ASCO 2012 Multiple Myeloma Update – Day Three: Carfilzomib And Pomalidomide

Results from many important multiple myeloma studies were presented this morning during the third day of the American Society of Clinical Oncology (ASCO) annual meeting. Most of the talks were about potential new anti-myeloma drugs.
This update will summarize the presentations about carfilzomib (Kyprolis) and pomalidomide (Pomalyst), two of the most promising new treatments being developed for multiple myeloma. Both of these drugs have been submitted to the U.S. Food and Drug Administration for potential approval as new myeloma treatments.
Carfilzomib
The first three presentations were about carfilzomib. Like Velcade (bortezomib), carfilzomib belongs to the class of drugs known as proteasome inhibitors.
The session started with a presentation by Dr. Philippe Moreau from the University Hospital in Nantes, France. Dr. Moreau presented results from a Phase 1/2 clinical trial testing carfilzomib in combination with melphalan (Alkeran) and prednisone in elderly newly diagnosed multiple myeloma patients (abstract).
The goal of the study was to identify the best dose for carfilzomib when used in this combination. Among the 24 patients included in Phase 1 of the trial, the maximum tolerated dose was 36 mg/m2 of carfilzomib.
An additional 16 patients were enrolled in Phase 2 of the trial. Among the 35 patients in both phases of the trial who were evaluated for response, the overall response rate was 89 percent, with 3 percent achieving a complete response, 40 percent achieving a very good partial response, and 46 percent a partial response.
The second presentation was by Dr. Joseph Mikhael from the Mayo Clinic in Scottsdale, Arizona. He presented results from the Phase 2 portion of a Phase 1/2 trial testing a regimen known as “CYCLONE.” The regimen consists of carfilzomib in combination with cyclophosphamide (Cytoxan), thalidomide (Thalomid), and dexamethasone (Decadron) (abstract).
Twenty-seven newly diagnosed myeloma patients eligible for stem cell transplantation were enrolled in the study. Among the 24 patients evaluated for response, the overall response rate was 96 percent. Specifically, 29 percent achieved a complete response, 46 percent a very good partial response, and 21 percent a partial response.
The most common severe side effects were fatigue, low white blood cell counts, blood clots, and muscular weakness. Additionally, 29 percent developed mild peripheral neuropathy (pain, tingling, or loss of sensation in the extremities, and a common side effect of Velcade).
Dr. Jakubowiak from the University of Chicago gave the final presentation about carfilzomib. He presented long-term follow-up results from a Phase 1/2 study of carfilzomib in combination with Revlimid (lenalidomide) and low-dose dexamethasone (abstract).
Fifty-three newly diagnosed myeloma patients were included in the study. Patients could enroll in the study regardless if they were transplant eligible or ineligible.
Thus far, 98 percent of patients have responded to the treatment. Forty two percent have achieved a stringent complete response, and an additional 20 percent have achieved a near complete response. Among the 22 patients who achieved a complete response, 91 percent had no evidence of residual disease.
The progression-free survival rate was 97 percent at one year and 92 percent at two years.
Among patients who received more than eight cycles of the combination therapy, the most common side effects were low white blood cell counts and fatigue. Dr. Jakubowiak reported that peripheral neuropathy was limited, with 11 percent of patients experiencing mild or moderate neuropathy.
In a presentation that also took place during this morning's session, Dr. Robert Orlowski of the M.D. Anderson Cancer Center reviewed the three carfilzomib studies. During his talk, he said that the three studies showed attractive response rates and, in some cases, deeper responses than in comparable previous trials that used Velcade instead of carfilzomib.
In addition, carfilzomib may offer a better side effect profile than Velcade. However, Dr. Orlowski believes future comparisons between the two drugs should account for the fact that Velcade is increasingly being administered subcutaneously and just once a week, which noticeably improves its side effect profile. (As a courtesy to The Beacon's readers, Dr. Orlowski has made his presentation (PowerPoint format) available for download and viewing.)
Pomalidomide
Later in the session, Dr. Ravi Vij from Washington University School of Medicine in St. Louis presented results from a Phase 2 study of pomalidomide for advanced myeloma patients (abstract).
The study included 221 relapsed and refractory myeloma patients with a median of five previous lines of therapy. Half were treated initially with pomalidomide alone, while the other half were treated with pomalidomide plus low-dose dexamethasone. Results from the trial were presented last year at the American Society of Hematology meeting (see related Beacon news).
Today, Dr. Vij presented an analysis of outcomes of the patients treated with pomalidomide and low-dose dexamethasone who were refractory (resistant) to previous treatment with Revlimid, Velcade, or both. Seventy-seven percent were refractory to Revlimid, 73 percent to Velcade, and 61 percent to both. Additionally, 42 percent were refractory to both and also had received a stem cell transplant.
