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Blood, 1 January 2005, Vol. 105, No. 1, pp. 289-291. Prepublished online as a Blood First Edition Paper on June 24, 2004; DOI 10.1182/blood-2004-02-0651. This Article Abstract Full Text (PDF) All Versions of this Article: 2004-02-0651v1 105/1/289    most recent Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Rights and Permissions Citing Articles Citing Articles via HighWire Citing Articles via CrossRef Citing Articles via Google Scholar Google Scholar Articles by Lin, T. S. Articles by Byrd, J. C. Search for Related Content PubMed PubMed Citation Articles by Lin, T. S. Articles by Byrd, J. C. Related Collections Immunobiology Neoplasia Clinical Trials and Observations Social Bookmarking                   What's this?  Previous Article  |  Table of Contents  |  Next Article  NEOPLASIA FCGR3A and FCGR2A polymorphisms may not correlate with response to alemtuzumab in chronic lymphocytic leukemia Thomas S. Lin, Ian W. Flinn, Rama Modali, Teresa A. Lehman, Jennifer Webb, Sharon Waymer, Mollie E. Moran, Margaret S. Lucas, Sherif S. Farag, and John C. Byrd From the Department of Medicine, Division of Hematology-Oncology, and the Department of Pharmacy, Division of Medicinal Chemistry, The Ohio State University, Columbus; the Department of Oncology, Division of Hematologic Malignancies, Johns Hopkins University, Baltimore, MD; and BioServe Biotechnologies, Laurel, MD.    Abstract Top Abstract Introduction Patients, materials, and methods Results Discussion References   The in vivo mechanism of action of alemtuzumab (anti-CD52; Campath-1H) remains unclear. With rituximab, FCGR3A and FCGR2A high-affinity polymorphisms have been associated with clinical response in lymphoma but not in CLL, suggesting potential divergent mechanisms of action between these 2 diseases. Herein, we examined FCGR3A (V/V, n = 4; V/F, n = 10; F/F, n = 19) and FCGR2A (A/A, n = 5; H/A, n = 22; H/H, n = 6) polymorphisms in 36 patients with relapsed CLL who were treated with thrice-weekly alemtuzumab for 12 weeks to assess the potential influence these high-affinity FcR receptor polymorphisms had on response to alemtuzumab. Response to alemtuzumab was similar regardless of FCGR3A polymorphism (V/V, 25%; V/F, 40%; F/F, 32%) or FCGR2A polymorphism (A/A, 40%; H/A, 32%; H/H, 33%). These findings indicate that FCGR3A and FCGR2A polymorphisms may not predict response to alemtuzumab in CLL. Future studies examining larger cohorts of alemtuzumab-treated patients with CLL will be required to definitively determine the predictive value of specific FCGR polymorphisms to treatment response. (Blood. 2005;105:289-291)    Introduction Top Abstract Introduction Patients, materials, and methods Results Discussion References   The CD52 antigen is a 21- to 28-kDa glycopeptide expressed on the surfaces of more than 95% of human lymphocytes, monocytes, and macrophages.1-3 CD52 is also expressed on all chronic lymphocytic leukemia (CLL) cells and indolent B-cell non-Hodgkin lymphoma (NHL) cells.4,5 Alemtuzumab (Campath-1H) is a humanized anti-CD52 monoclonal antibody that effectively fixes complement and depletes normal lymphocytes, lymphoma cells, and CLL cells.6-8 Alemtuzumab exhibits clinical activity in previously untreated9 and fludarabine-refractory CLL,10,11 with a 33% response rate in the pivotal phase 2 study.12 Antibody binding of CD52 in vitro elicits profound complement activation, antibody-dependent cellular cytotoxicity (ADCC), and apoptosis.13-15 To date, detailed studies examining the mechanism of alemtuzumab-mediated tumor clearance have not been examined in CLL. Studies with the anti-CD20 antibody rituximab in NHL suggest that ADCC, complement-dependent cytotoxicity (CDC), and a direct proapoptotic effect may contribute to cell death observed with this therapy. Recent studies in NHL have provided strong implication