Skip to main content
Journal cover image

Heart rate decrease during crizotinib treatment and potential correlation to clinical response.

Publication ,  Journal Article
Ou, S-HI; Tong, WP; Azada, M; Siwak-Tapp, C; Dy, J; Stiber, JA
Published in: Cancer
June 1, 2013

BACKGROUND: Crizotinib is used for the treatment of advanced anaplastic lymphoma kinase (ALK)-rearranged nonsmall cell lung cancer (NSCLC). Sinus bradycardia (SB) is a side effect listed in its package insert. We investigated the frequency and timing of SB, patient characteristics associated with SB during crizotinib treatment, and potential correlation between heart rate (HR) changes and clinical response to crizotinib. METHODS: A retrospective chart review was conducted of the timing and frequency of SB, patient characteristics, and clinical response of patients to crizotinib treatment. RESULTS: Forty-twp patients who had ALK-rearranged or mesenchymal epithelial transition (MET)-amplified NSCLC and received treatment with oral crizotinib 250 mg twice daily who were enrolled in 2 crizotinib trials (PROFILE 1001 and PROFILE 1005) were analyzed. There was an average decrease of 26.1 beats per minute (bpm) from the pretreatment HR among all patients during crizotinib treatment. Twenty-nine patients (69%) experienced at least 1 episode of SB (HR, <60 bpm). The average time to the lowest HR recorded was 18.6 weeks (range, 5-72 weeks). Patients who experienced SB were significantly older (aged 55.8 years vs 47.8 years; P = .0336), had a lower pretreatment HR (mean, 77.9 bpm vs 100.6 bpm; P = .002), and were on crizotinib longer (52.9 weeks vs 24.6 weeks; P = .0050) than patients who did not experience SB. The overall response rate (P = .0195) and the maximum tumor shrinkage (P = .0205) were significantly greater in patients who experienced SB. CONCLUSIONS: HR decrease is common during crizotinib treatment. It remains to be determined whether the correlation between HR decrease and clinical response to crizotinib reflects a biomarker of drug efficacy or a time/cumulative dose-dependent phenomenon.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

Cancer

DOI

EISSN

1097-0142

Publication Date

June 1, 2013

Volume

119

Issue

11

Start / End Page

1969 / 1975

Location

United States

Related Subject Headings

  • Retrospective Studies
  • Receptor Protein-Tyrosine Kinases
  • Pyridines
  • Pyrazoles
  • Protein Kinase Inhibitors
  • Oncology & Carcinogenesis
  • Middle Aged
  • Male
  • Lung Neoplasms
  • Humans
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Ou, S.-H., Tong, W. P., Azada, M., Siwak-Tapp, C., Dy, J., & Stiber, J. A. (2013). Heart rate decrease during crizotinib treatment and potential correlation to clinical response. Cancer, 119(11), 1969–1975. https://doi.org/10.1002/cncr.28040
Ou, Sai-Hong Ignatius, Wilson P. Tong, Michele Azada, Christina Siwak-Tapp, Joni Dy, and Jonathan A. Stiber. “Heart rate decrease during crizotinib treatment and potential correlation to clinical response.Cancer 119, no. 11 (June 1, 2013): 1969–75. https://doi.org/10.1002/cncr.28040.
Ou S-HI, Tong WP, Azada M, Siwak-Tapp C, Dy J, Stiber JA. Heart rate decrease during crizotinib treatment and potential correlation to clinical response. Cancer. 2013 Jun 1;119(11):1969–75.
Ou, Sai-Hong Ignatius, et al. “Heart rate decrease during crizotinib treatment and potential correlation to clinical response.Cancer, vol. 119, no. 11, June 2013, pp. 1969–75. Pubmed, doi:10.1002/cncr.28040.
Ou S-HI, Tong WP, Azada M, Siwak-Tapp C, Dy J, Stiber JA. Heart rate decrease during crizotinib treatment and potential correlation to clinical response. Cancer. 2013 Jun 1;119(11):1969–1975.
Journal cover image

Published In

Cancer

DOI

EISSN

1097-0142

Publication Date

June 1, 2013

Volume

119

Issue

11

Start / End Page

1969 / 1975

Location

United States

Related Subject Headings

  • Retrospective Studies
  • Receptor Protein-Tyrosine Kinases
  • Pyridines
  • Pyrazoles
  • Protein Kinase Inhibitors
  • Oncology & Carcinogenesis
  • Middle Aged
  • Male
  • Lung Neoplasms
  • Humans