Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

E-Poster Display

1662P - Outcomes and prognostic factors in localized soft tissue sarcoma: Prospective observational study

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Sarcoma

Presenters

Mathighatta Shivashankara

Citation

Annals of Oncology (2020) 31 (suppl_4): S914-S933. 10.1016/annonc/annonc288

Authors

M.S. Shivashankara1, S. Viswanath2, S. Pandalanghat1, A.N. Patel1, B. Guleria1, A. Rathore1, M. Kumar1, A. Pathak3

Author affiliations

  • 1 Medical Oncology Department, Army Hospital Research And Referral, 110010 - New Delhi/IN
  • 2 Medical Oncology Department, Command Hospital (NC), Lucknow/IN
  • 3 Medical Oncology Department, Army Hospital Research & Referal, 110010 - New Delhi/IN

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 1662P

Background

There is a lacuna of studies on adult soft tissue sarcoma (STS) patient’s disease patterns and factors influencing survival outcomes from developing countries in published literature.

Methods

This a single centre prospective observational study conducted at Army Hospital Research & Referral, New Delhi, from Apr 2017 to Mar 2019. One hundred and five consecutive cases of histologically proven Localized STS (excluding Metastatic disease, GIST, Rhabdomyosarcoma, and Ewing’s sarcoma) were included. Baseline demographic and clinical details were noted. Patients were treated with standard protocols after a multidisciplinary tumor board decision. Recurrence-free survival (PFS) and overall survival (OS) were analyzed for the outcome. Statistical analysis was done using SPSS software version 25.

Results

The median age at presentation was 45 years. Extremity (41.8%) was the common primary anatomical site closely followed by retroperitoneum (16%). The most common histopathologic subtype was undifferentiated pleomorphic STS (19%) closely followed by synovial sarcoma (18.1%). Of 105 localized patients, 97 patients underwent surgery, 21 patients received neoadjuvant therapy and reported partial response in 38% (8/21) patients; the remaining 62% (13/21) patients had stable disease. After a median follow up fourteen months, 16 patients had local recurrence, 22 patients had distant metastases, and six patients had died. Two-year RFS and OS rate estimates were 37.3% ± 7.3% and 91.2% ± 3.7%, respectively. On univariate analysis for recurrence-free survival the significant factors were tumor size (>10 cm vs ≤10 cm), HR for recurrence 2.378 (95% CI 1.27 to 4.45, p=0.007), Ki 67 (>20% vs ≤20%), HR for recurrence 2.88 (95% CI 1.52 to 5.44, p=0.001). Age, sex, ECOG PS, histopathological subtype, FNLCC grades, and resection margin status did not significantly predict recurrence. On multivariate analysis, both tumor size and Ki 67 remained statistically significant independent predictors of recurrence-free survival.

Conclusions

Median age is a decade earlier than data from western literature. Tumor size and Ki 67 are the strong independent predictors of recurrence-free survival.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.