for the role of ADCC in lymphoma tumor clearance. Specifically, in a xenograft model of human lymphoma, knocking out the FcR loci in mice completely abrogated the response to rituximab, whereas knocking out the inhibitory FcRIIb enhanced the response to rituximab in the same xenograft model.16 Similar studies with alemtuzumab have been reported with adult T-cell leukemia (ATL) cells in an in vivo murine model, demonstrating the importance of ADCC for this tumor type.17 However, neither this nor any other xenograft model is representative of CLL. Additional supporting data for the importance of ADCC in the clearance of NHL cells has come from correlating high-affinity FCGR polymorphisms with clinical response to rituximab. Indeed, the presence of genomic polymorphisms corresponding to phenotypic expression of valine (V) or phenylalanine (F) at amino acid 158 of FcIIIa and of histidine (H) or arginine (A) at amino acid 131 of FcIIa greatly influences the affinity of IgG for the Fc receptor.18,19 Expression of the high-affinity V allele at 158 results in tighter binding of FcIIIa to IgG1 and IgG3, whereas the low-affinity F allele is associated with decreased binding of FcRIIIa to IgG. Similarly, the high-affinity H allele at 131 results in greater affinity of FcRIIa for IgG2, whereas the low-affinity A allele correlates with decreased binding. Correlation of these high-affinity polymorphisms has been associated with clinical response in 2 studies of NHL.20 In contrast to NHL, we recently demonstrated that these high-affinity polymorphisms do not appear to influence response to single-agent rituximab in CLL.21 These findings, along with other studies by our group and others, suggest that apoptosis and CDC may contribute more to rituximab-induced tumor clearance in CLL.22-24 To our knowledge, no studies have examined the correlation of high-affinity polymorphisms with response to alemtuzumab. Herein, we describe a series of patients with CLL treated with alemtuzumab; as in our previous study with rituximab, preliminary examination of these polymorphisms suggested little influence on clinical outcome to this antibody therapy.    Patients, materials, and methods Top Abstract Introduction Patients, materials, and methods Results Discussion References   Patient samples and cell processing Patients with relapsed CLL, as defined by National Cancer Institute (NCI) 96 criteria,25 were enrolled and provided written consent to participate in this previously reported institutional review board (Johns Hopkins University and The Ohio State University)-approved protocol. Alemtuzumab was administered as previously reported for the CAM211 study.12 The alemtuzumab dose was stepped up from 3 mg to 30 mg during the first week and then was given at 30 mg thrice weekly for 12 weeks. Blood counts were monitored weekly. CLL response was assessed by NCI 96 criteria.25 Analysis of FCGR3A and FCGR2A polymorphisms Cells were obtained before alemtuzumab treatment, and mononuclear cells were isolated from blood using density-gradient centrifugation (Ficoll-Paque Plus; Pharmacia Biotech, Piscataway, NJ). Cells were then viably cryopreserved in 10% dimethyl sulfoxide (DMSO), 40% fetal calf serum and 50% RPMI media. DNA was extracted using the QIAamp kit, according to the manufacturer's instructions (Qiagen, Valencia, CA). Assessment of FCGR3A and FCGR2A polymorphisms was performed as previously described.20 All samples were analyzed in duplicate with identical results.    