Open Access

Long-term complete remission with belinostat in a patient with chemotherapy refractory peripheral t-cell lymphoma

Journal of Hematology & Oncology20136:69

DOI: 10.1186/1756-8722-6-69

Received: 9 August 2013

Accepted: 9 September 2013

Published: 10 September 2013


Peripheral T/NK-cell lymphomas (PTCL) are rare malignancies with a poor prognosis. Due to the lack of randomised studies, standard therapy has not been established. First-line treatment with anthracycline-based polychemotherapy followed by consolidation with high-dose therapy and autologous stem cell transplant in responding patients has demonstrated good feasibility with low toxicity in prospective studies and is widely used in eligible patients. In relapsed and refractory patients, who are not candidates for transplant approaches, therapeutic options are limited and are usually palliative. Several new agents are currently under investigation to improve the outcome of PTCL in the first line and salvage settings. Belinostat, a histone deacetylase (HDAC) inhibitor, has demonstrated broad antineoplastic activity in preclinical studies, and promising results in advanced relapsed/refractory lymphomas.

Here, we report the case of a 73 year old patient with heavily pre-treated refractory PTCL in complete remission with belinostat for 39 months.


Peripheral T-cell lymphoma Belinostat HDAC inhibitor


Peripheral T-cell lymphomas (PTCL) are rare malignancies representing approximately 10%-15% of all non-Hodgkin’s lymphomas (NHL) in Western countries[13]. With the exception of ALK (anaplastic lymphoma kinase) positive anaplastic large cell lymphoma, PTCL exhibits an aggressive course and patients have a poor outcome after conventional chemotherapy[47] with a median overall survival (OS) of 9 to 42 months[810]. Although anthracycline-based regimens are widely used as first-line therapy, their benefit has not been established prospectively in PTCL. In the absence of randomised trials, high-dose therapy with autologous stem cell transplantation is widely used as consolidation. For relapsed or refractory PTCL, autologous and allogeneic stem cell transplantation is the standard of care for eligible patients. However, chemotherapy-refractory patients are not good candidates for this approach. Several prospective trials have shown chemo-sensitivity to be the most important prognostic factor in the transplant setting and patients without at least a partial remission at transplantation have a poor outcome following either autologous or allogeneic stem cell transplantation. New approaches that include novel agents are urgently needed, and several different agents are currently under investigation to improve the outcome of patients with PTCL.

Belinostat is a potent inhibitor of histone deacetylase (HDAC) enzymes, which alter acetylation levels of histone and non-histone proteins. HDAC enzymes regulate multiple cellular processes and play a role in cancer cell proliferation and survival. Belinostat has demonstrated broad antineoplastic activity in preclinical studies and has been investigated in several Phase I and II studies in patients with solid and hematologic neoplasms. In 20 patients with refractory and relapsed PTCL, Pohlman et al. reported an overall response rate of 25% with a median duration of response of about 5 months[11]. Preliminary results of the large multicenter, open-label belinostat trial in relapsed and refractory PTCL were recently presented at the Annual Meeting of the American Society of Oncology[12].

We report the case of a 73 year old female patient with refractory PTCL, who remains in complete remission following treatment with belinostat for 39 months.

Case presentation

In June 2009, a 69 year old female patient was diagnosed with PTCL not otherwise specified (PTCL-NOS) after complaining of hoarseness. Staging procedures revealed a single manifestation with involvement of the epipharynx with no evidence of B symptoms (Ann Arbor stage IE A). The international prognostic index (IPI) and the prognostic index for T-cell lymphoma (PIT) were low (age above 60 years as the only risk factor). The patient was otherwise healthy with no relevant concomitant diseases. Following two cycles of chemotherapy with CHOP-21 (cyclophosphamide 750 mg/m2 day 1, vincristine 1.4 mg/m2 day 1, doxorubicin 50 mg/m2 day 1, and prednisolone 100 mg absolute day 1–5), she achieved a partial remission, but showed progressive disease after completing six cycles CHOP-21 with new enlarged cervical lymph nodes on both sides of the neck. The patient was scheduled for myeloablative chemotherapy with autologous stem cell transplant using a DHAP protocol (cisplatin 100 mg/m2 day 1, cytarabine 2.000 mg/m2 bid day 2, and dexamethasone 40 mg absolute days 1–4) for tumor reduction and stem cell collection. Following two courses of DHAP, the patient again had progressive disease showing further increase of the cervical lymph nodes and new supraclavicular lymph nodes. A third line chemotherapy regimen with DexaBEAM (dexamethasone 8 mg absolute TID day 1–10, carmustine 60 mg/m2 day 2, melphalan 20 mg/m2 day 3, etoposide 75 mg/m2 day 4–7, and cytarabine 100 mg/m2 BID day 4–7) did not result in lymphoma remission; due to chemo-refractory disease, the myeloablative concept was abandoned (Figure 1).
Figure 1

CT scan of the neck before starting belinostat therapy (January 2010) showing multiple lymph nodes mainly at the right site of the neck (arrow).

