Weekly dose reduces targeted drug's side effects, but not its activity against acute lymphocytic leukemia
MD Anderson News Release 12/10/2012
MD Anderson News Release 12/10/12
A potent chemotherapy agent wrapped within a monoclonal antibody selectively destroys the malignant cells responsible for acute lymphocytic leukemia (ALL) in either weekly or monthly dosing, researchers report at the 54th ASH Annual Meeting and Exposition.
This 'Trojan horse' assault on the cancer cells has significantly increased the response rate among patients with ALL, and now a clinical trial finds that weekly dosing works well and reduces side effects.
"The CD22 antigen is a specific marker for B-cell malignancies and is expressed in more than 90 percent of patients who have acute lymphocytic leukemia," said Susan O'Brien, M.D., professor in The University of Texas MD Anderson Department of Leukemia. "The antigen's specificity for B-cell cancers makes it a promising therapeutic target for intervention."
Bound to a potent toxin
The humanized antibody, known as inotuzumab ozogamicin, is attached to the toxin calicheamicin and binds to CD22. "After binding to the B cell, the antibody is internalized and the linker hydrolyzed, releasing the calicheamicin into only the malignant B cell," O'Brien said. "This enables us to bring in a very potent toxin that could not be given systemically and direct that toxin to the malignant B cell."
The experimental drug was first used in patients with B cell lymphoma. The main toxicity seen in the lymphoma trials was myelosuppression due primarily to deficiency of platelets.
"Myelosuppression is much less of an issue with acute leukemia, whether ALL or acute myelogenous leukemia, because you want to transiently wipe out the bone marrow to eradicate the leukemic cells," O'Brien said. "You expect to have myelosuppression as part of the therapy."
For this study, the researchers used the dose defined as tolerable in the lymphoma trials-1.8 mg/m2-as a starting point.
"We observed very good activity in this relapse/refractory population and an overall response rate of 57 percent," O'Brien said. "The main toxicities were infusion reactions either during or shortly after infusion of the antibody. Patients developed fever sometimes associated with a drop in blood pressure. These were generally grade 1-2 so they were mild and easily treatable." The treatment was also associated with grade 1-2 elevations of transaminases, enzymes that reflect liver function, which had also occurred in the lymphoma trials.
The researchers amended their protocol in an attempt to minimize toxicities. "We wondered whether we could reduce infusion reactions and liver function test elevations by giving the agent on a weekly basis instead of as a bolus every three to four weeks," O'Brien said. "The maximal plasma levels potentially would be lower, but the area under the curve might be the same because we would be giving the same total dose, just spread over three weeks."
Under the new protocol, the researchers gave the same total dose spread out over three weeks: .8 mg/m2 on Day 1 and .5 mg/m2 on Day 8 and Day 15. "We found exactly the same response rate with the weekly dose as with the monthly dose," O'Brien said. "But we did notice that the infusion reactions and the elevations in the transaminases were less frequent with the weekly schedule. This is probably because the side effects are most likely related to the peak concentrations of the drug, and when you spread it over three weeks the peak concentrations are not as high."
"We observed impressive activity in a relapsed, refractory population," O'Brien said. "The toxicities were acceptable and were mainly grade 1-2 reactions to the drug itself, which is not uncommon because most antibodies are associated with mild infusion reactions. Transaminase elevations were predominately grade 1-2, and in the trial as a whole, fewer than five percent of the patients experienced grade 3-4 liver elevations."
O'Brien added that a new trial at MD Anderson is incorporating the antibody with low-dose chemotherapy as a frontline regimen for ALL in patients over age 65.
"One of the biggest complications in treating older patients with ALL is that the treatments cause myelosuppression, which makes patients more vulnerable to infection, and older patients are particularly susceptible to this and other complications," she said. "The idea is to take a very well-tolerated antibody and combine it with chemotherapy. That way we might not have to use full-dose chemo and can reduce side effects."
The clinical trial is funded by Pfizer, Inc., which developed inotuzumab.
Co-investigators with O'Brien are Deborah Thomas, M.D., Farhad Ravandi, M.D., Stefan Faderl, M.D., Jorge Cortes, M.D., Elias Jabbour, M.D., Hagop Kantarjian, M.D., Monica Kwari, B.S.N., Sergernne York, R.N., and Rebecca Garris, BSc, all of MD Anderson's Department of Leukemia; and Jeffrey Jorgensen, M.D., Ph.D., of MD Anderson's Department of Hemopathology; and Partow Kebriaei, M.D., of MD Anderson's Department of Stem Cell Transplantation and Cellular Therapy.