It is the objective of these studies to improve the treatment outcomes for patients with newly diagnosed Hodgkin's disease and to continue to monitor the late effects of treatment on adults and children participating in past and present clinical trials. We intend to accomplish these goals through the conduct of novel therapeutic studies and the maintenance of a database on over 2500 Hodgkin's disease patients. The proposed clinical studies build upon our previous research efforts in Hodgkin's disease. A novel treatment for adults with early stage disease has been designed to maintain high cure rates, limit staging, and reduce late effects. This treatment, which consists of just eight weeks of chemotherapy followed by lower dose, modified involved field irradiation, is based on the success of abbreviated chemotherapy and limited irradiation in advanced stage disease. We plan to continue to study the abbreviated chemotherapy program, Stanford U, alone or in combination with irradiation in unfavorable and advanced stage Hodgkin's disease. Preliminary data indicate that this treatment approach is highly effective and, to date, has not been associated with serious morbidity. In the adult studies we plan to incorporate potentially more sensitive nuclear imaging for the identification of Hodgkin's disease and assessing the risk for relapse following the described treatments. Similar to adults, children with Hodgkin's disease will be treated according to risk group on clinical trials conducted at Stanford University, St. Jude Children's Research Hospital and the Dana Farber Cancer Center. Those patients with favorable, limited disease will receive four cycles of chemotherapy and low dose irradiation while an alternating chemotherapy program and low dose irradiation will be used for patients with unfavorable or advanced disease. Follow-on studies are planned for each of the clinical trials in progress in adults and children. An integral part of this application is the continued follow up of patients enrolled on prospective clinical trials at Stanford University since 1962. This includes the description of relapses, subsequent therapies, late morbidity, fatal treatment complications, causes of death and survival in over 2500 treated patients. These data, which have allowed Stanford investigators to make seminal observations on late effects such as second malignancy and cardiac disease, are maintained in a sophisticated database, representing a national resource for the efficacy and complications of the treatment of Hodgkin's disease.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA056060-07
Application #
2654089
Study Section
Experimental Therapeutics Subcommittee 1 (ET)
Program Officer
Wu, Roy S
Project Start
1992-02-07
Project End
2002-01-31
Budget Start
1998-03-17
Budget End
1999-01-31
Support Year
7
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Stanford University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Advani, R H; Hoppe, R T; Baer, D et al. (2013) Efficacy of abbreviated Stanford V chemotherapy and involved-field radiotherapy in early-stage Hodgkin lymphoma: mature results of the G4 trial. Ann Oncol 24:1044-8
Koontz, Michael Zach; Horning, Sandra J; Balise, Raymond et al. (2013) Risk of therapy-related secondary leukemia in Hodgkin lymphoma: the Stanford University experience over three generations of clinical trials. J Clin Oncol 31:592-8
Advani, Ranjana H; Hoppe, Richard T; Maeda, Lauren S et al. (2011) Stage I-IIA non-bulky Hodgkin's lymphoma. Is further distinction based on prognostic factors useful? The Stanford experience. Int J Radiat Oncol Biol Phys 81:1374-9
Ekstrand, Bradley C; Lucas, Jennifer B; Horwitz, Steven M et al. (2003) Rituximab in lymphocyte-predominant Hodgkin disease: results of a phase 2 trial. Blood 101:4285-9
Horning, Sandra J; Hoppe, Richard T; Breslin, Sheila et al. (2002) Stanford V and radiotherapy for locally extensive and advanced Hodgkin's disease: mature results of a prospective clinical trial. J Clin Oncol 20:630-7
Donaldson, S S; Hancock, S L; Hoppe, R T (1999) The Janeway lecture. Hodgkin's disease--finding the balance between cure and late effects. Cancer J Sci Am 5:325-33
Yuen, A R; Rosenberg, S A; Hoppe, R T et al. (1997) Comparison between conventional salvage therapy and high-dose therapy with autografting for recurrent or refractory Hodgkin's disease. Blood 89:814-22
Horning, S J; Hoppe, R T; Mason, J et al. (1997) Stanford-Kaiser Permanente G1 study for clinical stage I to IIA Hodgkin's disease: subtotal lymphoid irradiation versus vinblastine, methotrexate, and bleomycin chemotherapy and regional irradiation. J Clin Oncol 15:1736-44
Rosenberg, S A (1996) The management of Hodgkin's disease: half a century of change. The Kaplan Memorial Lecture. Ann Oncol 7:555-60
Horning, S J; Rosenberg, S A; Hoppe, R T (1996) Brief chemotherapy (Stanford V) and adjuvant radiotherapy for bulky or advanced Hodgkin's disease: an update. Ann Oncol 7 Suppl 4:105-8

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