Efficacy and safety of nivolumab in the treatment of relapsed/refractory classical Hodgkin’s lymphoma: Pavlov First Saint Petersburg State Medical University experience
https://doi.org/10.17650/1818-8346-2019-13-4-17-26
Abstract
Background . Using modern first-line chemotherapy more than 80 % of patients with classical Hodgkin’s lymphoma can be cured, however, in 15–20 % of cases there is a relapsed/refractory disease. The use of nivolumab in international clinical practice has significantly improved treatment results of patients with relapsed/refractory classical Hodgkin’s lymphoma.
Objective of this study is to evaluate the results of therapy with nivolumab in the сlinic of Pavlov First Saint Petersburg State Medical University.
Materials and methods . The retrospective analysis included treatment results of 101 patients with relapsed/refractory classical Hodgkin’s lymphoma who received nivolumab in Raisa Gorbacheva Memorial Research Institute of Children Oncology, Hematology and Transplantation from February 2016 to August 2018. The group included 90 patients who received nivolumab as part of an named patient program. Therapy response was assessed using CT/PET-CT in accordance with LYRIC criteria for response assessment of malignant lymphomas to immunotherapy. Safety and tolerability were assessed by registering adverse events in accordance with NCI CTCAE version 4.03 criteria. Results . Median follow-up was 25 months. The response was registered in 64 % of patients: in 32 (31.6 %) – complete response and in 33 (32.7 %) – partial response. Stabilization and progression as the best response were registered in 5 (4.9 %) and 10 (9.8 %) patients, respectively. Indeterminate response was observed in 21 (20.6 %) patients. The 2-year overall survival was 96 %; the median of overall survival was not achieved. Progression-free survival (PFS) in studied patients was 40.6 %. The median of PFS was 17.9 months. There were no significant differences in PFS between patients with a partial and indeterminate response. Adverse events were reported in 87.1 % of patients. Severe adverse events (III–IV grade) occur in 18.8 % of patients.
Conclusion . The results of a retrospective study of nivolumab therapy in Russian patients with relapsed/refractory classical Hodgkin’s lymphoma are consistent with published international data. Nivolumab demonstrates high efficacy as a monotherapy for relapsed/refractory classical Hodgkin’s lymphoma, regardless of previous therapy type and duration with well tolerance. Pseudo-progression phenomena during immunotherapy require revision of the traditional Hodgkin’s lymphoma therapy response criteria.
About the Authors
K. V. LepikRussian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
N. V. Mikhailova
Russian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
E. V. Kondakova
Russian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
L. A. Tsvetkova
Russian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
Yu. R. Zalyalov
Russian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
E. S. Borzenkova
Russian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
I. S. Moiseev
Russian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
V. V. Baykov
Russian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
B. A. Afanasyev
Russian Federation
6–8 L’va Tolstogo St., 197022 Saint Petersburg
References
1. Canellos G.P., Anderson J.R., Propert K.J. et al. Chemotherapy of advanced Hodgkin’s disease with MOPP, ABVD, or MOPP alternating with ABVD. N Engl J Med 1992;327(21):1478–84. DOI: 10.1056/NEJM199211193272102. PMID: 1383821.
2. Diehl V., Franklin J., Pfreundschuh M. et al. Standard and increased-dose BEACOPP chemotherapy compared with COPP-ABVD for advanced Hodgkin’s disease. N Engl J Med 2003;348(24):2386–95. DOI: 10.1056/NEJMoa022473. PMID: 12802024.
3. Linch D.C., Winfield D., Goldstone A.H. et al. Dose intensification with autologous bone-marrow transplantation in relapsed and resistant Hodgkin’s disease: results of a BNLI randomised trial. Lancet 1993;341(8852):1051–4. PMID: 8096958.
4. Schmitz N., Pfistner B., Sextro M. et al. Aggressive conventional chemotherapy compared with high-dose chemotherapy with autologous haemopoietic stem-cell transplantation for relapsed chemosensitive Hodgkin’s disease: a randomized trial. Lancet 2002;359(9323):2065–71. DOI: 10.1016/S0140–6736(02)08938–9. PMID: 12086759.
5. André M. Henry-Amar M., Pico J.L. et al. Comparison of high-dose therapy and autologous stem-cell transplantation with conventional therapy for Hodgkin’s disease induction failure: a case-control study. Société Francaise de Greffe de Moelle. J Clin Oncol 1999;17(1):222–9. DOI: 10.1200/JCO.1999.17.1.222. PMID: 10458237.
6. Rothe A., Sasse S., Goergen H. et al. Brentuximab vedotin for relapsed or refractory CD30-positive hematologic malignancies: the German Hodgkin Study Group experience. Blood 2012;120(7): 1470–2. DOI: 10.1182/blood-2012-05-430918. PMID: 22786877.
7. Myakova N.V., Evstratov D.A., Abramov D.S. et al. Brentuximab vedotin in children and adolescents with Hodgkin’s lymphoma and anaplastic large cell lymphoma – literature review and own experience. Onkogematologiya = Oncohematology 2016;11(1):8–13. (In Russ.). DOI: 10.17650/1818-8346-2016-11-1-8-13.