Results Top Abstract Introduction Patients, materials, and methods Results Discussion References   Patient population Thirty-six patients with relapsed CLL who received alemtuzumab were examined (Table 1). Median age was 61 years (range, 42-74 years), and 29 (81%) patients were male. Patients had received a median of 3 previous therapies (range, 1-12), and 29 (81%) patients had fludarabine-refractory disease. Seventy-five percent of the patients had Rai stage IV (n = 24) or III (n = 3) disease. Twelve (33%) patients had deletion of 17p13.1 detected by interphase cytogenetic analysis. View this table: [in this window] [in a new window]   Table 1.. Patient demographics and response to alemtuzumab therapy   Response Eleven (31%) responses were observed, including 2 complete responses (CRs) and 9 partial responses (PRs). One patient who achieved CR underwent autologous stem cell transplantation; median duration of response in the other 10 patients was 9.5 months (range, 3-36 months). Results are summarized in Table 1. FCGR3A and FCGR2A polymorphisms FCGR3A and FCGR2A polymorphism data were available on 32 patients (Table 2). FCGR3A polymorphism information alone was available on 1 patient, and FCGR2A information alone was available on 1 patient. Two patients had no polymorphism data. Analysis of V/F 158 FCGR3A showed V/V (n = 4), V/F (n = 10), and F/F (n = 19), and analysis of H/A 131 FCGR2A showed A/A (n = 5), H/A (n = 22), and H/H (n = 6). There was no concordance between FCGR3A and FCGR2A polymorphisms. No significant difference in response to alemtuzumab based on V/F 158 FCGR3A polymorphism was observed; response rates were 25% (V/V), 40% (V/F), and 32% (F/F). Similarly, H/A 131 FCGR2A polymorphism did not predict response to alemtuzumab, with response rates of 40% (A/A), 32% (H/A), and 33% (H/H). View this table: [in this window] [in a new window]   Table 2.. Response by FCGR3A and FCGR2A polymorphisms      Discussion Top Abstract Introduction Patients, materials, and methods Results Discussion References   Our report is the first preliminary investigation of the impact of FCGR polymorphisms on clinical response to alemtuzumab. No difference in response to alemtuzumab was observed in our 36 patients with CLL based on FCGR3A or FCGR2A polymorphisms (Table 2). Thus, similar to our previously published study of rituximab in CLL,21 our preliminary results suggest that these polymorphisms may not be predictive of improved response to alemtuzumab in CLL. The findings of our study should not be interpreted to minimize the importance of ADCC in mediating alemtuzumab tumor clearance; rather, the FCGR polymorphisms may be of less importance if our data are confirmed by larger, more definitive studies. Indeed, an HTLV leukemia in vivo murine model suggests that ADCC is important.17 In this study, ATL-bearing FcR-/- mice failed to respond to a 4-week course of alemtuzumab, with all FcR knockout mice dying by 22 days irrespective of alemtuzumab therapy. In contrast, alemtuzumab significantly prolonged survival in ATL-bearing wild-type FcR mice. Although all untreated ATL-bearing wild-type FcR mice died by 30 days, 8 of 10 wild-type FcR mice treated with alemtuzumab were alive at 40 days. Other clinical studies performed previously with anti-CD52 antibodies with different immunoglobulin G (IgG) and IgM isoforms also support the contribution of ADCC to the mechanism of action of alemtuzumab.26,27 The first, by Dyer et al,27 demonstrated little activity with an IgM anti-CD52 antibody with potent complement-dependent cytotoxicity but absent ADCC mediating ability. The second, by Isaacs et al,26 administered an IgG4 anti-CD52 antibody, followed 8 days later by an IgG1 anti-CD52 antibody, in patients with refractory rheumatoid arthritis. This study demonstrated modest CD4 cell depletion with the IgG4 antibody that should not mediate complement or ADCC but marked depletion with later treatment using the IgG1 antibody. Thus, the data presented herein and previously reported by others17,26,27 suggest that alemtuzumab may exert its effects through several pathways not inclusive or exclusive of ADCC. With respect to the importance of FCGR polymorphisms, this study represents an initial assessment of these, which now require larger