The patient was enrolled in January 2010 in the multicenter, open-label BELIEF-trial (Phase II study PXD101-CLN-19). Belinostat was started at a dose of 1000 mg/m2 for days 1–5 in a 21 day cycle. In April 2010 following two cycles of belinostat, the patient achieved a complete response (CR, Figure 2). After 1 year of belinostat therapy (~ 12 cycles), the interval between cycles was extended from 21 days to 42 days due to the long lasting remission, and to avoid potential toxicities. The patient has received a total of 28 cycles with the last cycle completed in December 2012, and maintains a CR at her last follow-up in July 2013.
Figure 2

CT scan of the neck after 2 cycles of belinostat (April 2010) showing a complete response.

In general, belinostat therapy was tolerated and administered for 28 cycles. Hematologic side effects were mild without any toxicity more than CTC grade 2. However, after cycle 2 the patient developed > 2 grade non-hematologic toxicity: CTC grade 3 relapsing bipulmonary alveolitis which was successfully treated with steroids: CTC grade 3 repeated episodes of Clostridium difficile toxin-associated diarrhoea during the first 4 months of treatment, that responded to metronidazole: CTC grade 3 antibiotic resistant atypical pneumonia while on steroid medication, that responded to treatment with voriconacole, suggesting pulmonary fungal infection. All of the non-hematologic adverse events except for the alveolitis were not considered related to belinostat treatment.


Here we report a patient with chemo-refractory PTCL, status post 2 cycles of CHOP-21, 2 cycles of DHAP, and 1 cycle of DexaBEAM, who achieved a remarkably long lasting CR (39 months) after treatment with the novel HDAC inhibitor, belinostat. After attaining a CR following 2 cycles of belinostat and receiving a total of 28 cycles, the patient has remained disease-free for 8 months after treatment discontinuation. To date, this is by far the longest period a patient has been treated with belinostat, and is the first report of durable response with this agent in relapsed or refractory PTCL.


Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.



Anaplastic lymphoma kinase


Twice a day [bis in die]


Cyclophosphamide, vincristine, doxorubicin, and prednisolone


Complete response


Dexamethasone, carmustine, melphalan, etoposide, and cytarabine


Cisplatin, cytarabine, and dexamethasone


Histone deacetylase


International prognostic index


Non-Hodgkin’s lymphomas


Overall survival


Prognostic index for peripheral T-cell lymphoma


Peripheral T/NK-cell lymphomas


PTCL not otherwise specified


Three times a day [ter in die].



The reported case represents one patient from the multicenter, open-label BELIEF-trial (Phase II study; protocol number: PXD101-CLN-19). In this trial patients with relapsed or refractory peripheral T-cell lymphoma were treated with the HDAC inhibitor belinostat at a dose of 1000 mg/m2 given intravenously for days 1–5 in a 21 day cycle until progression of disease or unacceptable toxicity. The primary objective of this study was to determine the objective response.

Authors’ Affiliations

Klinik für Hämatologie, Internistische Onkologie und Stammzelltransplantation, Evangelisches Krankenhaus Essen-Werden gGmbH
Spectrum Pharmaceuticals


