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world cancer report - iarc

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Fig. 5.106 Five-year relative survival rates after<br />

diagnosis of Hodgkin disease.<br />

Fig. 5.107 Five-year relative survival rates after<br />

diagnosis of non-Hodgkin lymphoma.<br />

REFERENCES<br />

1. Cartwright RA, Gilman EA, Gurney KA (1999) Time<br />

trends in incidence of haematological malignancies and<br />

related conditions. Br J Haematol, 106: 281-295.<br />

2. Baris D, Zahm SH (2000) Epidemiology of lymphomas.<br />

Curr Opin Oncol, 12: 383-394.<br />

3. Jaffe ES, Lee Harris N, Stein H, Vardiman JW, eds<br />

(2001) World Health Organization Classification of<br />

Tumours. Pathology and Genetics of Tumours of<br />

Haematopoietic and Lymphoid Tissues, Lyon, IARCPress.<br />

4. Harris NL, Jaffe ES, Stein H, Banks PM, Chan JK, Cleary<br />

ML, Delsol G, Wolf-Peeters C, Falini B, Gatter KC (1994) A<br />

revised European-American classification of lymphoid neoplasms:<br />

a proposal from the International Lymphoma Study<br />

therapy protocols, so-called “second and<br />

third generation regimens”, have met with<br />

little success. However, the introduction<br />

of the International Prognostic Index may<br />

help to identify patients who will benefit<br />

from more aggressive strategies [9]. In<br />

patients who relapse after conventional<br />

therapy, and who still have “sensitive disease”,<br />

high-dose chemotherapy with stem<br />

cell rescue appears to offer a reasonable<br />

salvage option.<br />

Hodgkin disease<br />

In contrast to non-Hodgkin lymphomas,<br />

the management of Hodgkin disease is<br />

usually dictated by the stage of disease<br />

rather than the histology [10,11]. Most<br />

centres would use radiotherapy for early<br />

stage (IA or IIA) disease, although there is<br />

a trend towards considering limited<br />

chemotherapy as an option. All other<br />

stages should have chemotherapy, and<br />

the traditional “gold standard” MOPP<br />

(mustine, vincristine, procarbazine and<br />

prednisone) therapy has been superseded<br />

by ABVD (adriamycin [doxorubicin],<br />

bleomycin, vinblastine and dacarbazine)<br />

which appears to be as efficacious without<br />

the adverse effects (particularly related<br />

to fertility and the development of second<br />

malignancies). The German Hodgkin<br />

Disease Study Group has proposed a<br />

prognostic model for advanced stage disease,<br />

and has identified seven factors<br />

which influence outcome. These are age,<br />

sex, histology, B symptoms, number of<br />

Group. Blood, 84: 1361-1392.<br />

5. Macintyre EA, Delabesse E (1999) Molecular<br />

approaches to the diagnosis and evaluation of lymphoid<br />

malignancies. Semin Hematol, 36: 373-389.<br />

6. Bierman PJ, Armitage JO (1996) Non-Hodgkin's lymphoma.<br />

Curr Opin Hematol, 3: 266-272.<br />

7. Pinkerton CR (1999) The continuing challenge of treatment<br />

for non-Hodgkin's lymphoma in children. Br J<br />

Haematol, 107: 220-234.<br />

8. Zucca E, Bertoni F, Roggero E, Cavalli F (2000) The<br />

gastric marginal zone B-cell lymphoma of MALT type.<br />

Blood, 96: 410-419.<br />

9. International Non-Hodgkin's Lymphoma Prognostic<br />

Factors Project (1993) A predictive model for aggressive<br />

involved sites, bulk of disease and erythrocyte<br />

sedimentation rate. Using such<br />

models it may be possible to identify poor<br />

prognosis patients who will benefit from<br />

more aggressive high-dose therapies,<br />

such as Stanford V (doxorubicin, vinblastine,<br />

mustard, bleomycin, vincristine,<br />

etoposide and prednisone) or BEACOPP<br />

(bleomycin, etoposide, adriamycin [doxorubicin],<br />

cyclophosphamide, oncovin<br />

[vincristine], procarbazine and prednisone)<br />

from the outset (Medical oncology,<br />

p281).<br />

Survival for both Hodgkin disease and<br />

non-Hodgkin lymphomas has improved<br />

markedly with time, in response to the<br />

development of more effective<br />

chemotherapy and bone marrow transplantation.<br />

Five-year survival after diagnosis<br />

of non-Hodgkin lymphoma patients in<br />

most developed countries is more than<br />

50%, but only 17-35% in developing countries<br />

(Fig. 5.107). Currently, survival of<br />

Hodgkin disease patients is related to<br />

extent of disease at diagnosis; overall, at<br />

five years it is between 70% and 90% in<br />

North America and Europe, but only 30-<br />

55% in developing countries (Fig. 5.106).<br />

non-Hodgkin's lymphoma. The International Non-<br />

Hodgkin's Lymphoma Prognostic Factors Project. N Engl J<br />

Med, 329: 987-994.<br />

10. Horwitz SM, Horning SJ (2000) Advances in the treatment<br />

of Hodgkin's lymphoma. Curr Opin Hematol, 7: 235-240.<br />

11. Aisenberg AC (1999) Problems in Hodgkin's disease<br />

management. Blood, 93: 761-779.<br />

Lymphoma<br />

241

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