Education and Training

A Frontline Therapy Trial in Participants With Advanced Classical Hodgkin Lymphoma

This open-label, randomized, 2-arm, multicenter, phase 3 study has the primary objective of comparing the modified progression-free survival (mPFS) obtained with brentuximab vedotin (ADCETRIS®) plus AVD (doxorubicin [Adriamycin], vinblastine, and dacarbazine; abbreviated A+AVD) versus that obtained with ABVD (doxorubicin [Adriamycin],bleomycin, vinblastine, and dacarbazine) for the frontline treatment of advanced classical Hodgkin lymphoma(HL)

Stanford is currently not accepting patients for this trial.

Intervention(s):

  • drug: brentuximab vedotin
  • drug: doxorubicin
  • drug: bleomycin
  • drug: vinblastine
  • drug: dacarbazine

Eligibility


Inclusion Criteria:

   1. Treatment-naïve participants with Ann Arbor Stage III or IV HL.

   2. Histologically confirmed classical Hodgkin Lymphoma (HL) according to the current
   World Health Organization (WHO) classification.

   3. Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to
   (<=) 2.

   4. Bidimensional measurable disease as documented by radiographic technique per the
   International Working Group Revised Criteria for Response Assessment for Malignant
   Lymphoma.

Exclusion Criteria:

   1. Nodular lymphocyte predominant Hodgkin lymphoma.

   2. Cerebral/meningeal disease, including signs and symptoms of progressive
   multifocalleukoencephalopathy (PML).

   3. Sensory or motor peripheral neuropathy.

   4. Prior immunosuppressive chemotherapy, therapeutic radiation, or any immunotherapy
   within 12 weeks of first study drug dose.

   5. Known human immunodeficiency virus (HIV) positive.

   6. Known hepatitis B surface antigen-positive, or known or suspected active hepatitis C
   infection.

Please note that there are additional exclusion criteria. The study center will determine
if you meet all of the criteria.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting