Levels of proteins C and S do not decline subsequent to first line chemotherapy in lymphoma patients

Hematol Oncol. 1997 Aug;15(3):121-7. doi: 10.1002/(sici)1099-1069(199708)15:3<121::aid-hon606>3.0.co;2-d.

Abstract

Thromboembolic complications and decrease in protein C and S have been observed in patients while receiving combination chemotherapy for breast cancer. We investigated whether initial cytotoxic treatment of non-Hodgkin's lymphoma (NHL) and Hodgkin's disease (HD) is also associated with changes in these anticoagulant parameters. For this purpose 25 patients with intermediate to high grade NHL and seven with HD, undergoing primary treatment with cytotoxic drugs were evaluated at three time-points: pre-therapy, mid-therapy and post-therapy. In contrast to the breast cancer patients, no significant changes in protein C, protein S and antithrombin III levels were observed in the NHL patients during the various stages of therapy. However in HD patients, the mean protein C values had a tendency to be higher at mid-therapy compared to pre-therapy and protein S levels had a tendency to be higher at mid-therapy compared to post-therapy. In lymphoma patients receiving primary cytotoxic treatment we did not find changes in anticoagulant parameters that can explain a chemotherapy-induced hypercoagulable state, as has been reported in breast cancer patients.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Antithrombin III / analysis
  • Bleomycin / administration & dosage
  • Bleomycin / adverse effects
  • Combined Modality Therapy
  • Cyclophosphamide / administration & dosage
  • Cyclophosphamide / adverse effects
  • Doxorubicin / administration & dosage
  • Doxorubicin / adverse effects
  • Etoposide / administration & dosage
  • Etoposide / adverse effects
  • Female
  • Fibrin Fibrinogen Degradation Products / analysis
  • Hodgkin Disease / blood
  • Hodgkin Disease / complications
  • Hodgkin Disease / drug therapy
  • Hodgkin Disease / radiotherapy
  • Humans
  • Leucovorin / administration & dosage
  • Leucovorin / adverse effects
  • Lymphoma / blood*
  • Lymphoma / complications
  • Lymphoma / drug therapy
  • Lymphoma / radiotherapy
  • Lymphoma, Non-Hodgkin / blood
  • Lymphoma, Non-Hodgkin / complications
  • Lymphoma, Non-Hodgkin / drug therapy
  • Lymphoma, Non-Hodgkin / radiotherapy
  • Male
  • Mechlorethamine / administration & dosage
  • Mechlorethamine / adverse effects
  • Methotrexate / administration & dosage
  • Methotrexate / adverse effects
  • Middle Aged
  • Mitoxantrone / administration & dosage
  • Mitoxantrone / adverse effects
  • Partial Thromboplastin Time
  • Plasminogen / analysis
  • Prednisone / administration & dosage
  • Prednisone / adverse effects
  • Procarbazine / administration & dosage
  • Procarbazine / adverse effects
  • Protein C / analysis*
  • Protein S / analysis*
  • Thrombophilia / chemically induced*
  • Time Factors
  • Vinblastine / administration & dosage
  • Vinblastine / adverse effects
  • Vincristine / administration & dosage
  • Vincristine / adverse effects
  • alpha-2-Antiplasmin / analysis

Substances

  • Fibrin Fibrinogen Degradation Products
  • Protein C
  • Protein S
  • alpha-2-Antiplasmin
  • Bleomycin
  • Procarbazine
  • Mechlorethamine
  • Vincristine
  • Vinblastine
  • Etoposide
  • Doxorubicin
  • Cyclophosphamide
  • Antithrombin III
  • Plasminogen
  • Mitoxantrone
  • Leucovorin
  • Prednisone
  • Methotrexate

Supplementary concepts

  • CEMP protocol
  • CHOP protocol
  • COMP protocol
  • MACOP-B protocol
  • MOPP-ABV protocol