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Indian Journal of Medical and Paediatric Oncology
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EDITORIAL COMMENTARY
Year : 2019  |  Volume : 40  |  Issue : 4  |  Page : 461-462  

First-line immunotherapy in advanced non-small-cell lung cancer


1 Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India
2 Department of Medical Oncology/Hematology/BMT, Asian Institute of Medical Sciences, Faridabad, Haryana, India
3 Department of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India
4 Malignant Diseases Treatment Centre, Army Hospital Research and Referral, New Delhi, India

Date of Submission15-Oct-2019
Date of Decision19-Dec-2019
Date of Acceptance03-Jan-2020
Date of Web Publication17-Feb-2020

Correspondence Address:
Vanita Noronha
Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijmpo.ijmpo_210_19

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How to cite this article:
Noronha V, Mehta P, Malik PS, Patel A. First-line immunotherapy in advanced non-small-cell lung cancer. Indian J Med Paediatr Oncol 2019;40:461-2

How to cite this URL:
Noronha V, Mehta P, Malik PS, Patel A. First-line immunotherapy in advanced non-small-cell lung cancer. Indian J Med Paediatr Oncol [serial online] 2019 [cited 2020 Apr 2];40:461-2. Available from: http://www.ijmpo.org/text.asp?2019/40/4/461/278512



Although immune checkpoint blockers (ICBs) were discovered in the 1990s, the initial reports of their efficacy in non-small-cell lung cancer (NSCLC) came through in 2012, when nivolumab (BMS-936558) showed responses in a Phase 1 study. From then on, there has been a constant flow of data pertaining ICBs in a multitude of previously treated malignancies.

ICBs have completely transformed care for untreated advanced NSCLC and now have entered the first-line therapeutic armamentarium based on convincing data. An encouraging update of Keynote-001 presented at the 2019 American Society of Clinical Oncology meeting showed that 23.2% overall and 29.6% of patients with a programmed death ligand (PD-L1) staining of >50% treated with pembrolizumab (P) upfront were alive at 5 years. We will be looking at some of the landmark trials of immunotherapy in treatment-naive NSCLC in relation to common clinical situations.


  Untreated Non-Small-Cell Lung Cancer With Programmed Death Ligand Staining ≥50% Top


In the Phase 3 Keynote-24, 305 patients with untreated advanced NSCLC with PD-L1 tumor proportion score ≥50% (22C3, Dako), with no sensitizing epidermal growth factor receptor (EGFR) mutations or anaplastic lymphoma kinase (ALK) translocations, and with no untreated central nervous system (CNS) metastases were randomized (1:1) toP200 mg once every 3 weeks for up to 35 cycles or histology-based platinum doublet (chemotherapy [CT]) for 4–6 cycles.

The response rates favored P(44.8% vs. 27.8%). The median progression-free survival (PFS) was 4.3 months more with P(10.3 vs. 6 months, P < 0.001, hazard ratio [HR]: 0.50), whereas the 12-month PFS was 48% versus 15%.

Similarly, the median overall survival (OS) was 30 months versus 14.2 months (P < 0.002, HR: 0.63), whereas the 24-month OS was 54% versus 34.5%, an increment of about 20% at 2 years.

Based on these findings, as of now, the most prudent choice for this patient subgroup is monotherapy with P. Although there may be a consideration for chemo-immunotherapy in severely symptomatic high-risk patients, there is no head-to-head comparison between P alone and with CT in this population.

About 30% of advanced NSCLC patients who have this level of PD-L1 expression are eligible for this strategy.

Although cross-trial comparisons can be misleading, the outcomes of PD-L1 high subgroup of Keynote-189 with chemo-immunotherapy were comparable to those in P arm of Keynote-24, with the 12-month OS rate being about 70% in both trials. Still, this will remain a point of contention awaiting concrete evidence.

