Low-dose (12 Gy) TSEBT+Vorinostat Versus Low-dose TSEBT Monotherapy in Mycosis Fungoides
Cutaneous Lymphoma, Cutaneous T-cell Lymphoma
About this trial
This is an interventional treatment trial for Cutaneous Lymphoma focused on measuring Cutaneous T-cell Lymphoma
Eligibility Criteria
INCLUSION CRITERIA
- Biopsy-confirmed mycosis fungoides (MF); clinical stage IB; IIA; IIB; or IIIB.
- Patients must have failed or have been intolerant to at least one prior systemic or skin-directed therapy. This may include topical steroids if used as primary therapy for MF.
- 18 years of age or older.
- Eastern Cooperative Oncology Group (ECOG) of ≤ 2.
- White blood cell (WBC) > 2000/uL
- Platelet count > 75,000/mm3
- Absolute neutrophil count (ANC) > 1000.
- Bilirubin ≤ 1.5 x upper limit of normal (ULN)
- Aspartate aminotransferase (AST) ≤ 2.5 x UNL
- Alanine aminotransferase (ALT) ≤ 2.5 x UNL
- Alkaline phosphatase (liver fraction) ≤ 2.5 x ULN
- Creatinine ≤ 1.5 x UNL OR creatinine clearance ≤ 60 mL/min for patients with creatinine levels > 1.5 x institutional ULN
- Potassium level between 3.5 and 4.5
- Magnesium level between 1.5 and 2.5
Required washout period for prior therapies
- Topical therapy: 2 weeks
- Systemic biologic, monoclonal antibody, or chemotherapy: 4 weeks
- Phototherapy or radiotherapy (excluding TSEBT): 4 weeks
- Other investigational therapy: 4 weeks
- Note: patients with rapidly progressive disease may be treated earlier than required washout period; however, such circumstance must be discussed and approved by the protocol director at the primary site (Stanford).
- Women of child-bearing potential (WOCBP) must have negative serum pregnancy test.
- WOCBP must agree to use effective contraception, defined as oral contraceptives, intrauterine devices, double barrier method (condom plus spermicide or diaphragm) or abstain from sexual intercourse. WOCBP includes any female who has experienced menarche and who has not undergone successful surgical sterilization or is not postmenopausal (defined as amenorrhea for 12 consecutive months).
- Male subjects must be willing to use an appropriate method of contraception (eg, condoms) or abstain from sexual intercourse and inform any sexual partners that they must also use a reliable method of contraception (eg, birth control pills) during the study.
- Ability to understand and sign a written informed consent document.
- Ability to comply with the treatment schedule
EXCLUSION CRITERIA
- Prior courses of TSEBT (Note : localized skin-directed radiotherapy is allowed if administered at least 4 weeks prior to initiation on study).
- Concomitant use of any anti-cancer therapy or immune modifier.
- Receiving colony stimulating factors.
- Prior allogeneic or autologous transplant.
- Active infection or have received intravenous antibiotics, antiviral, or antifungal agents within 2 weeks prior to the start of the study drug.
- Known history of human immunodeficiency virus (HIV), hepatitis B or C.
- History of prior malignancy with the exception of cervical intraepithelial neoplasia, non-melanoma skin cancer, and adequately treated localized prostate carcinoma (PSA < 1.0). Patients with a history of other malignancies must have undergone potentially curative therapy and have no evidence of that disease for 5 years.
- Uncontrolled intercurrent illness, condition, or circumstances that could limit compliance with the study, including, but not limited to the following: active infection, acute or chronic graft versus host disease, symptomatic congestive heart failure, unstable angina pectoris, medically significant cardiac arrhythmia, uncontrolled diabetes mellitus or hypertension, or psychiatric conditions.
- Medically significant cardiac event in prior 6 months (ie, myocardial infarction, cardiac surgery.
- Congenital long QT syndrome.
- QTc interval > 480 msec on screening ECG.
- Proven or suspected stage IV disease including patients with B2 (Sezary syndrome); N3 (frank LN disease); or M1 (visceral disease) categories; presence of reactive or dermatopathic lymphadenopathy (N1-2) or limited blood involvement (B1) is permitted.
- Pregnant or lactating.
- Unwilling to use reliable birth control methods.
- Any other medical issue, including laboratory abnormalities, deemed by the Investigator to be likely to interfere with patient participation.
- Unwilling or unable to provide informed consent.
Sites / Locations
- Stanford University School of Medicine
- Yale University School of Medicine
- MD Anderson Cancer Center
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
TSEBT & Vorinostat
TSEBT only
Total skin electron beam therapy (TSEBT) will be performed per institution guidelines. Vorinostat will be administered at a dose of 400 mg/day, starting one day prior to the initiation of TSEBT. During TSEBT, vorinostat should be taken in the morning and preferably prior to TSEBT.
Total skin electron beam therapy (TSEBT) will be administered according to the Stanford 6-field technique or equivalent technique per institutional standards. Patients will receive a planned total skin dose of 12 grey (Gy) fractionated at 2 Gy/cycle (each cycle requiring 2 days of treatment); 4 days each week; for a total of 3 weeks. Supplements will routinely be applied to the perineum and soles as well as any other "shadowed" sites involved by disease, such as the inframammary regions (1-2 Gy fractions to a total dose of 12 Gy). Discrete tumors may receive additional "boost" treatment not to exceed 12 Gy.