Analysis of Serious Weight Gain in Patients Using Alectinib for ALK-Positive Lung Cancer

被引:14
作者
de Leeuw, Simon P. [1 ,2 ]
Pruis, Melinda A. [1 ,2 ]
Sikkema, Barend J. [2 ]
Mohseni, Mostafa [3 ,4 ]
Veerman, G. D. Marijn [2 ]
Paats, Marthe S. [1 ]
Dumoulin, Daphne W. [1 ]
Smit, Egbert F. [5 ]
Schols, Annemie M. W. J. [6 ]
Mathijssen, Ron H. J. [2 ]
van Rossum, Elisabeth F. C. [3 ,4 ]
Dingemans, Anne-Marie C. [1 ,7 ]
机构
[1] Univ Med Ctr Rotterdam, Erasmus MC Canc Inst, Dept Pulm Med, Rotterdam, Netherlands
[2] Univ Med Ctr Rotterdam, Erasmus MC Canc Inst, Dept Med Oncol, Rotterdam, Netherlands
[3] Univ Med Ctr Rotterdam, Erasmus MC, Dept Internal Med, Div Endocrinol, Rotterdam, Netherlands
[4] Univ Med Ctr Rotterdam, Erasmus MC, Obes Ctr CGG, Rotterdam, Netherlands
[5] Leiden Univ, Dept Pulm Med, Med Ctr, Leiden, Netherlands
[6] Maastricht Univ, Sch Nutr & Translat Res Metab, Med Ctr, Maastricht, Netherlands
[7] Erasmus MC, Dept Pulm Med, dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands
关键词
Alectinib; Weight; Body composition; Obesity; Non-small cell lung cancer; BODY-MASS INDEX; SARCOPENIC OBESITY; METABOLIC SYNDROME; ABDOMINAL OBESITY; ADIPOSE-TISSUE; OPEN-LABEL; J-ALEX; CRIZOTINIB; RISK; DURATION;
D O I
10.1016/j.jtho.2023.03.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Alectinib is a standard-of-care treatment for metastatic ALK+ NSCLC. Weight gain is an unexplored side effect reported in approximately 10%. To prevent or intervene alectinib-induced weight gain, more insight in its extent and etiology is needed. Methods: Change in body composition was analyzed in a prospective series of 46 patients with ALK+ NSCLC, treated with alectinib. Waist circumference, visceral adipose tissue (VAT), subcutaneous adipose tissue (SAT), and skeletal muscle were quantified using sliceOmatic software on computed tomography images at baseline, 3 months (3M), and 1 year (1Y). To investigate an exposure-toxicity relationship, alectinib plasma concentrations were quantified. Four patients with more than 10 kg weight gain were referred to Erasmus MC Obesity Center CGG for in-depth analysis (e.g., assessments of appetite, dietary habits, other lifestyle, medical and psycho social factors, and extensive metabolic and endocrine assessments, including resting energy expenditure).Results: Mean increase in waist circumference was 9 cm (9.7%, p < 0.001) in 1Y with a 40% increase in abdominal obesity (p = 0.014). VAT increased to 10.8 cm2 (15.0%, p = 0.003) in 3M and 35.7 cm2 (39.0%, p < 0.001) in 1Y. SAT increased to 18.8 cm2 (12.4%, p < 0.001) in 3M and 45.4 cm2 (33.3%, p < 0.001) in 1Y. The incidence of sarcopenic obesity increased from 23.7% to 47.4% during 1Y of treatment. Baseline waist circumference was a positive predictor of increase in VAT (p = 0.037). No exposure toxicity relationship was found. In-depth analysis (n = 4) revealed increased appetite in two patients and metabolic syndrome in all four patients.Conclusions: Alectinib may cause relevant increased sarcopenic abdominal obesity, with increases of both VAT and SAT, quickly after initiation. This may lead to many serious metabolic, physical, and mental disturbances in long surviving patients.& COPY; 2023 Published by Elsevier Inc. on behalf of International Association for the Study of Lung Cancer.
