Selinexor in combination with carboplatin and paclitaxel in patients with advanced solid tumors: Results of a single-center, multi-arm phase Ib study

被引:4
|
作者
Thein, Kyaw Z. [1 ,2 ]
Karp, Daniel D. [1 ]
Tsimberidou, Apostolia [1 ]
Gong, Jing [1 ]
Sulovic, Selma [1 ]
Shah, Jatin [3 ]
Milton, Denai R. [4 ]
Hong, David S. [1 ]
Janku, Filip [1 ]
McQuinn, Lacey [1 ]
Stephen, Bettzy A. [1 ]
Colen, Rivka [5 ]
Carter, Brett W. [6 ]
Yap, Timothy A. [1 ]
Piha-Paul, Sarina A. [1 ]
Fu, Siqing [1 ]
Meric-Bernstam, Funda [1 ]
Naing, Aung [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Invest Canc Therapeut, Houston, TX 77030 USA
[2] Oregon Hlth & Sci Univ, Knight Canc Inst, Div Hematol & Med Oncol, Portland, OR 97201 USA
[3] Karyopharm Therapeut, Newton, MA USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Diagnost Radiol, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Thorac Imaging, Div Diagnost Imaging, Houston, TX 77030 USA
关键词
Selinexor; Carboplatin; Paclitaxel; Metastatic solid tumors; Selective inhibitor of nuclear export (SINE); NUCLEAR EXPORT; INHIBITOR SELINEXOR; SELECTIVE INHIBITOR; CRM1; EXPRESSION; 1ST-IN-CLASS;
D O I
10.1007/s10637-021-01188-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Carboplatin and paclitaxel (CT) is one of the standard chemotherapy regimens used in various tumor types. Preclinical models have suggested that selinexor, a first-in-class oral potent selective inhibitor of nuclear export Exportin-1, and CT exerts antitumor activity in multiple malignancies. Methods. This was a single-center, multi-arm phase Ib study utilizing a "basket type" expansion. CT and selinexor was employed as one of the 13 parallel arms. Advanced relapsed/refractory solid tumors following standard therapy or where the addition of selinexor to standard regimens deemed appropriate, were eligible. Results. Of 13 patients treated, 12 patients were evaluable for response. The most common cancers were breast (n = 4), esophageal (n = 2), ovarian (n = 2) and non-small cell lung cancers (n = 2). All 13 patients had at least one treatment-related adverse events (TRAEs) and the most common were neutropenia (85%), leukopenia (85%), thrombocytopenia (85%), anemia (69%), nausea (54%), vomiting (46%), and fatigue (46%). One patient at 60 mg QW experienced DLT with grade 3 nausea and vomiting lasting 3 days. Unconfirmed partial response (uPR) was observed in 3 patients; one patient each with esophageal, breast, and ovarian cancer. One patient with esophageal adenocarcinoma had confirmed PR, however, was discontinued from the study due to clinical progression. Five patients achieved stable disease (SD). Disease control rate was 8%. Majority of patients (77%), including two patients who had uPR, had prior exposure to carboplatin and/or paclitaxel. Time-to-treatment failure (TTF) ranged from 1 to 153 weeks. Conclusion. The RP2D of selinexor was 60 mg QW in combination with CT. The combination conferred viable clinical activity with durable objective responses which should further be explored in tumor types for which CT is used as standard of care. Trial information.
引用
收藏
页码:290 / 299
页数:10
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