albumin-bound paclitaxel / Generic mfg. 
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  • ||||||||||  irinotecan / Generic mfg., albumin-bound paclitaxel / Generic mfg., gemcitabine / Generic mfg.
    Molecular landscape and site of metastasis in PDAC. (Hall A; Poster Bd #: 139) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_3888;    
    When comparing pancreatic LM to OM sites, our data reinforces the observation that OS is better in OM vs LM and response to ICI was better in OM vs. LM. Significant differences were observed in molecular landscape, TME and signatures that are predictive of immunotherapy response (TIS and IFG scores).
  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD), MK-0482 / Merck (MSD)
    Phase 1 study of anti (Hall A; Poster Bd #: 119) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_3869;    
    P1
    The 4-drug combination showed increased clinical efficacy compared with that historically observed for chemotherapy regimens. Further evaluation is needed to confirm the clinical activities observed.
  • ||||||||||  albumin-bound paclitaxel / Generic mfg.
    NALIRIFOX versus nab-paclitaxel and gemcitabine in treatment-na (Hall A; Poster Bd #: 116) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_3866;    
    P3
    In this 29-month follow-up of NAPOLI 3, NALIRIFOX continued to demonstrate improved OS compared with Gem+NabP, with 11 patients still receiving the NALIRIFOX regimen. These data confirm NALIRIFOX as a new possible standard of care and reference regimen for the first-line treatment of patients with mPDAC.
  • ||||||||||  Tevimbra (tislelizumab-jsgr) / BeiGene, Keytruda (pembrolizumab) / Merck (MSD)
    Neoadjuvant immunotherapy (PD-1) combined with chemotherapy for locally advanced thoracic esophageal carcinoma (EC): A single-arm, open-label, phase II study. (Hall A; Poster Bd #: 55) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_3806;    
    P
    In this phase 2 study, patients (pts) with histopathologically confirmed ESCC, diagnosed as clinical stage cT1-3N1-3M0 and ECOG PS 0-1 were enrolled to receive two cycles of neoadjuvant chemoimmunotherapy with PD-1 blockade (Pembrolizumab/Tislelizumab on d1) plus nab-paclitaxel (260mg/m 2 in total on d1 and d8) and cisplatin (60mg/m 2 in total on d1-3) of each 21-day cycle, followed by esophagectomy. Combining PD-1 blockade with nab-paclitaxel and cisplatin is feasible and effective in patients with locally advanced resectable ESCC, and might be a promising approach for neoadjuvant treatment.
  • ||||||||||  Tevimbra (tislelizumab-jsgr) / BeiGene, Avastin (bevacizumab) / Roche
    A phase II, two-cohort study of neoadjuvant chemotherapy plus tislelizumab  (Hall A; Poster Bd #: 327) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_3323;    
    P2
    The Ki value derived from dynamic total-body FDG PET/CT proved instrumental in guiding the addition of bevacizumab to neoadjuvant therapy. Both cohorts exhibited promising responses to neoadjuvant therapy, suggesting that neoadjuvant chemotherapy plus tislelizumab
  • ||||||||||  Tevimbra (tislelizumab-jsgr) / BeiGene
    The safety and efficacy of induction chemoimmunotherapy in initially unresectable stage III non-small cell lung cancer. (Hall A; Poster Bd #: 320) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_3316;    
    Patients received 3 to 4 cycles (Q3W) of chemoimmunotherapy including carboplatin (area under the curve [AUC] 5mg/mL/min), nab-paclitaxel (squamous NSCLC, 260mg/m 2 ) or pemetrexed (non-squamous NSCLC, 500mg/m 2 ), and tislelizumab(200mg). The findings of this study indicate encouraging antitumor activity and manageable safety of induction chemoimmunotherapy, and the response-adapted strategy requires further exploration in locally advanced unresctable non-small cell lung cancer.
  • ||||||||||  Tevimbra (tislelizumab-jsgr) / BeiGene
    A phase II study of tislelizumab (TIS) and chemotherapy as neoadjuvant therapy for potentially resectable stage IIIA/IIIB non-small cell lung cancer (NSCLC). (Hall A; Poster Bd #: 286) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_3283;    
    Patients (pts) with stage IIIA/IIIB EGFR/ALK/ROS wild-type NSCLC received 2 cycles of neoadjuvantchemoimmunotherapy (PD-1 inhibitor TIS, nab-paclitaxel, and cisplatin/carboplatin) and were reassessed for surgery.Thereafter, pts underwent surgery within 6 weeks and continued 2 cycles of TIS plus chemotherapy, followed by up to 15 cycles of TIS monotherapy. Neoadjuvant TIS plus chemotherapy increased surgical opportunities and survival benefits in potentially resectable locally advanced stage IIIA/IIIB NSCLC.
