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Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents.
Moreno, Lucas; DuBois, Steven G; Glade Bender, Julia; Mauguen, Audrey; Bird, Nick; Buenger, Vickie; Casanova, Michela; Doz, François; Fox, Elizabeth; Gore, Lia; Hawkins, Douglas S; Izraeli, Shai; Jones, David T W; Kearns, Pamela R; Molenaar, Jan J; Nysom, Karsten; Pfister, Stefan; Reaman, Gregory; Smith, Malcolm; Weigel, Brenda; Vassal, Gilles; Zwaan, Christian Michel; Paoletti, Xavier; Iasonos, Alexia; Pearson, Andrew D J.
Afiliação
  • Moreno L; Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • DuBois SG; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.
  • Glade Bender J; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Mauguen A; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Bird N; Solving Kids' Cancer UK, London, United Kingdom.
  • Buenger V; Coalition Against Childhood Cancer (CAC2), Philadelphia, PA.
  • Casanova M; Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
  • Doz F; Université Paris Cité, Paris, France.
  • Fox E; SIREDO Centre (Care, Innovation Research in Pediatric, Adolescent and Young Adults Oncology), Institut Curie, Paris, France.
  • Gore L; St Jude Children's Research Hospital, Memphis, TN.
  • Hawkins DS; Children's Hospital Colorado, Aurora, CO.
  • Izraeli S; University of Colorado, Aurora, CO.
  • Jones DTW; Seattle Children's Hospital, Seattle, WA.
  • Kearns PR; Children's Oncology Group.
  • Molenaar JJ; Rina Zaizov Pediatric Hematology Oncology Division, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
  • Nysom K; Hematological Malignancies Centre of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Pfister S; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
  • Reaman G; NIHR Birmingham Biomedical Research Centre, University of Birmingham, Birmingham, United Kingdom.
  • Smith M; Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
  • Weigel B; Department of Pharmaceutical Sciences Utrecht University, Utrecht, the Netherlands.
  • Vassal G; Division of Pediatric Neurooncology, DKFZ, KiTZ.
  • Zwaan CM; Righospitalet, Copenhagen, Denmark.
  • Paoletti X; Clinical Trial Unit and Childhood Brain Tumors, Heidelberg University Hospital, Heidelberg, Germany.
  • Iasonos A; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
  • Pearson ADJ; Division of Pediatric Glioma Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.
J Clin Oncol ; 41(18): 3408-3422, 2023 06 20.
Article em En | MEDLINE | ID: mdl-37015036
ABSTRACT

PURPOSE:

There is an increasing need to evaluate innovative drugs for childhood cancer using combination strategies. Strong biological rationale and clinical experience suggest that multiple agents will be more efficacious than monotherapy for most diseases and may overcome resistance mechanisms and increase synergy. The process to evaluate these combination trials needs to maximize efficiency and should be agreed by all stakeholders.

METHODS:

After a review of existing combination trial methodologies, regulatory requirements, and current results, a consensus among stakeholders was achieved.

RESULTS:

Combinations of anticancer therapies should be developed on the basis of mechanism of action and robust preclinical evaluation, and may include data from adult clinical trials. The general principle for combination early-phase studies is that, when possible, clinical trials should be dose- and schedule-confirmatory rather than dose-exploratory, and every effort should be made to optimize doses early. Efficient early-phase combination trials should be seamless, including dose confirmation and randomized expansion. Dose evaluation designs for combinations depend on the extent of previous knowledge. If not previously evaluated, limited evaluation of monotherapy should be included in the same clinical trial as the combination. Randomized evaluation of a new agent plus standard therapy versus standard therapy is the most effective approach to isolate the effect and toxicity of the novel agent. Platform trials may be valuable in the evaluation of combination studies. Patient advocates and regulators should be engaged with investigators early in a proposed clinical development pathway and trial design must consider regulatory requirements.

CONCLUSION:

An optimized, agreed approach to the design and evaluation of early-phase pediatric combination trials will accelerate drug development and benefit all stakeholders, most importantly children and adolescents with cancer.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias / Antineoplásicos Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Child / Humans Idioma: En Revista: J Clin Oncol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias / Antineoplásicos Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Child / Humans Idioma: En Revista: J Clin Oncol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Espanha