  1. Ascani S, Zinzani PL, Gherlinzoni F, Sabattini E, Briskomatis A, de Vivo A, Piccioli M, Fraternali Orcioni G, Pieri F, Goldoni A, Piccaluga PP, Zallocco D, Burnelli R, Leoncini L, Falini B, Tura S, Pileri SA: Peripheral T-cell lymphomas: clinico-pathologic study of 168 cases diagnosed according to the R.E.A.L. classification. Ann Oncol. 1997, 8: 583-592. 10.1023/A:1008200307625.View ArticlePubMedGoogle Scholar
  2. Anonymous: A clinical evaluation of the International Lymphoma Study Group classification of non-Hodgkin’s lymphoma: the Non-Hodgkin’s Lymphoma Classification Project. Blood. 1997, 89: 3909-3918.Google Scholar
  3. Rüdiger T, Weisenburger DD, Anderson JR, Armitage JO, Diebold J, MacLennan KA, Nathwani BN, Ullrich F, Müller-Hermelink HK: Non-Hodgkin's Lymphoma Classification Project: Peripheral T-cell lymphoma (excluding anaplastic large-cell lymphoma): results from the Non-Hodgkin's Lymphoma Classification Project. Ann Oncol. 2002, 13: 140-149. 10.1093/annonc/mdf033.View ArticlePubMedGoogle Scholar
  4. Coiffier B, Brousse N, Peuchmaur M, Berger F, Gisselbrecht C, Bryon PA, Diebold J: Peripheral T-cell lymphomas have a worse prognosis than B-cell lymphomas: a prospective study of 361 immunophenotyped patients treated with the LNH-84 regimen. The GELA (Groupe d'Etude des Lymphomes Agressives). Ann Oncol. 1990, 1: 45-50.PubMedGoogle Scholar
  5. Armitage J, Vose JM, Weisenburger D: International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes. J Clin Oncol. 2008, 26: 4124-4130.View ArticlePubMedGoogle Scholar
  6. Gascoyne RD, Aoun P, Wu D, Chhanabhai M, Skinnider BF, Greiner TC, Morris SW, Connors JM, Vose JM, Viswanatha DS, Coldman A, Weisenburger DD: Prognostic significance of anaplastic lymphoma kinase (ALK) protein expression in adults with anaplastic large cell lymphoma. Blood. 1999, 93: 3913-3921.PubMedGoogle Scholar
  7. Falini B, Pileri S, Zinzani PL, Carbone A, Zagonel V, Wolf-Peeters C, Verhoef G, Menestrina F, Todeschini G, Paulli M, Lazzarino M, Giardini R, Aiello A, Foss HD, Araujo I, Fizzotti M, Pelicci PG, Flenghi L, Martelli MF, Santucci A: ALK + lymphoma: clinico-pathological findings and outcome. Blood. 1999, 93: 2697-2706.PubMedGoogle Scholar
  8. Huang HQ, Peng YL, Lin XB, Sun XF, Lin TY, Xia ZJ, Li YH, Cai QQ, He YJ, Jiang WQ, Guan ZZ: Clinical outcomes of 106 patients with peripheral T-cell lymphoma treated by standard CHOP regimen. Ai Zheng. 2004, 23 (suppl 11): 1443-1447.PubMedGoogle Scholar
  9. Kim K, Kim WS, Jung CW, Kim K, Kim WS, Jung CW, Im YH, Kang WK, Lee MH, Park CH, Ko YH, Ree HJ, Park K: Clinical features of peripheral T-cell lymphomas in 78 patients diagnosed according to the Revised European-American lymphoma (REAL) classification. Eur J Cancer. 2002, 38: 75-81.View ArticlePubMedGoogle Scholar
  10. López-Guillermo A, Cid J, Salar A, López-Guillermo A, Cid J, Salar A, López A, Montalbán C, Castrillo JM, González M, Ribera JM, Brunet S, García-Conde J, de Fernández Sevilla A, Bosch F, Montserrat E: Peripheral T-cell lymphomas: initial features, natural history, and prognostic factors in a series of 174 patients diagnosed according to the R.E.A.L. Classification. Ann Oncol. 1998, 9: 849-855. 10.1023/A:1008418727472.View ArticlePubMedGoogle Scholar
  11. Pohlman B, Advani R, Duvic M, Hymes KB, Intragumtornchai T, Lekhakula A, Shpilberg O, Lerner A, Ben-Yehuda D, Beylot-Barry M, Hillen U, Fagerberg J, Foss FM: Final results of a phase II trial of belinostat (PXD101) in patients with recurrent or refractory peripheral or cutaneous T-cell lymphoma [abtract]. Blood. 2009, 114 (22): s379-Google Scholar
  12. O'Connor OA, Masszi T, Savage KJ, Pinter-Brown LC, Foss FM, Popplewell L, Cashen AF, Doorduijn J, Chawla S, Knoblauch P, Zinzani PL, Brown P, Hess G, Van Hoof A, Horwitz SM, Shustov AR: Belinostat, a novel pan-histone deacetylase inhibitor (HDACi), in relapsed or refractory peripheral T-cell lymphoma (R/R PTCL): Results from the BELIEF trial [abtract]. J Clin Oncol. 2013, 31: s850-Google Scholar


© Reimer and Chawla; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.