Aggressive lymphomas with renal involvement: a study of 48 patients treated with the LNH-84 and LNH-87 regimens. Groupe d'Etude des Lymphomes de l'Adulte

Br J Cancer. 1994 Jul;70(1):154-9. doi: 10.1038/bjc.1994.267.

Abstract

In order to describe renal involvement in aggressive non-Hodgkin's lymphomas (NHLs) and its prognostic significance, we reviewed the outcome of 48 patients with renal involvement treated with the LNH-84 or LNH-87 regimen. Histology was diffuse large cell in 29 (60%) patients; immunoblastic, diffuse mixed cell and lymphoblastic in four each; follicular large cell, diffuse small cleaved cell and diffuse small non-cleaved cell in one each; and unclassified in four. Ann Arbor stage was IV in 44 patients, and IE or IIE in four. Tumour mass > or = 10 cm, performance status (ECOG scale) > 2 and increased LDH level were present in 69%, 20% and 76% of patients respectively. Fifteen patients (31%) had multiple intraparenchymal nodules, 14 (29%) had direct spread into the kidney from a perirenal mass, ten (21%) had a single intraparenchymal nodule and nine (19%) had diffuse infiltration. Twenty-one patients (43%) presented with bilateral lesions. Three patients (6%) presented with acute renal failure. Ten other patients (21%) had serum creatinine > 120 mumol l-1. In 12 of these 13 patients renal function was restored with chemotherapy. Twenty-eight patients (57%) achieved complete remission. Estimated 4 year disease-free survival was 39%. Disease-free survival and actuarial survival at 4 years were estimated to be 58% respectively. Two renal parameters had adverse prognostic significance for survival: renal hilum involvement (P = 0.02) and diffuse renal infiltration (P = 0.01). A Cox model identified only two independent prognostic factors for survival, namely performance status > or = 2 and tumour size > or = 10 cm. We conclude that alteration in renal function occurs in 27% of patients with renal involvement. Systemic chemotherapy improves renal function rapidly. Long-term outcome is similar to that expected in NHL patients presenting with the same prognostic factors.

Publication types

  • Clinical Trial
  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • Actuarial Analysis
  • Adolescent
  • Adult
  • Aged
  • Antibiotics, Antineoplastic / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Bleomycin / administration & dosage
  • Chi-Square Distribution
  • Creatinine / blood
  • Cyclophosphamide / administration & dosage
  • Doxorubicin / administration & dosage
  • Female
  • Humans
  • Kidney / physiopathology
  • Kidney Neoplasms / drug therapy*
  • Kidney Neoplasms / physiopathology
  • Kidney Neoplasms / secondary*
  • L-Lactate Dehydrogenase / blood
  • Lymphoma, Follicular / drug therapy
  • Lymphoma, Large B-Cell, Diffuse / drug therapy
  • Lymphoma, Large-Cell, Immunoblastic / drug therapy
  • Lymphoma, Non-Hodgkin / drug therapy*
  • Lymphoma, Non-Hodgkin / pathology
  • Male
  • Methotrexate / administration & dosage
  • Methylprednisolone / administration & dosage
  • Middle Aged
  • Neoplasm Staging
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy
  • Prednisolone / administration & dosage
  • Prognosis
  • Proportional Hazards Models
  • Remission Induction
  • Survival Analysis
  • Survival Rate
  • Treatment Outcome
  • Vindesine / administration & dosage

Substances

  • Antibiotics, Antineoplastic
  • Bleomycin
  • Doxorubicin
  • Cyclophosphamide
  • Prednisolone
  • Creatinine
  • L-Lactate Dehydrogenase
  • Vindesine
  • Methylprednisolone
  • Methotrexate

Supplementary concepts

  • LNH 84 protocol
  • LNH87-2 protocol