Complementary Medicine Use Amongst Patients with Metastatic Cancer Enrolled in Phase III Clinical Trials

Author:

Wells J Connor1ORCID,Sidhu Aven2,Ding Keyue3,Smoragiewicz Martin3,Heng Daniel Y C4,Shepherd Frances A5,Ellis Peter M6ORCID,Bradbury Penelope A7,Jonker Derek J8,Siu Lillian L5,Gelmon Karen A8ORCID,Karapetis Christos9,Shapiro Jeremy10,Nott Louise11,O’Callaghan Christopher J3,Parulekar Wendy R3,Seymour Lesley3ORCID,Monzon Jose G4

Affiliation:

1. Queen’s University, Kingston, ON, Canada

2. Fraser Health and Veralife Health Centre, Surrey, BC, Canada

3. Canadian Cancer Trials Group, Kingston, ON, Canada

4. Tom Baker Cancer Centre, University of Calgary, Calgary, AB, Canada

5. Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada

6. Juravinski Hospital and Cancer Centre, McMaster University, Hamilton, ON, Canada

7. The Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada

8. BC Cancer Agency, Vancouver, BC, Canada

9. Flinders Medical Centre and Flinders University, Adelaide, Australia

10. Cabrini Health, Melbourne, Australia

11. Royal Hobart Hospital, Tasmania, Australia

Abstract

Abstract Background Complementary medicines (CM) are frequently used by patients with cancer. Controversy exists over the effectiveness and risk that CM may add to conventional cancer therapy. The incidence of CM use among patients enrolled in phase III clinical trials is unknown. Methods Medication lists from 6 international phase III clinical trials were retrospectively reviewed to identify patients using CM. Patients had metastatic breast, colorectal, or lung cancers. Quality of life, adverse events, overall survival, and progression-free survival were compared between CM users and non-users. Baseline differences between groups were adjusted with propensity score matching groups. Results Seven hundred and six of 3446 patients (20.5%) used at least one CM. CM use was highest among patients with breast cancer (35.6%). CM users had more favorable baseline prognostic factors (ECOG 0-1, non-smoking status, younger age, and fewer metastases). CM use was associated with lower rates of adverse events (50% vs. 62%, P = .002) and quality of life was similar between both groups. After adjustment with propensity score matching, CM use was also associated with longer overall survival in patients with lung cancer (adjusted hazard ratio 0.80, 95%CI, 0.68-0.94, P =.0054). However, several key control variables like EGFR status were not available. Conclusion One in 5 patients in phase III clinical trials report using CM. CM was not associated with worse cancer-specific outcomes. However, CM users had more favorable baseline prognostic factors, and likely other confounders that may have contributed to improved outcomes observed in the lung cohort. Physicians should monitor for CM use and potential interactions with clinical trial drugs.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Reference45 articles.

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