The Keynote-042 was a similar study in patients with PD-L1 staining ≥1%; although it did show a similar benefit of P monotherapy, the benefit was primarily driven by PD-L1-high patients. Thus, P monotherapy remains a less suitable choice for PD-L1 <50% and combination approaches need to be utilized in such a scenario.


  Untreated Nonsquamous Non-Small-Cell Lung Cancer With Programmed Death Ligand Staining <50% Top


The Keynote-189 randomized 616 patients with untreated Stage IV nonsquamous NSCLC with no actionable EGFR/ALK alterations and no symptomatic CNS metastases to pemetrexed (Pem) + platinum + placebo versus Pem + platinum agent + P followed by Pem + P maintenance (up to 35 cycles). The median PFS in the combination arm was 8.8 months versus 4.9 months in the CT arm (P < 0.001, HR: 0.52). The 1-year OS was 73% versus 48.1%, the benefit was apparent in all PD-L1 subgroups. An updated analysis showed a median OS of 22.0 versus 10.7 months (P < 0.00001, HR: 0.56). Despite 54% of CT-alone arm receiving ICB in second line, this difference was maintained. The PFS2 was also significantly longer (17 months vs. 9 months) in the combination arm.

Adverse events were 67.2% in combination group versus 65.8% in CT-placebo group.

Another noteworthy trial, IMpower150, studied addition of atezolizumab, a PD-L1 blocker, in combination with paclitaxel/carboplatin ± bevacizumab (ACP vs. ABCP vs. BCP) followed by maintenance. The median PFS of ABCP versus BCP was 8.3 months versus 6.8 months (P < 0.0001, HR: 0.59), whereas the 18-month PFS was 27% versus 8%. The median OS was 19.8 versus 14.9 months (HR: 0.76). Importantly, patients with EGFR and ALK aberrations who had progressed or were intolerant to tyrosine-kinase inhibitor were not excluded from the study population. ABCP could represent a possible option for this subgroup.

Overall, in patients with PD-L1 expression <50%, a combination approach is more beneficial.


  Untreated Squamous Non-Small-Cell Lung Cancer With Programmed Death Ligand Staining <50% Top


The Keynote-407 randomized 559 patients with advanced squamous NSCLC to P+ paclitaxel/nab-paclitaxel + carboplatin or paclitaxel/nab-paclitaxel + carboplatin + placebo (P + CT followed byPfor up to 31 cycles vs. CT). Again, the median OS favored the combination (15.9 vs. 11.3 months, P < 0.001, HR: 0.64). The median PFS was similarly superior, 6.4 versus 4.8 months (HR: 0.56).

The Impower131 studied a similar population utilizing atezolizumab as the ICB. Although the median PFS was marginally better in the trial, an OS advantage could not be demonstrated.

Overall, combinations of ICBs and CT have been proven superior except in PD-L1-high patients. Although the Food and Drug Administration (FDA) has approved P as monotherapy in PD-L1 >1%, this may not be a wise choice in the PD-L1 <50% cohort, while P monotherapy does remain the standard of care for PD-L1-high (≥50%) population.


  Immuno-Oncology–immuno-Oncology Combination Top


A recent update of Checkmate-227 studying nivolumab + ipilimumab versus platinum doublet in advanced NSCLC demonstrated an OS advantage for the immuno-oncology (IO) combination irrespective of PD-L1 expression, though the toxicity of IO–IO combination will be a concern with this approach.

In the end, and most importantly, we need to remember that these trials have included only up to Eastern Cooperative Oncology Group-performance status (PS) one patients with no actionable mutations. We really need to choose wisely and be cautious if we are going to extrapolate the available data to PS-2/3 patients. In addition, Prequires Dako PD-L1 immunohistochemistry 22C3 pharmDx assay as the PD-L1 testing platform as per the FDA approval. Toxicities of ICBs can be sometimes very serious and if not treated in time may be fatal, so careful preinfusion assessment, follow-up, monitoring, and patient and family education are always essential in the context of these drugs.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.






 

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