SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:uu-172441"
 

Search: onr:"swepub:oai:DiVA.org:uu-172441" > Activity ex vivo of...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist
  • Cashin, Peter H,1984-Uppsala universitet,Kolorektalkirurgi,Peritoneal Carcinomatos Forskargrupp (author)

Activity ex vivo of cytotoxic drugs in patient samples of peritoneal carcinomatosis with special focus on colorectal cancer

  • Article/chapterEnglish2013

Publisher, publication year, extent ...

  • 2013-09-24
  • Springer Science and Business Media LLC,2013
  • electronicrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-172441
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-172441URI
  • https://doi.org/10.1186/1471-2407-13-435DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Background: The optimal choice of cytotoxic drugs for intraperitoneal chemotherapy (IPC) in conjunction with cytoreductive surgery (CRS) for treatment of peritoneal carcinomatosis(PC) is poorly defined. We investigated drug sensitivity ex vivo in patient samples of various PC tumor types and correlated clinical outcome to drug sensitivity within the subset of PC fromcolorectal cancer (CRC). Methods: PC tissue samples (n = 174) from mesothelioma, pseudomyxoma peritonei (PMP), ovarian cancer, CRC or appendix cancer were analyzed ex vivo for sensitivity to oxaliplatin, cisplatin, mitomycin C, melphalan, irinotecan, docetaxel, doxorubicin and 5-FU. Clinicopathological variables and outcome data were collected for the CRC subset. Results: Mesothelioma and ovarian cancer were generally more drug sensitive than CRC, appendix cancer and PMP. Oxaliplatin showed the most favorable ratio between achievable IPC concentration and ex vivo drug sensitivity. Drug sensitivity in CRC varied considerably between individual samples. Ex vivo drug sensitivity did not obviously correlate to time-to-progression (TTP) in individual patients. Conclusions: Drug-sensitivity varies considerably between PC diagnoses and individual patients arguing for individualized therapy in IPC rather than standard diagnosis-specific therapy. However, in the current paradigm of treatment according to diagnosis, oxaliplatin is seemingly the preferred drug for IPC from a drug sensitivity and concentration perspective. Inthe CRC subset, analysis of correlation between ex vivo drug sensitivity and TTP was inconclusive due to the heterogeneous nature of the data.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Mahteme, HaileUppsala universitet,Kolorektalkirurgi(Swepub:uu)hailmaht (author)
  • Graf, WilhelmUppsala universitet,Kolorektalkirurgi(Swepub:uu)wilhgraf (author)
  • Karlsson, HenningUppsala universitet,Klinisk farmakologi(Swepub:uu)henka962 (author)
  • Larsson, RolfUppsala universitet,Klinisk farmakologi(Swepub:uu)rolflars (author)
  • Nygren, PeterUppsala universitet,Enheten för onkologi(Swepub:uu)peterng (author)
  • Uppsala universitetKolorektalkirurgi (creator_code:org_t)

Related titles

  • In:BMC Cancer: Springer Science and Business Media LLC13, s. 435-1471-2407

Internet link

Find in a library

  • BMC Cancer (Search for host publication in LIBRIS)

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Find more in SwePub

By the author/editor
Cashin, Peter H, ...
Mahteme, Haile
Graf, Wilhelm
Karlsson, Hennin ...
Larsson, Rolf
Nygren, Peter
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Cancer and Oncol ...
Articles in the publication
BMC Cancer
By the university
Uppsala University

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view