Evaluation of Uracil Mustard in Children with Hodgkin's Disease, Lymphosarcoma, and Soft Tissue Sarcoma

1972 ◽  
Vol 12 (4) ◽  
pp. 169-173 ◽  
Author(s):  
D. H. BERRY ◽  
W. W. SUTOW ◽  
T. J. VIETTI ◽  
D. J. FERNBACH ◽  
M. P. SULLIVAN ◽  
...  
1988 ◽  
Vol 14 (4) ◽  
pp. 224-230 ◽  
Author(s):  
Shelia Hoar Zahm ◽  
Aaron Blair ◽  
F F Holmes ◽  
C D Boysen ◽  
R J Robel

Cancer ◽  
1984 ◽  
Vol 53 (2) ◽  
pp. 232-236 ◽  
Author(s):  
Edward C. Halperin ◽  
Mortimer S. Greenberg ◽  
Herman D. Suit

1983 ◽  
Vol 69 (5) ◽  
pp. 473-476 ◽  
Author(s):  
Marcello Zanini ◽  
Roberto Zucali ◽  
Alberto Banfi

Prolonged follow-up of large series of patients treated for Hodgkin's disease with an intensive therapeutic approach has demonstrated an incidence of second tumors of around 5–10%. Acute leukemia is the most frequent second neoplasia, and treatments including alkylating agents and radiotherapy seem to be correlated with a higher risk of this fatal complication. Bone and soft tissue sarcomas have rarely been observed after treatment of Hodgkin's disease, and only a few cases are described in the literature. Four cases observed at the Istituto Nazionale Tumori of Milano in a large series of nearly 800 patients treated over the last two decades with different modalities are presented. One case of chondrosarcoma and 3 cases of soft tissue sarcomas were diagnosed after a median and mean interval of 50 and 70 months, respectively (range 49–96). Three patients had been treated with radiotherapy plus chemotherapy (MOPP, 2 cases; ABVD, 1 case), and one with radiotherapy alone. The site of the second tumor was always within an irradiated area, which had received a dose ranging from 10 to 43 Gy. Prognosis of secondary bone and soft tissue sarcomas is very poor. Three of our cases died 14, 15 and 19 months after diagnosis; only one patient is alive, 3 months after diagnosis of a chondrosarcoma. The problem of second tumors in patients treated for Hodgkin's disease requires a careful evaluation of aggressive treatment modalities to minimize the risks of this severe complication.


CHEST Journal ◽  
1987 ◽  
Vol 91 (1) ◽  
pp. 136-137 ◽  
Author(s):  
Julian R. Vainright ◽  
John N. Diaconis ◽  
Phillip J. Haney

Author(s):  
J. P. Brunschwig ◽  
R. M. McCombs ◽  
R. Mirkovic ◽  
M. Benyesh-Melnick

A new virus, established as a member of the herpesvirus group by electron microscopy, was isolated from spontaneously degenerating cell cultures derived from the kidneys and lungs of two normal tree shrews. The virus was found to replicate best in cells derived from the homologous species. The cells used were a tree shrew cell line, T-23, which was derived from a spontaneous soft tissue sarcoma. The virus did not multiply or did so poorly for a limited number of passages in human, monkey, rodent, rabbit or chick embryo cells. In the T-23 cells, the virus behaved as members of the subgroup B of herpesvirus, in that the virus remained primarily cell associated.


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