First results of durvalumab after chemoradiotherapy in locally advanced non-small-cell lung cancer in Russia

Author:

Yudin D. I.1ORCID,Laktionov K. K.2ORCID,Moiseenko F. V.3ORCID,Ponomarenko D. M.4ORCID,Chekh E. A.5ORCID,Chubenko V. A.6ORCID,Levchenko N. V.6ORCID,Kozlov V. V.5ORCID,Stepanova E. О.6ORCID,Sarantseva K. A.1ORCID,Denisova E. S.1ORCID,Ardzinba M. S.1ORCID,Yukalchuk D. Yu.4ORCID

Affiliation:

1. Blokhin National Medical Research Center of Oncology

2. Blokhin National Medical Research Center of Oncology; Pirogov Russian National Research Medical University

3. Saint Petersburg Clinical Research and Practice Centre for Specialized Care (Oncological); Petrov National Medical Cancer Research Centre; North-Western State Medical University named after I.I. Mechnikov

4. Regional Oncological Dispensary

5. Novosibirsk Regional Oncology Dispensary

6. Saint Petersburg Clinical Research and Practice Centre for Specialized Care (Oncological)

Abstract

Introduction. The addition of durvalumab after chemoradiation therapy in unresectable stage III non-small-cell lung cancer (NSLC) is a new standard of care.Aim. Study the features and outcomes of durvalumab maintenance treatment after chemoradiotherapy in patients with unresectable stage III NSCLC in the real-world clinical practice in Russia.Materials and methods. 50 patients with unresectable III stage NSCLC after concurrent or sequential chemoradiotherapy (CRT) were enrolled in this observational retrospective study. Median follow up time at primary analysis was 12.4 months.Results. A mean age of the patients in the study was 61.2 years (58.4-64.1; 95% CI). Most of the patients had received sequential CRT (76%, n = 38). Median time of durvalumab start from the end of CRT varied from 22 to 50 days (overall - 35 days). Estimated median PFS and OS were 10.86 months (7.78-14.01, 95% CI) and 26 months (20.19-31.81, 95% CI), respectively. There was a trend toward increased PFS in patients with smoking history: 12 months (9.79-14.2; 95% CI) versus 4,9 months (0.0-12.47; 95% CI), p = 0.2. Half of the patients without smoking history (5/10) had targetable mutations (EGFR ex 19, ALK, ROS1, cMET). Most common reported adverse events of special interest were pneumonitis grade 1-2 (36%, n = 18), leading permanent treatment discontinuation to in 6% of patients (n = 3). There were no reported cases of grade 3-4 adverse events.Conclusions. Real-world characteristic of patients in our study were different from PACIFIC trial. Sequential CRT is the most frequent treatment option in locally advanced unresectable NSCLC in Russia. Estimated PFS was shorter than in PACIFIC, but there were less cases of pneumonitis.

Publisher

Remedium, Ltd.

Subject

General Medicine

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