Recombinant erythropoietin for the anaemia of patients with advanced Gastrointestinal Stromal Tumours (GIST) receiving imatinib: an active agent only in non progressive patients
Clinical Sarcoma Research volume 2, Article number: 11 (2012)
Recombinant erythropoietin for the anaemia of patients with advanced Gastrointestinal Stromal Tumours (GIST) receiving imatinib : an active agent only in non progressive patients.
Imatinib is a standard treatment for advanced/metastatic GIST and in adjuvant setting. Anaemia is frequently observed in patients with advanced GIST, and is one of the most frequent side effects of imatinib with grade 3–4 anaemia in 10% of patients. Whether EPO treatment is useful in the management of GIST patients receiving imatinib treatment is unknown.
A retrospective study of EPO treatment in GIST patients receiving imatinib was undertaken in 4 centres. Thirty four patients received EPO treatment among the 319 GIST patients treated with imatinib in clinical trials or with compassionate use between 2001 and 2003. The efficacy of EPO on the anaemia of patients with GIST treated with imatinib was analyzed.
There were 18 males and 16 females with a median age of 59 years. Median WHO-PS was 1. Primary tumour sites were mainly gastric (32%) and small bowel (29%). Sites of metastases were mainly liver (82%) and peritoneum (79%). The median delay between the initiation of imatinib treatment and EPO was 58 days (range 0–553). Median haemoglobin (Hb) level prior to EPO was 9 g/dL (range 6,9-11,8) and 11,7 g/dL (range 6,8-14,4) after 2 months. An increase of more than 2 g/dL was observed in 18 (53%) of patients. None of the 7 patients who progressed (PD) under imatinib treatment (400 mg/day) experienced HB response, as compared to 66% (18/27) of the remaining patients (PR + SD) (p = 0,002). Primary tumour site, liver metastases, peritoneal metastases, age, gender did not correlate with HB response to EPO. Response to EPO was observed in 2/11 patients receiving high-dose imatinib (800 mg/day) vs 16/23 of others. Using logistic regression, only PD before EPO treatment was retained as a predictive factor for EPO response.
EPO enables to increase Hb in most anaemic GIST patients who do not progress under imatinib, but not in patients with progressive disease.
Imatinib (Glivec® / Gleevec®, Novartis) is an orally administered small molecule tyrosine kinase inhibitor active against BCR-ABL, KIT, and PDGF. It has proven to be remarkably effective in gastrointestinal stromal tumours (GIST) patients with advanced/metastatic disease [1–5], as well as in adjuvant phase . Imatinib is approved worldwide for use in GIST, with a usual recommended dose of 400 mg daily . Overall, imatinib is well tolerated, but severe side effects are reported in 2-5% of patients . Anaemia is one of the most frequent side effects observed in imatinib treated patients with GIST (90% of patients), mostly mild to moderate, while this drug is associated with severe grade 3–4 anaemia in less than 10% of patients . Erythropoietin (EPO) is well demonstrated to improve anaemia associated with chemotherapy in solid tumours and quality of life in anaemic patients with cancer . It reduces the need of red blood cell transfusion in cancer patients. Whether EPO treatment is useful in the management of GIST patients receiving imatinib is unknown.
In the present retrospective study, the impact of EPO treatment on the symptomatic anaemia of GIST patients treated with imatinib and the predictive factors of EPO efficacy was investigated.
Patients and method
This retrospective study of EPO treatment in GIST patients receiving imatinib was performed in 4 French centers (Institut Gustave Roussy, Villejuif, Hôpital E. Hérriot, Lyon, Centre Léon Bérard, Lyon, Hôpital La Timone, Marseille). Patients with histologically proven advanced unresectable and/or metastatic GIST characterized by KIT expression (assessed by DAKO assay based on immunohistochemistry), receiving imatinib (Glivec®) in clinical trials or with compassionate use,and who developed anaemia (haemoglobin ≤ 11 g/dL) were treated with EPO. All patients had measurable disease as defined by Response Evaluation Criteria in Solid Tumours (RECIST).
Treatment plan and dose modifications
Patients were treated for anaemia with weekly doses of 30,000U EPO subcutaneously (epoetin alpha, n = 30, 88% or epoietin beta, n = 2, 6%) or 150 μg/week of darbepoetin alpha (n = 2, 6%) until the haemoglobin (Hb) level increase up to 11–13 g/dL according to the recommendations for clinical use. EPO was discontinued if the Hb levels remained stable at 11–13 g/dL or higher. For patients with suspected iron-deficient anaemia (based on clinical history and red blood cell parameters), levels of serum iron, iron-binding capacity, and serum ferritin were evaluated, as was any possible cause of blood loss, before EPO was considered. Only patients with iron-deficient anaemia received iron supplementation. Serum EPO levels were not screened before the initiation of EPO therapy.
