RecruitingPhase 2NCT03548428

Stereotaxic Body Irradiation of Oligometastase in Sarcoma (Stereosarc)

Randomized Phase II, 2-arm Study of Immunomodulation with Atezolizumab Concomitant with High Dose Radiation (SBRT) Versus SBRT Alone in Patients with Oligometastatic Sarcomas


Sponsor

Centre Antoine Lacassagne

Enrollment

103 participants

Start Date

Jun 4, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

Up to 50% of soft tissue sarcoma (STS) patients will develop metastases in the course of their disease. Cytotoxic therapy is a standard treatment in this setting but yields average tumor response rates of 25% at first line and ≤10% at later lines. It is also limited in the number of lines and courses by tolerance issues. Trials include poly/oligometastases indistinctively and suggest that consolidation ablation is used in \~20% of patients with residual oligometastases refractory to chemotherapy. Oligometastases represent a stage of disease between completely absent and widely metastatic, and which might be cured if the limited numbers of metastatic sites are eradicated. Ablative strategies to treat patients with oligometastases from sarcomas yield prolonged survival times and stereotactic body radiation therapy (SBRT) is associated with excellent tolerance. Surgery may be offered in selected metastatic cases. Alternatively and increasingly, SBRT yields high control rates at treated sites (≥ 80%). The so-called radioresistance of sarcomas is overcome by the high doses per fraction made possible owing to the high precision achieved with SBRT. SBRT is an accepted treatment strategy provided that tumor burden remains limited in the number and size of metastases. Systemic treatment can be combined with SBRT. SBRT may produce abscopal effects where tumors outside the irradiation area also demonstrate tumor shrinkage in some occurrences. SBRT produces systemic antitumoral immune response in certain conditions and enhances radiation-induced tumor cell death compared to conventional lower dose irradiation. Abscopal effects have been potentialized with SBRT/immunotherapy in several tumor models. Sarcomas are a privileged target tumor given their high metastatic propensity. Several potent immunomodulators that skew the tumor immune microenvironment toward a proimmunity context are being investigated in STS either alone or in combination with chemotherapy or targeted therapy. The PD-1 receptor is present within the tumor microenvironment, and limits the activity of infiltrating cytotoxic T lymphocytes, thus blocking effective immune responses. The action of PD-1 is triggered upon binding to its ligands. PD-1 can stimulate the immunosuppressive function of regulatory T cells. Moreover, blockade of PD-1 can stimulate anti-tumor immune responses. Significant responses have been obtained in several sarcomas with acceptable tolerance. Preliminary clinical experience suggests that immunotherapy can be efficient in refractory leiomyosarcomas. Several drugs targeting the PD-1/PD-L1/2 axis are ongoing either as single agents or in combination with ipilimumab, kinase inhibitors, or chemotherapy in STS subtypes. Combination of radiotherapy with immunotherapy is included as a means of increasing tumor antigen release in metastatic STS. Immunomodulated SBRT is a particularly attractive strategy, given the potential of radiation to induce cytotoxicity in tumors and induce abscopal effects. A phase II radiation trial showed increased apoptosis-, intra-tumoral dendritic cells and accumulation of intratumoral T cells in STS with correlation with tumor-specific immune responses. We here propose a randomized phase II study to prolong progression-free survival (PFS) with the combination of SBRT/immunotherapy in oligometastatic STS patients. SBRT is well-tolerated with hardly any severe toxicity (fewer than 5% acute and late grade 3 toxicities). It is performed in an ambulatory setting in only a few treatment fractions. Associations between irradiation and immunomodulatory agents appear to be synergistic and show favorable tolerance profiles. Immunomodulatory agents have a more favorable toxicity profile than cytotoxic agents with about 65% overall acute toxicities. Immunotherapy selectively binds to PD-L1 and competitively blocks its interaction with PD-1. Compared with anti-PD-1 antibodies that target T-cells, immunotherapy targets tumor cells, and is therefore may induce fewer side effects, including a lower risk of autoimmune-related safety issues, as blockade of PD-L1 leaves the PD-L2 - PD-1 pathway intact to promote peripheral self-tolerance. Stereotactic irradiation is associated with an excellent tolerance with rates of grade 3 or more toxicities below 5%. Preliminary data of toxicity with the association of stereotactic irradiation and immunotherapy show no cumulative toxicity in association with immunotherapy. However, their incidence and characteristics are no different from that observed with stereotactic irradiation alone. Moreover, intracranial metastases are exceptional in sarcomas. The toxicity of the association for extracranial stereotactic irradiation does not seem to be increased either.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying whether focused, high-dose radiation treatment (called stereotactic body radiation, or SBRT) combined with an immunotherapy drug can help people with soft-tissue sarcoma (a type of muscle or tissue cancer) that has spread to 1–5 other parts of the body. **You may be eligible if...** - You are 18 or older - You have been diagnosed with a soft-tissue sarcoma such as leiomyosarcoma, liposarcoma, or undifferentiated sarcoma - Your cancer has spread to no more than 5 spots in the body, with none larger than 5 cm - You are in generally good health and able to carry out daily activities - Your blood counts and organ function (liver, kidneys) are within acceptable ranges - You are on your first or second round of treatment for metastatic disease - You are willing to use effective birth control during and after the study **You may NOT be eligible if...** - You have been on an immunotherapy drug like pembrolizumab or ipilimumab before - You have an active autoimmune disease or are on immune-suppressing medications - You have HIV, active hepatitis B, or hepatitis C - You are pregnant, breastfeeding, or planning to become pregnant during the study - You received major surgery or radiation in the past 4 weeks - A tumor is located very close to your spinal cord - You have another active cancer that is progressing Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAtezolizumab

1200mg IV every 3 weeks for 4 months

RADIATIONSBRT

3 to 5 fractions depending on tumor size


Locations(17)

Institut Bergonié

Bordeaux, France

Centre François BACLESSE

Caen, France

Centre Georges François LECLERC

Dijon, France

Centre Oscar LAMBRET

Lille, France

Centre Léon BERARD

Lyon, France

AP-HM CHU La Timone

Marseille, France

Institut Paoli CALMETTES

Marseille, France

Institut de cancérologie de Montpellier

Montpellier, France

Centre Antoine LACASSAGNE

Nice, France

APHP La Pitié

Paris, France

CHU de Poitiers

Poitiers, France

Centre Eugene MARQUIS

Rennes, France

Centre Henri BECQUEREL

Rouen, France

Institut de cancérologie Strasbourg Europe

Strasbourg, France

Institut Claudius REGAUD

Toulouse, France

Institut de Cancérologie de Lorraine

Vandœuvre-lès-Nancy, France

Institut Gustave ROUSSY

Villejuif, France

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NCT03548428


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