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Novel Options in Melanoma and Multiple Myeloma

Evidence-Based OncologyThe American Society of Clinical Oncology Annual Meeting, 2015
Volume 21
Issue SP10

Immuno-oncology continues to deliver results in oncology, as seen from results presented at the annual meeting of the American Society of Clinical Oncology. The combination of nivolumab and ipilimumab significantly improved survival in melanoma, while elotozumab showed encouraging results in relapsed refractory multiple myeloma.

Checkmate 67 Results Push Nivolumab Closer to First Line in Melanoma

The much-anticipated phase 3 results from the CheckMate 067 trial were presented during the Plenary Session on the third day of the annual meeting of the American Society of Clinical Oncology, held at the McCormick Convention Center, Chicago, May 29-June 2, 2015. A late-breaking abstract, “Efficacy and Safety Results From a Phase III Trial of Nivolumab Alone or Combined With Ipilimumab Versus Ipilimumab Alone in Treatment-Naïve Patients With Advanced Melanoma,” was presented by Jedd D. Wolchok, MD, PhD, chief, melanoma and immunotherapeutics service at Memorial Sloan Kettering Cancer Center.

CheckMate 67 is an ongoing randomized double-blind study designed to evaluate the efficacy of nivolumab as first-line therapy in advanced melanoma, alone or in combination with ipilimumab.

The trial methods were as follows: 945 treatment-naïve patients, a majority of whom were male, were randomized to receive either nivolumab alone, ipilimumab alone, or nivolumab and ipilimumab, until progression or unacceptable toxicity. Patients were stratified by PD-L1 status, BRAF mutation status, and disease stage. Primary end points were progression-free survival (PFS) and overall survival (OS). Secondary end points were objective response rate (ORR) and safety. During the Plenary Session, Wolchok reported PFS and ORR data (Table); the trial is ongoing to estimate OS.

At a minimum follow-up of 9 months, patients treated with the combination of nivolumab and ipilimumab, as well as those treated with nivolumab alone, had significantly improved PFS and ORR compared with patients treated with ipilimumab alone, said Wolchok.

Table. Primary and Secondary End Points in Checkmate 067 Trial

Nivolumab + ipilimumab



PFS (months)*

11.5 (8.9-16.7)

6.9 (4.3-9.5)

2.9 (2.8-3.4)

ORR (%)*

57.6 (52.0-63.2)

43.7 (38.1-49.3)

19.0 (14.9-23.8)

CR rate (%)




CR indicates complete response; ORR, objective response rate; PFS, progression-free survival.

*PFS and ORR presented as median (95% CI).

Furthermore, a higher number of patients treated with the combination had a partial response compared with nivolumab or ipilimumab alone. While progressive disease was highest with ipilimumab and lowest with the combination, duration of response had not been reached because the follow-up period was not long enough.

When the response rate was analyzed in relation to high PD-L1 expression, Wolchok said that the combination treatment resulted in a higher response rate (72.1%) compared with nivolumab alone (57.5%). Similar trends were observed with low PD-L1-expressing tumors.

The safety profile of the combination, he said, was consistent with earlier results, and the combination did show a higher incidence of adverse events. There were no new safety signals or drug-related deaths observed with the combination, while the monotherapies had 1 death each. “The current evidence suggests that the combination presents a means to improve outcomes versus using nivolumab alone, especially in patients with low (<5%) PD-L1 expression,” Wolchok concluded.

Elotozumab Presents Promise in Multiple Myeloma

A poster presented on the second day of the annual meeting of the American Society of Clinical Oncology, held from May 29 to June 2, 2015, in Chicago, evaluated the advantage of incorporating the monoclonal antibody, elotuzumab, into a treatment regimen of bortezomib/dexamethasone in relapsed-refractory multiple myeloma (RRMM) patients. These results were from a phase 2 open-label study from 83 centers across the United States and Europe, and included 152 patients.1

Interaction of elotuzumab with the signaling lymphocytic activation molecule F7 results in myeloma cell death, with minimal effects on normal tissue. Previous studies from a preclinical myeloma model found enhanced activity of elotuzumab combined with bortezomib, as well as good phase 1 results. The current study investigated the efficacy and safety of elotuzumab ± bortezomib/dexamethasone in RRMM patients.

The primary objective of the study was to compare PFS between the treatment arms in the intent-to-treat population, and the secondary objective to estimate differences in response rates between the arms. Additionally, the researchers explored safety, time to response, duration of response, and OS.

Patients with RRMM who had progressed on at least 1 to 3 prior therapies, and who met Eastern Cooperative Oncology Group status ≤ 2, were eligible for participation.1

The authors showed that the study met its primary end point of PFS: median PFS was 9.7 months in the elotozumab/bortezomib/dexamethasone—treated group versus 6.9 months when elotuzumab was left out. ORR was 65% when elotuzumab was included in the treatment, versus 63% when it was not. The 1-year OS rate was 85% versus 74%, with and without elotuzumab, respectively.1

At the time of analysis, 40 patients had died following disease progression, of which 17 were on the elotuzumab/bortezomib/dexamethasone arm. The authors did not see any differences in adverse events between the 2 trial arms.1

Based on this analysis, the authors concluded that the study met its primary end point. Elotuzumab significantly improved PFS when combined with bortezomib/dexamethasone, and elotuzumab-treated patients had a 28% reduction in their risk of disease progression. Additionally, the authors consider the available OS data encouraging as well. Long-term outcomes studies are ongoing.1


1. Jakubowiak AJ, Offidani M, Pegourie B, et al. A randomized phase II study of bortezomib (Btz)/dexamethasone (dex) with or without elotuzumab (Elo) in patients (pts) with relapsed/refractory multiple myeloma (RRMM). J Clin Oncol. 2015;33(suppl): abstract 8573.

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