For the purpose of the current analysis, a favourable response to EPO was considered as a sustained (i.e. lasting > 4 weeks) increase in the Hb level ≥ 2 g/dL from the pre-treatment values. Dose reductions of imatinib for non haematological or haematological toxic effects were initiated according to the clinical trials recommendations [3–5]. No dose interruptions or dose reductions were indicated for anaemia alone. Patients were followed with complete blood counts (CBC) weekly during the first 4 weeks of imatinib therapy and then every 2–4 weeks.
A univariate analysis was performed on the following variables: age at diagnosis, sex, site of metastases, initial dose of imatinib, and response to imatinib. Statistical significance was determined using the Fisher exact test. To identify the potential predictive factors of EPO efficacy, a logistic regression model was performed.
Thirty four patients who developed anaemia (Hb level ≤ 11 g/dL) among the 319 (11%) GIST patients treated with imatinib in clinical trials or with compassionate use in the 4 French centres, between July 2001 and August 2003, received EPO therapy. The median time from the initiation of imatinib to the initiation of EPO was 58 days (range, 0–553 days). 2 patients started imatinib and Epo on the same day. Demographic and clinical characteristics are presented in Table 1. There were 18 males and 16 females with a median age of 59 years (range, 29–85 years) and a median WHO-PS of 1 (range, 0–3). Thirty two patients had a metastatic GIST and two patients had a locally advanced disease. The primary tumour sites were gastric (n = 11, 32%) and small bowel (n = 10, 29%). Of note, a relative large proportion of patients had primary mesenteric or peritoneal GIST (10, 30%). The sites of metastases were mainly liver (82%) and peritoneum (79%). Ten out of 34 (29%) patients required red blood transfusion before starting EPO treatment.
Response to the EPO treatment is presented in Table 2. Median Hb level prior to EPO was 9 g/dL (range, 6.9-11.8 g/dL) and 11.7 g/dL (range, 6.8-14.4 g/dL) after 2 months. Of the 34 patients receiving EPO, 18 (53%) had an increase in Hb levels of ≥ 2 g/dL. Eight additional patients had an increase in Hb levels of 1–1.9 g/dL. Therefore, only 8 of 34 (23.5%) patients had no response at all to EPO therapy. None of the 7 patients who had previously progressed (PD) under imatinib (400 mg/day) obtained an Hb increase after EPO treatment, as compared to 66% (18/27) of the remaining patients (patients with a partial response to imatinib or with a disease stabilization, \PR + SD]) (p = 0,002). There were no differences in responses between the three recombinant EPO used, but there were only 2 patients treated with Epo beta, and darbepoietin respectively. No patient discontinued imatinib therapy because of anaemia. Six non-responding patients to EPO required red blood cells transfusion.
An important question is whether EPO administration is active on the anaemia induced by imatinib, on the anaemia induced by the tumor through iron loss or inflammation, or both. The efficacy of EPO in patients who initiated EPO treatment within the first 2 months of imatinib initiation, between 2 and 6 months and beyond was compared: no significant difference was observed between the three groups (p = 0,3, not shown), indicating that EPO is active also in patients who develop anaemia as a consequence of imatinib treatment,
Primary tumour site, liver and peritoneal metastases, age and gender did not correlate with Hb response to EPO. Response to EPO was observed in 2/9 (22%) patients receiving high-dose imatinib as initial treatment (800 mg/day) versus 16/25 (64%) of others (p = 0.05). Using logistic regression analysis, disease progression (PD) before EPO treatment was the only parameter retained as a predictive factor for EPO response.
Anaemia is a frequently reported haematological side effect in clinical trials with imatinib in GIST [1–4]. To our knowledge, the capacity of EPO to improve the anaemia observed in patients treated with imatinib in GISTs has not been reported, and no article has been reported on this topic within Pubmed (date of access 25/3/2012).