Among these patients, 20 percent achieved at least a partial response, median progression-free survival was 3.5 months, and the one-year survival rate was 59 percent. These outcomes were similar regardless of whether patients were refractory to Revlimid or Velcade, both, or had a previous transplant.
Dr. Vij said that these results suggest that patients resistant to Revlimid will not necessarily be resistant to pomalidomide, despite that the two drugs are chemically related to one another.
Dr. Vij has made his presentation available to The Beacon as a courtesy to the Beacon's readers.
Myeloma presentations from today and the rest of the ASCO meeting will be summarized in additional ASCO daily updates. Further coverage of key research results from the meeting will continue throughout the rest of the week in individual, topic-specific news articles. For all Beacon articles related to this year’s ASCO meeting, see The Beacon’s full ASCO 2012 coverage.
Related Articles:
- Once-Weekly High-Dose Kyprolis Yields Deeper Responses And Longer Remissions Than Twice-Weekly Kyprolis (ASCO & EHA 2018)
- ASCO 2018 Update – Expert Perspectives On The Key Multiple Myeloma-Related Oral Presentations
- Nelfinavir-Velcade Combination Very Active In Advanced, Velcade-Resistant Multiple Myeloma
- Nelfinavir Shows Only Limited Success In Overcoming Revlimid Resistance In Multiple Myeloma Patients
- Common Measures Of Heart And Blood Vessel Health May Predict Risk Of Heart-Related Side Effects During Treatment With Kyprolis
So is Carfilzomib going to be released as a first line treatment or initially only for refractory application?
Onyx applied to the Food and Drug Administration to have carfilzomib approved for treatment of relapsed and refractory multiple myeloma patients who have had at least two prior therapies. So if carfilzomib gets approved by the end of July based on the current submission, it will be only for relapsed and refractory myeloma.
Regarding the CRd studies, I was wondering about the following:
(1) What percentage of patients who attained an sCR maintained an sCR at 1 and 2 years?
(2) Similarly what percent of patients that attained sCR progressed at 1 and 2 years. I know that the rate was 92 and 97 percent for nCR and sCR -- but what about sCR alone? Did it matter?
(3) Regardless, it will be more than interesting to see whether -- akin to total therapy a la Barlogie -- patients who maintain an sCR for say 3-4 years are operationally cured. Let's keep our fingers crossed.
Hi Dan,
Are your questions about NDMM patients or R/R patients?
The data that has been sent to FDA for approval is with R/R patients. Trials and data on NDMM is ongoing in several trials presently.
NDMM -- where the high rate of sCR was observed -- including I think for you?
Same response as Shane for your SR.
Why just R/R patients on the FDA submission and not ND patients as well?
Sorry SR: Let me be clearer, as my message was garbled. What I was looking for were the results for newly diagnosed patients.
The trials for NDMM patients were not completed. This is typical and we can see the same for lenalidamide as well, it too has no indication to date for NDMM.
Trials are expensive as you know. Once the mfgr receives approval for one indication, clinicians can and will, as you know, use the agent beyond the initial indication.
Yes, Shane
..also true for Kevin.
Hi Steve,
The goal was to receive approval as quickly as possible. That often times means submission with data that has been completed. That can be a good thing for patients as many others, outside of clinical trial setting, would have access to the drug, as opposed to having to continue to wait for therapy outside of a clinical trial.
Hi Dan,
Jakobuwiak presented data at ASH 2011 and ASCO 2012 on NDMM patients. The Beacon did write ups also.
http://www.oncologystat.com/news/Phase_II_Results_Continue_to_Support_Carfilzomib_in_Myeloma.html
http://www.myelomabeacon.com/news/2011/12/19/ash-2011-multiple-myeloma-update-day-three-afternoon-carfilzomib-and-pomalidomide/
Well, let's hope it gets approved next month, so physicians have the option to use it for NDMM patients (even if officially approved for RR patients).
This same situation is already the case for revlimid of course.
This study was published in 2011 and shows a great PFS curve for patients that had a stringent CR plus Immunophenotypic response (IR) from Induction only. Figure 3 shows this. European studies have been showing this for some time. Achieving sCR does not appear to improve outcomes over CR or VGPR but IR with sCR does.
http://jco.ascopubs.org/content/29/12/1627.full
Dan D - 3-4 years or remission is too short of a time period to think a patient is operationally cured in the non-Allo setting IMO. This Italian study showing Molecular Responses first being lost after 4 years of remission. Also, UAMS studies are showing PFS curves with patients staying on therapy. In the Allo setting most PFS curves flatten after 5 years of Remission with no therapy. Since patients in the non-Allo setting do not have a Donor immune system to protect against relapse, I could not imagine 3-4 years of remission in the non-Allo setting could ever be considered a functional cure until we have better testing techniques.
https://ash.confex.com/ash/2011/webprogram/Paper36584.html
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