Trial Search Results

CytoreductiveSurgery & HIPEC w/Gemcitabine+Chemotherapy w/Dacarbazine in Uterine Leiomyosarcoma

The purpose of this study is to find out if giving a dose of heated chemotherapy in the abdomen immediately after surgery that is done to remove uterine leiomyosarcoma type of cancer will help lower the risk of the cancer coming back in the future.

Stanford is currently accepting patients for this trial.

Lead Sponsor:

Stanford University

Stanford Investigator(s):

Intervention(s):

  • Drug: Gemcitabine
  • Drug: Dacarbazine
  • Procedure: Cytoreductive Surgery
  • Behavioral: Functional Assessment of Cancer Therapy (FACT) G questionnaire
  • Procedure: Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) Scan
  • Drug: Gadolinium

Phase:

Phase 2

Eligibility


Inclusion Criteria:

   1. Histologically confirmed diagnosis of uterine leiomyosarcoma (LMS) with evidence of
   local recurrence.

   2. Imaging provides evidence of locally recurrent uterine LMS.

   3. Candidate for potentially radical, maximal effort cytoreductive surgery at the
   discretion and expertise of the treating physician.

   4. Age ≥ 18 years.

   5. Life expectancy > 3 months.

   6. Women of childbearing potential (WOCBP) will have a negative pregnancy test ≤ 7 days
   prior to surgery (this test can be omitted if subject is post menopausal by either
   surgery or elevated FSH)

   7. Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 2.

   8. Hemoglobin (HGB) ≥ 9 g/dL.

   9. White blood cell count (WBC) ≥ 3.0 K/ul.

10. Absolute neutrophil count (ANC) ≥ 1.5 K/ul.

11. Platelets (PLT) ≥ 100 K/ul.

12. Total bilirubin within normal institutional limits.

13. Serum glutamic oxaloacetic transaminase (SGOT/Serum glutamic pyruvic transaminase
   (SGPT) < 2.5 x institutional upper limit of normal (ULN).

14. Creatinine < 1.5 x ULN or creatinine clearance > 60 mL/min according to Cockroft Gault
   formula.

15. Prothrombin Time (PT) such that international normalized ratio (INR) is < 1.5 (or an
   in range INR, usually between 2 and 3, if a subject is on a stable dose of therapeutic
   warfarin or low molecular weight heparin) and a partial thromboplastin time (PTT) <
   1.2 times control.

16. Serum albumin ≥ 2.5 g/dL.

17. Ability to understand and the willingness to personally sign the written IRB approved
   informed consent document.

Note that this study does not allow the use of a legally authorized representative

Exclusion Criteria:

   1. Recurrence of LMS within less than 6 months after the last dose of gemcitabine.

   2. Active extra abdominal disease including active malignant pleural effusion. Subjects
   who have been successfully treated with neoadjuvant chemotherapy and no longer have
   (malignant) pleural effusions may be included.

   3. Prior gemcitabine given in non adjuvant setting.

   4. Prior treatment with dacarbazine.

   5. Active infection requiring antibiotics.

   6. Unresolved toxic effects of prior therapy (except alopecia). Resolution is considered
   ≤ Grade 1 per NCI CTCAE, version 5.0.

   7. Pregnant.

   8. Breast feeding.

   9. Presence of metastatic liver disease

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

Female

Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Maria Ahern
650-725-6413
Recruiting