Palbociclib in Patients With Non-Small-Cell Lung Cancer With CDKN2A Alterations: Results From the Targeted Agent and Profiling Utilization Registry Study

被引:62
|
作者
Ahn, Eugene R. [1 ]
Mangat, Pam K. [2 ]
Garrett-Mayer, Elizabeth [2 ]
Halabi, Susan [3 ]
Dib, Elie G. [4 ]
Haggstrom, Daniel E. [5 ]
Alguire, Kathryn B. [6 ]
Calfa, Carmen J. [7 ]
Cannon, Timothy L. [8 ]
Crilley, Pamela A. [9 ]
Gaba, Anu G. [10 ]
Marr, Alissa S. [11 ]
Sangal, Ashish [12 ]
Thota, Ramya [13 ]
Antonelli, Kaitlyn R. [2 ]
Islam, Samiha [2 ]
Rygiel, Andrew L. [2 ]
Bruinooge, Suanna S. [2 ]
Schilsky, Richard L. [2 ]
机构
[1] Canc Treatment Ctr Amer, Chicago, IL USA
[2] Amer Soc Clin Oncol, 2318 Mill Rd, Alexandria, VA 22314 USA
[3] Duke Univ, Med Ctr, Durham, NC USA
[4] Michigan Canc Res Consortium, Ypsilanti, MI USA
[5] Levine Canc Inst, Charlotte, NC USA
[6] Canc Res Consortium West Michigan, Grand Rapids, MI USA
[7] Sylvester Comprehens Canc Ctr, Plantation, FL USA
[8] Inova Schar Canc Inst, Fairfax, VA USA
[9] Canc Treatment Ctr Amer, Philadelphia, PA USA
[10] Sanford Hlth, Sioux Falls, SD USA
[11] Univ Nebraska Med Ctr, Omaha, NE USA
[12] Canc Treatment Ctr Amer, Phoenix, AZ USA
[13] Intermt Healthcare, Salt Lake City, UT USA
关键词
GENETIC ALTERATIONS;
D O I
10.1200/PO.20.00037
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSEThe Targeted Agent and Profiling Utilization Registry (TAPUR) Study is a phase II pragmatic basket trial evaluating antitumor activity of commercially available targeted agents in patients with advanced cancer with genomic alterations known to be drug targets. Results in a cohort of patients with non-small-cell lung cancer (NSCLC) with CDKN2A alterations treated with palbociclib are reported.METHODSEligible patients were >= 18 years old with advanced NSCLC, no remaining standard treatment options, measurable disease, Eastern Cooperative Oncology Group performance status of 0 to 2, and adequate organ function. Patients with NSCLC with CDKN2A alterations and no Rb mutations received palbociclib 125 mg orally once daily for 21 days, followed by 7 days off. Simon's two-stage design was used with a primary study end point of objective response or stable disease (SD) of at least 16 weeks in duration. Secondary end points are progression-free survival (PFS), overall survival (OS), and safety.RESULTSTwenty-nine patients were enrolled from January 2017 to June 2018; two patients were not evaluable for response but were included in safety analyses. One patient with partial response and six patients with SD were observed, for a disease control rate of 31% (90% CI, 19% to 40%). Median PFS was 8.1 weeks (95% CI, 7.1 to 16.0 weeks), and median OS was 21.6 weeks (95% CI, 14.1 to 41.1 weeks). Eleven patients had at least 1 grade 3 or 4 adverse event (AE) or serious AE (SAE) possibly related to palbociclib (most common, cytopenias). Other AEs or SAEs possibly related to the treatment included anorexia, fatigue, febrile neutropenia, hypophosphatemia, sepsis, and vomiting.CONCLUSIONPalbociclib monotherapy demonstrated evidence of modest antitumor activity in heavily pretreated patients with NSCLC with CDKN2A alterations. Additional investigation is necessary to confirm efficacy and utility of palbociclib in this population.
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收藏
页码:757 / 766
页数:10
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