Lymphocyte Support to SBRT in Patients With Oligo-metastatic Solid Cancer

Last updated: July 11, 2024
Sponsor: Gustave Roussy, Cancer Campus, Grand Paris
Overall Status: Active - Recruiting

Phase

1/2

Condition

N/A

Treatment

all-trans retinoic acid

Stereotactic Body Radiation Therapy

Clinical Study ID

NCT06439888
2022-500680-13-00
2022/3511
  • Ages > 18
  • All Genders

Study Summary

The goal of this clinical trial is to assess safety of pan-metastases directed SBRT combined with ATRA and the lympho-protective efficacy of ATRA upon radiation-induced lymphopenia.

This is a French bicentric, open label, phase I/II clinical study that will comprise two parts. Part I will evaluate the safety of the combination based on a single-arm safety run design, while Part II will be randomized (ratio 1:1) and will study SBRT with or without ATRA.

Patients enrolled will be treated with:

  • SBRT to all lesions more than 1.5cm, on week days (from Monday to Friday), over a maximum of 2 weeks,

  • With or without (for part II patients randomized in the control arm) ATRA therapy: ATRA 150 mg/m^2/day for 3 days every 3 weeks for a maximum of 4 cycles (about 3 months), starting on the first day of radiation therapy.

The expected rate of patients who will have lymphopenia of grade 2 or higher in the control arm at 6 weeks post-radiotherapy is 50%.

At a one-sided level of statistical significance of 0.07, the randomization of 52 patients (26 patients in each arm) will provide 85% power to detect a decrease in this rate to 15% in the SBRT+ATRA arm, using Fisher's exact test.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adult male or female patients (older than 18 years of age at inclusion);

  • Histologically or cytologically proven solid cancer at the oligo-metastatic stageamenable to pan-lesion SBRT, as defined by:

  1. 2 to 5 tumor lesions measurable as per RECIST V1.1 (including primary) with alargest diameter comprised between 1.5 and 5 cm,

  2. The disease can be either genuinely oligo-metastatic, oligo-progressive, or aninduced oligo-metastatic disease,

  3. All tumor lesions that match criterion I2a must be eligible to SBRT in terms oflocation and radiotherapy constraints,

  4. SBRT to all lesions must be feasible over a two-week period,

  5. Whatever the primary tumor type;

  • Patients must agree to comply with biopsy and blood sampling for research purpose;

  • Minimal wash-out periods from last administration of treatments to the first day ofSBRT must be:

  1. Systemic chemotherapy including cytotoxic, immunotherapy, targeted therapy,hormone therapy, any investigational agent during the last 4 weeks,

  2. Immunosuppressive medication during the last 4 weeks, with the exceptions ofintranasal, topical, and inhaled corticosteroids or systemic corticosteroids atphysiological doses, which are not to exceeding 10 mg/day of prednisone, or anequivalent corticosteroid,

  3. Live attenuated vaccination during the last 4 weeks,

  4. Major surgery during the last 4 weeks;

  • World Health Organization (WHO) 0 or 1 and Eastern Cooperative Oncology Group (ECOG)Performance Status 0 or 1;

  • Patients must have adequate organ function defined as follows:

  1. White blood cell count of equal to or higher than 1,500/mm^3,

  2. Lymphocyte count of equal to or higher than 800/mm^3,

  3. Platelet count of equal to or higher than 100,000/mm^3,

  4. Hemoglobin higher than 9 g/dL,

  5. Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) equalto or less than 2.5 upper level norm (or if liver metastases are present mustbe equal to or less than 5x upper level norm)

  6. Serum creatinine clearance higher than 40 mL/min by the Cockcroft-Gault formula (Cockcroft and Gault 1976) or by 24-hour urine collection for determination ofcreatinine clearance;

  • Female patients must either be of non-reproductive potential or must have a negativeserum pregnancy test within 3 days prior to the initiation of the study drug.Fertile men with a female partner of childbearing potential must agree to use malecondom plus spermicide and childbearing potential women must have agreed to use atleast one highly effective contraceptive method during treatment on this trial andfor up to 1 month after the last dose of ATRA; Pregnancy testing and contraceptioncounseling should be repeated monthly throughout the period of ATRA treatment.

