Hot flushes are common in women with a history of breast cancer. Hormonal therapies are known to reduce these symptoms but are not recommended in women with a history of breast cancer due to their potential adverse effects. The efficacy of non-hormonal therapies is still uncertain. To assess the efficacy of non-hormonal therapies in reducing hot flushes in women with a history of breast cancer. We searched the Cochrane Breast Cancer Group Specialised Register, CENTRAL (The Cochrane Library), MEDLINE, EMBASE, LILACS, CINAHL, PsycINFO (August 2008) and WHO ICTRP Search Portal. We handsearched reference lists of reviews and included articles, reviewed conference proceedings and contacted experts. Randomized controlled trials (RCTs) comparing non-hormonal therapies with placebo or no therapy for reducing hot flushes in women with a history of breast cancer. Two authors independently selected potentially relevant studies, decided upon their inclusion and extracted data on participant characteristics, interventions, outcomes and the risk of bias of included studies. Sixteen RCTs met our inclusion criteria. We included six studies on selective serotonin (SSRI) and serotonin-norepinephrine (SNRI) reuptake inhibitors, two on clonidine, one on gabapentin, two each on relaxation therapy and homeopathy, and one each on vitamin E, magnetic devices and acupuncture. The risk of bias of most studies was rated as low or moderate. Data on continuous outcomes were presented inconsistently among studies, which precluded the possibility of pooling the results. Three pharmacological treatments (SSRIs and SNRIs, clonidine and gabapentin) reduced the number and severity of hot flushes. One study assessing vitamin E did not show any beneficial effect. One of two studies on relaxation therapy showed a significant benefit. None of the other non-pharmacological therapies had a significant benefit. Side-effects were inconsistently reported. Clonidine, SSRIs and SNRIs, gabapentin and relaxation therapy showed a mild to moderate effect on reducing hot flushes in women with a history of breast cancer.
1 February 2018 in Journal of Biomedical Informatics
With the increasing amount and growing variety of healthcare data, multimodal machine learning supporting integrated modeling of structured and unstructured data is an increasingly important tool for clinical machine learning tasks. However, it is non-trivial to manage the differences in dimensionality, volume, and temporal characteristics of data modalities in the context of a shared target task. Furthermore, patients can have substantial variations in the availability of data, while existing multimodal modeling methods typically assume data completeness and lack a mechanism to handle missing modalities. We propose a Transformer-based fusion model with modality-specific tokens that summarize the corresponding modalities to achieve effective cross-modal interaction accommodating missing modalities in the clinical context. The model is further refined by inter-modal, inter-sample contrastive learning to improve the representations for better predictive performance. We denote the model as Attention-based cRoss-MOdal fUsion with contRast (ARMOUR). We evaluate ARMOUR using two input modalities (structured measurements and unstructured text), six clinical prediction tasks, and two evaluation regimes, either including or excluding samples with missing modalities. Our model shows improved performances over unimodal or multimodal baselines in both evaluation regimes, including or excluding patients with missing modalities in the input. The contrastive learning improves the representation power and is shown to be essential for better results. The simple setup of modality-specific tokens enables ARMOUR to handle patients with missing modalities and allows comparison with existing unimodal benchmark results. We propose a multimodal model for robust clinical prediction to achieve improved performance while accommodating patients with missing modalities. This work lays a foundation for future work to study the effective incorporation of multiple modalities of clinical data into a single model.