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Phase 3 N=271 Randomized Treatment

Alisertib (MLN8237) or Investigator's Choice in Patients With Relapsed/Refractory Peripheral T-Cell Lymphoma

Relapsed Peripheral T-Cell Lymphoma · Refractory Peripheral T-Cell Lymphoma

Enrolled (actual)
271
Serious AEs
54.9%
Results posted
Jul 2018
Primary outcome: Primary: Overall Response Rate (ORR) Based on Independent Review Committee (IRC) Assessment — 33; 45 percentage of participants — p=0.038

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Alisertib (Drug); Pralatrexate (Drug); Gemcitabine (Drug); Romidepsin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Millennium Pharmaceuticals, Inc.
Primary completion
Jun 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Response Rate (ORR) Based on Independent Review Committee (IRC) Assessment
33; 45 0.038 sig
PRIMARY
Progression-Free Survival (PFS) Based on IRC Assessment
115; 104 0.177
SECONDARY
Overall Survival (OS)
415; 367 0.338
SECONDARY
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
136; 126; 75; 69
SECONDARY
Number of Participants With Clinically Important Abnormal Laboratory Values Reported as AEs
18; 14; 17; 10; 6; 5
SECONDARY
Number of Participants With Clinically Important Vital Sign Measurements Reported as AEs
1; 0; 0; 1; 4; 6
SECONDARY
Complete Response (CR) Rate
18; 27
SECONDARY
Time to Disease Progression (TTP)
162; 116 0.362
SECONDARY
Duration of Response (DOR)
225; 172
SECONDARY
Time to Response
62; 64
SECONDARY
Time to Subsequent Antineoplastic Therapy
336; 233
SECONDARY
Plasma Concentration-time Data to Contribute to Future Population Pharmacokinetics (PK) Analysis
SECONDARY
Change Form Baseline in Reported Symptoms and Quality of Life (QoL) Assessment Per Functional Assessment of Cancer Therapy-Lymphoma (FACT-LYM) for Functioning and Symptoms
-2.4; -1.3; -0.3; 0.0; -1.4; -0.8

Summary

This is a phase 3, randomized, 2-arm, open-label, international trial evaluating alisertib compared with single-agent treatment, as selected by the investigator from the offered options of pralatrexate or gemcitabine or romidepsin, in participants with relapsed or refractory peripheral T-cell lymphoma (PTCL). Note: romidepsin was not used as a single-agent comparator outside the United States of America (USA) as supply was not available.

Eligibility Criteria

Inclusion Criteria

  • Male or female participants age 18 or older
  • Participants with Peripheral T cell lymphoma (PTCL) (selected subtypes) according to World Health Organization (WHO) criteria and have relapsed or are refractory to at least 1 prior systemic, cytotoxic therapy for PTCL. Participants must have received conventional therapy as a prior therapy. Cutaneous-only disease is not permitted. Participants must have documented evidence of progressive and measurable disease.
  • Tumor biopsy available for central hematopathologic review
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
  • Female participants who are post menopausal for at least 1 year, surgically sterile, or agree to practice 2 effective methods of contraception through 30 days after the last dose of study drug or agree to abstain from heterosexual intercourse.
  • Male participants who agree to practice effective barrier contraception through 6 months after the last dose of alisertib or agree to abstain from heterosexual intercourse
  • Suitable venous access
  • Voluntary written consent

Exclusion Criteria

  • Known central nervous system lymphoma
  • Systemic antineoplastic therapy, immunotherapy, investigational agent or radiation therapy within 4 weeks of first dose of study treatment or concomitant use during study
  • Prior administration of an Aurora A kinase-targeted agent, including alisertib; or all of the 3 comparator drugs (pralatrexate, or romidepsin or gemcitabine; or known hypersensitivity)
  • History of uncontrolled sleep apnea syndrome or other conditions that could result in excessive daytime sleepiness
  • Cardiac condition as specified in study protocol, including left ventricular ejection fraction (LVEF) <40%
  • Concomitant use of other medicines as specified in study protocol
  • Participants with abnormal gastric or bowel function who require continuous treatment with H2-receptor antagonists or proton pump inhibitors
  • Known active infection with human immunodeficiency virus (HIV), hepatitis B virus, or hepatitis C
  • Autologous stem cell transplant less than 3 months prior to enrollment
  • Participants who have undergone allogeneic stem cell or organ transplantation any time
  • Inadequate blood levels, bone marrow or other organ function as specified in study protocol
  • The participant must have recovered to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Grade ≤ 1 toxicity, to participant's baseline status (except alopecia), or deemed irreversible from the effects of prior cancer therapy
  • Major surgery, serious infection, or infection requiring systemic antibiotic therapy within 14 days prior to the first dose of study treatment
  • Female participants who are breastfeeding or pregnant
  • Coexistent second malignancy or history of prior solid organ malignancy within previous 3 years
  • Serious medical or psychiatric illness or laboratory abnormality that could, in the investigator's opinion, potentially interfere with the completion of treatment according to the protocol
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01482962). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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