Phase II Study of Everolimus in Metastatic Malignant Melanoma (NCCTG-N0377, Alliance).

LESSONS LEARNED: Everolimus does not have sufficient activity to justify its use as single agent in metastatic melanoma.Patients treated with 10 mg per day dose were most likely to require dose reductions.Everolimus appeared to reduce the numbers of regulatory T cells in approximately half of the treated patients; unfortunately, these effects were not correlated with clinical outcomes.
BACKGROUND: Everolimus (RAD-001) is an orally active rapamycin analogue shown in preclinical data to produce cytostatic cell inhibition, which may be potentially beneficial in treating melanoma. We conducted a phase II study to evaluate the efficacy and safety of everolimus in patients with unresectable metastatic melanoma (MM).
METHODS: This study included two cohorts; cohort 1 received 30 mg of everolimus by mouth (PO) weekly, and cohort 2 was dosed with 10 mg of everolimus PO daily. The endpoints of the study were safety, 16-week progression-free survival (PFS), overall survival (OS), and measures of immunomodulatory/antiangiogenic properties with therapy. Tumor samples before therapy and at week 8 of treatment were analyzed. Peripheral blood plasma or mononuclear cell isolates collected prior to therapy and at weeks 8 and 16 and at time of tumor progression were analyzed for vascular endothelial growth factor and regulatory T-cell (Treg) measurements.
RESULTS: A total of 53 patients were enrolled in cohort 1 (n = 24) and cohort 2 (n = 29). Only 2 patients of the first 20 patients enrolled in cohort 2 had treatment responses (25%; 95% confidence interval, 8.6%-49.1%); this result did not allow full accrual to cohort 2, as the study was terminated for futility. Median OS was 12.2 months for cohort 1 versus 8.1 months in cohort 2; no PFS advantage was seen in either group (2.1 months vs. 1.8 months). Dose-limiting toxicities included grade 4 myocardial ischemia (3.4%); grade 3 fatigue, mucositis, and hyperglycemia (10.3%); and anorexia and anemia (6.9%). Everolimus significantly reduced the number of Tregs in approximately half of the treated patients; however, these effects were not correlated with clinical outcomes.
CONCLUSION: Everolimus does not have sufficient single-agent activity in MM; however, we have identified evidence of biological activity to provide a potential rationale for future combination studies. © AlphaMed Press; the data published online to support this summary are the property of the authors.

Discussion

Melanoma is the most malignant form of skin cancer, the fifth most common cancer in men and sixth in women in the U.S., with its highest incidence in the white population [1], [2], [3].

In preclinical studies by our group, inhibitors of mammalian target of rapamycin (mTOR) demonstrated a potent inhibitory effect on tumor growth, improved survival, an inhibitory effect of rapamycin on angiogenesis, and significant decrease in the number of capillaries perfusing the tumor [4], [5], [6]. The results of the current study demonstrate that single‐agent therapy with RAD‐001 does not have sufficient activity to justify its use as a single agent in the treatment of metastatic melanoma. Our data also suggest that patients treated with the 10 mg per day dose were most likely to require dose reductions. The treatment did appear to modulate aspects of both immunity and angiogenesis; however, in view of the insufficient clinical efficacy of treatment, these findings can only be viewed as exploratory and illustrative of the potential utility of everolimus in combination with other agents. Everolimus significantly reduced the numbers of Tregs in approximately half of the treated patients; unfortunately, these effects were not correlated with clinical outcomes.

Kaplan‐Meier plot. Overall survival (OS) and PFS comparing cohort 1, 30 mg by mouth (PO) weekly (n = 24), with cohort 2, 10 mg PO daily (n = 9). Median OS was 12.2 months versus 8.1 months, respectively; no PFS advantage was seen in either group (2.1 months vs. 1.8 months).

Abbreviation: PFS, progression‐free survival.

Investigating the benefits of everolimus as a single agent is the first step toward incorporating this agent into a combination regimen to treat melanoma. Because the 10 mg per day dose appeared to be excessively toxic in this population, future studies will need to use a lower dose. The toxicity profile of everolimus does not overlap with other melanoma therapies.

Trial Information

Melanoma

Metastatic/Advanced

No designated number of regimens

Phase I/II

Phase II study

Safety

Overall response rate

Progression‐free survival

Correlative endpoint

Drug Information

Everolimus (RAD‐001)

Novartis

Small molecule

mTOR

30 milligrams (mg) per flat dose

PO

Doses: Cohort 1 received 30 mg of everolimus PO weekly, and cohort 2 was dosed with 10 mg of everolimus PO daily.

37

16

IV

Median (range): 61 years (21.0-81.0)

0 — 31

1 — 20

2 — 2

3 —

Unknown —

Malignant melanoma

Primary Assessment Method for Phase I Control

Total Patient Population

53

53

RECIST, version 1.0

n = 0

n = 1

n = 0

n = 52

Adverse Events

Dose‐Limiting Toxicities

Assessment, Analysis, and Discussion

Study completed

Inactive because results did not meet primary endpoint

Although the inhibition of PI3K/mammalian target of rapamycin (mTOR)/AKT pathway is a therapeutic strategy for several cancer types, the current study demonstrates that single‐agent therapy with everolimus does not have sufficient activity to justify its use in the treatment of metastatic melanoma. This was our conclusion, despite literature showing that the mTOR pathway is activated in malignant melanoma as opposed to benign nevi [7]. Efforts to evaluate the efficacy of everolimus with other regimens have been performed by different groups; for example, the use of everolimus in combination with temozolamide was evaluated in a single‐arm phase II multi‐institution trial; although the regimen was well tolerated, it failed to meet or exceed the study threshold for promising clinical activity in patients with metastatic melanoma [8]. A subsequent phase II trial combining paclitaxel, carboplatin, and everolimus showed activity in the first‐line treatment of metastatic melanoma; unfortunately, the duration of benefit was brief for most patients [7]. A recent study evaluated the addition of everolimus to carboplatin, paclitaxel, and bevacizumab; this combination was found to be ineffective in metastatic melanoma because of inability to give the full dose of everolimus, predominantly because of cytopenias [9]. Although it was a negative study, the investigators reported that the everolimus combination arm performed exceptionally well, receiving >30 cycles of therapy [9].

Interestingly, the use of everolimus in a preclinical model demonstrated increased programmed death‐ligand 1(PD‐L1) expression in renal cell carcinoma, and the addition of everolimus to anti‐PD‐L1 significantly reduced tumor burden compared with everolimus alone; [10] the use of immunotherapy in combination with everolimus in patients with melanoma warrants further investigation.

Summary of correlative studies. Effects of RAD‐001 therapy on peripheral blood‐derived parameters of immune homeostasis. Peripheral blood plasma or mononuclear cell isolates collected prior to therapy, at weeks 8 and 16 of therapy as well as at the time of tumor progression, were analyzed. For most measured parameters, RAD‐001 therapy did not appear to significantly influence the measurements; however, therapy did appear to significantly reduce the numbers of regulatory T cells (Treg) in approximately half of the treated patients. These effects were not correlated with clinical outcomes.

Abbreviation: PFS, progression‐free survival.

Table 1.

Patient characteristics