Abstract
Goal of the work
Anemia is a common side effect of chemotherapy. Limited information exists about its incidence and risk factors. The objective of this study was to evaluate the incidence of anemia and risk factors for anemia occurrence in patients with early breast cancer who received adjuvant chemotherapy.
Materials and methods
We evaluated risk factors for anemia in pre- and post/perimenopausal patients with lymph node-positive early breast cancer treated with adjuvant chemotherapy in two randomized trials. All patients received four cycles of doxorubicin and cyclophosphamide (AC) followed by three cycles of cyclophosphamide, methotrexate, fluorouracil (CMF). Anemia incidence was related to baseline risk factors. Multivariable analysis used logistic and Cox regression.
Main results
Among the 2,215 available patients, anemia was recorded in 11% during adjuvant chemotherapy. Grade 2 and 3 anemia occurred in 4 and 1% of patients, respectively. Pretreatment hemoglobin and white blood cells (WBC) were significant predictors of anemia. Adjusted odds ratios (logistic regression) comparing highest versus lowest quartiles were 0.18 (P < 0.0001) for hemoglobin and 0.52 (P = 0.0045) for WBC. Age, surgery type, platelets, body mass index, and length of time from surgery to chemotherapy were not significant predictors. Cox regression results looking at time to anemia were similar.
Conclusions
Moderate or severe anemia is rare among patients treated with AC followed by CMF. Low baseline hemoglobin and WBC are associated with a higher risk of anemia.


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Acknowledgment
We thank the patients, physicians, nurses, data managers, and trial coordinators who participate in the International Breast Cancer Study Group trials and Joie Celano for central data management. Supported in part by the Swiss Group for Clinical Cancer Research, Frontier Science and Technology Research Foundation, The Cancer Council Australia, Australian New Zealand Breast Cancer Trials Group, National Health and Medical Research Council of Australia (grants 940892, 980380, 100925), United States National Cancer Institute (CA-75362), Swedish Cancer Society, Foundation for Clinical Research of Eastern Switzerland, Cancer Association of South Africa (for South African patients), Orion-Farmos (for medication for trial 14–93).
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IBCSG Trials 13-93 and 14-93 Participants and Authors
IBCSG Trials 13-93 and 14-93 Participants and Authors
Trial 13-93 Study Chair: Marco Colleoni; Trial 14-93 Study Chairs: Edda Simoncini, Olivia Pagani; Scientific Committee: A. Goldhirsch, A.S. Coates (Co-Chairs); Foundation Council: B. Thürlimann (President), M. Castiglione, A.S. Coates, J.P. Collins, H. Cortés Funes, R.D. Gelber, A. Goldhirsch, M. Green, A. Hiltbrunner, S.B. Holmberg, D. K. Hossfeld, I. Láng, J. Lindtner, C.-M. Rudenstam, R. Stahel, H.-J. Senn, A. Veronesi; Coordinating Center (Bern, Switzerland): M. Castiglione-Gertsch (CEO), A. Hiltbrunner (Director), G. Egli, M. Rabaglio, R. Studer, B. Ruepp, R. Maibach, M. Strausak, E. Marbot; Statistical Center (Harvard School of Public Health and Dana-Farber Cancer Institute, Boston, MA, USA): R.D. Gelber (Group Statistician), K.N. Price (Director of Scientific Administration), B.F. Cole, S. Gelber, M.M. Regan, D. Zahrieh, Z. Sun, A. Giobbie-Hurder; Quality of Life Office (Bern, Switzerland): J. Bernhard, G. Egli, Ch. Hürny, D. Gerber; Pathology Office: B. Gusterson, G. Viale; Data Management Center (Frontier Science & Tech. Res. Found., Amherst, NY, USA): L. Blacher (Director), J. Celano, M. Isley, R. Hinkle, S. Lippert, K. Scott; Centro di Riferimento Oncologico Aviano, Italy: A. Veronesi, D. Crivellari, S. Monfardini, E. Galligioni, M.D. Magri, A. Buonadonna, S. Massarut, C. Rossi, E. Candiani, A. Carbone, R. Volpe, M. Roncadin, M. Arcicasa, F. Coran, S. Morassut; Spedali Civili & Fondazione Beretta, Brescia, Italy: E. Simoncini, G. Marini, P. Marpicati, M. Braga, P. Grigolato, L. Lucini; Istituto Europeo di Oncologia, Milano, Italy: A. Goldhirsch, M. Colleoni, G. Martinelli, G. Viale, L. Orlando, F. Nolè, R. Torrisi, T. De Pas, F. de Braud, S. Cinieri, F. Peccatori, A. Luini, R. Orecchia, G. Renne, F. de Braud, A. Costa, S. Zurrida, P. Veronesi, V. Sacchini, V. Galimberti, M. Intra, U. Veronesi; Ospedale Infermi Rimini, Italy: A. Ravaioli, D. Tassinari, G. Oliverio, F. Barbanti, P. Rinaldi, E. Pini, G. Drudi; Ospedale S. Eugenio Roma, Italy: M. Antimi, M. Minelli, V. Bellini, R. Porzio, E. Pernazza,G. Santeusanio, L.G. Spagnoli; General Hospital, Gorizia, Italy: S. Foladore, L. Foghin, G. Pamich, C. Bianchi, B. Marino, A. Murgia, V. Milan; West Swedish Breast Cancer Study Group, Göteborg, Sweden: C.M. Rudenstam, A. Wallgren, S. Ottosson-Lönn, R. Hultborn, G. Colldahl-Jädeström, E. Cahlin, J. Mattsson, S. B.Holmberg, O. Ruusvik, L.G. Niklasson, S. Dahlin, G. Karlsson, B. Lindberg, A. Sundbäck, S. BergegÂrdh, O. Groot, L.O. Dahlbäck, H. Salander, C. Andersson, M. Heideman, A. Nissborg, A. Wallin, G. Claes, T. Ramhult, J.H. Svensson, P. Liedberg, A. Nilsson, G. Havel, G. Oestberg, S. Persson, M. Suurküla, J. Matusik; The Institute of Oncology, Ljubljana, Slovenia: J. Lindtner, D. Erzen, T. Cufer, J. Cervek, O. Cerar, B. Zakotnik, E. Majdic, R. Golouh, J. Lamovec, J. Jancar, I. Vrhovec, M. Kramberger; Groote Schuur Hospital, Cape Town, Rep. of South Africa: E. Murray, I.D. Werner, D.M. Dent, A. Gudgeon, E. Panieri, E. McEvoy, J. Toop, R. Bowen; Sandton Oncology Center, Johannesburg, South Africa: D. Vorobiof, M. Chasen, G. Fotheringham, G. de Muelenaere, B. Skudowitz, C. Mohammed, A. Rosengarten; Madrid Breast Cancer Group, Madrid, Spain: H. Cortès-Funes, C. Mendiola, C. Gravalos, Colomer, M. Mendez, F. Cruz Vigo, P. Miranda, A. Sierra, F. Martinez-Tello, A. Garzon, S. Alonso, A. Ferrero, C. Vargas; SAKK (Swiss Group for Clinical Cancer Research): Inselspital, Bern: M.F. Fey, M. Castiglione-Gertsch, E. Dreher, H. Schneider, S. Aebi, K. Buser, J. Ludin, G. Beck, A. Haenel, J.M. Lüthi, H.J. Altermatt, M. Nandedkar; Kantonsspital, St. Gallen: H.J. Senn, B. Thürlimann, Ch. Oehlschlegel, G. Ries, M. Töpfer, U. Lorenz, A. Ehrsam, B. Späti, E. Vogel; Ospedale San Giovanni, Bellinzona: F. Cavalli, O. Pagani, H. Neuenschwander, L. Bronz, C. Sessa, M. Ghielmini, T. Rusca, P. Rey, J. Bernier, E. Pedrinis, T. Gyr, L. Leidi, G. Pastorelli, A. Goldhirsch; Kantonsspital, Basel: R. Herrmann, C.F. Rochlitz, J.F. Harder, O. 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Tattersall; St George Hospital. Kogarah, NSW: P. de Souza; Auckland Hospital, Auckland, New Zealand: V.J. Harvey, P. Thompson, D. Porter
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Gianni, L., Cole, B.F., Panzini, I. et al. Anemia during adjuvant non-taxane chemotherapy for early breast cancer: Incidence and risk factors from two trials of the International Breast Cancer Study Group. Support Care Cancer 16, 67–74 (2008). https://doi.org/10.1007/s00520-007-0295-y
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DOI: https://doi.org/10.1007/s00520-007-0295-y