Review Article

Optimization of the Therapeutic Approach to Patients with Sarcoma: Delphi Consensus

Table 5

Recommendations for retroperitoneal sarcomas.

RecommendationPhaseType of consensus (% agreement)

Performance of core needle biopsy for the diagnosis of retroperitoneal sarcoma (RS)
 (i) Must always be carried out if neoadjuvant therapy is planned (radiation therapy and/or chemotherapy)1Yes (95)
 (ii) It must not be replaced by FNA, as it provides little diagnostic information and can cause delays in starting potential treatment1Yes (90)
(iii) Has minimal risk of dissemination in the needle tract, so this should not be a reason for not performing this procedure1Yes (75)
Patients with RS should always be referred to a tertiary care facility or one renowned for its expertise and known to have a multidisciplinary team/committee with extensive surgical experience in the management of tumors at this location1Yes (mode: 85)
The procedure to be followed in patients who are referred for assessment after inadequate RS surgery (no en-bloc resection, R0, etc.) performed at a hospital center lacking the necessary experience depends on the grade:
 (i) Low-grade RS: performance of CT TAP scan and follow up closely in the absence of clear disease data until development of macroscopic lesions, at which time a new surgery should be performed1Yes (mode: 50%)
 (ii) High-grade RS: treatment should be tailored to each case, as there are no clear recommendations in this regard1Yes (mode: 50%)
Rescue surgery should be considered as treatment for local RS recurrence in cases in which the disease is resectable and R0 can be achieved1Yes (mode: 80%)
Complementary radiation therapy cannot be used as standard treatment for patients who have potentially resectable RS; if after individualized assessment it is indicated, preoperative radiation therapy will be administered in every case as long as it is possible to meet the radiation field requirements2Yes (93.8)
Neoadjuvant chemotherapy should be considered for high-grade RS with potential sensitivity to chemotherapy (leiomyosarcoma, angiosarcoma, synovial sarcoma, etc.) that are at the limits of resectability1Yes (75)
Given the absence of evidence to show increase in survival, adjuvant chemotherapy cannot be considered standard treatment for resected RS; hence, if considered as an option in individual cases, the factors that should be assessed are (in decreasing order of importance) as follows:
 (i) Risk of relapse2Yes (mean: 4.0; CV: 28.9%)
 (ii) Histology2Yes (mean: 3.9; CV: 22.8%)
 (iii) Histological grade2Yes (mean: 3.3; CV: 32.5%)
In the event that the decision is made to treat resected RS with adjuvant chemotherapy, the regimen to be administered would consist of a combination of an anthracycline and ifosfamide1Yes (mode: 50%)