studies for definitive determination of their importance in predicting response to alemtuzumab. Interestingly, however, the FCGR3A polymorphism (V/V 158) associated with high-affinity binding to IgG correlated with the lowest response rate to rituximab and alemtuzumab in our 2 series (herein and in Farag et al21), in contrast to previously reported findings in NHL.20 Similarly, we did not observe an improved response rate to rituximab or alemtuzumab in patients with CLL with the H/H 131 FCGR2A polymorphism (herein and in Farag et al21), contrary to the findings of a recent report in NHL patients treated with rituximab.28 Preliminary data from our laboratory suggest that alemtuzumab effectively induces apoptosis in CLL through a caspase-dependent mechanism.29 The CD52 antigen is also expressed at high density on CLL cells, and it is feasible that CDC may also partially contribute to alemtuzumab-induced tumor clearance in vivo. Given the promising results of alemtuzumab in refractory CLL and its ability to eliminate highly resistant p53 mutant CLL cells,30,31 further investigations of the in vivo mechanism of action of alemtuzumab are warranted.    Footnotes   Submitted February 25, 2004; accepted May 8, 2004. Prepublished online as Blood First Edition Paper, June 24, 2004; DOI 10.1182/blood-2004-02-0651. Supported by the National Cancer Institute (P01 CA95426-01A), The Sidney Kimmel Cancer Research Foundation, The Leukemia and Lymphoma Society of America, and The D. Warren Brown Foundation. J.C.B. is a Clinical Scholar of the Leukemia and Lymphoma Society of America. The publication costs of this article were defrayed in part by page charge payment. Therefore, and solely to indicate this fact, this article is hereby marked "advertisement" in accordance with 18 U.S.C. section 1734. Reprints: John C. Byrd, Division of Hematology-Oncology, Starling Loving Hall, Rm B-302, The Ohio State University, Columbus, OH 43210; e-mail: byrd-3{at}medctr.osu.edu.    References Top Abstract Introduction Patients, materials, and methods Results Discussion References   Treumann A, Lifely MR, Schneider P, Ferguson MA. Primary structure of CD52. J Biol Chem. 1995;270: 6088-6099.[Abstract/Free Full Text] Domagala A, Kurpisz M. CD52 antigen: a review. Med Sci Monit. 2001;7: 325-331.[Medline] [Order article via Infotrieve] Rowan W, Tite J, Topley P, Brett SJ. Cross-linking of the CAMPATH-1 antigen (CD52) mediates growth inhibition in human B- and T-lymphoma cell lines, and subsequent emergence of CD52-deficient cells. Immunology. 1998;95: 427-436.[CrossRef][Medline] [Order article via Infotrieve] Hale G, Swirsky D, Waldmann H, Chan LC. Reactivity of rat monoclonal antibody CAMPATH-1 with human leukaemia cells and its possible application for autologous bone marrow transplantation. 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Campath-1H-induced complete remission of chronic lymphocytic leukemia despite p53 gene mutation and resistance to chemotherapy. N Engl J Med. 2002;347: 452-453.[Free Full Text] Lozanski G, Heerema NA, Flinn IW, et al. Alemtuzumab is an effective therapy for chronic lymphocytic leukemia with p53 mutations and deletions. Blood. 2004;103: 3278-3281.[Abstract/Free Full Text] CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    What's this? This article has been cited by other articles: F. Bibeau, E. Lopez-Crapez, F. Di Fiore, S. Thezenas, M. Ychou, F. Blanchard, A. Lamy, F. Penault-Llorca, T. Frebourg, P. Michel, et al. Impact of Fc{gamma}RIIa-Fc{gamma}RIIIa Polymorphisms and KRAS Mutations on the Clinical Outcome of Patients With Metastatic Colorectal Cancer Treated With Cetuximab Plus Irinotecan J. Clin. Oncol., March 1, 2009; 27(7): 1122 - 1129. [Abstract] [Full Text] [PDF] A. Musolino, N. Naldi, B. Bortesi, D. Pezzuolo, M. Capelletti, G. Missale, D. Laccabue, A. 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