospectively accrued data were used to identify patients with primary STS age >or=65 years (n = 325) who underwent complete macroscopic resection at our institution (1996-2007). Univariable and multivariable analyses were performed to identify prognostic factors.
RESULTS: Median age at presentation was 72 years; 179 patients (55.1%) had associated comorbidities with an ASA score of >or=3. Extremity was the most common site (57.1%; n = 186), undifferentiated pleomorphic sarcoma the most common histology (60.4%; n = 197); 232 (71.2%) were high grade, 222 (68.3%) were >5 cm. Thirty-day postoperative mortality was 0.9% (n = 3); overall complication rate was 30.7% (n = 100), and mean postoperative hospital stay was 9 days (range, 1-84). Estimated median survival was 96 months, 5-year disease-specific survival (DSS) was 63%. Multivariable analysis identified age >or=75 year (HR = 2.03), tumor size: 5-15 vs <5 cm (HR = 3.54), or >15 vs <5 cm (HR = 10.33), and high-grade (HR = 5.53) as significant independent adverse prognostic factors. Compared with patients aged 65-74 years, older patients had more high grade tumors (P = .04), received chemotherapy less often (P < .0001), developed different patterns of recurrence (P < .05), and exhibited a shorter median survival (70 months; P = .05).
CONCLUSIONS: Properly selected elderly patients can safely undergo extensive STS resections. Until more effective therapies become available, surgery in the elderly is indicated and remains the best means for STS control.

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Year:  2009        PMID: 19557478     DOI: 10.1245/s10434-009-0574-6

Source DB:  PubMed          Journal:  Ann Surg Oncol        ISSN: 1068-9265            Impact factor:   5.344


  20 in total

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Journal:  Int J Clin Oncol       Date:  2018-02-27       Impact factor: 3.402

9.  Managing soft tissue sarcomas in a developing country: are prognostic factors similar to those of developed world?

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Journal:  World J Surg Oncol       Date:  2012-09-13       Impact factor: 2.754

10.  Characterization of PD-1/PD-L1 immune checkpoint expression in soft tissue sarcomas.

Authors:  Kazuhiko Hashimoto; Shunji Nishimura; Tomohiko Ito; Masao Akagi
Journal:  Eur J Histochem       Date:  2021-07-02       Impact factor: 3.188

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