CClinicalTrials.gg
Status unknownNCT00941200Updated Jan 14, 2014

Pharmacogenetic DNA Bank

An observational study in Cancer, sponsored by National University Hospital, Singapore. Status unknown at 1 site in Singapore. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-01-14.

Sponsored by National University Hospital, Singapore · Observational

The sponsor has not verified this record recently (last verified Jan 2014), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-crossover
Time perspective
Cross-sectional
Enrollment
5,000
Ages
18 Years and older
Sex
All
01

Study summary

Aims of Research Proposal:

  1. To build a DNA bank in association with a comprehensive database of treatment outcomes and toxicities of cancer patients.
  2. To carry out genotyping of potential candidate genes in relation to specific anti-cancer agents and to correlate genotype with treatment outcomes and toxicities.

The investigators hypothesize that genetic variations between different individuals and ethnic groups may account for inter-individual and inter-ethnic differences in treatment response and toxicities to anti-cancer therapy. The understanding of the contribution of these genetic variations may help to individualize therapy to optimize treatment outcomes and reduce toxicities. Patients will be recruited from the National University Hospital Cancer Centre. Any individual aged 18 or above who has been diagnosed with cancer is eligible. 20 ml of blood will be collected from each subject for DNA extraction and pharmacogenetics analysis. At the time of recruitment, demographic characteristics, cancer history, and past and present cancer treatment history of the study subject will be collected. The patients' progress will be followed up periodically (approximately every 6 months) through the medical records, and subsequent cancer treatments, progression of cancer, and survival outcome will be updated. Follow-up will occur until death. Important treatment information that will be collected include the drug regimen, drug doses, intent of treatment, aematologic and non-haematologic toxicities, and hospitalization episodes that may be related to treatment. Known functional single nucleotide polymorphisms (SNPs) of drug metabolizing enzymes, transporters and targets of different anti-cancer agents will be characterized. More comprehensive genotyping will be carried out in 'outliers' who experience exceptional toxicity or biological response to identify novel functional SNPs using high throughput sequencing techniques. Correlation will be made between genotype and treatment-related outcomes (tumor response, progression-free survival) and toxicities. For selected patients, lymphoblastoid transformation will be carried out to maintain an infinite supply of DNA.

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Conditions studied

  • Cancer
03

In context

Lead sponsor

National University Hospital, Singapore is the lead sponsor of 444 studies on the registry; 96 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Any individual who has been diagnosed with cancer is eligible.

Inclusion criteria

  • Any cancer patient who is aged >=18 is eligible.

Exclusion criteria

Exclusion Criteria:

  • Cancer patients who are below age 18 will be excluded.
05

Study design

Observational model
Case-crossover
Time perspective
Cross-sectional
Enrollment
5,000 participants
Biospecimen retention
Samples with dna

Groups and cohorts

  • Blood collection

    Biological: Blood collection

Interventions

  • BiologicalBlood collection
06

Study locations

1 of 1 sites recruiting
  • National University Hospital
    Singapore, 119074, Singapore
    • Soo Chin Lee, MBBS, MRCP · Contact · Soo_Chin_Lee@nuhs.edu.sg · 65 6772 4629
    • Soo Chin Lee, MBBS, MRCP · Principal investigator
    Recruiting
07

References and documents

Publications

  • Wei X, McLeod HL, McMurrough J, Gonzalez FJ, Fernandez-Salguero P. Molecular basis of the human dihydropyrimidine dehydrogenase deficiency and 5-fluorouracil toxicity. J Clin Invest. 1996 Aug 1;98(3):610-5. doi: 10.1172/JCI118830. PubMed 8698850 ↗
  • Goetz MP, Knox SK, Suman VJ, Rae JM, Safgren SL, Ames MM, Visscher DW, Reynolds C, Couch FJ, Lingle WL, Weinshilboum RM, Fritcher EG, Nibbe AM, Desta Z, Nguyen A, Flockhart DA, Perez EA, Ingle JN. The impact of cytochrome P450 2D6 metabolism in women receiving adjuvant tamoxifen. Breast Cancer Res Treat. 2007 Jan;101(1):113-21. doi: 10.1007/s10549-006-9428-0. Epub 2006 Nov 18. PubMed 17115111 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 14, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00941200
Lead sponsor
National University Hospital, Singapore
First posted
Jul 17, 2009
Start date
Apr 2009
Primary completion
Dec 2015 (estimated)
Completion
Dec 2015 (estimated)
Last update
Jan 14, 2014

Study contacts

Soo Chin Lee, MBBS, MRCP
Contact
Soo_Chin_Lee@nuhs.edu.sg
65 6772 4629
Soo Chin Lee, MBBS, MRCP
principal investigator · National University Hospital, Singapore

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2014. You cannot join it, but the record below documents what was studied.

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