Sequential Neoadjuvant Chemotherapy in Soft Tissue Sarcoma

NCT ID: NCT04776525

Last Updated: 2025-08-14

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 49 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-04-27
• Study Completion Date: 2036-09-30

Brief Summary

Nearly half of patients with high-grade, localized soft tissue sarcoma (STS) of extremities and trunk wall develop disease recurrence after local therapy. Adjuvant chemotherapy with ifosfamide and doxorubicin may improve long-term disease-free survival, but the benefit of adjuvant treatment is limited and predictive factors for treatment response are lacking. The aim of this study is to explore sequential treatment with ifosfamide and doxorubicin in a neoadjuvant setting and to investigate biomarkers predictive of treatment response.

Conditions

Soft Tissue Sarcoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Sequential ifosfamide and doxorubicin

Four cycles ifosfamide 9 g/m2 and four cycles doxorubicin 80 mg/m2. Each cycle has a duration of 14 days.

Group Type: EXPERIMENTAL

Ifosfamide

Intervention Type: DRUG

3 g/m2 each day for three days

Doxorubicin

Intervention Type: DRUG

80 mg/m2 over four hours day 1

Interventions

Ifosfamide

3 g/m2 each day for three days

Intervention Type: DRUG

Doxorubicin

80 mg/m2 over four hours day 1

Intervention Type: DRUG

Other Intervention Names

Holoxan; Adriamycin

Eligibility Criteria

Inclusion Criteria

1. ≥ 18 years of age at the time of informed consent.

2. Histological diagnosis of soft tissue sarcoma belonging to one of the following histotypes:

1. Leiomyosarcoma

2. Malignant peripheral nerve sheath tumor

3. Undifferentiated pleomorphic sarcoma

4. Myxofibrosarcoma

5. Synovial sarcoma

6. Pleomorphic liposarcoma

7. Pleomorphic rhabdomyosarcoma

8. Unclassified spindle cell sarcoma

3. Malignancy grade ≥ 2 according to the Fédération Nationale des Centres de Lutte Contre le Cancer (FNCLCC) grading system.

4. Tumor localized in extremity, girdle and/or trunk wall.

5. Primary tumor size ≥5.0 cm as measured in the longest diameter on diagnostic MRI or CT scan.

6. Primary tumor location below the superficial fascia or involving the superficial fascia, i.e. deep-seated according to the World Health Organization (WHO) Classification of Tumors of Soft Tissue and Bone (4th edition, 2013).

7. The primary tumor must be available for biopsy collection at protocol inclusion.

8. Patients must have a measurable tumor according to RECIST v1.1.

9. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

10. Before patient registration, written informed consent must be given according to national and local regulations.

11. Adequate organ function and bone marrow reserve as indicated by the following laboratory assessments:

1. Hemoglobin ≥ 8.0 g/dL

2. Neutrophil count ≥ 1.0 x 109/L

3. Platelet count ≥ 75 x 109/L

4. Total bilirubin ≤ 1.5 x the upper limit of normal (ULN)

5. Creatinine clearance ≥ 60 ml/min based on Cockcroft Gault estimation or direct measurement

12. Negative Hepatitis B and C and HIV serology.

13. Adequate contraception in women of childbearing potential (WOCBP) and their fertile partners during the study and until 6 months after end of study treatment. WOCBP should have a negative highly sensitive serum or urine pregnancy test within 72 hours prior to receiving the first dose of study medication. A woman is considered fertile following menarche and until becoming post-menopausal unless permanently sterile. WOCBP should be willing to use one of the mentioned highly effective methods of birth control mentioned below or be surgically sterile, or abstain from heterosexual activity for the course of the study through 1 year after the last dose of study medication. Methods considered as highly effective birth control methods include combined (estrogen and progestogen containing) or progestogen-only hormonal contraception associated with inhibition of ovulation (oral, intravaginal, injectable, implantable or transdermal), intrauterine device (including hormone-releasing), male condom, bilateral tubal occlusion, vasectomised partner or sexual abstinence (see appendix 5 for definitions).

Exclusion Criteria

1. Any prior therapy for soft tissue sarcoma.

2. Locoregional or distant metastasis as assessed by CT and/or MRI at time of diagnosis. Patients with lung nodules <10 mm of uncertain etiology may be included.

3. Clinical evidence of serious coagulopathy. Prior arterial/venous thrombosis or embolism does not exclude patients from inclusion, unless patient is considered unfit by study oncologist.

4. Urinary obstruction.

5. Known hypersensitivity towards ifosfamide, doxorubicin or pegfilgrastim, their metabolites and other ingredients in the drug administration formulation.

6. New York Heart Association class II-IV heart disease, myocardial infarction within 6 months of diagnosis of soft tissue sarcoma, active ischemia or any other uncontrolled cardiac condition such as angina pectoris, clinically significant cardiac arrhythmia requiring therapy, uncontrolled hypertension or congestive heart failure.

7. Left ventricular ejection fraction (LVEF) < 50%.

8. Patients with a prior or concurrent malignant disease whose natural history or treatment have the potential to interfere with the safety or efficacy assessment of this clinical trial are not eligible. Patients with a history of breast cancer, requiring continued hormonal treatment (e.g. anti-estrogen or an aromatase inhibitor) may be included. Patients with a history of prostate cancer, requiring continued support with luteinizing hormone releasing hormone (LHRH) agonists, with or without androgens, may be included.

9. Patients not able to give an informed consent or comply with study regulations as deemed by study investigator.

10. Any other significant comorbidities, such as active infection, uncontrolled pulmonary or liver disease, active cystitis, or any other condition, that based on the assessment of the treating physician could compromise compliance with the protocol or predispose the patient to safety risks.

11. Pregnant or lactating patients.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Haukeland University Hospital

OTHER

Sponsor Role: collaborator

Oslo University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Kjetil Boye

Senior Consultant

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Kjetil Boye, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Oslo University Hospital

Locations

Haukeland University Hospital

Bergen, , Norway

Site Status: RECRUITING

Oslo University Hospital

Oslo, , Norway

Site Status: RECRUITING

Countries

Norway

Central Contacts

Kjetil Boye, MD PhD

Role: CONTACT

kjetil.boye@ous-hf.no

+4722934000

Facility Contacts

Tor-Christian Johannessen, MD

Role: primary

tor-christian.aase.johannessen@helse-bergen.no

Kjetil Boye, MD PhD

Role: primary

kjetil.boye@ous-hf.no

Other Identifiers

44-2020

Identifier Type: -

Identifier Source: org_study_id