引用
收藏
页码:1017 / 1030
页数:14
相关论文
共 67 条
  • [1] The number of years lived with obesity and the risk of all-cause and cause-specific mortality
    Abdullah, Asnawi
    Wolfe, Rory
    Stoelwinder, Johannes U.
    de Courten, Maximilian
    Stevenson, Christopher
    Walls, Helen L.
    Peeters, Anna
    [J]. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2011, 40 (04) : 985 - 996
  • [2] The duration of obesity and the risk of type 2 diabetes
    Abdullah, Asnawi
    Stoelwinder, Johannes
    Shortreed, Susan
    Wolfe, Rory
    Stevenson, Christopher
    Walls, Helen
    de Courten, Maximilian
    Peeters, Anna
    [J]. PUBLIC HEALTH NUTRITION, 2011, 14 (01) : 119 - 126
  • [3] Improving the tolerability of osimertinib by identifying its toxic limit
    Agema, Bram C.
    Veerman, G. D. Marijn
    Steendam, Christi M. J.
    Lanser, Daan A. C.
    Preijers, Tim
    van der Leest, Cor
    Koch, Birgit C. P.
    Dingemans, Anne-Marie C.
    Mathijssen, Ron H. J.
    Koolen, Stijn L. W.
    [J]. THERAPEUTIC ADVANCES IN MEDICAL ONCOLOGY, 2022, 14
  • [4] Harmonizing the Metabolic Syndrome A Joint Interim Statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity
    Alberti, K. G. M. M.
    Eckel, Robert H.
    Grundy, Scott M.
    Zimmet, Paul Z.
    Cleeman, James I.
    Donato, Karen A.
    Fruchart, Jean-Charles
    James, W. Philip T.
    Loria, Catherine M.
    Smith, Sidney C., Jr.
    [J]. CIRCULATION, 2009, 120 (16) : 1640 - 1645
  • [5] How can we measure insulin sensitivity/resistance?
    Antuna-Puente, B.
    Disse, E.
    Rabasa-Lhoret, R.
    Laville, M.
    Capeau, J.
    Bastard, J. -P.
    [J]. DIABETES & METABOLISM, 2011, 37 (03) : 179 - 188
  • [6] Clinical Management of Adverse Events Associated with Lorlatinib
    Bauer, Todd M.
    Felip, Enriqueta
    Solomon, Benjamin J.
    Thurm, Holger
    Peltz, Gerson
    Chioda, Marc D.
    Shaw, Alice T.
    [J]. ONCOLOGIST, 2019, 24 (08) : 1103 - 1110
  • [7] Benjamin JS, 2019, J CLIN ONCOL, V37
  • [8] Overweight, obesity, and mortality from cancer in a prospectively studied cohort of US adults
    Calle, EE
    Rodriguez, C
    Walker-Thurmond, K
    Thun, MJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (17) : 1625 - 1638
  • [9] Brigatinib versus Crizotinib in ALK-Positive Non-Small-Cell Lung Cancer
    Camidge, D. R.
    Kim, H. R.
    Ahn, M. -J.
    Yang, J. C. -H.
    Han, J. -Y.
    Lee, J. -S.
    Hochmair, M. J.
    Li, J. Y. -C.
    Chang, G. -C.
    Lee, K. H.
    Gridelli, C.
    Delmonte, A.
    Garcia Campelo, R.
    Kim, D. -W.
    Bearz, A.
    Griesinger, F.
    Morabito, A.
    Felip, E.
    Califano, R.
    Ghosh, S.
    Spira, A.
    Gettinger, S. N.
    Tiseo, M.
    Gupta, N.
    Haney, J.
    Kerstein, D.
    Popat, S.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (21) : 2027 - 2039
  • [10] Lorlatinib Exposure-Response Analyses for Safety and Efficacy in a Phase I/II Trial to Support Benefit-Risk Assessment in Non-Small Cell Lung Cancer
    Chen, Joseph
    Ruiz-Garcia, Ana
    James, Leonard P.
    Peltz, Gerson
    Thurm, Holger
    Clancy, Jill
    Hibma, Jennifer
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2021, 110 (05) : 1273 - 1281