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

Primary Purpose

Soft Tissue Sarcoma, Non Metastatic Disease

Status
Unknown status
Phase
Phase 2
Locations
Sweden
Study Type
Interventional
Intervention
doxorubicin , ifosfamide
doxorubicin, ifosfamide
doxorubicin, ifosfamide
doxorubicin, ifosfamide
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Soft Tissue Sarcoma focused on measuring Soft-tissue sarcomas, prognostic factors, adjuvant, chemotherapy, radiotherapy, metastases-free survival, toxicity, High malignancy grade, High-risk for metastases, Adult

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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)

Sites / Locations

  • Scandinavian Sarcoma Group SecretariatRecruiting
  • Scandinavian Sarcoma Group centersRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Arm 2

Arm 3

Group B

Arm 1

Arm Description

<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle and radiotherapy 36Gy (1.8Gy per fraction, two fractions daily) will be given between cycle 3 and 4. (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)

<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle and radiotherapy 45Gy (1.8Gy per fraction, two fractions daily) will be given between cycle 3 and 4. (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)

<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle and radiotherapy 36Gy (1.8Gy per fraction, two fractions daily) will be given between cycle 2 and 3. (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)

<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)

Outcomes

Primary Outcome Measures

Metastases-free survival

Secondary Outcome Measures

cumulative incidence of local recurrence,overall survival,acute and late toxicity,secondary malignancies

Full Information

First Posted
November 12, 2008
Last Updated
July 3, 2011
Sponsor
Oslo University Hospital
Collaborators
Scandinavian Sarcoma Group
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1. Study Identification

Unique Protocol Identification Number
NCT00790244
Brief Title
A Scandinavian Sarcoma Group Protocol for Patients With High-risk Soft Tissue Sarcoma of the Extremities and Trunk Wall
Acronym
SSGXX
Official Title
A Scandinavian Sarcoma Group Treatment Protocol for Adult Patients With Non-metastatic High-risk Soft Tissue Sarcoma of the Extremities and Trunk Wall
Study Type
Interventional

2. Study Status

Record Verification Date
November 2008
Overall Recruitment Status
Unknown status
Study Start Date
October 2007 (undefined)
Primary Completion Date
October 2012 (Anticipated)
Study Completion Date
October 2022 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Oslo University Hospital
Collaborators
Scandinavian Sarcoma Group

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Soft Tissue Sarcoma, Non Metastatic Disease
Keywords
Soft-tissue sarcomas, prognostic factors, adjuvant, chemotherapy, radiotherapy, metastases-free survival, toxicity, High malignancy grade, High-risk for metastases, Adult

