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Three-Drug Regimen Produces High Response Rate in Relapsed/Refractory Multiple Myeloma

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Key Points

  • The combination of bendamustine with bortezomib and dexamethasone in patients with relapsed/refractory multiple myeloma produced an overall response rate of 60.9% of patients in a phase II trial.
  • The short time to response (31 days) and to best response (111 days) is considered clinically relevant, because rapid tumor control usually corresponds with fast improvement of clinical symptoms.

A phase II trial to evaluate the combination of bendamustine (Treanda) with bortezomib (Velcade) and dexamethasone in patients with relapsed/refractory multiple myeloma “showed a remarkable response rate of 60.9%, and, when minor responses were included in 75.9% of patients,” researchers reported in Blood. “The short time to response (31 days) and to best response (111 days) is clinically relevant, because rapid tumor control usually corresponds with fast improvement of clinical symptoms,” the investigators noted.

The 79 study patients were enrolled by nine participating centers in Austria and the Czech Republic. The patients’ median age was 64. Most had stage I (34.2%) or stage II disease (39.2%). The median number of prior treatment lines was two.

Treatment consisted of bendamustine at 70 mg/m2 on day 1 and 4, bortezomib at 1.3 mg/m2 on days 1, 4, 8, 11 intravenously, and dexamethasone at 20 mg on days 1, 4, 8, and 11. Cycles were repeated every 4 weeks until a maximum of eight cycles. In case of patients with no response, treatment was discontinued at cycle 4, the investigators explained.

Complete response occurred in 12 patients, very good partial response in 16 patients, and partial response in 20 patients, yielding the overall response rate of 60.9%. Adding the minor responses in 12 patients resulted in the overall response rate of 75.9%. The overall response rate was similar in patients who had been previously exposed to bortezomib, lenalidomide (Revlimid), and to both bortezomib and lenalidomide.

Relatively Well Tolerated

The overall response rate was lower for patients with adverse cytogenetic features than for those without such aberrations, as defined by fluorescence in situ hybridization (53% vs 67%). Progression-free survival of 9.7 months, and overall survival of 25.6 months; these endpoints did not differ significantly according to adverse cytogenetic features. “Multivariate analysis showed high LDH, ≥ 3 prior treatment lines, and low platelet counts correlating with short survival,” the investigators noted.

The treatment regimen was relatively well tolerated, although grade 3/4 hematologic toxicities were seen in up to one-third of patients, the authors noted. Grade 3 to 5 infections were observed in 23% of our patients, two of whom had fatal outcomes. “Hence, G-CSF [Neupogen] prophylaxis should be considered particularly in elderly frail patients. Herpes zoster prophylaxis is mandatory but clinical virus reactivation may occur even during adequate prophylaxis.”

Grade < 2 polyneuropathy increased with duration of therapy, from 19% at baseline to 52% at cycle 8. Other nonhematologic side effects, mostly grade 1/2, included insomnia/fatigue, nausea, emesis, and constipation.

Heinz Ludwig, MD, of Wilhelminenspital in Vienna, Austria, is corresponding author of the Blood article.

The study was supported by the Austrian Forum Against Cancer. For full disclosures of the study authors, visit bloodjournal.hematologylibrary.org.

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.


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