Trials of Anti-PD-L1 in NSCLC Are Well Under Way

July 30, 2014
Special Reports, NSCLC (Issue 3), Volume 3, Issue 1

Despite standard chemotherapy and the availability of targeted therapies such as bevacizumab, cetuximab, and tyrosine kinase inhibitors (TKIs) such as erlotinib, afatinib, and crizotinib, survival rates are far from optimal for patients with NSCLC.

David R. Spigel, MD

Despite standard chemotherapy and the availability of targeted therapies such as bevacizumab, cetuximab, and tyrosine kinase inhibitors (TKIs) such as erlotinib, afatinib, and crizotinib, survival rates are far from optimal for patients with non-small cell lung cancer (NSCLC). In fact, 5-year relative survival rates are 49%, 16%, and 2% for local, regional, and distant disease, respectively.1-3

However, development of immunotherapies that can alter the activity of T cells by targeting checkpoint pathways, and determining their level of activity is well under way.4Tumor cells include evolved mechanisms to evade attack by the immune system, and one such tactic is high cell-surface expression of the programmed death receptor-ligand 1 (PD-L1).5The PD-1 receptor is expressed on the surface of tumor-invading T cells, and when activated by the ligand, sends a signal leading to decreased T-cell proliferation and reduction of cytokine synthesis, inducing a degree of immunosuppression within the tumor.

Under normal circumstances, this inhibitory checkpoint pathway is thought to protect healthy tissue from T-cell attack and the induction of autoimmunity,6but when tumor-invading T cells interact with PD-L1, they are inactivated, permitting tumor cell replication and tumor growth. The microenvironment within a tumor may also stimulate invading T cells to increase expression of PD-1 versus T cells in normal tissue and peripheral blood.7Additionally, PD-L1 is a ligand for B7-1 (CD 80), which also inhibits T-cell proliferation and cytokine synthesis.8

“Early data from multiple studies suggest to us that PD-L1 expression can predict for a higher response (particularly to an anti-PD-L1 therapy),” said David R. Spigel, MD, director of the lung cancer research program at the Sarah Cannon Research Institute in Nashville, Tennessee. “However, these same studies show that patients without PD-L1 overexpression can still benefit from these agents, so it remains unclear that their PD-L1 expression by immunohistochemistry is going to be the optimal biomarker and a way to select patients for immunotherapy treatment.”

The high levels of expression of PD-L1 in lung cancer tumor cells has led to the development of monoclonal antibodies that prevent the ligand from binding to its receptors, including PD-1 and B7.1, thereby facilitating a vigorous T-cell immune response against the tumor.9Table 1contains a list of anti-PDL1 agents in clinical trials. Two of these agents are in the advanced stages of development: MPDL3280A, an antibody that has been modified to remove its antibody-dependent cell-mediated cytotoxicity function, and MEDI4736, a human IgG1 monoclonal antibody.

TABLE 1. Anti-PD-L1 Agents in Clinical Trials

A phase I study of MPDL3280A (NCT01375842) in patients with locally advanced or metastatic solid tumors demonstrated Response Evaluation Criteria In Solid Tumors (RECIST) responses in patients with NSCLC and other tumor types, and the treatment was well tolerated. Patients with PD-L1—positive tumors showed an overall response rate (ORR) of 39%, and a progressive disease (PD) rate of 12%. Patients with PD-L1–negative tumors had an ORR of 13% with a PD rate of 59%. The results suggested a correlation between response to the agent and PD-L1 status.9,10

In an ongoing, multicenter, dose-escalation study of MEDI4736 (NCT01693562) in patients with advanced solid tumors (13 NSCLC, 8 melanoma, 5 other), treatment resulted in a disease control rate of 46% and 4 partial responses (3 NSCLC, 1 melanoma). The safety profile was acceptable and tumor shrinkage occurred at all doses tested, was durable, and was seen as early as 6 weeks.11

Currently recruiting, the ATLANTIC (NCT02087423) is a single-arm, phase II global study of efficacy and safety of MEDI4736 in patients with locally advanced or metastatic NSCLC who have received at least 2 prior chemotherapies, one of which had to be platinum-based. The primary outcome measure is ORR, and secondary measures include response duration, progression-free survival (PFS), overall survival (OS), safety, and pharmacokinetics. The estimated primary completion date is April 2015.

In addition, there are several early phase I studies in NSCLC of MEDI4736 in combination with gefitinib (NCT02088112), tremelimumab (NCT02000947), an anticytotoxic T-lymphocyte—associated antigen 4 monoclonal antibody, and MEDI0680 (NCT02118337), an anti-PD-1 monoclonal antibody (in advanced malignancies).

