A B S T R A C TFemale recipients of hematopoietic cell transplant (HCT) may develop lower genital tract (LGT) dysplasia or new malignancies. A comprehensive systematic review to delineate the occurrence and risk factors for post-HCT LGT precancer and cancer in women was conducted via electronic search of the Cochrane Library, PubMed, Embase, Wiley Online Library, from 1990 to 2018. All studies on the risk, presentation, or incidence of LGT (cervix, vulva, vagina) precancer or cancer post-HCT were included. Reviews, case reports, meta-analysis, book chapters, and studies without the relevant clinical outcomes were excluded. Post-HCT incidence and risk factors for developing LGT precancer or cancer were assessed and determined. Twenty-two out of the original 344 studies met the selection criteria. The risk of LGT cancers in allo-HCT recipients was found to be significantly higher than in the general population, with the standardized incidence ratios of 1.5-48 for cervical cancer and from 19 to 287 for dysplasia. Our review portrays an increased risk of premalignant and malignant neoplasms of female LGT, which have an incompletely described epidemiology and outcomes. Similar to other immunocompromised states, HCT recipients require specific cervical screening guidelines and can greatly benefit from HPV vaccinations. However, there is a lack of prospective data regarding optimum cervical screening in HCT recipients and limited programs offer HPV vaccinations worldwide.Peer review under responsibility of the International Academy for Clinical Hematology and biopsy of lesions enables early identification and treatment of premalignant lesions which, in turn, could decrease the risk of cervical and other LGT cancers in long-term survivors of allo-HCT [2].HPV is the most common sexually transmitted infection, with a 27% estimated overall prevalence in women aged 14-59 years in North American and European populations [3,4]. The HPV prevalence increases from 20% in teenagers to 45% in women aged 20-24 years and declines to 5% in women over 50 years [5][6][7]. Ninety percent of HPV infections clear spontaneously within 2 years, but persistent HPV confers a significant risk of development of highgrade lesions and cancer. Additionally, HPV may reactivate and cause neoplasms later in life [8]. HPV-related disease typically takes 10 to 30 years to progress from initial epithelial changes to invasive cancer [9], illustrating how screening to identify and treat premalignant lesions in the general population can enable prevention of cervical cancer. Whether the time to these cancers is shorter in women post-HCT is not known.Cervical cancer is the second most common cancer worldwide in women [10]. Vulvar and vaginal cancer are rare and account for only 7% of all gynecological malignancies [10] and HPV plays an important role in their development. High-risk HPV types (16, 18, 31, 33, 34, 45, 52, and 58) are responsible for 95% of cervical Pdf_Folio:142