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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Clin Cancer Res. Author manuscript; available in PMC 2010 October 20.
Published in final edited form as:
PMCID: PMC2957892
NIHMSID: NIHMS99477

Letter to the Editor - Response

To the Editor

We are grateful to Arai and colleagues for their comments.

We agree that payment to phase 0 oncology trial participants must be carefully considered. However, to the extent that healthy volunteers are paid to participate in research that does not offer the prospect of direct benefit, the same modest incentives should be considered for cancer patients who are enrolled in nonbeneficial studies. Research in the developing world raises additional concerns; yet, insofar as people in developing countries are offered compensation for participating in research, phase 0 oncology trial participants in these regions should not be overlooked. Paying patients is a potential strategy for combating the therapeutic misconception in nonbeneficial research, and one of the key arguments against paying subjects, their receipt of medical treatment, is not applicable in the context of phase 0 trials [1].

Aria and colleagues rightly point out that the population likely recruited to participate in phase 0 trials, terminally ill cancer patients, will not benefit directly from the research. Extending post-trial access to drugs that prove successful in phase III trials to patients who were enrolled in earlier-phase research is certainly worth evaluating; nevertheless, it may not be the best strategy to maximize benefits to participants. Many drugs fail before reaching even late-phase trials, and the late-stage cancer patients who participate in phase 0 trials may not survive to see successful drugs reach efficacy studies. One important policy to implement is to ensure that participants are not excluded from trials that may benefit them merely because of their previous participation in phase 0 studies [2, 3].

References

1. Dickert N, Grady C. What’s the price of a research subject. Approaches to payment for research participation. N Engl J Med. 1999;341:198–203. [PubMed]
2. Kinders R, Parchment RE, Ji J, et al. Phase 0 clinical trials in cancer drug development: from FDA guidance to clinical practice. Mol Interv. 2007;7:325–31. [PubMed]
3. Kummar S, Kinders R, Rubinstein L, et al. Compressing drug development timelines in oncology using phase ‘0’ trials. Nat Rev Cancer. 2007;7:131–9. [PubMed]