Pavani Chalasani

ORCID: 0000-0002-7953-2979
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • HER2/EGFR in Cancer Research
  • Advanced Breast Cancer Therapies
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Treatment and Pharmacology
  • Estrogen and related hormone effects
  • Radiopharmaceutical Chemistry and Applications
  • Breast Cancer Treatment Studies
  • Lung Cancer Research Studies
  • Biosimilars and Bioanalytical Methods
  • Inflammatory mediators and NSAID effects
  • Chronic Lymphocytic Leukemia Research
  • Cancer Risks and Factors
  • Brain Metastases and Treatment
  • Cancer, Stress, Anesthesia, and Immune Response
  • Cancer survivorship and care
  • Cancer-related cognitive impairment studies
  • Childhood Cancer Survivors' Quality of Life
  • Glioma Diagnosis and Treatment
  • PARP inhibition in cancer therapy
  • Cancer Genomics and Diagnostics
  • Cancer, Hypoxia, and Metabolism
  • Bone health and treatments
  • Colorectal Cancer Treatments and Studies
  • Cancer-related Molecular Pathways
  • Family Support in Illness

University of Arizona
2015-2025

University of Arizona Cancer Center
2015-2025

George Washington University
2023-2024

Wayne State University
2024

Rochester College
2024

Tucson Medical Center
2022

Medizinische Hochschule Hannover
2021

The University of Texas Health Science Center at San Antonio
2017-2020

Mays Cancer Center at UT Health San Antonio
2020

Seattle Cancer Care Alliance
2019

Adjuvant abemaciclib combined with endocrine therapy (ET) previously demonstrated clinically meaningful improvement in invasive disease-free survival (IDFS) and distant relapse-free (DRFS) hormone receptor-positive, human epidermal growth factor receptor 2-negative, node-positive, high-risk early breast cancer at the second interim analysis, however follow-up was limited. Here, we present results of prespecified primary outcome analysis an additional analysis.This global, phase III,...

10.1016/j.annonc.2021.09.015 article EN cc-by-nc-nd Annals of Oncology 2021-10-16

Abstract Purpose: ANG1005, a novel taxane derivative, consists of three paclitaxel molecules covalently linked to Angiopep-2, designed cross the blood–brain and blood–cerebrospinal barriers penetrate malignant cells via LRP1 transport system. Preclinical clinical evidence efficacy with ANG1005 has been previously shown. Patients Methods: A multicenter, open-label phase II study in adult patients measurable recurrent brain metastases from breast cancer (BCBM), or without leptomeningeal...

10.1158/1078-0432.ccr-19-3258 article EN Clinical Cancer Research 2020-01-22

Objective: The purpose of this study was to test two 2-month psychosocial interventions (Telephone Interpersonal Counseling [TIPC] and Supportive Health Education [SHE]) improve quality life (QOL) outcomes for Latinas with breast cancer their informal caregivers. Methods: Two hundred forty-one caregivers were assessed at baseline, immediately after the intervention, 4 6 months baseline. QOL psychological distress, symptoms social support. Results: Linear mixed effects models showed that...

10.1080/08870446.2019.1626395 article EN Psychology and Health 2019-06-12

Abstract Samuraciclib is a selective oral CDK7-inhibitor. A multi-modular, open-label Phase I study to evaluate safety and tolerability of samuraciclib in patients with advanced malignancies was designed (ClinicalTrials.gov: NCT03363893). Here we report results from dose escalation 2 expansion cohorts: Module 1A paired biopsy cohort solid tumor patients, 1B-1 triple negative breast cancer (TNBC) monotherapy expansion, 2A fulvestrant combination HR+/HER2− post-CDK4/6-inhibitor. Core primary...

10.1038/s41467-023-40061-y article EN cc-by Nature Communications 2023-07-24

Abstract PF-06804103 is an anti-HER2 antibody–drug conjugate with auristatin payload. We evaluated its safety, tolerability, and antitumor activity in patients advanced/unresectable or metastatic breast gastric cancers. This multicenter, open-label, first-in-human, phase 1 study (NCT03284723) comprised dose escalation (P1) expansion (P2). In P1, adults HER2+ cancer received 0.15–5.0 mg/kg intravenously once/21 days (Q3W); P2, HER2-low (IHC 1+ IHC 2+/ISH−) 3.0 4.0 Q3W. The primary endpoints...

10.1158/1535-7163.mct-23-0101 article EN cc-by-nc-nd Molecular Cancer Therapeutics 2023-07-07

Abstract Vaccines against SARS-CoV-2 have shown high efficacy, but immunocompromised participants were excluded from controlled clinical trials. We compared immune responses to the Pfizer/BioNTech mRNA vaccine in solid tumor patients (n=53) on active cytotoxic anti-cancer therapy a control cohort (n=50) as an observational study. Using live assays, neutralizing antibodies detected 67% and 80% of cancer after first second immunizations, respectively, with 3-fold increase median titers...