  • Patient should understand, sign, and date the written voluntary informed consentform prior to any protocol-specific procedures performed. Patient should be able andwilling to comply with study visits and procedures as per protocol;

  • Patients must be affiliated to a social security system or beneficiary of the same

Exclusion

Exclusion Criteria:

  • Evidence of disease rapidly progressing at the time of screening according to thetwo last best-fitted imaging modalities (CT-scans, MRI, positron emissiontomography), at the discretion of the investigator and the multidisciplinary board (RCP);

  • Any evidence of brain metastasis;

  • Any situation where irradiation of the target site(s) would imply re-irradiation ofa formerly irradiated tumor site;

  • Bone metastasis located in a femoral bone if risk of pending fracture is high;

  • Liver metastasis adjacent to the stomach or small bowel and liver metastasis thatleads to a volume of uninvolved liver less than 700 cc;

  • Patients with any concurrent severe condition (grade 3 or beyond according to CTCAEV5.0) and/or uncontrolled medical condition that could compromise participation inthe study;

  • Any psychiatric illness or social situations that would limit compliance with studyrequirements or compromise the ability of the subject to give written informedconsent;

  • Active secondary malignancy unless the malignancy is not expected to interfere withthe evaluation of safety and is approved by the Sponsor. Examples of the latterinclude basal or squamous cell carcinoma of the skin, in-situ carcinoma of thecervix, and isolated elevation of prostate-specific antigen. Patients with acompletely treated prior malignancy who are no longer treated (including maintenancetherapy) and no evidence of disease for at least 2 years are eligible;

  • Chronic treatment with systemic corticosteroids or another immunosuppressantincluding, but not limited to systemic corticosteroids at doses exceeding 10 mg/dayof prednisone or equivalent, methotrexate, azathioprine, and tumor necrosis factor-α (TNF-α) blockers. Use of immunosuppressive medications for the management ofinvestigational product-related Adverse Events or in subjects with contrastallergies is acceptable. The use of topical, inhaled and intranasal corticosteroidsis permitted;

  • Patients with tumor(s) that invade major vessels, as shown unequivocally by imagingstudies;

  • Patients with central lung metastasis (i.e within 2 cm from hilum) that are cavitaryas shown unequivocally by imaging studies;

  • Persisting significant toxicities related to prior treatments i.e. Grade 2 andhigher adverse event according to CTCAE V5.0 criteria, except for alopecia andbiological values defined in inclusion criteria I6;

  • Known allergy or hypersensitivity to the study drug. The study drug iscontraindicated in patients with soy or peanut allergy;

  • Positive test for human immunodeficiency virus (HIV) or known acquiredimmunodeficiency syndrome (AIDS);

  • Patients at risk of QT prolongation (including patients with hypokaliemia, baselineQT/corrected QT interval more than 470 ms (for women) and more than 450 ms (formen));

  • Pregnant or breastfeeding women;

  • Persons deprived of their freedom or under guardianship, or for whom it would beimpossible to undergo the medical follow-up required by the trial, for geographic,social or psychological reasons.

Study Design

Total Participants: 58
Treatment Group(s): 2
Primary Treatment: all-trans retinoic acid
Phase: 1/2
Study Start date:
July 11, 2024
Estimated Completion Date:
January 31, 2027

Study Description

Ablative radiotherapy - also called stereotactic body radiation therapy (SBRT) - can achieve durable control of tumor lesions and appears as a highly promising strategy to extend overall survival of patients with oligo-metastatic diseases. Radiotherapy has recognized immunomodulatory effects: it triggers immunogenic cell death and reprogramming of the tumor immune microenvironment, which eventually results in a systemic antitumor response following focal radiation treatment. This is called the abscopal effect (distant out-of-the-field lesions that shrink after focal irradiation). Unfortunately, evidences show that this is directly counteracted by the toxic effects of radiotherapy on cytotoxic lymphocytes, which are highly radiosensitive.

Recent data support the fact that radiation-induced lymphopenia is mostly driven by the deregulation of the myeloid-lymphoid imbalance following radiation therapy, with aberrant myelopoiesis and high levels of tumor infiltration by myeloid-derived suppressive cells (MDSC). In preclinical models, pharmacological blockade of MDSC combined with radiation therapy successfully abrogated radiation-induced lymphopenia and significantly improved survival outcomes.

All trans retinoic acid (ATRA, also known as tretinoin) is a vitamin A derivative that has a market authorization for the treatment of acute promyelocytic leukemia as it efficiently induces differentiation of abnormal promyelocytes. Similarly, several clinical studies report that ATRA can differentiate MDSCs into mature myeloid cells, with a positive effect on the count of activated cluster of differentiation 8 (CD8+) lymphocytes.

This clinical trial will provide the clinical proof-of-concept that adding ATRA to pan-metastases SBRT is safe in humans, prevents severe and prolonged lymphopenia and therefore, may foster a radiation-induced systemic anticancer immune response sufficient to increase survival in patients with cancer at the oligo-metastatic stage.

Connect with a study center

  • Centre Léon Bérard

    Lyon, 69000
    France

    Site Not Available

  • Gustave Roussy

    Villejuif, 94800
    France

    Active - Recruiting

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