Survival analysis of patients with Hodgkin lymphoma who failed high dose chemotherapy and autologous stem cell transplant

Ann Hematol. 2018 Jul;97(7):1229-1240. doi: 10.1007/s00277-018-3283-z. Epub 2018 Feb 26.

Abstract

Hodgkin lymphoma (HL) patients failing after high dose chemotherapy (HDC) and auto-SCT have a poor outcome. Some patients may still benefit from further treatments. From 1996 to 2016, 137 HL patients (39.5%) out of 347 transplanted experienced post auto-SCT failure. Males/female 61%:39%, median age at auto-SCT 23.4 years and median follow-up 55.6 months (9-153). Type of failure was progressive (46%), relapsed (35%) or persistent disease/refractory disease (19%). Median overall survival (OS) from the time of failure is 20 months; 35 patients (25.5%) are alive. One hundred and four patients received treatment; the response rate was 45%; complete remission in 41 (30%) and partial remission in 21 (15%) patients. 1st interventions post auto-SCT were chemotherapy (39%), radiation therapy (35%) or best supportive care (24%). Twenty-seven patients with 2nd-SCT (allogeneic (15), auto-SCT (2)) and/or brentuximab (18 patients) had superior OS (50.6 months) vs other treatments (22.5 months, P value 0.037). COX regression multivariate analysis identified post auto-SCT treatment failure before 12 months (hazard ratio (HR) 3.37, CI 1.7-6.6, P value < 0.001), presence of B symptoms (HR 2.55, CI 1.4-4.6, P value 0.002), stages III-IV (HR 2.7, CI 1.5-4.9, P value 0.001), albumin < 4 g/dl (HR 1.76, CI 1.1-2.9, P value 0.027) and tumor > 5 cm (HR 1.1.9, CI 1.13-3.25, P value 0.015) as significant risk factors; P value < 0.001. KM OS with 0-1 factor (148.6 months): 2 factors (23.6 months) and 3-5 factors (9.4 months) (P value < 0.001). OS was 63%:25%:7% respectively with 0-1:2:3-5 factors respectively (P value < 0.001). Despite high-risk factors, 2nd-SCT/brentuximab use post HDC auto-SCT failure may result in durable survival.

Keywords: Auto/allogeneic-SCT; Brentuximab; Hodgkin lymphoma; Prognostic model; Relapsed after auto-SCT.

MeSH terms

  • Adolescent
  • Adult
  • Allografts
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bleomycin / administration & dosage
  • Brentuximab Vedotin
  • Carmustine / administration & dosage
  • Cisplatin / administration & dosage
  • Combined Modality Therapy
  • Cytarabine / administration & dosage
  • Dacarbazine / administration & dosage
  • Disease-Free Survival
  • Doxorubicin / administration & dosage
  • Drug Resistance, Neoplasm
  • Etoposide / administration & dosage
  • Female
  • Hematopoietic Stem Cell Transplantation*
  • Hodgkin Disease / drug therapy
  • Hodgkin Disease / mortality*
  • Hodgkin Disease / radiotherapy
  • Hodgkin Disease / therapy
  • Humans
  • Immunoconjugates / therapeutic use
  • Kaplan-Meier Estimate
  • Male
  • Melphalan / administration & dosage
  • Methylprednisolone / administration & dosage
  • Middle Aged
  • Proportional Hazards Models
  • Remission Induction
  • Retrospective Studies
  • Salvage Therapy
  • Transplantation Conditioning
  • Transplantation, Autologous
  • Vinblastine / administration & dosage
  • Young Adult

Substances

  • Immunoconjugates
  • Cytarabine
  • Bleomycin
  • Vinblastine
  • Etoposide
  • Dacarbazine
  • Brentuximab Vedotin
  • Doxorubicin
  • Cisplatin
  • Melphalan
  • Carmustine
  • Methylprednisolone

Supplementary concepts

  • ABVD protocol
  • BEAM regimen
  • ESAP protocol