[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100588761":3},{"organization":4,"armGroups":7,"interventions":26,"overallOfficials":10,"centralContacts":10,"locations":10,"responsibleParty":37,"collaborators":10,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":43,"sex":49,"minAge":50,"maxAge":10,"enrollmentInfo":51,"targetDuration":10,"studyType":54,"phases":10,"briefSummary":55,"conditions":56,"keywords":10,"overallStatus":58,"whyStopped":10,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":10},{"fullName":5,"class":6},"IRCCS San Raffaele","OTHER",[8,14,18,22],{"label":9,"type":10,"description":11,"interventionNames":12},"Cervical Cancer (K cervix) with pregnancy",null,"Patients with cervical cancer (k cervix) with one or more previous pregnancies",[13],"Drug: ICI monotherapy or combinations of chemo- immunotherapy",{"label":15,"type":10,"description":16,"interventionNames":17},"Endometrial Cancer (K endometrium) with pregnancy","Patients with endometrial cancer (K endometrium) with one or more previous pregnancies",[13],{"label":19,"type":10,"description":20,"interventionNames":21},"Cervical Cancer (K cervix)","Patients with cervical cancer (K cervix)",[13],{"label":23,"type":10,"description":24,"interventionNames":25},"Endometrial Cancer (K endometrium)","Patients with endometrial cancer (K endometrium)",[13],[27],{"type":28,"name":29,"description":29,"armGroupLabels":30,"otherNames":31},"DRUG","ICI monotherapy or combinations of chemo- immunotherapy",[19,9,23,15],[32,33,34,35,36],"immunotherapy, combination of chemotherapy with immunotherapy","PD-1\u002FPD-L1 inhibitors","immunotherapy","chemotherapy","immune checkpoint inhibitors",{"type":38,"investigatorFullName":39,"investigatorTitle":40,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Roberto Ferrara","M.D. Specialist in Medical Oncology","100588761","the-effect-of-previous-pregnancies-in-patients-with-gynecological-neoplasms-treated-with-pd-1pd-l1-inhibitors-100588761",false,"NCT06945601","The Effect of Previous Pregnancies in Patients With Gynecological Neoplasms Treated With PD-1\u002FPD-L1 Inhibitors","Observational Study on the Effect of One or More Previous Pregnancies in Patients With Gynecological Neoplasms Treated With PD-1\u002FPD-L1 Inhibitors","FECONDE","Inclusion Criteria:\n\n* For patients past-pregnant and nulliparous:\n\n  * Age 18 years or older\n  * Female sex\n  * Confirmed cytological\u002Fhistological diagnosis of endometrial or cervical cancer\n  * Treatment with ICI monotherapy or in combination with chemotherapy\n  * Written informed consent for living patients Only for patients past-pregnant:\n  * Available obstetric history\n\nExclusion Criteria:\n\n* Not eligible for treatment with ICI either in monotherapy or in combination with chemotherapy.","FEMALE","18 Years",{"count":52,"type":53},150,"ESTIMATED","OBSERVATIONAL","Despite the fact that immunotherapy has radically changed the therapeutic landscape in multiple types of tumors, to date the only predictive factor for response to treatment with immune checkpoint inhibitors (ICI), although with many limitations and very different specificity among different pathologies, remains the expression of PD-L1. Several meta- analyses of randomized studies have shown that the female sex is associated with less benefit compared to the male sex in patients with melanoma and NSCLC. Reviewing the available data in the literature, this reduced efficacy is confirmed only in the mono- immunotherapy settings, while when chemo-immune combinations are administered, women seem to benefit more than men. Pregnancy, being associated with immunological changes that can last over time (e.g., mechanisms of immuno-tolerance, antigen sharing between the placenta and neoplasia, fetal microchimeric cells, etc.), could partly explain the impact of sex on the outcome of immune checkpoint inhibitors. In particular, some mechanisms of immunotolerance, such as the increase of T-regulatory cells specific to oncofetal antigens in the endometrium, could potentially suggest a lower efficacy of immunotherapy in women. The current study, by characterizing the impact of previous pregnancies on oncological outcomes, could contribute to providing the basis for future research aimed at defining the biological mechanisms underlying the effect of pregnancy on the immune system and the efficacy of immune checkpoint inhibitors.\n\nThe study has an observational, retrospective\u002Fprospective, multicenter design. Female patients with endometrial and cervical cancer will be included. All these patients will be treated with ICIs either as monotherapy or in combination with chemo-immunotherapy. Clinical and oncological anamnesis information will be collected for each patient (type of neoplasm, line of therapy, age at the start of therapy, weight, height, smoking habits, comorbidities, performance status, number and site of metastases, concomitant non- oncological therapies); anatomical-pathological parameters will also be collected (level of PD-L1 expression, molecular and mutational profile of the tumor). Additionally, information regarding the woman's pregnancy and fertility history will be gathered (age at menarche\u002Fmenopause, number of pregnancies, age at first pregnancy, age at last pregnancy, any HRT or contraceptive therapy, any gynecological surgery).",[57],"Gynecologic Cancers","NOT_YET_RECRUITING","2025-04-18",{"date":61,"type":62},"2025-04-25","ACTUAL",{"date":64,"type":53},"2025-05",{"date":66,"type":53},"2030-05",{"name":5,"class":6}]