Abstract

Purpose: We evaluated a Trop-2-targeting antibody conjugated with SN-38 in metastatic small cell lung cancer (mSCLC) patients.Experimental Design: Sacituzumab govitecan was studied in patients with pretreated (median, 2; range, 1-7) mSCLC who received either 8 or 10 mg/kg i.v. on days 1 and 8 of 21-day cycles. The primary endpoints were safety and objective response rate (ORR); duration of response, progression-free survival (PFS), and overall survival (OS) were secondary endpoints.Results: Sixty percent of patients showed tumor shrinkage from baseline CTs. On an intention-to-treat basis (N = 50), the ORR was 14% (17% for the 10-mg/kg group); the median response duration, 5.7 months; the clinical benefit rate (CBR ≥4 months), 34%; median PFS, 3.7 months; and median OS, 7.5 months. There was a suggested improvement in PR, CBR, and PFS with sacituzumab govitecan in second-line patients who were sensitive to first-line therapy, but no difference between first-line chemosensitive versus chemoresistant patients in the overall population. There was a statistically significant higher OS in those patients who received prior topotecan versus no topotecan therapy in a small subgroup. Grade ≥3 adverse events included neutropenia (34%), fatigue (13%), diarrhea (9%), and anemia (6%). Trop-2 tumor staining was not required for patient selection. No antibodies to the drug conjugate or its components were detected on serial blood collections.Conclusions: Sacituzumab govitecan appears to have a safe and effective therapeutic profile in heavily pretreated mSCLC patients, including those who are chemosensitive or chemoresistant to first-line chemotherapy. Additional studies as a monotherapy or combination therapy are warranted. Clin Cancer Res; 23(19); 5711-9. ©2017 AACR.

Highlights

  • IntroductionSmall cell lung cancer (SCLC), originating from neuroendocrine progenitor cells, comprises approximately 15% of all lung cancers, yet has one of the lowest 5-year survival rates at 6% [1, 2]

  • Small cell lung cancer (SCLC), originating from neuroendocrine progenitor cells, comprises approximately 15% of all lung cancers, yet has one of the lowest 5-year survival rates at 6% [1, 2].This is because of its highly aggressive nature, with about two thirds of patients already having metastatic disease at diagnosis [3]

  • We evaluated a novel antibody–drug conjugate (ADC), sacituzumab govitecan (IMMU-132), composed of an antibody targeting Trop-2 and containing the active metabolite of irinotecan, SN-38

Read more

Summary

Introduction

Small cell lung cancer (SCLC), originating from neuroendocrine progenitor cells, comprises approximately 15% of all lung cancers, yet has one of the lowest 5-year survival rates at 6% [1, 2]. This is because of its highly aggressive nature, with about two thirds of patients already having metastatic disease at diagnosis [3]. Graham Cancer Center & Research Institute, Newark, Delaware. Graham Cancer Center & Research Institute, Newark, Delaware. 6Weill Cornell Medicine, New York, New York. 7University of Florida Health Cancer Center, Orlando, Florida. 8Columbia University Medical Center-Herbert Irving Comprehensive Cancer Center, New York, New York. 9Immunomedics, Inc., Morris Plains, New Jersey.

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call