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Asciminib is approved by the USFDA for newly diagnosed chronic myeloid leukemia
Asciminib is approved by the USFDA for newly diagnosed chronic myeloid leukemia

On October 29, 2024, the FDA granted accelerated approval to asciminib (Scemblix) for adults with newly diagnosed Philadelphia chromosome-positive chronic myeloid leukemia in chronic phase....

Zolbetuximab-clzb with chemotherapy is approved by the USFDA for gastric or gastroesophageal junction adenocarcinoma
Zolbetuximab-clzb with chemotherapy is approved by the USFDA for gastric or gastroesophageal junction adenocarcinoma

On October 18, 2024, the FDA approved zolbetuximab-clzb (Vyloy) combined with fluoropyrimidine- and platinum-based chemotherapy for first-line treatment of adults with locally advanced unresectable or...

Inavolisib with palbociclib and fulvestrant for endocrine-resistant, PIK3CA-mutated, HR-positive, HER2-negative, advanced breast cancer
Inavolisib with palbociclib and fulvestrant for endocrine-resistant, PIK3CA-mutated, HR-positive, HER2-negative, advanced breast cancer

On October 10, 2024, the FDA approved inavolisib (Itovebi) combined with palbociclib and fulvestrant for adults with endocrine-resistant, PIK3CA-mutated, HR-positive, HER2-negative advanced breast cancer. The...

Neoadjuvantadjuvant nivolumab for resectable non-small cell lung cancer
Neoadjuvant/adjuvant nivolumab is approved by the USFDA for resectable non-small cell lung cancer

  On October 3, 2024, the Food and Drug Administration sanctioned nivolumab (Opdivo, Bristol Myers Squibb Company) in conjunction with platinum-doublet chemotherapy as neoadjuvant therapy,...

Selpercatinib is approved by the USFDA for medullary thyroid cancer with a RET mutation
Selpercatinib is approved by the USFDA for medullary thyroid cancer with a RET mutation

On September 27, 2024, the FDA granted traditional approval to selpercatinib (Retevmo) for treating advanced or metastatic medullary thyroid cancer (MTC) with RET mutations in...

Latest therapies in the treatment of blood cancer
Latest therapies in the treatment of hematological malignancies

  Introduction Hematological malignancies, such as leukemias, lymphomas, and multiple myeloma, are a heterogeneous group of cancers that arise in the bone marrow and lymphatic...

Osimertinib is approved by the USFDA for locally advanced, unresectable (stage III) non-small cell lung cancer following chemoradiation therapy
Osimertinib is approved by the USFDA for locally advanced, unresectable (stage III) non-small cell lung cancer following chemoradiation therapy

On September 25, 2024, the FDA approved osimertinib (Tagrisso) for adults with locally advanced, unresectable stage III non-small cell lung cancer (NSCLC) with specific EGFR...

Isatuximab-irfc with bortezomib, lenalidomide, and dexamethasone is approved by the USFDA for newly diagnosed multiple myeloma
Isatuximab-irfc with bortezomib, lenalidomide, and dexamethasone is approved by the USFDA for newly diagnosed multiple myeloma

The FDA has licensed isatuximab-irfc in combination with bortezomib, lenalidomide, and dexamethasone (Isa-VRd) for patients with newly diagnosed multiple myeloma who are not candidates for...

Amivantamab-vmjw with carboplatin and pemetrexed is approved by the USFDA for non-small cell lung cancer with EGFR exon 19 deletions or L858R mutations
Amivantamab-vmjw with carboplatin and pemetrexed is approved by the USFDA for non-small cell lung cancer with EGFR exon 19 deletions or L858R mutations

The FDA has approved Amivantamab-vmjw in combination with carboplatin and pemetrexed for the first-line treatment of adult patients with non-small cell lung cancer (NSCLC) with...

Pembrolizumab with chemotherapy is approved by the USFDA for unresectable advanced or metastatic malignant pleural mesothelioma
Pembrolizumab with chemotherapy is approved by the USFDA for unresectable advanced or metastatic malignant pleural mesothelioma

The FDA approved pembrolizumab (Keytruda) in combination with chemotherapy for the treatment of unresectable, advanced, or metastatic malignant pleural mesothelioma. This is a great leap...

Kisqali with an aromatase inhibitor and Kisqali Femara Co-Pack is approved by the USFDA for early high-risk breast cancer
Kisqali with an aromatase inhibitor and Kisqali Femara Co-Pack is approved by the USFDA for early high-risk breast cancer

The FDA has approved Kisqali (ribociclib) plus an aromatase inhibitor and the Kisqali-Femara Co-Pack for early, high-risk breast cancer. The approval extends the use of...

Bridging The Gaps In CAR T Cell therapy
Bridging The Gaps In CAR T Cell therapy

Chimeric Antigen Receptor (CAR) T-cell therapy has transformed the treatment of hematologic malignancies but is confronting hurdles in the context of solid tumors because of...

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