Role of Neoadjuvant Immunotherapy Being Refined in Resectable NSCLC

Tina Cascone, MD, PhD

Tina Cascone, MD, PhD

Neoadjuvant immunotherapy can offer promise to patients with resectable non—small cell lung cancer (NSCLC), but further investigation is required for optimal use, Tina Cascone, MD, PhD, said in a presentation during the 14th Annual New York Lung Cancers Symposium^®.¹

“We have learned that immune checkpoint inhibitors have an important role in the neoadjuvant setting, but there are a lot of questions that remain, such as the best therapy, number of doses, sequence versus combination, as well as the spatiotemporal modulation of the immune tumor microenvironment with these agents,” said Cascone, an assistant professor of thoracic and head and neck cancer at The University of Texas MD Anderson Cancer Center.

However, neoadjuvant immunotherapy is a highly active area of investigation and evolving data from preclinical models and clinical trials are expected to yield answers. For example, the ongoing, phase III Checkmate-77T (NCT04025879), KEYNOTE-671 (NCT03425643), IMpower030 (NCT034056063), and AEGEAN (NCT03800134) studies are evaluating nivolumab (Opdivo), pembrolizumab (Keytruda), atezolizumab (Tecentriq), and durvalumab (Imfinzi), respectively, in combination with chemotherapy in patients with stage II to stage III resectable disease.

“These trials will give us an opportunity to evaluate major pathologic response (MPR) and pathologic complete response (pCR) as surrogate endpoints for improved survival after neoadjuvant therapy,” Cascone said. “[In NSCLC], MPR [has been recognized] as predictive of improvement in long-term overall survival.”

Establishing surrogate endpoints for clinical benefit is of paramount importance in NSCLC, because “trials can take decades to complete and are expensive,” Cascone added.

Surrogate endpoints should be sufficiently well correlated with clinical endpoints, in order to justify their employment, and they should capture the full net effect of the treatment on the clinical outcome, Cascone said, adding that the FDA may approve an agent based on an improvement in a surrogate endpoint.²

Cascone highlighted the phase II Lung Cancer Mutation Consortium (LCMC3; NCT02927301) and NEOSTAR (NCT03158129) studies as those in which MPR was a key predictor of response to immunotherapy.

LCMC3 investigators evaluated neoadjuvant atezolizumab in 180 patients with operable stage IB to IIIB NSCLC. The agent induced an MPR in 19% and a pCR in 5% of patients in the primary efficacy population (n = 77) who went on to have complete surgical resection. Atezolizumab had positive activity and a favorable safety profile, affirming the PD-L1 inhibitor to be a viable treatment option in the neoadjuvant setting.³ Notably, LCMC3 was the first study to release findings on preoperative atezolizumab in resectable NSCLC.

Cascone was the lead author of NEOSTAR, which randomized 44 patients with operable stage I to IIIA NSCLC to either single-agent nivolumab or nivolumab with ipilimumab (Yervoy). NEOSTAR’s study of neoadjuvant nivolumab/ipilimumab was predicated on earlier evidence showing that treatment is more efficacious when given earlier and in combination with another agent.

“In murine models of lung cancer, we have tested neoadjuvant and adjuvant therapies and found that neoadjuvant combined treatment is superior to neoadjuvant monotherapy and adjuvant therapy in improving survival and reducing lung metastases,” Cascone said.

Beyond lung cancer, Liu et al have noted the superiority of neoadjuvant anti—PD-1 therapy to adjuvant therapy in eradicating metastases in a murine breast cancer model.⁴ Neoadjuvant immunotherapy is an attractive treatment modality because it increases PD-L1 expression. Targeting PD-L1 on cancer cells reverses CD8-positive tumor-infiltrating lymphocyte (TIL) dysfunction and suppresses metastases.⁵

Results from the phase I CheckMate-012 trial (NCT01454102) of nivolumab plus ipilimumab in advanced NSCLC corroborated the positive activity previously witnessed in the murine models: the doublet elicited high response rates and prolonged progression-free survival. Findings from the murine models and CheckMate-012 provided the motivation for the NEOSTAR study, Cascone said.

In NEOSTAR, investigators observed a combined MPR and pCR of 25% (11 patients) in the intent-to-treat population (n = 44).⁶ The joint MPR and pCR rate was 17% (95% CI, 0.05-0.39) in the nivolumab arm and 33% (95% CI, 0.15-0.57) in the nivolumab/ipilimumab arm, causing NEOSTAR to meet its prespecified trial efficacy boundary. The combination of nivolumab/ipilimumab as neoadjuvant therapy was associated with higher frequencies of CD3-positive TILs and increases in CD8-positive/CD103-positive (TRM) and CD4-positive/CD28-positive cell compartments.

As the investigators further define the role of neoadjuvant immunotherapy in NSCLC, combinations that include an immune checkpoint inhibitor and an anti—CTLA-4 agent, or an intratumoral immunotherapy, or even a simulator of interferon genes protein agonist, will warrant further investigation, Cascone said. The same is true for biomarkers predictive of patient response to neoadjuvant therapy. “Translational analyses are critical for biomarker discovery and subsequent patient selection in the next-generational trials,” she added.

Adjuvant treatment is intended to eliminate micrometastatic disease; neoadjuvant therapy has the potential to “downstage” primary tumors, thereby augmenting the efficacy of adjuvant therapy, Cascone said. Moreover, a neoadjuvant approach might also decrease the morbid effects of surgery and enable subsequent analysis of the treated tumor.

The central role of neoadjuvant immunotherapy in the investigative push to further define the role of this therapy in resectable NSCLC and advance the field is evidenced by the bevy of phase II trials currently exploring immune checkpoint inhibitors, such as the NEOMUN (NCT03197467) and NADIM (NCT03081689) studies, as well as the platform NeoCOAST (NCT03794544) trial, Cascone said.

References

1. Cascone T. Perioperative immunotherapy for non—small cell lung cancer. Presented at: 14th Annual New York Lung Cancers Symposium^®; November 9, 2019; New York, New York.
2. Blumenthal GM, Bunn PA Jr, Chaft JE, et al. Current status and future perspectives on neoadjuvant therapy in lung cancer. J Thorac Oncol. 2018;13(12):1818-1831. doi: 10.1016/j.jtho.2018.09.017.
3. Kwiatkowski DJ, Rusch VW, Chaft JE, et al. Neoadjuvant atezolizumab in resectable non-small cell lung cancer (NSCLC): Interim analysis and biomarker data from a multicenter study (LCMC3). J Clin Oncol. 2019;37(suppl; abstr 8503). doi: 10.1200/JCO.2019.37.15_suppl.8503.
4. Chen L, Gibbons DL, Goswami S, et al. Metastasis is regulated via microRNA-200/ZEB1 axis control of tumour cell PD-L1 expression and intratumoral immunosuppression. Nat Commun. 2014;5:5241. doi: 10.1038/ncomms6241.
5. Liu J, Blake SJ, Yong MC, et al. Improved efficacy of neoadjuvant compared to adjuvant immunotherapy to eradicate metastatic disease. Cancer Discov. 2016;6(12):1382-1399. doi: 10.1158/2159-8290.CD-16-0577.
6. Cascone T, William WN, Weissferdt A, et al. Neoadjuvant nivolumab (N) or nivolumab plus ipilimumab (NI) for resectable non-small cell lung cancer (NSCLC): Clinical and correlative results from the NEOSTAR study. J Clin Oncol. 2019;37(suppl; abstr 8504).

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