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
188 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm 2
Arm Type
Experimental
Arm Description
<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle and radiotherapy 36Gy (1.8Gy per fraction, two fractions daily) will be given between cycle 3 and 4. (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)
Arm Title
Arm 3
Arm Type
Experimental
Arm Description
<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle and radiotherapy 45Gy (1.8Gy per fraction, two fractions daily) will be given between cycle 3 and 4. (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)
Arm Title
Group B
Arm Type
Experimental
Arm Description
<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle and radiotherapy 36Gy (1.8Gy per fraction, two fractions daily) will be given between cycle 2 and 3. (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)
Arm Title
Arm 1
Arm Type
Experimental
Arm Description
<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)
Intervention Type
Drug
Intervention Name(s)
doxorubicin , ifosfamide
Other Intervention Name(s)
Doxorubicin, Holoxan
Intervention Description
doxorubicin 60mg/m2+ifosfamide 6g/m2 every third week
Intervention Type
Drug
Intervention Name(s)
doxorubicin, ifosfamide
Other Intervention Name(s)
Doxorubicin, Holoxan
Intervention Description
Doxorubicin and Ifosfamide given every three weeks, totally 6 courses.
Intervention Type
Drug
Intervention Name(s)
doxorubicin, ifosfamide
Other Intervention Name(s)
Doxorubicin, Holoxan
Intervention Description
<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle and radiotherapy 36Gy (1.8Gy per fraction, two fractions daily) will be given between cycle 3 and four. (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)
Intervention Type
Drug
Intervention Name(s)
doxorubicin, ifosfamide
Other Intervention Name(s)
Doxorubicin, Holoxan
Intervention Description
<70y: 6 cycles with doxorubicin 60mg/m2+ifosfamide 6g/m2 of each 21day cycle and radiotherapy 36Gy (1.8Gy per fraction, two fractions daily) will be given between cycle 2 and 3. (>=70y: doxorubicin 50mg/m2+ifosfamide 5g/m2)
Primary Outcome Measure Information:
Title
Metastases-free survival
Time Frame
time frame from start of treatment until the events metastases or death of any cause
Secondary Outcome Measure Information:
Title
cumulative incidence of local recurrence,overall survival,acute and late toxicity,secondary malignancies
Time Frame
for ten years from start of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kirsten Sundby Hall, MD, PhD
Phone
+4722934000
Email
k.s.hall@klinmed.uio.no
First Name & Middle Initial & Last Name or Official Title & Degree
Mikael Eriksson, MD,PhD
Phone
+4646177507
Email
mikael.eriksson@onk.lu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kirsten Sundby Hall, MD,PhD
Organizational Affiliation
c/o: Scandinavian Sarcoma Group, Southern Swedish Regional Tumor Registry, Lund University Hospital, SE-221 85 Lund
Official's Role
Principal Investigator
Facility Information:
Facility Name
Scandinavian Sarcoma Group Secretariat
City
Lund University Hospital
State/Province
Lund
ZIP/Postal Code
SE-221 85
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kirsten Sundby Hall, MD,PhD
Phone
+4722934000
Email
k.s.hall@klinmed.uio.no
First Name & Middle Initial & Last Name & Degree
Mikael Eriksson, MD,PhD
Phone
+4646 177507
Email
mikael.eriksson@onk.lu.se
First Name & Middle Initial & Last Name & Degree
Kirsten Sundby Hall, MD,PhD
Facility Name
Scandinavian Sarcoma Group centers
City
Lund
ZIP/Postal Code
221 85
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kirsten Sundby Hall, MD, PhD
Phone
+4722934000
Email
k.s.hall@klinmed.uio.no
First Name & Middle Initial & Last Name & Degree
Mikael Eriksson, MD,PhD
Phone
+4646177507
Email
mikael.eriksson@onk.lu.se
First Name & Middle Initial & Last Name & Degree
Kirsten Sundby Hall, MD,PhD
First Name & Middle Initial & Last Name & Degree
Mikael Eriksson, MD,PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
17627813
Citation
Engellau J, Samuelsson V, Anderson H, Bjerkehagen B, Rissler P, Sundby-Hall K, Rydholm A. Identification of low-risk tumours in histological high-grade soft tissue sarcomas. Eur J Cancer. 2007 Sep;43(13):1927-34. doi: 10.1016/j.ejca.2007.05.018. Epub 2007 Jul 12.
Results Reference
background
PubMed Identifier
16153463
Citation
Engellau J, Bendahl PO, Persson A, Domanski HA, Akerman M, Gustafson P, Alvegard TA, Nilbert M, Rydholm A. Improved prognostication in soft tissue sarcoma: independent information from vascular invasion, necrosis, growth pattern, and immunostaining using whole-tumor sections and tissue microarrays. Hum Pathol. 2005 Sep;36(9):994-1002. doi: 10.1016/j.humpath.2005.07.008.
Results Reference
background
PubMed Identifier
33292545
Citation
Hall KS, Bruland OS, Bjerkehagen B, Lidbrink E, Jebsen N, Hagberg H, Papworth K, Hagberg O, Trovik C, Bauer H, Eriksson M. Preoperative accelerated radiotherapy combined with chemotherapy in a defined cohort of patients with high risk soft tissue sarcoma: a Scandinavian Sarcoma Group study. Clin Sarcoma Res. 2020 Nov 17;10(1):22. doi: 10.1186/s13569-020-00145-5.
Results Reference
derived
PubMed Identifier
29929092
Citation
Sundby Hall K, Bruland OS, Bjerkehagen B, Zaikova O, Engellau J, Hagberg O, Hansson L, Hagberg H, Ahlstrom M, Knobel H, Papworth K, Zemmler M, Goplen D, Bauer HCF, Eriksson M. Adjuvant chemotherapy and postoperative radiotherapy in high-risk soft tissue sarcoma patients defined by biological risk factors-A Scandinavian Sarcoma Group study (SSG XX). Eur J Cancer. 2018 Aug;99:78-85. doi: 10.1016/j.ejca.2018.05.011. Epub 2018 Jun 19.
Results Reference
derived
Links:
URL
http://www.ssg-org.net
Description
Scandinavian Sarcoma Group

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

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