Marrow transplantation following escalating doses of fractionated total body irradiation and cyclophosphamide--a phase I trial. 1992

F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
Department of Medicine, University of Washington, School of Medicine, Seattle.

Thirty-six patients with advanced hematologic malignancy were entered into a Phase I study designed to define the maximum tolerated dose of unshielded total body irradiation delivered from dual 60 Cobalt sources at an exposure rate of 8 cGy/min and given in fractions twice daily for total doses ranging from 12 Gy to 17 Gy. All patients received cyclophosphamide, 120 mg/kg administered over 2 days before total body irradiation. Allogeneic marrow was infused from HLA-identical siblings (n = 29) or one locus HLA incompatible family members (n = 3); three patients received cryopreserved autologous marrow and one patient received syngeneic marrow. The maximum tolerated dose of total body irradiation given as 2 Gy fractions twice a day was 16 Gy. One of eight patients receiving 12 Gy, none of four receiving 14 Gy, three of 20 receiving 16 Gy, and two of four receiving 17 Gy developed severe (Grade 3-4) regimen-related toxicity. The primary dose limiting toxicity was pneumonitis, followed by veno-occlusive disease of the liver, renal impairment, and mucositis. Five patients (14%) are alive, four disease-free 798-1522 days posttransplant. Twenty (56%) relapsed posttransplant. Further investigation of regimens containing 16 Gy of hyperfractionated total body irradiation is warranted to assess anti-tumor efficacy.

UI MeSH Term Description Entries
D007938 Leukemia A progressive, malignant disease of the blood-forming organs, characterized by distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemias were originally termed acute or chronic based on life expectancy but now are classified according to cellular maturity. Acute leukemias consist of predominately immature cells; chronic leukemias are composed of more mature cells. (From The Merck Manual, 2006) Leucocythaemia,Leucocythemia,Leucocythaemias,Leucocythemias,Leukemias
D008223 Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. Germinoblastoma,Lymphoma, Malignant,Reticulolymphosarcoma,Sarcoma, Germinoblastic,Germinoblastic Sarcoma,Germinoblastic Sarcomas,Germinoblastomas,Lymphomas,Lymphomas, Malignant,Malignant Lymphoma,Malignant Lymphomas,Reticulolymphosarcomas,Sarcomas, Germinoblastic
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D003037 Cobalt Radioisotopes Unstable isotopes of cobalt that decay or disintegrate emitting radiation. Co atoms with atomic weights of 54-64, except 59, are radioactive cobalt isotopes. Radioisotopes, Cobalt
D003131 Combined Modality Therapy The treatment of a disease or condition by several different means simultaneously or sequentially. Chemoimmunotherapy, RADIOIMMUNOTHERAPY, chemoradiotherapy, cryochemotherapy, and SALVAGE THERAPY are seen most frequently, but their combinations with each other and surgery are also used. Multimodal Treatment,Therapy, Combined Modality,Combined Modality Therapies,Modality Therapies, Combined,Modality Therapy, Combined,Multimodal Treatments,Therapies, Combined Modality,Treatment, Multimodal,Treatments, Multimodal
D003520 Cyclophosphamide Precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent that must be activated in the LIVER to form the active aldophosphamide. It has been used in the treatment of LYMPHOMA and LEUKEMIA. Its side effect, ALOPECIA, has been used for defleecing sheep. Cyclophosphamide may also cause sterility, birth defects, mutations, and cancer. (+,-)-2-(bis(2-Chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-Oxide Monohydrate,B-518,Cyclophosphamide Anhydrous,Cyclophosphamide Monohydrate,Cyclophosphamide, (R)-Isomer,Cyclophosphamide, (S)-Isomer,Cyclophosphane,Cytophosphan,Cytophosphane,Cytoxan,Endoxan,NSC-26271,Neosar,Procytox,Sendoxan,B 518,B518,NSC 26271,NSC26271
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

Related Publications

F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
September 1989, Bone marrow transplantation,
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
September 1992, American journal of hematology,
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
January 1985, Leukemia research,
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
November 1989, Bone marrow transplantation,
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
June 1994, American journal of hematology,
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
November 1993, European journal of pediatrics,
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
November 1983, British journal of haematology,
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
March 1995, Bone marrow transplantation,
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
December 1986, Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al],
F B Petersen, and H J Deeg, and C D Buckner, and F R Appelbaum, and R Storb, and R A Clift, and J E Sanders, and W I Bensinger, and R P Witherspoon, and K M Sullivan
January 1992, Bone marrow transplantation,
Copied contents to your clipboard!