Key result
Intensive chemotherapy followed by mediastinal irradiation induced persistent subclinical pulmonary and cardiac damage, including radiographic parenchymal damage in 51% of patients.
Why the study?
Does intensive chemotherapy followed by mediastinal irradiation induce cardiopulmonary toxicity in patients with advanced Hodgkin's disease?
Cohort (n=39)
Does intensive chemotherapy followed by mediastinal irradiation induce cardiopulmonary toxicity in patients with advanced Hodgkin's disease?
Intensive chemotherapy combined with mediastinal irradiation in advanced Hodgkin's disease induces persistent, subclinical reductions in LVEF and pulmonary diffusion capacity.
May warrant enhanced cardiopulmonary surveillance in Hodgkin survivors; leaves open effects of modern dose-reduced regimens.
Mediastinal irradiation combined with chemotherapy in patients with Hodgkin's disease have been associated with cardiopulmonary toxic effects that can last over the years. In this study we monitored pulmonary and cardiac function in 39 patients affected by advanced Hodgkin's disease (stage II B-III and IV) with mediastinal involvement and submitted to an intensive chemotherapy regimen (epirubicin, vincristine, ciclophosphamide, and etoposide) followed by involved field irradiation. Pulmonary function was verified with chest x-ray, spirometric parameters, arterial blood gas analysis, single breath CO transfer factor (DLCO), and its components Dm and Vc. Cardiac function was verified with electrocardiogram (EKG) and left ventricular ejection fraction (LVEF) by means of radionuclide angiocardiography. The median follow-up was 40 months. Spirometric parameters did no show modifications at the end of treatment, on the contrary they improved during the follow-up. Chest x-ray showed radiographic parenchimal damage in 51% of patients. DLCO remained constantly decreased. sEKG did not show significant modification, whereas LVEF significantly decreased at the end of treatment and remained persistently decreased during follow-up. None of the patients with reduction of DLCO or LVEF showed clinical symptoms of heart and pulmonary dysfunctions. One patient, 49 years old, suffered from myocardial infarction 25 months after the completion of radio-chemotherapy. These data indicate that this combined regimen can induce persistent pulmonary and cardiac damages at subclinical level.
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Villani et al. (2003) conducted a cohort in Advanced Hodgkin's disease (n=39). Intensive chemotherapy and mediastinal irradiation was evaluated on Radiographic parenchymal damage. Intensive chemotherapy followed by mediastinal irradiation induced persistent subclinical pulmonary and cardiac damage, including radiographic parenchymal damage in 51% of patients.
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