Abstract |
Therapy for steroid-refractory acute graft-versus-host disease (SR-aGVHD) remains suboptimal. Preclinical data demonstrate increased CD30 expression on activated CD8+ T cells during aGVHD. Brentuximab vedotin (BV) is an antibody-drug conjugate targeting CD30. We conducted a multicenter phase 1 trial in 34 patients to establish the maximum tolerated dose (MTD) of BV for SR-aGVHD treatment. A 3+3 cohort design was conducted initially with BV given weekly × 3 doses followed by maintenance dosing (initial dose 0.6 mg/kg IV weekly). Six patients were treated with the initial weekly dosing scheme; 2 of these patients died of neutropenic sepsis complications. The trial was subsequently revised to escalating cohorts of 5 patients treated every 2 weeks × 4 doses with a 4-week dose-limiting toxicity (DLT) period. Twenty-eight patients were treated with every-2-week dosing (n = 10 at 0.6 mg/kg; n = 18 at 0.8 mg/kg). MTD was defined at 0.8 mg/kg with 1 DLT observed ( sepsis). At day 28, the overall response rate was 38.2% with 5 complete responses (CRs; 14.7%) and 8 very-good-partial responses (23.5%). An additional 7 patients achieved CR by day 56. With 12 months' follow-up on all patients, overall survival was 41% (95% confidence interval [CI], 25%-57%) at 6 months and 38% (95% CI, 22%-54%) at 12 months. CD30 expression on central memory CD8+, central memory CD4+, and regulatory T-lymphocyte subsets at enrollment was not associated with clinical response. BV is tolerable and has activity in SR-aGVHD and merits further investigation. This trial was registered at www.clinicaltrials.gov as #NCT01940796.
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Authors | Yi-Bin Chen, Miguel-Angel Perales, Shuli Li, Maria Kempner, Carol Reynolds, Jami Brown, Yvonne A Efebera, Steven M Devine, Areej El-Jawahri, Steven L McAfee, Thomas R Spitzer, Robert J Soiffer, Jerome Ritz, Corey Cutler |
Journal | Blood
(Blood)
Vol. 129
Issue 24
Pg. 3256-3261
(06 15 2017)
ISSN: 1528-0020 [Electronic] United States |
PMID | 28473406
(Publication Type: Clinical Trial, Phase I, Journal Article, Multicenter Study)
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Copyright | © 2017 by The American Society of Hematology. |
Chemical References |
- Immunoconjugates
- Ki-1 Antigen
- Brentuximab Vedotin
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Topics |
- Acute Disease
- Adult
- Aftercare
- Aged
- Allografts
- Brentuximab Vedotin
- CD8-Positive T-Lymphocytes
(immunology, pathology)
- Female
- Graft vs Host Disease
(drug therapy, immunology, pathology)
- Hematopoietic Stem Cell Transplantation
- Humans
- Immunoconjugates
(administration & dosage, adverse effects)
- Ki-1 Antigen
(immunology)
- Male
- Maximum Tolerated Dose
- Middle Aged
- Neoplasms
(immunology, therapy)
- T-Lymphocytes, Regulatory
(immunology, pathology)
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