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Hypofractionated Radiotherapy in Locally Advanced Myxoid Liposarcomas of Extremities or Trunk Wall (LIPO-MYX Trial) (LIPOMYX)

Primary Purpose

Myxoid Liposarcoma

Status
Active
Phase
Phase 2
Locations
Poland
Study Type
Interventional
Intervention
Hypofractionated radiotherapy
Sponsored by
Maria Sklodowska-Curie National Research Institute of Oncology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myxoid Liposarcoma focused on measuring Dose Hypofractionation, Neoadjuvant Therapy, Sarcoma, Dose Fractionation, Dose-Response Relationship

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ≥ 18 years old;
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2;
  • pathologically confirmed diagnosis of localized, potentially resectable myxoid liposarcoma;
  • primary tumor without previous treatment;
  • extremity or trunk wall localization of the tumor;
  • eligibility for limb-sparing surgery;
  • >= 5cm in the longest diameter at imaging staging (MRI);
  • adequate hematologic, liver, and renal function;
  • women of childbearing potential must have a negative pregnancy test on the day of registration for study;
  • female subjects who are breastfeeding should discontinue nursing prior to the first day of study treatment and during the whole radiotherapy treatment;
  • no co-existing malignancy within the last 2 years except for adequately treated basal cell carcinoma of the skin or carcinoma in situ of the cervix;
  • the absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before randomization in the trial;
  • before patient randomization, written informed consent must be given according to ICH/GCP.

Exclusion Criteria:

  • history of radiation to the affected volume;
  • previous or planned neoadjuvant chemotherapy;
  • contraindications to radiotherapy, or surgery;
  • metastatic disease.

Sites / Locations

  • Maria Sklodowska-Curie Institute - Oncology Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Hypofractionated radiotherapy

Arm Description

5x5 Gy radiotherapy and delayed surgery (after 6-8 weeks)

Outcomes

Primary Outcome Measures

Wound complication rate
Wound complication rate

Secondary Outcome Measures

Percentage of tumor necrosis
Local control rate
Local control rate at 5 years

Full Information

First Posted
January 22, 2019
Last Updated
June 14, 2019
Sponsor
Maria Sklodowska-Curie National Research Institute of Oncology
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1. Study Identification

Unique Protocol Identification Number
NCT03816475
Brief Title
Hypofractionated Radiotherapy in Locally Advanced Myxoid Liposarcomas of Extremities or Trunk Wall (LIPO-MYX Trial)
Acronym
LIPOMYX
Official Title
Hypofractionated 5x5 Gy Radiotherapy With Prolonged Gap Before Surgery in Preoperative Treatment of Patients With Locally Advanced Myxoid Liposarcomas of Extremities or Trunk Wall
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 24, 2015 (Actual)
Primary Completion Date
March 1, 2019 (Actual)
Study Completion Date
February 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maria Sklodowska-Curie National Research Institute of Oncology

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
After a screening, which consists of pathology confirmation, physical examination, magnetic resonance imaging (MRI), body computed tomography (CT) scan, blood tests, and case analysis on Multidisciplinary Team (MDT) meeting, patient will be irradiated 5x5 Gy and after radiotherapy and then referred for surgery 6-8 weeks after the radiotherapy completion.
Detailed Description
Myxoid liposarcoma has been reported to be more radiosensitive compared with other soft tissue sarcomas (STS). Response to preoperative treatment involves in decrease in tumor size, a large percentage in tumor necrosis (which according to some reports has a beneficial effect on the reduction of local recurrence rates) and also among other in a change in vasculature of the tissue. Hypofractionation represents a variation of radiotherapy fractionation in which the total dose is divided into fewer fractions with an increased fraction dose. Such treatment may lead to additional biological effects when compared to conventionally fractionated radiotherapy (eg. vascular damage, increased immunogenicity, and antigenicity). The main advantages of hypofractionation are those related to the decreased overall treatment time what is more convenient for both patients and physicians, increased compliance and makes the treatment more cost-effective. Intriguing, such an approach may provide an additional benefit when treating non-radiosensitive tumors with a low alpha/beta ratio (eg. sarcomas). The use of preoperative hypofractionated radiotherapy 5x5 Gy for five consecutive days, and then immediate surgery in patients with locally advanced soft tissue sarcomas showed in a published study a good local control rate, with a favorable amount of late toxicities. In this patient population, there were 22 patients with primary myxoid liposarcoma and the local control rate in this group was 86%. In the proposed study we plan to increase the gap between the end of radiotherapy and surgery to commonly applied five weeks to better assess the changes occurring in the tumor after treatment and to evaluate the impact of longer treatment interval on reducing the proportion of early complications of treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myxoid Liposarcoma
Keywords
Dose Hypofractionation, Neoadjuvant Therapy, Sarcoma, Dose Fractionation, Dose-Response Relationship

