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Appropriate dose of regorafenib based on body weight of colorectal cancer patients: a retrospective cohort study.
Nakashima, Masayuki; Li, Kan; Chen, Qichen; de Silva, Sajith; Li, Hal; Kawakami, Koji; Wei, Qingyi; Luo, Sheng; Zhao, Hong.
Afiliação
  • Nakashima M; Department of Pharmacoepidemiology, Graduate School of Medicine and Public Health, Kyoto University, Kyoto, Japan.
  • Li K; MRL, Merck & Co., Inc, North Wales, PA, USA.
  • Chen Q; Department of Hepatobiliary Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • de Silva S; MRL, Merck & Co., Inc, North Wales, PA, USA.
  • Li H; MRL, Merck & Co., Inc, North Wales, PA, USA.
  • Kawakami K; Department of Pharmacoepidemiology, Graduate School of Medicine and Public Health, Kyoto University, Kyoto, Japan.
  • Wei Q; Duke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
  • Luo S; Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
  • Zhao H; Department of Population Health Sciences, Duke University, Durham, NC, USA.
BMC Cancer ; 23(1): 1268, 2023 Dec 21.
Article em En | MEDLINE | ID: mdl-38129822
ABSTRACT

PURPOSE:

Previous randomized studies have shown a survival benefit of using regorafenib but a high rate of adverse events in unresectable colorectal cancer patients. To reduce these adverse events and improve the tolerability, we examined the appropriate dose of regorafenib based on body weight.

METHODS:

We used a nationwide claims database in Japan and examined the efficacy and safety of regorafenib for patients with metastatic colorectal cancer between groups divided by body weight (60 kg) and median average dose (120 mg) between 2013 and 2018. We also assessed overall survival (OS) and adverse events between these groups.

RESULTS:

We identified 2530 Japanese patients (heavy weight/high dose 513, light weight/low dose 921, heavy weight/low dose 452, and light weight/high dose 644). There was no significant difference in the adverse events and OS after inverse probability treatment weighting (IPTW) adjustment between heavy weight/high dose group and light weight/low dose group (hazard ratio, HR=0.97). Among the light-weight patients, higher average dose was associated with shorter OS (IPTW adjusted HR=1.21, 95% CI 1.05 - 1.39, Table 3) while among the heavy-weight patients, there was no significant difference in OS between high and low dose groups (IPTW adjusted HR=1.14, 95% CI 0.95 - 1.37).

CONCLUSION:

The findings suggest that a low dose of regorafenib for light-weight patients may be as safe and effective as high doses for heavy-weight patients. Further studies should be conducted to identify an appropriate dose based on each patient's physique and condition.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piridinas / Neoplasias Colorretais Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piridinas / Neoplasias Colorretais Idioma: En Ano de publicação: 2023 Tipo de documento: Article