Abstract

The risk of late complications including secondary malignancies is increased in long-term survivors of allogeneic hematopoietic stem cell transplants (HSCT). There is limited literature on the biological behavior and clinical features of squamous cell carcinoma (SCC) of head and neck post-HSCT. We present the clinical and pathologic characteristics on six patients who were diagnosed with SCC while in remission following an allogeneic HSCT. Median follow-up was 8 years. Five patients (83%) developed SCC of tongue and one developed esophageal SCC. Five patients had oral chronic graft-versus-host disease (cGvHD). The conventional risk factors of alcohol, tobacco, and human papillomavirus were absent. The most common presenting finding was the new-onset focal oral pain and ulcerated plaques clinically indistinguishable from a flare of their oral cGvHD lesions. We demonstrated that the SCC in three patients was of donor origin.

Highlights

  • Advances in hematopoietic stem cell transplants (HSCT) are curing an increasing number of patients with hematologic malignancies leading to an increase in the number of long-term survivors

  • In a large reported cohort of HSCT recipients, the oral cavity was one of the most common squamous cell carcinoma (SCC) sites accounting for 15% of all solid cancers [5]

  • This study and other small series have identified a strong association between oral SCC and chronic graft-versus-host disease [6,7,8,9]

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Summary

Introduction

Advances in hematopoietic stem cell transplants (HSCT) are curing an increasing number of patients with hematologic malignancies leading to an increase in the number of long-term survivors. Survivors are developing late complications following the HSCT, including an increase in delayed cardiovascular morbidity, late pulmonary complications, and an increased risk of secondary solid cancers[1,2,3]. The risk of secondary solid cancers is increased both with total body irradiation (TBI) and non-TBI-based conditioning regimens [3, 4]. The advent of reduced-intensity conditioning (RIC) has greatly expanded the scope of HSCT but the risk of secondary malignancies after RIC HSCT is similar to patients who receive a myeloablative conditioning regimen [4]. We report on six patients who developed SCC and review the literature of reports of SCCs. This study and other small series have identified a strong association between oral SCC and chronic graft-versus-host disease (cGvHD) [6,7,8,9].

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