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Pembrolizumab Improves Long-term Overall Survival over Docetaxel in Advanced NSCLC

Pembrolizumab significantly prolongs overall survival in previously treated patients with advanced NSCLC
15 Dec 2018
Immunotherapy
Thoracic Malignancies

Patients with previously treated advanced non-small cell lung cancer (NSCLC) who received pembrolizumab showed significantly longer overall survival (OS) compared to those treated with docetaxel, researchers reported at the ESMO Immuno-Oncology Congress 2018 in Geneva, Switzerland. Roy S. Herbst, Medical Oncology, Yale University School of Medicine in New Haven, USA presented long-term findings from the global, open-label, phase II/III KEYNOTE-010 trial (NCT01905657).

KEYNOTE-010 enrolled adult patients with previously treated advanced NSCLC and PD-L1 tumour proportion scores (TPS) ≥1% who were randomised 1:1:1 to receive pembrolizumab at 10 mg/kg or 2 mg/kg every 3 weeks for up to 35 cycles, or to docetaxel at 75 mg/m2 every 3 weeks for the maximum number of cycles allowed per local guidelines, until disease progression or intolerable toxicity. Response assessments per RECIST v1.1 were made every 9 weeks by independent central review, and survival was evaluated every 2 months post-treatment. No difference between pembrolizumab doses was demonstrated in the primary analysis, thus doses were pooled in this analysis.

Previously reported results from this trial showed OS was improved with pembrolizumab over docetaxel in subgroups of patients with high and low PD-L1 expression levels, defined as PD-L1 TPS ≥50% and ≥1% with median follow-up of 13.1 months.

At ESMO Immuno-Oncology Congress 2018, Dr. Herbst reported updated OS and safety results with 43 months median follow-up in the study overall, and long-term results for patients who had completed 35 cycles or approximately 2 years of pembrolizumab, and for patients who received a second course of pembrolizumab therapy.

Patients completing the 35-cycle (2 year) course of pembrolizumab showed extremely high rates of response and OS

After median follow-up of 42.6 months (range, 35.2 to 53.2 months), OS in the overall population of 1033 patients was improved with pembrolizumab over docetaxel.

Patients with PD-L1 TPS ≥50% demonstrated significantly improved OS with pembrolizumab compared to docetaxel. Median OS was 16.9 (95% confidence interval [CI], 12.3–21.4) months with pembrolizumab versus 8.2 (95% CI 6.4–9.8) months with docetaxel (hazard ratio [HR] 0.53; 95% CI 0.42–0.66; p < 0.00001). In this cohort, the 36-month OS rates were 35% versus 13%, respectively.

Similarly, OS was improved with pembrolizumab versus docetaxel in patients with TPS ≥1% (HR 0.69; 95% CI, 0.60–0.80; p < 0.00001).

Thirty-five cycles or 2 years of pembrolizumab were delivered to 79 of 690 patients. Among these patients, the 36-month OS rate was 99%. Ninety-five percent of these patients achieved complete or partial response as the best response, and 48 (64%) had an ongoing response. The median duration of response was not reached (range, 4 to 46+ months).

Among patients who completed 35 cycles or 2 years of pembrolizumab, 72 (91%) patients remained alive. Progressive disease was observed in 25 (32%) patients, per investigator. A second course of pembrolizumab was delivered to 14 patients, of whom 5 patients completed 17 cycles. In this group, 11 (79%) patients remained alive, with 6 (43%) patients achieving partial response, and 5 (36%) patients showing stable disease.

The safety profile was similar to that reported for the primary analysis. Grades 3 to 5 treatment-related adverse events (TRAEs) occurred in 16% of pembrolizumab-treated patients overall compared to 37% of docetaxel patients.

Treatment Duration and Time to Response Among Patients Who Completed 35 cycles (2 Years) of Pembrolizumaba
Pembrolizumab Improves Long-term Overall Survival over Docetaxel in Advanced NSCLC

2 years of pembrolizumab treatment provided durable response and long-term disease control.

© Roy S. Herbst.

Conclusion 

With 43 months of follow-up, pembrolizumab continued to prolong OS compared to docetaxel in patients with previously treated, PD-L1–expressing advanced NSCLC. Manageable long-term safety was also demonstrated. Most of the patients completing 35 cycles of pembrolizumab had a durable response.

The majority of patients experiencing progressive disease by investigator review who received a second course of pembrolizumab remained alive and showed either partial response or stable disease.

Reference

LBA4 – Herbst RS, Garon EB, Kim D-W, et al. Long-term follow-up in the KEYNOTE-010 study of pembrolizumab (pembro) for advanced NSCLC, including in patients (pts) who completed 2 years of pembro and pts who received a second course of pembro.

Last update: 15 Dec 2018

Funding from Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA was reported.

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