Treatment of refractory Hodgkin's disease with an anti-CD16/CD30 bispecific antibody. 1997

F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
Medizinische Klinik I, Universitätskliniken des Saarlandes, Homburg, Germany.

Fifteen patients with refractory Hodgkin's disease were treated in a phase I/II trial with the natural killer (NK)-cell-activating bispecific monoclonal antibody HRS-3/A9, which is directed against the Fc(gamma)-receptor III (CD16 antigen) and the Hodgkin's-associated CD30 antigen, respectively. Median counts of NK cells and of all lymphocyte subsets were considerably decreased in the patients before therapy. HRS-3/A9 was administered 4 times every 3 to 4 days, starting with 1 mg/m2. The treatment was well tolerated, and the maximum tolerated dose was not reached at 64 mg/m2, the highest dose administered because of the limited amounts of HRS-3/A9 available. Side effects were rare and consisted of fever, pain in involved lymph nodes, and a maculopapulous rash. A total of 9 patients developed human antimouse Ig antibodies, and 4 patients developed an allergic reaction after attempted retreatment. A total of 1 complete and 1 partial remission (lasting 6 and 3 months, respectively) [corrected], 3 minor responses (1 to 11+ months), and 1 mixed response were achieved. There was no clear-cut dose-side effect or dose-response correlation. Our results encourage further clinical trials with this novel immunotherapeutic approach and emphasize the necessity to reduce the immunogenicity of the murine bispecific antibodies.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D012074 Remission Induction Therapeutic act or process that initiates a response to a complete or partial remission level. Induction of Remission,Induction, Remission,Inductions, Remission,Remission Inductions
D005260 Female Females
D006689 Hodgkin Disease A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen. Granuloma, Hodgkin,Granuloma, Malignant,Hodgkin Lymphoma,Lymphogranuloma, Malignant,Granuloma, Hodgkin's,Granuloma, Hodgkins,Hodgkin Lymphoma, Adult,Hodgkin's Disease,Hodgkin's Lymphoma,Hodgkins Disease,Lymphocyte Depletion Hodgkin's Lymphoma,Lymphocyte-Rich Classical Hodgkin's Lymphoma,Mixed Cellularity Hodgkin's Lymphoma,Nodular Lymphocyte-Predominant Hodgkin's Lymphoma,Nodular Sclerosing Hodgkin's Lymphoma,Adult Hodgkin Lymphoma,Disease, Hodgkin,Disease, Hodgkin's,Disease, Hodgkins,Hodgkin Granuloma,Hodgkin's Granuloma,Hodgkins Granuloma,Hodgkins Lymphoma,Lymphocyte Rich Classical Hodgkin's Lymphoma,Lymphogranulomas, Malignant,Lymphoma, Hodgkin,Lymphoma, Hodgkin's,Malignant Granuloma,Malignant Granulomas,Malignant Lymphogranuloma,Malignant Lymphogranulomas,Nodular Lymphocyte Predominant Hodgkin's Lymphoma
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000911 Antibodies, Monoclonal Antibodies produced by a single clone of cells. Monoclonal Antibodies,Monoclonal Antibody,Antibody, Monoclonal
D016131 Lymphocyte Subsets A classification of lymphocytes based on structurally or functionally different populations of cells. Lymphocyte Subpopulations,Lymphocyte Subpopulation,Lymphocyte Subset,Subpopulation, Lymphocyte,Subpopulations, Lymphocyte,Subset, Lymphocyte,Subsets, Lymphocyte

Related Publications

F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
April 2001, Cancer immunology, immunotherapy : CII,
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
July 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology,
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
May 1992, Lancet (London, England),
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
November 1993, International journal of cancer,
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
June 2007, Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi,
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
September 1998, British journal of haematology,
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
June 2002, Clinical cancer research : an official journal of the American Association for Cancer Research,
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
July 2021, Clinical cancer research : an official journal of the American Association for Cancer Research,
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
June 2015, Blood,
F Hartmann, and C Renner, and W Jung, and C Deisting, and M Juwana, and B Eichentopf, and M Kloft, and M Pfreundschuh
August 1989, Journal of clinical oncology : official journal of the American Society of Clinical Oncology,
Copied contents to your clipboard!