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Rituximab plus liposomal doxorubicin in HIV-infected patients with KSHV-associated multicentric Castleman disease.

Authors :
Uldrick TS
Polizzotto MN
Aleman K
Wyvill KM
Marshall V
Whitby D
Wang V
Pittaluga S
O'Mahony D
Steinberg SM
Little RF
Yarchoan R
Source :
Blood [Blood] 2014 Dec 04; Vol. 124 (24), pp. 3544-52. Date of Electronic Publication: 2014 Oct 20.
Publication Year :
2014

Abstract

Kaposi sarcoma (KS) herpesvirus-associated multicentric Castleman disease (KSHV-MCD) is a lymphoproliferative disorder, most commonly seen in HIV-infected patients, that has a high mortality if untreated. Concurrent KS is common. Although rituximab has reported activity in KSHV-MCD, its use is often associated with KS progression. Within a natural history study of KSHV-MCD, we prospectively evaluated rituximab 375 mg/m(2) combined with liposomal doxorubicin 20 mg/m(2) (R-Dox) every 3 weeks in 17 patients. Patients received a median of 4 cycles (range 3-9). All received antiretroviral therapy, 11 received consolidation interferon-α, and 6 received consolidation high-dose zidovudine with valganciclovir. Using NCI KSHV-MCD response criteria, major clinical and biochemical responses were attained in 94% and 88% of patients, respectively. With a median 58 months' potential follow-up, 3-year event-free survival was 69% and 3-year overall survival was 81%. During R-Dox therapy, cutaneous KS developed in 1 patient, whereas 5 of 6 patients with it had clinical improvement. R-Dox was associated with significant improvement in anemia and hypoalbuminemia. KSHV viral load, KSHV viral interleukin-6, C-reactive protein, human interleukin-6, and serum immunoglobulin free light chains decreased with therapy. R-Dox is effective in symptomatic KSHV-MCD and may be useful in patients with concurrent KS. This trial was registered at www.clinicaltrials.gov as #NCT00092222.

Details

Language :
English
ISSN :
1528-0020
Volume :
124
Issue :
24
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
25331113
Full Text :
https://doi.org/10.1182/blood-2014-07-586800