• Users Online: 538
  • Print this page
  • Email this page


 
 
Table of Contents
LETTER TO EDITOR
Year : 2020  |  Volume : 3  |  Issue : 1  |  Page : 119-120

Addressing the unmet need of improving survival outcomes of bone and soft tissue tumors


Department of Surgical Oncology, Cancer Institute (WIA), Chennai, Tamil Nadu, India

Date of Submission06-Jan-2020
Date of Decision06-Jan-2020
Date of Acceptance16-Jan-2020
Date of Web Publication24-Feb-2020

Correspondence Address:
Arvind Krishnamurthy
Department of Surgical Oncology, Cancer Institute (WIA), 38, Sardar Patel Road, Adyar, Chennai - 600 036, Tamil Nadu
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/CRST.CRST_14_20

Get Permissions


How to cite this article:
Krishnamurthy A, Karthik V. Addressing the unmet need of improving survival outcomes of bone and soft tissue tumors. Cancer Res Stat Treat 2020;3:119-20

How to cite this URL:
Krishnamurthy A, Karthik V. Addressing the unmet need of improving survival outcomes of bone and soft tissue tumors. Cancer Res Stat Treat [serial online] 2020 [cited 2020 Apr 8];3:119-20. Available from: http://www.crstonline.com/text.asp?2020/3/1/119/279094



The previous issue of Cancer Research, Statistics, and Treatment featured two articles addressing the larger issue of the oncological outcomes of bone and soft tissue tumors, which, despite the limited numbers and retrospective design, added to the limited available published Indian literature.[1],[2],[3] The rarity and, more importantly, the heterogeneity of these tumors make an in-depth study of their clinical behavior difficult.[4]

The article by Pareekutty et al.[1] interestingly demonstrated a better survival in the cohort of patients who had undergone unplanned excisions (uP), and the authors have attributed this to a combination of multiple adverse factors though none of the individual factors studied, i.e., tumor size, grade, and histology, were found to be statistically significant between the two groups (planned versus the uP groups). The mean tumor size in the uP group was >9 cm, which is much more than the traditional believed 5 cm thumb size rule of suspecting a soft tissue tumor to be a possible sarcoma. This understanding among surgeons managing soft tissue tumors would go a long way in bringing down the number of unplanned excisions, and further, this sound clinical practice could definitely save the patients the psychological trauma and the resultant additional costs of having to undergo a repeat surgery to achieve clear margins, among other benefits. The reasons for the better outcomes in the 'uP' excision group, other than a 'pattern of referral' bias, are definitely worth exploring.

Further, the authors passingly mentioned that the patients in the 'uP' group had limited metastases and could be salvaged by a metastatectomy. However, the authors have not elaborated much on the same. It is worthwhile to mention that an important determinant of overall survival for any cancer is the ability to potentially salvage such recurrences.

The other article in the issue by Ankalkoti et al.[2] audits the life and limb salvage outcomes in a tertiary care center. Nearly a third of the recurrences in that series could be salvaged, which included three cases of pulmonary metastasis. It is important to note that about 30%–40% of the patients with extremity osteosarcoma relapse and >80% of these localize in the lungs; there is a need for consideration of pulmonary metastasectomy in carefully selected patients of extremity osteosarcomas.

Further improvements in the survival outcomes in bone and soft tissue sarcomas could possibly stem from the use of novel systemic therapies through predictive biomarker development.[5],[6] While there are hardly any robust choices of second-line systemic therapies in extremity osteosarcomas,[5] histology-directed therapies have shown promise in the management of metastatic soft tissue sarcomas.[6],[7] There is, thus, a huge unmet need pertaining to the development of precision medicine and targeted therapies (both patient-specific biomarker driven and tumor-agnostic) in the population of patients of soft tissue as well as bony sarcomas.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Pareekutty NM, Kattepur AK, Alapett JJ, Satheesan B. Unplanned excision in soft-tissue sarcomas – Is it the unkindest cut of all? Cancer Res Stat Treat 2019;2:152-7.  Back to cited text no. 1
  [Full text]  
2.
Ankalkoti B, Pareekutty NM, Kattepur AK, Kumbakara R, Vazhayil R, Balasubramanian S. Life and limb after limb salvage surgery for osteosarcoma in an Indian tertiary cancer center. Cancer Res Stat Treat 2019;2:145-51.  Back to cited text no. 2
  [Full text]  
3.
Tiwari A. Management of bone and soft-tissue sarcomas: From state of practice to state of art. Cancer Res Stat Treat 2019;2:215-6.  Back to cited text no. 3
  [Full text]  
4.
Sidappa KT, Krishnamurthy A. Adult soft-tissue sarcomas of the head and neck. Indian J Cancer 2011;48:284-8.  Back to cited text no. 4
[PUBMED]  [Full text]  
5.
Harrison DJ, Geller DS, Gill JD, Lewis VO, Gorlick R. Current and future therapeutic approaches for osteosarcoma. Expert Rev Anticancer Ther 2018;18:39-50.  Back to cited text no. 5
    
6.
Haddox CL, Riedel RF. Individualizing systemic therapy for advanced soft tissue sarcomas based on tumor histology and biology. Expert Rev Anticancer Ther 2020;20:5-8.  Back to cited text no. 6
    
7.
Turkar S. Current treatment landscape and emerging management options for extremity sarcoma. Cancer Res Stat Treat 2018;1:121-38.  Back to cited text no. 7
  [Full text]  




 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
References

 Article Access Statistics
    Viewed83    
    Printed1    
    Emailed0    
    PDF Downloaded13    
    Comments [Add]    

Recommend this journal