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Safety, tolerability and pharmacokinetics of crizotinib in combination with cytotoxic chemotherapy for pediatric patients with refractory solid tumors or anaplastic large cell lymphoma (ALCL): a Children's Oncology Group phase 1 consortium study (ADVL1212).
Greengard, Emily; Mosse, Yael P; Liu, Xiaowei; Minard, Charles G; Reid, Joel M; Voss, Stephan; Wilner, Keith; Fox, Elizabeth; Balis, Frank; Blaney, Susan M; Adamson, Peter C; Weigel, Brenda J.
Afiliação
  • Greengard E; Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA. emilyg@umn.edu.
  • Mosse YP; St Jude Children's Research Hospital, Memphis, TN, USA.
  • Liu X; Children's Oncology Group, Monrovia, CA, USA.
  • Minard CG; Baylor College of Medicine, Houston, TX, USA.
  • Reid JM; Mayo Clinic, Rochester, MN, USA.
  • Voss S; Dana Farber Cancer Institute, Boston, MA, USA.
  • Wilner K; Pfizer, Inc, Bentonville, AR, USA.
  • Fox E; St Jude Children's Research Hospital, Memphis, TN, USA.
  • Balis F; St Jude Children's Research Hospital, Memphis, TN, USA.
  • Blaney SM; Baylor College of Medicine, Houston, TX, USA.
  • Adamson PC; St Jude Children's Research Hospital, Memphis, TN, USA.
  • Weigel BJ; Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Cancer Chemother Pharmacol ; 86(6): 829-840, 2020 12.
Article em En | MEDLINE | ID: mdl-33095287
ABSTRACT

PURPOSE:

This phase 1 study aimed to determine the safety, tolerability and recommended phase 2 dose (RP2D) of crizotinib in combination with cytotoxic chemotherapy for children with refractory solid tumors and ALCL.

METHODS:

Pediatric patients with treatment refractory solid tumors or ALCL were eligible. Using a 3 + 3 design, crizotinib was escalated in three dose levels 165, 215, or 280 mg/m2/dose BID. In Part A, patients received crizotinib oral solution (OS) in combination with topotecan and cyclophosphamide (topo/cyclo); in Part B, crizotinib OS was administered with vincristine and doxorubicin (vcr/dox). In Parts C and D, patients received topo/cyclo in combination with either crizotinib-formulated capsules (FC) or microspheres (cMS), respectively. Crizotinib pharmacokinetic evaluation was required.

RESULTS:

Forty-four eligible patients were enrolled, 39 were evaluable for toxicity. Parts A and B were terminated due to concerns regarding palatability and tolerability of the OS. In Part C, crizotinib, FC 215 mg/m2/dose BID, in combination with topo/cyclo was tolerated. In Part D, the maximum tolerated dose (MTD) was exceeded at 165 mg/m2/dose of crizotinib cMS. Pharmacokinetics of crizotinib in combination with chemotherapy was similar to single-agent crizotinib and exposures were not formulation dependent.

CONCLUSIONS:

The RP2D of crizotinib FCs in combination with cyclophosphamide and topotecan was 215 mg/m2/dose BID. The oral solution of crizotinib was not palatable in this patient population. Crizotinib cMS was palatable; however, patients experienced increased toxicity that was not explained by the relative bioavailability or exposure and warrants further investigation. CLINICAL TRIAL REGISTRY The trial is registered as NCT01606878 at Clinicaltrials.gov.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma Anaplásico de Células Grandes / Crizotinibe / Recidiva Local de Neoplasia Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Cancer Chemother Pharmacol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma Anaplásico de Células Grandes / Crizotinibe / Recidiva Local de Neoplasia Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Cancer Chemother Pharmacol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos
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