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
35 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hypofractionated radiotherapy
Arm Type
Experimental
Arm Description
5x5 Gy radiotherapy and delayed surgery (after 6-8 weeks)
Intervention Type
Radiation
Intervention Name(s)
Hypofractionated radiotherapy
Other Intervention Name(s)
5x5 Gy
Intervention Description
Preoperative hypofractionated 5x5 Gy radiotherapy (5 consecutive days) prescribed on planned target volume (tumor volume + elective margins + setup/error margin) with daily image guidance.
Primary Outcome Measure Information:
Title
Wound complication rate
Description
Wound complication rate
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Percentage of tumor necrosis
Time Frame
2 months
Title
Local control rate
Description
Local control rate at 5 years
Time Frame
60 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥ 18 years old; Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2; pathologically confirmed diagnosis of localized, potentially resectable myxoid liposarcoma; primary tumor without previous treatment; extremity or trunk wall localization of the tumor; eligibility for limb-sparing surgery; >= 5cm in the longest diameter at imaging staging (MRI); adequate hematologic, liver, and renal function; women of childbearing potential must have a negative pregnancy test on the day of registration for study; female subjects who are breastfeeding should discontinue nursing prior to the first day of study treatment and during the whole radiotherapy treatment; no co-existing malignancy within the last 2 years except for adequately treated basal cell carcinoma of the skin or carcinoma in situ of the cervix; the absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before randomization in the trial; before patient randomization, written informed consent must be given according to ICH/GCP. Exclusion Criteria: history of radiation to the affected volume; previous or planned neoadjuvant chemotherapy; contraindications to radiotherapy, or surgery; metastatic disease.
Facility Information:
Facility Name
Maria Sklodowska-Curie Institute - Oncology Center
City
Warsaw
State/Province
Mazovian
ZIP/Postal Code
02-781
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
25282099
Citation
Kosela-Paterczyk H, Szacht M, Morysinski T, Lugowska I, Dziewirski W, Falkowski S, Zdzienicki M, Pienkowski A, Szamotulska K, Switaj T, Rutkowski P. Preoperative hypofractionated radiotherapy in the treatment of localized soft tissue sarcomas. Eur J Surg Oncol. 2014 Dec;40(12):1641-7. doi: 10.1016/j.ejso.2014.05.016. Epub 2014 Sep 20.
Results Reference
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PubMed Identifier
19472403
Citation
Chung PW, Deheshi BM, Ferguson PC, Wunder JS, Griffin AM, Catton CN, Bell RS, White LM, Kandel RA, O'Sullivan B. Radiosensitivity translates into excellent local control in extremity myxoid liposarcoma: a comparison with other soft tissue sarcomas. Cancer. 2009 Jul 15;115(14):3254-61. doi: 10.1002/cncr.24375.
Results Reference
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PubMed Identifier
26802529
Citation
Messiou C, Bonvalot S, Gronchi A, Vanel D, Meyer M, Robinson P, Morosi C, Bloem JL, Terrier PH, Lazar A, Le Pechoux C, Wardelman E, Winfield JM, Boulet B, Bovee J, Haas RL. Evaluation of response after pre-operative radiotherapy in soft tissue sarcomas; the European Organisation for Research and Treatment of Cancer-Soft Tissue and Bone Sarcoma Group (EORTC-STBSG) and Imaging Group recommendations for radiological examination and reporting with an emphasis on magnetic resonance imaging. Eur J Cancer. 2016 Mar;56:37-44. doi: 10.1016/j.ejca.2015.12.008. Epub 2016 Jan 20.
Results Reference
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PubMed Identifier
27026512
Citation
Kosela-Paterczyk H, Szumera-Cieckiewicz A, Szacht M, Haas R, Morysinski T, Dziewirski W, Prochorec-Sobieszek M, Rutkowski P. Efficacy of neoadjuvant hypofractionated radiotherapy in patients with locally advanced myxoid liposarcoma. Eur J Surg Oncol. 2016 Jun;42(6):891-8. doi: 10.1016/j.ejso.2016.02.258. Epub 2016 Mar 18.
Results Reference
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Hypofractionated Radiotherapy in Locally Advanced Myxoid Liposarcomas of Extremities or Trunk Wall (LIPO-MYX Trial)

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