Αρχειοθήκη ιστολογίου

Αναζήτηση αυτού του ιστολογίου

Δευτέρα 18 Ιανουαρίου 2021

Broadening treatment options for patients with non-small-cell lung cancer

Cancer shared this article with you from Inoreader
The use of immune-checkpoint inhibitors targeting the CTLA-4, PD-1, or PD-L1 signalling axis in the modulation of anti-tumour T-cell activity has revolutionised the treatment of lung cancer in different settings.1 In patients with PD-L1 expression of at least 50%, pembrolizumab (anti PD-1) and atezolizumab (anti PD-L1) have been approved by the US Food and Drug Administration as first-line single-agent treatments because they significantly prolong overall survival compared with platinum-based chemotherapy, in patients with both squamous and non-squamous tumours without sensitising EGFR mutations or ALK rearrangements.
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First-line nivolumab plus ipilimumab combined with two cycles of chemotherapy in patients with non-small-cell lung cancer (CheckMate 9LA): an international, randomised, open-label, phase 3 trial

Cancer shared this article with you from Inoreader
Nivolumab plus ipilimumab with two cycles of chemotherapy provided a significant improvement in overall survival versus chemotherapy alone and had a favourable risk–benefit profile. These data support this regimen as a new first-line treatment option for patients with advanced NSCLC.
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Longitudinal study of intravenous versus subcutaneous immunoglobulin replacement therapy in hematological malignancy

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Longitudinal study of intravenous versus subcutaneous immunoglobulin replacement therapy in hematological malignancy

First longitudinal study on the clinical impact and patient perception of intravenous versus subcutaneous immunoglobulin replacement therapy in patients with acquired hypogammaglobulinemia secondary to hematological malignancy.


Abstract

Aim

To present findings from a longitudinal study on infection risk, mortality, and patient perspective of intravenous immunoglobulin (IVIg) and subcutaneous immunoglobulin (SCIg) treatment for patients with hypogammaglobulinemia secondary to hematological malignancy or its treatment (abbreviated as SID).

Methods

Observational study period included final year of IVIg (13 patients) and of the first 3 years of SCIg (17 patients) with SID. Data were collected on clinical outcomes from medical records and patient perception via study specific questionnaire.

Results

The median age was 63 years (53‐76 years), and for 82.4% of patients their hematological malignancy was in complete remission. The annual mean serum IgG trough levels remained stable over the 4 years and were 7.0 g/L (±2.77 g/L) with IVIg, and 8.0 g/L (±1.75 g/L), 8.7 g/L (±2.75 g/L), and 7.6 g/L (±2.89 g/L) (year 1, 2, and 3, respectively) with SCIg. While the annual infection rate was similar, the rate of hospitalization due to infection fluctuated, with 37%, 9%, 15%, and 32% in year 1, 2, 3, and 4 respectively. There were no systemic adverse events with IVIg or SCIg. Patients reported a strong preference for SCIg. One patient died due to progression of underlying disease and infection within the study period.

Conclusion

SCIg was the preferred treatment mode over IVIg in our cohort, but both were well tolerated without any systemic adverse events in 4‐year follow up. The dosage and serum IgG levels were stable throughout. However, the number of infections requiring hospitalization fluctuated. It is anticipated that these findings encourage more hospitals to offer SCIg for SID patients.

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To betray or to fight? The dual identity of the mitochondria in cancer

Cancer shared this article with you from Inoreader
Future Oncology, Ahead of Print.
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Correlations between serum cetuximab and EGFR-related markers, and skin disorders in head and neck cancer patients

Cancer shared this article with you from Inoreader

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Abstract

Purpose

Cetuximab inhibits epidermal growth factor receptor (EGFR) signaling in cancer and skin cells, thereby inducing anti-cancer effects and skin disorders. The present study aimed to evaluate the relationships between serum cetuximab and EGFR-related markers, and adverse effects in head and neck cancer patients.

Methods

Thirty-four head and neck cancer patients receiving weekly intravenous cetuximab were enrolled. Serum cetuximab levels were determined just before dosing. Blood samples for determination of serum EGFR-related markers including soluble epidermal growth factor receptor (sEGFR) and interleukin-6 (IL-6) were obtained. The severities of skin disorders, their medications, and hypomagnesemia treatment were also assessed.

Results

Serum levels of cetuximab and sEGFR were negatively and positively correlated with that of IL-6, respectively. The serum cetuximab level was twofold higher in the patients with a grade 2–3 skin rash than with a grade 0–1 rash. The serum cetuximab cutoff value related to severe skin rash was 71 μg/mL (sensitivity, 59%; and specificity, 94%). The use of a strong topical corticosteroid for skin rash was also associated with a higher serum cetuximab level. Serum levels of sEGFR and IL-6 had no correlations with the skin disorder severities or their medications. Hypomagnesemia treatment using intravenous magnesium sulfate was not related to serum cetuximab and EGFR-related markers.

Conclusions

Head and neck cancer patients with a higher serum IL-6 level tended to have a lower serum cetuximab level. Serum cetuximab had positive correlations to skin rash severity and its medication in the study population.

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