Trial Search Results

Low-dose (12 Gy) TSEBT+Vorinostat Versus Low-dose TSEBT Monotherapy in Mycosis Fungoides

The purpose of this study is to determine if vorinostat combined with low-dose total skin electron beam therapy (TSEBT) offers superior clinical benefit (efficacy & safety) over low-dose TSEBT alone in participants with mycosis fungoides (MF)

Treatment in this study is TSEBT +/- vorinostat, with participants stratified by MF stage.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Stanford University

Stanford Investigator(s):


  • Radiation: Total skin electron beam therapy (TSEBT)
  • Drug: Vorinostat


Phase 1/Phase 2



   - 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

   - Ability to understand and sign a written informed consent document.

   - Ability to comply with the treatment schedule


   - 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.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study


Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cutaneous Lymphoma Coordinator
Not Recruiting