In May 2014, AstraZeneca announced the start of a phase III study for its anti-PD-L1 monoclonal antibody, MEDI4736, versus placebo, in concert with the global double-blind PACIFIC trial (NCT02125461). The primary outcome measures are PFS and OS. Secondary outcome measures include duration of response and objective response rate. It is expected that 880 patients will be randomized, and the trial will use more than 100 sites. It will recruit patients with locally advanced, unresectable NSCLC, with no evidence of progression after completion of treatment with a course of chemoradiotherapy. Estimated primary completion date is May 2017.

A phase III trial of MPDL3280A (NCT02008227) is recruiting patients. This open-label, multicenter, global trial expects to enroll 850 patients and is designed to evaluate the efficacy and safety of MPDL3280A (1200 mg IV on day 1 of each 21-day cycle) versus an active comparator, docetaxel (75 mg/m2 IV on day 1 of each 21-day cycle) in patients with locally advanced or metastatic NSCLC following failure on a platinum-containing chemotherapy. The primary outcome measure is OS, and secondary outcome measures include adverse events, ORR, PFS, and duration of response. The estimated primary completion date is June 2018.

“To date, the efficacy and safety profiles are very encouraging for the anti-PD-1 and PD-L1 therapies. In terms of efficacy, so far there appears to be higher response rates in heavily pretreated patients than we would expect with single-agent systemic therapy,” said Spigel.

“It’s unclear whether this can translate into PFS and OS advantages, and we will learn more in ongoing studies,” Spigel stated.

In terms of safety, results have been encouraging, according to Spigel. “The agents appear to be well-tolerated across the board, although there have been rare serious events, including pneumonitis (with nivolumab in the initial phase I experience, leading to 2 fatalities). However, so far, this does not appear to be a general problem for any one agent or for the class. Immune-related toxicities have occurred, including thyroid abnormalities, but most of the toxicities have been mild and reversible.”

Inducing a robust T-cell response against NSCLC tumors using antibodies directed at PD-L1 is a promising approach to improving outcomes, and clinical data clarifying the benefits of this approach are expected from active clinical trials over the next 4 to 5 years.


  1. National Cancer Institute. General Information About Non-Small Cell Lung Cancer (NSCLC). Accessed July 19, 2014.
  2. American Cancer Society. Lung Cancer (Non-Small Cell). Chemotherapy for non-small cell lung cancer. Accessed July 20, 2014.
  3. American Cancer Society. Lung Cancer (Non-Small Cell). Targeted therapies for non-small cell lung cancer. Accessed July 20, 2014).
  4. Forde PM, Ettinger DS. Targeted therapy for non-small-cell lung cancer: past, present and future.Expert Rev Anticancer Ther. 2013;13(6):745-758.
  5. Pardoll DM. The blockade of immune checkpoints in cancer immunotherapy.Nat Rev Cancer. 2012;12(4):252-264.
  6. Sznol M, Chen L. Antagonist antibodies to PD-1 and B7-H1 (PD-L1) in the treatment of advanced human cancer.Clin Cancer Res. 2013;19(5):1021-1034.
  7. Ahmadzadeh M, Johnson LA, Heemskerk B, et al. Tumor antigen-specific CD8 T cells infiltrating the tumor express high levels of PD-1 and are functionally impaired.Blood. 2009;114(8):1537-1544.
  8. Butte MJ, Keir ME, Phamduy TB, Sharpe AH, Freeman GJ. Programmed death-1 ligand 1 interacts specifically with the B7-1 costimulatory molecule to inhibit T cell responses.Immunity. 2007;27(1):111-122.
  9. Spigel DR, Gettinger SN, Horm L, et al. Clinical activity, safety, and biomarkers of MPDL3280A, an engineered PD-L1 antibody in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC)J Clin Oncol. 2013;31(suppl): Abstract 8008.
  10. Herbst RS, Gordon MS, Fine GD, et al. A study of MPDL3280A, an engineered PD-L1 antibody in patients with locally advanced or metastatic tumorsJ Clin Oncol. 2013;31 (suppl):Abstract 3000.
  11. Jose Lutzky J, Antonia SJ, Blake-Haskins A, et al. A phase 1 study of MEDI4736 an anti-PD-L1 antibody in patients with advanced solid tumors.J Clin Oncol. 2014;32;5s (suppl): Abstract 3001.
  12. AstraZeneca. AstraZeneca initiates phase III immunotherapy study for MEDI4736 in patients with lung cancer. Accessed July 18, 2014.