Literature DB >> 3182915

Should i.m. injections be avoided during cancer chemotherapy?

P Kellokumpu-Lehtinen1, K O Söderström.   

Abstract

The intravascular transit of malignant tumor cells constitutes an important step in the formation of distant metastases. The development of tumors in extravascular tissues depends upon the exit of these cells from the circulation by crossing the barriers formed by endothelium and basement membrane and their growth in the extravascular environment. Cytostatic drugs may disturb the function of these barriers and some of them, as well as antiemetic drugs, are given as i.m. injections. Thus these both mechanically and chemically induced endothelial and extravascular tissue changes might facilitate tumor cell transit to extravascular tissues. These aspects are discussed in this case report of a young female patient with a mediastinal germ cell tumor. At 4 years after complete remission induced with chemotherapy and radiotherapy she developed recurrent germ cell tumor in the form of a s.c. gluteal abscess. This gluteal region is the most common site of i.m. injections during or after cancer chemotherapy.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3182915     DOI: 10.1007/bf00391508

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  12 in total

1.  A STUDY OF NORMAL, ATYPICAL AND NEOPLASTIC CELLS IN THE WHITE CELL CONCENTRATE OF THE PERIPHERAL BLOOD.

Authors:  K P NAGY
Journal:  Acta Cytol       Date:  1965 Jan-Feb       Impact factor: 2.319

2.  A QUANTITATIVE COMPARISON OF PROCESSING TECHNIQUES FOR STUDY OF CIRCULATING MALIGNANT CELLS.

Authors:  J C PRUITT; R V POWELL; T F PRATER
Journal:  Acta Cytol       Date:  1965 Mar-Apr       Impact factor: 2.319

3.  Mediastinal extragonadal germ cell tumors.

Authors:  J Recondo; H I Libshitz
Journal:  Urology       Date:  1978-04       Impact factor: 2.649

4.  Invasion of reconstituted basement membrane matrix by metastatic human tumor cells.

Authors:  R H Kramer; K G Bensch; J Wong
Journal:  Cancer Res       Date:  1986-04       Impact factor: 12.701

5.  The chemotactic response of tumor cells. A model for cancer metastasis.

Authors:  W C Lam; E J Delikatny; F W Orr; J Wass; J Varani; P A Ward
Journal:  Am J Pathol       Date:  1981-07       Impact factor: 4.307

Review 6.  Tumors: wounds that do not heal. Similarities between tumor stroma generation and wound healing.

Authors:  H F Dvorak
Journal:  N Engl J Med       Date:  1986-12-25       Impact factor: 91.245

7.  Promotion of pulmonary metastasis in mice by bleomycin-induced endothelial injury.

Authors:  F W Orr; I Y Adamson; L Young
Journal:  Cancer Res       Date:  1986-02       Impact factor: 12.701

8.  Treatment of disseminated germ-cell tumors with cisplatin, bleomycin, and either vinblastine or etoposide.

Authors:  S D Williams; R Birch; L H Einhorn; L Irwin; F A Greco; P J Loehrer
Journal:  N Engl J Med       Date:  1987-06-04       Impact factor: 91.245

9.  Mast cells and matrix degradation at sites of tumour invasion in rat mammary adenocarcinoma.

Authors:  M K Dabbous; R Walker; L Haney; L M Carter; G L Nicolson; D E Woolley
Journal:  Br J Cancer       Date:  1986-09       Impact factor: 7.640

10.  The treatment of metastatic germ-cell testicular tumours with bleomycin, etoposide and cis-platin (BEP).

Authors:  M J Peckham; A Barrett; K H Liew; A Horwich; B Robinson; H J Dobbs; T J McElwain; W F Hendry
Journal:  Br J Cancer       Date:  1983-05       Impact factor: 7.640

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.