Abstract

BackgroundHereditary haemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait, affects ~1 in 5,000, and causes multi-systemic vascular lesions and life-limiting complications. Life expectancy is surprisingly good, particularly for patients over 60ys. We hypothesised that individuals with HHT may be protected against life-limiting cancers.MethodsTo compare specific cancer rates in HHT patients and controls, we developed a questionnaire capturing data on multiple relatives per respondent, powered to detect differences in the four most common solid non skin cancers (breast, colorectal, lung and prostate), each associated with significant mortality. Blinded to cancer responses, reports of HHT-specific features allowed assignment of participants and relatives as HHT-subjects, unknowns, or controls. Logistic and quadratic regressions were used to compare rates of specific cancer types between HHT subjects and controls.Results1,307 participants completed the questionnaire including 1,007 HHT-subjects and 142 controls. The rigorous HHT diagnostic algorithm meant that 158 (12%) completed datasets were not assignable either to HHT or control status. For cancers predominantly recognised as primary cancers, the rates in the controls generally matched age-standardised rates for the general population. HHT subjects recruited through the survey had similar demographics to controls, although the HHT group reported a significantly greater smoking habit. Combining data of participants and uniquely-reported relatives resulted in an HHT-arm of 2,161 (58% female), and control-arm of 2,817 (52% female), with median ages of 66ys [IQR 53–77] and 77ys [IQR 65–82] respectively. In both crude and age-adjusted regression, lung cancers were significantly less frequent in the HHT arm than controls (age-adjusted odds ratio 0.48 [0.30, 0.70], p = 0.0012). Breast cancer prevalence was higher in HHT than controls (age-adjusted OR 1.52 [1.07, 2.14], p = 0.018). Overall, prostate and colorectal cancer rates were equivalent, but the pattern of colorectal cancer was modified, with a higher prevalence in younger HHT patients than controls.ConclusionsThese preliminary survey data suggest clinically significant differences in the rates of lung, breast and colorectal cancer in HHT patients compared to controls. For rare diseases in which longitudinal studies take decades to recruit equivalent datasets, this type of methodology provides a good first-step method for data collection.

Highlights

  • Hereditary haemorrhagic telangiectasia (HHT, known as Osler-Weber-Rendu syndrome) is inherited as an autosomal dominant trait, and affects approximately 1 in 5,000 people [1,2,3]

  • Additional HHT-related pathologies include pulmonary arterial hypertension (PAH) when the prognosis appears worse than for patients with PAH due to BMPR2 mutations [17], a higher risk of venous thromboemboli [18,19], and for patients with SMAD4 mutations, colon cancer and other gastrointestinal cancers related to their juvenile polyposis [20,21]

  • The smoking habit in terms of pack years smoked per smoker was significantly higher for HHT respondents than controls (Table 1)

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Summary

Introduction

Hereditary haemorrhagic telangiectasia (HHT, known as Osler-Weber-Rendu syndrome) is inherited as an autosomal dominant trait, and affects approximately 1 in 5,000 people [1,2,3]. Affected individuals have multi-systemic vascular lesions that cause major morbidity and mortality [4,5,6]. Cerebral, spinal and hepatic arteriovenous malformations (AVMs) affect high proportions of patients with HHT, and commonly cause complications including haemorrhagic [9], ischaemic [10] and infective strokes; [10,11,12] other major haemorrhage; [13] and maternal death in pregnancy [14]. Hereditary haemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait, affects ~1 in 5,000, and causes multi-systemic vascular lesions and life-limiting complications. We hypothesised that individuals with HHT may be protected against life-limiting cancers

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