S. Viviani et al., ALTERNATING VERSUS HYBRID MOPP AND ABVD COMBINATIONS IN ADVANCED HODGKINS-DISEASE - 10-YEAR RESULTS, Journal of clinical oncology, 14(5), 1996, pp. 1421-1430
Purpose: To compare, in a prospective randomized trial, the efficacy o
f two different sequences of mechlorethamine, vincristine, procarbazin
e, and prednisone (MOPP) and doxorubicin, bleomycin, vinblostine, and
dacarbazine (ABVD) chemotherapy in untreated advanced Hodgkin's diseas
e. Patients and Methods: From June 1982 to September 1990, 427 consecu
tive previously untreated patients with pathologic stage IB, IIA bulky
, IIB, III (A and B), and IV (A and B) disease were prospectively rand
omized to receive two different sequences of MOPP and ABVD for a minim
um of six cycles followed by radiotherapy (median dose, 30 Gy) to the
nodal site(s) of pretreatment bulky disease, Of 415 assessable patient
s, 211 received one cycle of MOPP monthly, alternated with one cycle o
f ABVD (alternating regimen), and 204 patients received one-half cycle
of MOPP alternated with one-half cycle of ABVD within a 1-month perio
d (hybrid regimen). Results. The complete remission (CR) rate was 91%
with the alternating regimen and 89% with the hybrid regimen. At 10 ye
ars, the freedom-from-progression (FFP) rate was 67% versus 69% and th
e overall survival (OS) rate was 74% versus 72%, respectively. After a
ttainment of CR, 85 patients relapsed in nodal (n = 60) versus extrano
dal with or without nodal (n = 25) sites, In patients given consolidat
ive radiation because of bulky lymphoma, the true recurrence rate was
13%. A total of 23 second malignancies (6%) were documented, including
11 Eases of acute nonlymphocytic leukemia. No cases of congestive hea
rt failure attributable to doxorubicin or pulmonary toxicity related t
o bleomycin were documented. Conclusion: By delivering MOPP and ABVD,
it is possible to cure approximately 70% of patients with advanced Hod
gkin's disease. The two different drug sequences yielded superimposabl
e results. (C) 1996 by American Society of Clinical Oncology.