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dc.contributor.advisorAzam, Faruque
dc.contributor.authorMahmud, Tanzim
dc.date.accessioned2023-07-09T09:56:05Z
dc.date.available2023-07-09T09:56:05Z
dc.date.copyright2022
dc.date.issued2022-08
dc.identifier.otherID: 18146005
dc.identifier.urihttp://hdl.handle.net/10361/18694
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2022.en_US
dc.descriptionCataloged from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 16-17).
dc.description.abstractAccording to the American Cancer Society's projections, there will be 339,250 cases of breast cancer and 43,250 women will pass away due to this cancer in the year 2022. Moreover, breast cancer is responsible for 15% of all cancer deaths. Cancer treatments are approved in the market after successfully passing through Phase III clinical trials. However, most of the cancer drugs fail in the real world despite showing promising efficacy in the clinical trials. We have collected 95 PFS (progression free survival) and ORR (overall response rate) data of different breast cancer molecular subtypes from 140 extracted articles reporting Phase II clinical trials. We have observed how the PFS and ORR values change in response to the combination size and different breast cancer subtypes as well. We have found a moderate positive correlation (r = 0.57) between PFS and ORR. Also, the PFS and ORR increase when treatment number in combination is increased. The highest ORR and PFS values are observed under HER2+ (Human epidermal growth factor receptor 2- positive) subtype in our research. On the contrary, these values were significantly lower for HR+ (Hormone receptor-positive) and TNBC (Triple negative breast cancer). Our study will certainly help clinical trial researchers to better understand how PFS and ORR vary in response to tumor subtypes and combination size.en_US
dc.description.statementofresponsibilityTanzim Mahmud
dc.format.extent17 pages
dc.language.isoenen_US
dc.publisherBrac Universityen_US
dc.rightsBrac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subjectBreast canceren_US
dc.subjectPFSen_US
dc.subjectORRen_US
dc.subjectHR+ subtypeen_US
dc.subjectHER2+ subtypeen_US
dc.subjectTNBC subtypeen_US
dc.subjectCombination sizeen_US
dc.subject.lcshBreast--Cancer--Patients
dc.subject.lcshBreast--Cancer--Treatment
dc.titleImpact of treatment size and molecular types of breast cancer on response rate and progression-free survivalen_US
dc.typeThesisen_US
dc.contributor.departmentDepartment of Pharmacy, Brac University
dc.description.degreeB. Pharmacy


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