In this study, we investigated the efficacy of EPO treatment on the anaemia of GIST patients treated with imatinib and the predictive factors of EPO efficacy. Hb levels increased in 76.5% of patients following EPO administration in this retrospective study. Of note, somepatients were given EPO with baseline Hb levels above 11 g/dL. This reflects practices which are no longer recommended following the recent clinical practice guidelines regarding EPO administration in cancer patients . EPO was reported as safe by the investigators of this retrospective study, and no severe complications possibly caused by imatinib were reported.
Surprisingly, an over representation of mesenteric GIST is observed in this relatively small series of patients, possibly because of a more aggressive behaviour of primary tumors occurring in these sites, resulting in a greater impact on the general status of the patient.
It has been reported that EPO improves anaemia induced by imatinib therapy in patients with chronic myeloid leukaemia in chronic phase . The present data confirm that EPO is also an efficient treatment in patients with GIST. However, only patients in whom imatinib induces tumor control were found to respond to EPO, and none of the patients progressing under imatinib achieved Hb response to EPO. Importantly, baseline Epo levels were not measured in this series. The role of the paraneoplastic inflammatory syndrome in the resistance to EPO in progressive patients was not investigated either. The impact of iron supplementation in non sideropenic patients, while controversial, was also not explored in this retrospective series, but may also be worth exploring in refractory patients.
For symptomatic and persistent anaemia associated with imatinib, EPO may therefore be considered. Further studies investigating the impact on other measures, such as quality of life and fatigue are needed to measure the benefits of this treatment, even though. Furthermore, the 62005 intergroup phase III trial from EORTC-STBSG  in advanced/metastatic GIST patients reported that Hb level is significantly correlated to imatinib response and to progression free survival (PFS) with high imatinib response and favourable PFS predicted by high Hb level. Whether EPO treatment improves imatinib antitumour activity in this context remains to be explored. It must be stressed however that EPO treatment has been reported to impact negatively on survival in a meta-analysis of all Epo trials . The present retrospective study is of course not adequate to address this important question.
It can be concluded that Epo treatment increases Hb level in patients with GIST receiving imatinib with anaemia, whether related to imatinib treatment or to the disease, but that this benefits only to patients achieving tumour control under imatinib treatment.
Demetri GD, von Mehren M, Blanke CD: Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumours. N Engl J Med. 2002, 347: 472-480. 10.1056/NEJMoa020461
Verweij J, van Oosterom A, Blay JY: Results from an EORTC STBSG phase II study. Eur J Cancer. 2003, 39: 2006-2011. 10.1016/S0959-8049(02)00836-5
Verweij J, Casali P, Zalcberg J, LeCesne A, Peter R, Blay J-Y, Issels7 R, van Oosterom A, Hogendoorn P, Van Glabbeke M, Judson I: Improved progression free survival in gastro-intestinal stromal tumours with high dose Imatinib. Results of a randomized phase III study of the EORTC, ISG and AGITG. Lancet. 2004, 364: 1127-1134. 10.1016/S0140-6736(04)17098-0
Blay JY, Le Cesne A, Ray-Coquard I, Bui B, Duffaud F, Delbaldo C, Adenis A, Viens P, Rios M, Bompas E, Cupissol D, Guillemet C, Kerbrat P, Fayette J, Chabaud S, Berthaud P, Perol D: Prospective multicentric randomized phase III study of imatinib in patients with advanced gastrointestinal stromal tumours comparing interruption versus continuation of treatment beyond 1 year: the French Sarcoma Group. J Clin Oncol. 2007, 25 (9): 1107-1113. 10.1200/JCO.2006.09.0183
Le Cesne A, Ray-Coquard I, Bui BN, Adenis A, Rios M, Bertucci F, Duffaud F, Chevreau C, Cupissol D, Cioffi A, Emile JF, Chabaud S, Pérol D, Blay JY: for the French Sarcoma Group. Discontinuation of imatinib in patients with advanced gastrointestinal stromal tumours after 3 years of treatment: an open-label multicentre randomised phase 3 trial. Lancet Oncol. 2010, 10: 942-949.
