Philip Morris
Directory of on-Going Research in Cancer Epidemiology 870000 Sero-Epidemiology of the Epstein-Barr Virus
Fields
- Author
- Parkin, D.M.
- Wahrendorf, J.
- Document File
- 2023234446/2023234895/Philip Morris: Witnesses C.R.W.
- Type
- REPT, REPORT, OTHER
- Area
- WALL,CHARLES/OFFICE
- Named Organization
- Childrens Hospital of Philadelphia
- Joseph Stokes Jr Research Inst
- Site
- N328
- Named Person
- Albeck, H.
- Barr
- Berkel, A.I.
- Burkitt
- Cheliak
- Demaret, E.
- Epstein
- Fleisher, G.
- Henle, G.
- Higashi
- Hirsch, M.S.
- Hodgkin
- Horwitz, C.A.
- Klein, G.
- Lanier, A.K.
- Levine, A.
- Merino, F.
- Nagytiborcz, A.
- Pearson, G.R.
- Schlaefer, K.
- Villhauerlehr, M.
- Whelan, S.
- Barr
- Author (Organization)
- Dkfz
- Iarc
- Master ID
- 2023234542/4594
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- Date Loaded
- 24 May 1999
- UCSF Legacy ID
- kht61f00
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DIRECTORY
OF ON-GOING RESEARCH
IN CANCER EPIDEMIOLOGY
1987
IARC
DKFZ
D. M. Parkin
J. Wahrendorf
In collaboration with
E. Demaret
A. Nagy-Tiborcz
K. Schlaefer
M. Villhauer-Lehr
S. Whelan
ttBRARY REFERENCE ONLY

UNITED STATES OF AMERICA Pennsylvania
TERM: Aetiology; Clinical Effects; Delayed Effects; Environment; Familial, Genetic; Folbw-Up;
Germinal'Mutation; Ti
Mutation Epidemiology; Sib; Treatment I
SITE: Wilms' Tumou !r
TIME: 1979 - `
L
f 1229 / 1987 / ID: 00022 T
Hanle, W.
Children s Hosp. of Philadelphia, The Joseph Stokes Jr. Research lnst:, Div. of Virology, 34th and
Civic Center Bivd, 1
. Philadelphia, PA 19104, USA (TeL:(215) 596-9435/3876180) k
COLL: Henle, G.; Fleisher, G.; Klein, G.;',Pearson; G.R:; Horwitz, C.A,; Hirsch, MS.; Berkel,
A.I.; Lanier, A.K:; L
Merino, F.; Albeck, H.; Levine, A. ! C
II C
Saro-Epid.miology of the Epstein-Barr Virus
i The aims of these studies are (1) to apply EBV-specific serological tests measunng antibodies of
different ~ C
immune globulin classes against several virus-coded antigens to the diagnosis, prognosis and
post-therapeutic j
monitoring of patients with EBV-associated cancers; i.e. Burkitt's tymphoma, nasopharyngeal
carcinoma and I
now also B cell lymphomas that arise with enhanced freqpency in immunologically compromised
patients.
Whenever possible, malignant cells in touch preparations made from biopsies will be examined for the
presence
of the EBV-associated nuclear antigen (EBNA); (2) to determine the effects of immunological
deficiencies, be
they of genetic (e.g., ataxia telangiectasia, or Cheliak-Higashi~Syndrome), therapeutic (organ
transplant reci-
pients), or disease-related origins (such as Hodgkin's disease or Aquired Immunodeficiency Syndrome)
upon
, the immune responses to primary or reactivation of persistent EBV infections in efforts to obtain
information on
the mechanism(s) leading to the setf-limitation of infectious mononucleosis and the control of the
regularly
ensuing latent viral carrier state and to evaluate the EBV-specific serology as another parameter in
the ~
assessment of immunological incompetence.
TERM: Aetiology; Antibodies: Antigens; Immunosuppression; Infection; Virus j
SITE: Burkitt'S Lymphoma; Hodgkin's Disease; Lymphomas; Nasopharynx Neoplasms
LOCA: Denmark; Greenland; Sweden; Turkey; United States of America; Venezuela
~ TIME: 1966 - } ~
:
1230/'1987/ID:02480 ~ ~
London, W.T.
Inst. for Cancer Research, Fox Chase Cancer Center; Univ: of Pennsylvania, School of Medicine,
Clinical Research
Div., 77018urholme Ave, Philadelphia, PA 19111, USA (Tel.:(215) 728-2204) ~
COLL: Ablin, A.A. l'
c
Rrlation of HBV Merkers In Children with Hspatoblastoma or Primary Hepetocpltular Carcinoma ~
Primary, cancers of the liver are rare in children. In ~ collaboratron with the Children's Cancer
Study Group an
investigation of HBV markers, including HBV DNA, in serum and liver tissue in children with these
tumours is E
being carried out. About 39 patients per year will be studied They will be drawn from hospitals in
the US
participating in a protocol for the treatment of hepatoblastoma and hepatocellular carcinoma in
children.
TERM: Case Characteristics; Child; Infection; Virus
SITE: Liver NeopVasms
TIME: 1980 - 1987
)
>
1231 / 1987 / 1D: 00318
Meadows, A.T-
Univ. of Pennsylvania, Children's Hosp., Div. ot Oncology, Childrens Cancer Research Center, 34th
and Civic
Center Blvd, Philadelphia, PA 19104, USA (Tel.:(215) 596-9644)
COLL: Banfi, A.; Baum, E.; d'Angio, G.J.; Green, D.; LeMerle, J.; Marsden, H.B.; Morris-Jones, P.H.;
NesbitM.;
Newton, W.A.;, Obringer, A.; Sallan, S.; Sandberg, A.; Siegef, S:; Vawter G.; Voute PA.;
Woods; W:;
Zipursky, A.
Late Eff.cts of Successful Cancer Therapy In Children
The success of multi-modal and adjuvant therapy in improving the prognosis of childhood cancer has
been
dramaticwith the current overall long-term survival proportion reaching 60%. Concomitant with
improvements in
survival rates, however~ has come the realization that children cured of primary malignancies may be
at
increased risk of second malignant neoplasms (SMN) which may be related to the radio/'chemotherapies
they
received6 to genetic predispositions or a combination of botti, A 12-member international consortium
of institu-
tions, the Late Effects Study Group, has been~ formed to study patterns of, occurrence and risk
factors for
development of, SMN among children, treated for a primary malignancy and surviving at least two
years post
diagnosis. A registry of suchipatients, now including 300 children, serves as the basis for
investigating (1) the
incidence of SMN; (2) histopathology of, SMN; (~) identification of risk factors for SMN, including
therapy and
genetic factors; (4) unusual tumour associations in children with SMN; (5) congenital anomalies
associated with
SMN;,(6) family history in,children with SMN, particularly with regard to cancer, genetic disorders,
and congenitat
anomalies. A paper appeared in Radiation, JiD. Boice Jr and J.F. Fraumeni, Jr; (Eds),
Carcinogenesis: Epide-
miology and'Biol; Significance, pp. 21 t224, Raven Press, New York 1984.
394
