Literature DB >> 28679770

Therapy of Small Cell Lung Cancer (SCLC) with a Topoisomerase-I-inhibiting Antibody-Drug Conjugate (ADC) Targeting Trop-2, Sacituzumab Govitecan.

Jhanelle E Gray1, Rebecca S Heist2, Alexander N Starodub3, D Ross Camidge4, Ebenezer A Kio3, Gregory A Masters5, W Thomas Purcell4, Michael J Guarino5, Jamal Misleh5, Charles J Schneider5, Bryan J Schneider6, Allyson Ocean6, Tirrell Johnson7, Leena Gandhi2, Kevin Kalinsky8, Ronald Scheff6, Wells A Messersmith4, Serengulam V Govindan9, Pius P Maliakal9, Boyd Mudenda9, William A Wegener9, Robert M Sharkey9, David M Goldenberg10.   

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. ©2017 American Association for Cancer Research.

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Year:  2017        PMID: 28679770     DOI: 10.1158/1078-0432.CCR-17-0933

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  32 in total

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4.  Antibody-drug conjugates in treating older patients suffering from cancer: what is the real value?

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5.  The Properties of Cysteine-Conjugated Antibody-Drug Conjugates Are Impacted by the IgG Subclass.

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Review 6.  Sacituzumab govitecan: antibody-drug conjugate in triple-negative breast cancer and other solid tumors.

Authors:  K M Fenn; K Kalinsky
Journal:  Drugs Today (Barc)       Date:  2019-09       Impact factor: 2.245

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8.  TROPHY-U-01: A Phase II Open-Label Study of Sacituzumab Govitecan in Patients With Metastatic Urothelial Carcinoma Progressing After Platinum-Based Chemotherapy and Checkpoint Inhibitors.

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Review 10.  The promising role of antibody drug conjugate in cancer therapy: Combining targeting ability with cytotoxicity effectively.

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