Abstract
Currently, there is limited data regarding the effectiveness of standard subsequent line therapies such as endocrine therapy, chemotherapy, or targeted agents after progression on CDK4/6 inhibitor-based regimens. This paper describes time-to-treatment failure beyond progression on palbociclib or palbociclib+endocrine therapy in patients enrolled in the phase II, multicenter TREnd trial. Our results indicate that there is limited benefit from post-palbociclib treatment, regardless of the type of therapy received. A small population of long responders were identified who demonstrated ongoing benefit from a subsequent line of endocrine therapy after progression to palbociclib-based regimens. A translational research program is ongoing on this population of outliers.
Keywords:
Best sequence; CDK4/6 inhibitors; Metastatic breast cancer; Palbociclib; TREnd trial.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents, Hormonal / administration & dosage
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Breast Neoplasms / drug therapy*
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Breast Neoplasms / metabolism
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Breast Neoplasms / mortality*
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Erb-b2 Receptor Tyrosine Kinases / metabolism
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Female
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Humans
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Kaplan-Meier Estimate
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Piperazines / administration & dosage
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Piperazines / adverse effects
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Piperazines / therapeutic use*
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Postmenopause
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Prognosis
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Pyridines / administration & dosage
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Pyridines / adverse effects
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Pyridines / therapeutic use*
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Receptors, Estrogen / metabolism
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Receptors, Progesterone / metabolism
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Treatment Outcome
Substances
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Antineoplastic Agents, Hormonal
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Piperazines
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Pyridines
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Erb-b2 Receptor Tyrosine Kinases
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Receptors, Estrogen
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Receptors, Progesterone
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palbociclib