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A Scandinavian Sarcoma Group Protocol for Patients With High-risk Soft Tissue Sarcoma of the Extremities and Trunk Wall

A Scandinavian Sarcoma Group Treatment Protocol for Adult Patients With Non-metastatic High-risk Soft Tissue Sarcoma of the Extremities and Trunk Wall

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00790244
Acronym
SSGXX
Enrollment
188
Registered
2008-11-13
Start date
2007-10-31
Completion date
2022-10-31
Last updated
2011-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Metastatic Disease, Soft Tissue Sarcoma

Keywords

Soft-tissue sarcomas, prognostic factors, adjuvant, chemotherapy, radiotherapy, metastases-free survival, toxicity, High malignancy grade, High-risk for metastases, Adult

Brief summary

SSG XX is a phase II trial for high-risk soft tissue sarcomas (STS) of the extremities and trunk wall. Prognostic factors (histopathological markers) are used to identify high-risk tumors. SSG XX will evaluate chemo- and radiotherapy given adjuvantly to these patients. In a specified group of patients also preoperatively given therapy will be studied.

Detailed description

SSG XX, the third adjuvant STS protocol by SSG, is a phase II non-randomized trial in patients with high risk to develop metastases. SSG XX is based on a previous SSG trial (SSG XIII) regarding use of prognostic markers to identify high-risk tumors and include very similar chemo- and radiotherapy treatment schedules compared to SSG XIII, but the new protocol also includes a treatment arm with preoperative chemo- and radiotherapy for patients with an obvious risk for intralesional surgery initially. Patients: In this new adjuvant protocol SSG adopts an inclusion decision algorithm based on the following criteria: 1.vascular invasion or 2. presence of at least two of the risk factors: tumor size =\>8 cm, necrosis or infiltrative growth(all defined microscopically by the pathologist. The system was developed retrospectively by evaluation of 434 primary histologically high grade (III-IV) STS from the SSG registry, and was later validated in a series of 175 patients in which patients with a high risk for metastases (\>40 %) and low risk (\<15 %) were separated (Engellau J et al.Eur J Ca 2007 43: 1927-34). Inclusion criteria: age ≥ 18 y and \<75 y. Primary end point is metastasis-free survival. Local recurrence and toxicity will also be studied. Treatment: Six cycles of doxorubicin 60mg/m2 and ifosfamide 6g/m2 will be given adjuvantly (to patients ≥ 70y: 50mg/m2 and 5g/m2 ). Dependent on surgical resection margins, 36Gy or 45Gy (1,8Gy per fraction, two fractions daily) will be given interpolated with chemotherapy. Conclusion: SSG XX will evaluate chemo-and radiotherapy given adjuvantly to patients with STS and high risk for metastases (arm A). In a specified group of patients also preoperatively given therapy will be studied(arm B). Other sarcoma centers are invited to participate in the study.

Interventions

DRUGdoxorubicin , ifosfamide

doxorubicin 60mg/m2+ifosfamide 6g/m2 every third week

DRUGdoxorubicin, ifosfamide

Doxorubicin and Ifosfamide given every three weeks, totally 6 courses.

Sponsors

Scandinavian Sarcoma Group
CollaboratorOTHER
Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

Group A: Histological high-grade malignancy soft tissue sarcomas of the extremity and trunk wall. Patients fulfilling the high-risk criteria defined above (see detailed description) Group B: Patients with histological high-grade malignancy soft tissue sarcomas of the extremity and trunk wall for whom surgery carries an obvious risk of intralesional margin Other inclusion criteria for therapy group A and group B * Age ≥ 18 y and ≤ 75 y * WHO grade 0-1 * Adequate cardiac function (LVEF ≥ 50%) * Normal GFR (clearance) * Adequate haematologic and liver function * All histotypes except those listed below

Exclusion criteria

The following histological types: * Extraskeletal osteosarcoma and - chondrosarcoma, Ewing/PNET, rhabdomyosarcoma, Kaposi´s sarcoma, malignant mesenchymoma, clear cell sarcoma, alveolar soft part sarcoma, epithelioid sarcoma * Radiation induced sarcoma * No previous anthracycline treatment * Less than 5 years free of another primary malignancy * More than 12 weeks have elapsed since primary surgery (Group A) * More than 4 weeks from diagnostic biopsy to start of chemotherapy (Group B)

Design outcomes

Primary

MeasureTime frame
Metastases-free survivaltime frame from start of treatment until the events metastases or death of any cause

Secondary

MeasureTime frame
cumulative incidence of local recurrence,overall survival,acute and late toxicity,secondary malignanciesfor ten years from start of treatment

Countries

Sweden

Contacts

Primary ContactKirsten Sundby Hall, MD, PhD
k.s.hall@klinmed.uio.no+4722934000
Backup ContactMikael Eriksson, MD,PhD
mikael.eriksson@onk.lu.se+4646177507

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026