8. Younes A., Gopal A.K., Smith S.E. et al. Results of a pivotal phase II study of brentuximab vedotin for patients with relapsed or refractory Hodgkin’s lymphoma. J Clin Oncol 2012;30(18):2183–9. DOI: 10.1200/JCO.2011.38.0410. PMID: 22454421.
9. Forero-Torres A., Holkova B., Goldschmidt J. et al. Phase 2 study of frontline brentuximab vedotin monotherapy in Hodgkin’s lymphoma patients aged 60 years and older. Blood 2015;126(26):2798–804. DOI: 10.1182/blood-2015-06-644336. PMID: 26377597.
10. Chen R., Gopal A.K., Smith S.E. et al. Five-year survival and durability results of brentuximab vedotin in patients with relapsed or refractory Hodgkin’s lymphoma. Blood 2016;128(12):1562–6. DOI: 10.1182/blood-2016-02-699850. PMID: 27432875.
11. Roemer M.G.M., Advani R.H., Ligon A.H. et al. PD-L1 and PD-L2 genetic alterations define classical Hodgkin’s lymphoma and predict outcome. J Clin Oncol 2016;34(23):2690–7. DOI: 10.1200/JCO.2016.66.4482. PMID: 27069084.
12. Yokosuka T., Takamatsu M., KobayashiImanishi W. et al. Programmed cell death 1 forms negative costimulatory microclusters that directly inhibit T cell receptor signaling by recruiting phosphatase SHP2. J Exp Med 2012;209(6):1201–17. DOI: 10.1084/jem.20112741. PMID: 22641383.
13. Ansell S.M., Lesokhin A.M., Borrello I. et al. PD-1 blockade with nivolumab in relapsed or refractory Hodgkin’s lymphoma. N Engl J Med 2015;372(4): 311–9. DOI: 10.1056/NEJMoa1411087. PMID: 25482239.
14. Armand P., Engert A., Younes A. et al. Nivolumab for relapsed/refractory classic Hodgkin’s lymphoma after failure of autologous hematopoietic cell transplantation: extended follow-up of the multicohort single-arm phase II CheckMate 205 Trial. J Clin Oncol 2018;36(14):1428–39. DOI: 10.1200/JCO.2017.76.0793. PMID: 29584546.
15. Beköz H., Karadurmus N., Paydas S. et al. Nivolumab for relapsed or refractory Hodgkin’s lymphoma: real-life experience. Ann Oncol 2017;28(10):2496–502. DOI: 10.1093/annonc/mdx341. PMID: 28961828.
16. Cheson B.D., Ansell S., Schwartz L. et al. Refinement of the Lugano Classification lymphoma response criteria in the era of immunomodulatory therapy. Blood 2016;128(21):2489–96. DOI: 10.1182/blood-2016-05-718528. PMID: 27574190.
17. Buder-Bakhaya K., Hassel J.C. Biomarkers for clinical benefit of immune checkpoint inhibitor treatment. A review from the melanoma perspective and beyond. Front Immunol 2018;9:1474. DOI: 10.3389/fimmu.2018.01474. PMID: 30002656.
18. Jenkins R.W., Barbie D.A., Flaherty K.T. Mechanisms of resistance to immune checkpoint inhibitors. Br J Cancer 2018;118(1):9–16. DOI: 10.1038/bjc.2017.434. PMID: 29319049.
19. Gnjatic S., Bronte V., Brunet L.R. et al. Identifying baseline immune-related biomarkers to predict clinical outcome of immunotherapy. J Immunother Cancer 2017;5:44. DOI: 10.1186/s40425-017-0243-4. PMID: 28515944.
20. Wang G.X., Guo L.Q., Gainor J.F., Fintelmann F.J. Immune checkpoint inhibitors in lung cancer: imaging considerations. AJR Am J Roentgenol 2017;209(3):567–75. DOI: 10.2214/AJR.16.17770. PMID: 28657846.
21. Cheson B.D., Fisher R.I., Barrington S.F. et al. Recommendations for initial evaluation, staging, and response assessment of Hodgkin’s and non-hodgkin lymphoma: the Lugano classification. J Clin Oncol 2014;32(27):3059–68. DOI: 10.1200/JCO.2013.54.8800. PMID: 25113753.
22. Haanen J.B.A.G., Carbonnel F., Robert C. et al. Management of toxicities from immunotherapy: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2017;28(Suppl 4):iv119–42. DOI: 10.1093/annonc/mdx225. PMID: 28881921.
Review
For citations:
Lepik K.V., Mikhailova N.V., Kondakova E.V., Tsvetkova L.A., Zalyalov Yu.R., Borzenkova E.S., Moiseev I.S., Baykov V.V., Afanasyev B.A. Efficacy and safety of nivolumab in the treatment of relapsed/refractory classical Hodgkin’s lymphoma: Pavlov First Saint Petersburg State Medical University experience. Oncohematology. 2018;13(4):17-26. (In Russ.) https://doi.org/10.17650/1818-8346-2019-13-4-17-26