Hydroxychloroquine in combination with platinum doublet chemotherapy as first-line treatment for extensive-stage small cell lung cancer (Study 15): A randomised phase II multicentre trial

72 patients were randomised (36 HCQ+chemotherapy and 36 chemotherapy alone). Median HCQ treatment duration was 4.4 months. HCQ did not improve PFS (HR 1·12 95 %CI 0·69-1.84; p = 0·64), with a median of 5.7 months (HCQ+chemotherapy) versus 6.2 months (chemotherapy). The corresponding median OS were 8.9 and 10.2 months (HR 0.83, 95 %CI 0.48-1.45, p = 0.52). Fewer patients in the HCQ arm completed four cycles of chemotherapy due to adverse events (64 % vs. 81 %). Grade ≥ 3 adverse events were higher in the HCQ+chemotherapy arm (83.3 % vs. 27.8 %), primarily anaemia, neutropenia, and thrombocytopenia, partly due to the initially higher gemcitabine dose used CONCLUSIONS: Combining HCQ with platinum doublet chemotherapy did not improve PFS or OS outcomes for ES-SCLC, resulting in more patients stopping chemotherapy due to increased adverse events. When considered alongside other randomised studies of HCQ in cancer, the evidence collectively indicates a limited role for HCQ as a therapeutic option.

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Publication Details

Journal
European Journal of Cancer
Published
2024-12-06
DOI
https://doi.org/10.1016/j.ejca.2024.115162
Citations
4
Primary Topic
Lung Cancer Research Studies
Type
article
Field-Weighted Citation Impact
1.13

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article

Hydroxychloroquine in combination with platinum doublet chemotherapy as first-line treatment for extensive-stage small cell lung cancer (Study 15): A randomised phase II multicentre trial

M. Förster, Alastair Greystoke, Allan Hackshaw, Siow Ming Lee et al.
4 citations
European Journal of Cancer
Lung Cancer Research Studies
1.13
article

Hydroxychloroquine in combination with platinum doublet chemotherapy as first-line treatment for extensive-stage small cell lung cancer (Study 15): A randomised phase II multicentre trial

M. Förster, Alastair Greystoke, Allan Hackshaw, Siow Ming Lee, Arvind Arora, Eleni Karapanagiotou, Dionysis Papadatos-Pastos, Laura Farrelly, Fion Bremner, Angel E. Garcı́a, Robin Young, Madeleine Hewish, Fiona Helen Blackhall, Amy Ford, Tanya Ahmad, S. Vaja, Robin Rudd, A.E. Hollingdale, Samreen Ahmed
article en
4 citations

Abstract

72 patients were randomised (36 HCQ+chemotherapy and 36 chemotherapy alone). Median HCQ treatment duration was 4.4 months. HCQ did not improve PFS (HR 1·12 95 %CI 0·69-1.84; p = 0·64), with a median of 5.7 months (HCQ+chemotherapy) versus 6.2 months (chemotherapy). The corresponding median OS were 8.9 and 10.2 months (HR 0.83, 95 %CI 0.48-1.45, p = 0.52). Fewer patients in the HCQ arm completed four cycles of chemotherapy due to adverse events (64 % vs. 81 %). Grade ≥ 3 adverse events were higher in the HCQ+chemotherapy arm (83.3 % vs. 27.8 %), primarily anaemia, neutropenia, and thrombocytopenia, partly due to the initially higher gemcitabine dose used CONCLUSIONS: Combining HCQ with platinum doublet chemotherapy did not improve PFS or OS outcomes for ES-SCLC, resulting in more patients stopping chemotherapy due to increased adverse events. When considered alongside other randomised studies of HCQ in cancer, the evidence collectively indicates a limited role for HCQ as a therapeutic option.

European Journal of CancerVol. 215
Glan Clwyd Hospital (GB), St Thomas' Hospital (GB), Royal Surrey County Hospital (GB), Royal Lancaster Infirmary (GB), Peterborough City Hospital (GB), Royal London Hospital (GB), Cancer Research UK (GB), Newcastle upon Tyne Hospitals NHS Foundation Trust (GB), University Hospitals of Leicester NHS Trust (GB), Weston Park Cancer Centre (GB), Nottingham City Hospital (GB), The Christie Hospital (GB), CRUK Lung Cancer Centre of Excellence (GB), University College London (GB)
Cancer Research UK, University College London
Good health and well-being
Openalex Percentile: Top 18%
Lung Cancer Research Studies
1.13
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