  • ||||||||||  Imjudo (tremelimumab) / AstraZeneca, Pfizer, Imfinzi (durvalumab) / AstraZeneca
    Impact of concurrent antibiotics on survival with immunotherapy in metastatic colorectal and pancreatic cancer. (Hall A; Poster Bd #: 88) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_3010;    
    P2
    Concurrent exposure to antibiotics, and specifically fluoroquinolones during ICI therapy was associated with a statistically significant improvement in OS in patients with metastatic CRC, but not metastatic pancreatic cancer. This is discrepant from prior reports in other tumor types and suggests that the gut microbiome may impact ICI efficacy uniquely in patient with CRC.
  • ||||||||||  albumin-bound paclitaxel / Generic mfg.
    Acupuncture for preventing progression of taxane-induced peripheral neuropathy (ATP): A phase II randomized, placebo-controlled trial. (Hall A; Poster Bd #: 279a) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_2901;    
    P2
    four weeks of paclitaxel or nab-paclitaxel weekly or biweekly planned, as standard of care and at treating physician's discretion; willing to adhere to requirement that no new pain medication or dose changes be taken throughout the first 12 weeks of the study period; and willing to adhere to all study-related procedures...With 80 patients we will have 80% power to detect a difference between arms as small as 10 points on the NPS, assuming a one-sided test, type I error of 5%, correlation between baseline and follow-up measurements of 0.5, SD of 17, and 15% attrition at week 4. Present accrual and target accrual: We accrued 43 participants in the intervention phase by the end of January 2024; the target accrual is 80 participants.
  • ||||||||||  albumin-bound paclitaxel / Generic mfg., gemcitabine / Generic mfg.
    Enrollment closed, Trial primary completion date, Combination therapy:  Nab-Paclitaxel and Gemcitabine for Recurrent/Refractory Sarcoma (clinicaltrials.gov) -  Apr 24, 2024   
    P2,  N=59, Active, not recruiting, 
    More prospective trials on fruquintinib are needed, especially on different pathological types and diverse combination regimens. Recruiting --> Active, not recruiting | Trial primary completion date: Dec 2024 --> Jan 2024
  • ||||||||||  Saltikva (attenuated Salmonella typhimurium expressing IL-2) / MD Biosciences, Salspera
    Enrollment closed, Metastases:  Saltikva for Metastatic Pancreatic Cancer (clinicaltrials.gov) -  Apr 24, 2024   
    P2,  N=60, Active, not recruiting, 
    Recruiting --> Active, not recruiting | Trial primary completion date: Dec 2024 --> Jan 2024 Recruiting --> Active, not recruiting
  • ||||||||||  carboplatin / Generic mfg., albumin-bound paclitaxel / Generic mfg., pirfenidone / Generic mfg.
    Retrospective data, Journal, Combination therapy:  A retrospective study of combination therapy with glucocorticoids and pirfenidone for PD-1 inhibitor-related immune pneumonitis. (Pubmed Central) -  Apr 23, 2024   
    George's Respiratory Questionnaire score and the recurrence rate of ICIP, but there was no significant difference between the 2 groups (P?>?.05). Adding pirfenidone to glucocorticoid treatment was shown to be safe and may be more beneficial than glucocorticoids alone for improving pulmonary interstitial lesions, reversing ICIP, and preventing its recurrence.
  • ||||||||||  Imfinzi (durvalumab) / AstraZeneca, abequolixron (RGX-104) / Inspirna
    Enrollment open, Combination therapy:  Abequolixron (RGX-104) and Durvalumab in Lung Cancer (clinicaltrials.gov) -  Apr 22, 2024   
    P1,  N=24, Recruiting, 
    Not yet recruiting --> Recruiting Not yet recruiting --> Recruiting
  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD)
    The tumor immune environment in advanced breast cancer following treatment with pembrolizumab and nab-paclitaxel (Exhibit Hall F1; Poster Board Number: B965) -  Apr 20, 2024 - Abstract #IMMUNOLOGY2024IMMUNOLOGY_2621;    
    The final results will determine intrinsic subtype signatures of each cohort and study crosstalk between different cell types in the TME. In conclusion, our approach aims to enhance the understanding of treatment response and TME's role in metastatic breast cancer for improved therapeutic strategies.