10.1101/2021.05.13.21257129 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2021-05-14

Objectives: AEG35156 is an antisense oligonucleotide (ASO) that targets the X-linked inhibitor of apoptosis mRNA. Preclinical studies showed potent activity in combination with gemcitabine pancreatic ductal adenocarcinoma (PDA). A phase I study was conducted to establish maximum-tolerated dose, safety, and antitumor plus metastatic PDA. Methods: Fourteen patients PDA were enrolled. Nine treated at 350 mg IV 5 500 AEG35156, 3 weeks on/1 week off a 28-day cycle. Gemcitabine administered 1000...

10.1097/coc.0b013e3182467a13 article EN American Journal of Clinical Oncology 2012-03-22

Abstract Bavituximab is a chimeric monoclonal antibody that targets phosphatidylserine (PS). PS externalized on cells in the tumor microenvironment when exposed to hypoxia and/or other physiological stressors. On attaching PS, bavituximab thought promote antitumor immunity through its effects receptors monocytes, and myeloid‐derived suppressor cells, as well trigger by inducing an antibody‐dependent cellular cytotoxicity tumor‐associated endothelial cells. We conducted phase I clinical trial...

10.1002/cam4.447 article EN cc-by Cancer Medicine 2015-03-31

Two-thirds of U.S. adult women are overweight or obese. High body mass index (BMI) and weight gain risk factors for a number chronic diseases, including postmenopausal breast cancer. The higher cancer in with elevated BMI is likely to be attributable related metabolic disturbances altered circulating sex steroid hormones adipokines, pro-inflammatory cytokines, insulin resistance. Metformin widely used antidiabetic drug that has demonstrated favorable effects on as such may lead lower obese...

10.1186/s12885-016-2551-3 article EN cc-by BMC Cancer 2016-07-18

Patients with breast cancer and brain metastases (BM) have a poor prognosis high clinical need for novel treatments; however, historically, studies often excluded these patients. Although the BEACON study did not meet its primary end point, treatment etirinotecan pegol vs chemotherapy of physician's choice patients advanced demonstrated significant improvement in overall survival (OS) prespecified patient subgroup preexisting, pretreated, nonprogressive BM.

10.1001/jamaoncol.2022.0514 article EN JAMA Oncology 2022-05-12

Background Little has been reported on suicides among seafarers and how they have changed over time. Aims To establish the causes, rates trends in at work UK merchant shipping from 1919 to 2005 compare suicide with general population employed non-UK shipping. Methods Examination of seafarers' death inquiry files, registers returns (for a total 11.90 million seafarer-years); literature reviews national statistics. Results The rate unexplained disappearances sea) fell 40–50 per 100 000 1920s...

10.1093/occmed/kqp133 article EN Occupational Medicine 2009-10-04

Abstract Introduction BAY 94‐9027 is an extended‒half‐life, site‐specifically PEGylated, B‐domain‒deleted recombinant factor VIII (FVIII). The PROTECT main study demonstrated efficacy of bleed control using extended‐interval prophylaxis with for 36 weeks. Aim To report long‐term and safety in a descriptive analysis the ongoing extension total treatment time up to >5 years. Methods Previously treated males aged 12‐65 years severe haemophilia A who completed were eligible open‐label...

10.1111/hae.13853 article EN cc-by-nc-nd Haemophilia 2019-10-17

Abstract Introduction: ZN-c3 is a selective and orally bioavailable small molecule WEE1 inhibitor. crucial component of the G2/M cell cycle checkpoint preventing cells from entering mitosis to allow repair DNA damage before progression. has demonstrated significant growth inhibition in vitro multiple lines various cancer types antitumor activity vivo human xenograft tumor models. Methods: ZN-c3-001 (NCT04158336) dose escalation, open-label, multicenter, Phase 1 clinical trial evaluating...

10.1158/1538-7445.am2021-ct016 article EN Cancer Research 2021-07-01

Abstract Purpose: To evaluate the effect of sulindac, a nonselective anti-inflammatory drug (NSAID), for activity to reduce breast density (BD), risk factor cancer. Experimental Design: An open-label phase II study was conducted test 12 months' daily sulindac at 150 mg twice on change in percent BD postmenopausal hormone receptor–positive cancer patients aromatase inhibitor (AI) therapy. Change contralateral, unaffected measured by noncontrast magnetic resonance imaging (MRI) and reported as...

10.1158/1078-0432.ccr-21-0732 article EN Clinical Cancer Research 2021-06-10
Coming Soon ...