TY - JOUR
T1 - CCNU, vinblastine, procarbazine and prednisone (CVPP) with extended- field radiotherapy in the treatment of early unfavorable Hodgkin's disease
T2 - A prospective study on behalf of the Gruppo Italiano per lo Studio dei Linfomi (GISL)
AU - Gobbi, P. G.
AU - Pieresca, C.
AU - Cavanna, L.
AU - Corbella, F.
AU - Vallisa, D.
AU - Federico, M.
AU - Formisano, R.
AU - Carotenuto, M.
AU - Merli, F.
AU - Callea, V.
AU - Angrilli, F.
AU - Silingardi, V.
PY - 1996
Y1 - 1996
N2 - Purpose. To test the adequacy of the CVPP four-drug regimen as ancillary chemotherapy associated with extended-field radiotherapy in the treatment of early, unfavorable, clinically staged Hodgkin's disease. Patients and Methods. The population of this prospective, multicenter study consisted of 49 patients with stage I-II disease, associated with bulky involvement or unfavorable histology (lymphocyte-depleted nodular sclerosis or lymphocyte depletion), systemic symptoms or extranodal involvement, or presenting with stage III A favorable-histology disease, with or without extranodal involvement. Results. Complete remission was achieved in 39 patients, partial remission in 2, while 8 patients did not respond. Four patients have relapsed so far (median follow-up: 43 months), all of whom were subsequently rescued with different salvage treatments. Dose intensity (mean±SD: 0.83±0.12) and hematological toxicity (including 2 deaths from infection) were higher when RT followed CT than when it was interposed in the middle of the 6 cycles. No growth factors were used. Non-hematological toxicity was very low and fully tolerable. Conclusions. Results confirmed the mild neurological and gastroenteric side effects of CVPP that make it an interesting MOPP-variant regimen. This combination seems most indicated when a regimen devoid of cardiac and pulmonary toxicity is required for association with full-dosage mediastinal radiotherapy, as is often the case in early, unfavorable Hodgkin's disease. The optimal sequence consists of radiotherapy administered after completion of the chemotherapy program. The use of growth factors for correction (or prevention) of marked leukopenia seems appropriate.
AB - Purpose. To test the adequacy of the CVPP four-drug regimen as ancillary chemotherapy associated with extended-field radiotherapy in the treatment of early, unfavorable, clinically staged Hodgkin's disease. Patients and Methods. The population of this prospective, multicenter study consisted of 49 patients with stage I-II disease, associated with bulky involvement or unfavorable histology (lymphocyte-depleted nodular sclerosis or lymphocyte depletion), systemic symptoms or extranodal involvement, or presenting with stage III A favorable-histology disease, with or without extranodal involvement. Results. Complete remission was achieved in 39 patients, partial remission in 2, while 8 patients did not respond. Four patients have relapsed so far (median follow-up: 43 months), all of whom were subsequently rescued with different salvage treatments. Dose intensity (mean±SD: 0.83±0.12) and hematological toxicity (including 2 deaths from infection) were higher when RT followed CT than when it was interposed in the middle of the 6 cycles. No growth factors were used. Non-hematological toxicity was very low and fully tolerable. Conclusions. Results confirmed the mild neurological and gastroenteric side effects of CVPP that make it an interesting MOPP-variant regimen. This combination seems most indicated when a regimen devoid of cardiac and pulmonary toxicity is required for association with full-dosage mediastinal radiotherapy, as is often the case in early, unfavorable Hodgkin's disease. The optimal sequence consists of radiotherapy administered after completion of the chemotherapy program. The use of growth factors for correction (or prevention) of marked leukopenia seems appropriate.
KW - Early stages
KW - Hodgkin's disease
KW - Multiple drug chemotherapy
KW - Radiotherapy
KW - Unfavorable prognosis
UR - http://www.scopus.com/inward/record.url?scp=0030323813&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0030323813&partnerID=8YFLogxK
M3 - Article
C2 - 9009437
AN - SCOPUS:0030323813
VL - 81
SP - 503
EP - 512
JO - Haematologica
JF - Haematologica
SN - 0390-6078
IS - 6
ER -