Dematteo RP, Ballman KV, Antonescu CR, Maki RG, Pisters PW, Demetri GD, Blackstein ME, Blanke CD, von Mehren M, Brennan MF, Patel S, McCarter MD, Polikoff JA, Tan BR, Owzar K: American College of Surgeons Oncology Group (ACOSOG) Intergroup Adjuvant GIST Study Team. Adjuvant imatinib mesylate after resection of localised, primary gastrointestinal stromal tumour: a randomised, double-blind, placebo-controlled trial. Lancet. 2009, 373: 1097-1104. 10.1016/S0140-6736(09)60500-6
Blay JY, Bonvalot S, Casali P, Choi H, Debiec-Richter M, Dei Tos AP, Emile JF, Gronchi A, Hogendoorn PC, Joensuu H, Le Cesne A, McClure J, Maurel J, Nupponen N, Ray-Coquard I, Reichardt P, Sciot R, Stroobants S, van Glabbeke M, van Oosterom A, Demetri GD: GIST consensus meeting panelists. Consensus meeting for the management of gastrointestinal stromal tumours. Report of the GIST Consensus Conference of 20–21 March 2004, under the auspices of ESMO. Ann Oncol. 2005, 16: 566-578. 10.1093/annonc/mdi127
Van Glabbeke M, Verweij J, Casali PG, Simes J, Le Cesne A, Reichardt P, Issels R, Judson IR, van Oosterom AT, Blay JY: Predicting toxicities for patients with advanced gastrointestinal stromal tumours treated with imatinib: a study of the European Organisation for Research and Treatment of Cancer, the Italian Sarcoma Group, and the Australasian Gastro-Intestinal Trials Group (EORTC-ISG-AGITG). Eur J Cancer. 2006, 42: 2277-2285. 10.1016/j.ejca.2006.03.029
Bokemeyer C, Aapro MS, Courdi A, Foubert J, Link H, Osterborg A, Repetto L, Soubeyran P: European Organisation for Research and Treatment of Cancer (EORTC) Taskforce for the Elderly. EORTC guidelines for the use of erythropoietic proteins in anaemic patients with cancer: 2006 update. Eur J Cancer. 2007, 43 (2): 258-270. 10.1016/j.ejca.2006.10.014
Bohlius J, Schmidlin K, Brillant C, Schwarzer G, Trelle S, Seidenfeld J, Zwahlen M, Clarke M, Weingart O, Kluge S, Piper M, Rades D, Steensma DP, Djulbegovic B, Fey MF, Ray-Coquard I, Machtay M, Moebus V, Thomas G, Untch M, Schumacher M, Egger M, Engert A: Recombinant human erythropoiesis-stimulating agents and mortality in patients with cancer: a meta-analysis of randomised trials. Lancet. 2009, 373 (9674): 1532-1539. 10.1016/S0140-6736(09)60502-X
Cortes J, O’Brien S, Quintas A: Erythropoietin is effective in improving the anemia induced by imatinib mesylate therapy in patients with chronic myeloid leukemia in chronic phase. Cancer. 2004, 100: 2396-2402. 10.1002/cncr.20292
Van Glabbeke M, Verweij J, Casali PG, Le Cesne A, Hohenberger P, Ray-Coquard I, Schlemmer M, van Oosterom AT, Goldstein D, Sciot R, Hogendoorn PC, Brown M, Bertulli R, Judson IR: Initial and late resistance to imatinib in advanced gastrointestinal stromal tumours are predicted by different prognostic factors: a European Organisation for Research and Treatment of Cancer-Italian Sarcoma Group-Australasian Gastrointestinal Trials Group study. J Clin Oncol. 2005, 23: 5795-5804. 10.1200/JCO.2005.11.601
JYB, FD, ALC, IRC have received research grants and honoraria from Roche, Novartis, Jansen and Amgen Supported in part by grants from LYRIC, LabEX DEvweCan, and Eurosarc FP-7 278742.
FlD established the protocol, contributed to obtain academic funding, participated to data collection and analysis, wrote the initial manuscript, and approved the final version. CE participated to data collection and analysis, and approved the final version; IRC participated to data collection and analysis, and approved the final version; EB participated to data collection and analysis, and approved the final version; TKH participated to data collection and analysis, and approved the final version; SS participated to data collection and analysis, and approved the final version; PC participated to data collection, and approved the final version; AD participated to data collection, and approved the final version; SB participated to data collection, and approved the final version; FrDuc participated to data collection, funding, animation of the research group and approved the final version; ALC participated to data collection and analysis, and approved the final version; JYB established the protocol, contributed to obtain academic funding, participated to data collection and analysis, contributed to the different version, and approved the final version. All authors read and approved the final manuscript.
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Duffaud, F., Even, C., Ray-Coquard, I. et al. Recombinant erythropoietin for the anaemia of patients with advanced Gastrointestinal Stromal Tumours (GIST) receiving imatinib: an active agent only in non progressive patients. Clin Sarcoma Res 2, 11 (2012). https://doi.org/10.1186/2045-3329-2-11