PMID- 12200356 OWN - NLM STAT- MEDLINE DCOM- 20021024 LR - 20210206 IS - 0006-4971 (Print) IS - 0006-4971 (Linking) VI - 100 IP - 6 DP - 2002 Sep 15 TI - Stanford V regimen and concomitant HAART in 59 patients with Hodgkin disease and HIV infection. PG - 1984-8 AB - A phase 2 prospective study was performed to evaluate the feasibility and activity of a short, dose-intensive chemotherapy regimen and radiotherapy (the Stanford V regimen) plus highly active antiretroviral therapy (HAART) and granulocyte colony-stimulating factor (G-CSF) support in patients with Hodgkin disease and HIV infection. Fifty-nine patients were enrolled. Stanford V was well tolerated and 69% of the patients completed treatment with no dose reduction or delayed chemotherapy administration. The most important dose-limiting side effects were bone marrow toxicity and neurotoxicity. Complete remission was achieved by 81% of the patients, and after a median follow-up of 17 months 33 patients (56%) were alive and disease-free. The estimated 3-year overall survival (OS), disease-free survival (DFS), and freedom from progression (FFP) were 51%, 68%, and 60%, respectively. Probability of FFP was significantly (P =.02) higher among patients with an International Prognostic Score (IPS) of 2 or lower than in those with an IPS higher than 2, and the percentages of FFP at 2 years in these groups were 83% and 41%, respectively. Similarly, the probability of OS was significantly (P =.0004) different in the 2 groups, and the percentages of OS at 3 years were 76% and 33%, respectively. Our data confirm that the Stanford V regimen with concomitant HAART is feasible and active in an HIV setting. However, a more intensive approach should be considered in patients with high IPSs. FAU - Spina, Michele AU - Spina M AD - Division of Medical Oncology A, National Cancer Institute, Via Pedemontana Occidentale 12, 33081 Aviano (PN), Italy. FAU - Gabarre, Jean AU - Gabarre J FAU - Rossi, Giuseppe AU - Rossi G FAU - Fasan, Marco AU - Fasan M FAU - Schiantarelli, Clara AU - Schiantarelli C FAU - Nigra, Ezio AU - Nigra E FAU - Mena, Maurizio AU - Mena M FAU - Antinori, Andrea AU - Antinori A FAU - Ammassari, Adriana AU - Ammassari A FAU - Talamini, Renato AU - Talamini R FAU - Vaccher, Emanuela AU - Vaccher E FAU - di Gennaro, Giampiero AU - di Gennaro G FAU - Tirelli, Umberto AU - Tirelli U LA - eng PT - Clinical Trial PT - Clinical Trial, Phase II PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't PL - United States TA - Blood JT - Blood JID - 7603509 RN - 11056-06-7 (Bleomycin) RN - 50D9XSG0VR (Mechlorethamine) RN - 5J49Q6B70F (Vincristine) RN - 5V9KLZ54CY (Vinblastine) RN - 6PLQ3CP4P3 (Etoposide) RN - 80168379AG (Doxorubicin) RN - VB0R961HZT (Prednisone) RN - Stanford V protocol SB - IM MH - Adult MH - Aged MH - Antineoplastic Combined Chemotherapy Protocols/administration & dosage/*therapeutic use/toxicity MH - Antiretroviral Therapy, Highly Active/*methods MH - Bleomycin/administration & dosage MH - Disease-Free Survival MH - Doxorubicin/administration & dosage MH - Etoposide/administration & dosage MH - HIV Infections/complications/*drug therapy/mortality MH - HIV-1 MH - Hodgkin Disease/*drug therapy/mortality/virology MH - Humans MH - Lymphoma, AIDS-Related/*drug therapy/mortality MH - Male MH - Mechlorethamine/administration & dosage MH - Middle Aged MH - Prednisone/administration & dosage MH - Prognosis MH - Prospective Studies MH - Remission Induction/methods MH - Survival Analysis MH - Survival Rate MH - Vinblastine/administration & dosage MH - Vincristine/administration & dosage EDAT- 2002/08/30 10:00 MHDA- 2002/10/31 04:00 CRDT- 2002/08/30 10:00 PHST- 2002/08/30 10:00 [pubmed] PHST- 2002/10/31 04:00 [medline] PHST- 2002/08/30 10:00 [entrez] AID - S0006-4971(20)50993-2 [pii] AID - 10.1182/blood-2002-03-0989 [doi] PST - ppublish SO - Blood. 2002 Sep 15;100(6):1984-8. doi: 10.1182/blood-2002-03-0989.