Full chemotherapy modules

Quick reference

Chemotherapy cheat sheet

Fast-lookup drug classes, mechanisms, toxicities, and concurrent chemoradiation regimens.

Drug classes

Platinum analogs

Platinums

Cisplatin, Carboplatin, Oxaliplatin

Cross-link DNA strands (G2 arrest) — classic radiosensitizers used concurrently with RT.

Cisplatin: nephrotoxicity (hydrate + replace magnesium), ototoxicity, severe nausea (high emetogenic). Carboplatin: thrombocytopenia. Oxaliplatin: cold-induced neuropathy.

Alkylating agents

Alkylators

Cyclophosphamide, Ifosfamide, Temozolomide, Carmustine (BCNU)

Transfer alkyl groups to DNA, causing cross-linking and strand breaks in all cell-cycle phases.

Myelosuppression, hemorrhagic cystitis (→ mesna), infertility, secondary malignancy risk. Temozolomide: daily 75 mg/m² during GBM RT (Stupp). BCNU: pulmonary toxicity.

Antimetabolites

Antimetabolites

5-FU, Capecitabine, Gemcitabine, Methotrexate, Pemetrexed, Cytarabine

Mimic endogenous bases and block DNA synthesis (S phase) — several are radiosensitizers.

Mucositis, diarrhea, hand-foot syndrome (capecitabine). Gemcitabine: potent radiosensitizer — severe toxicity with thoracic RT. Methotrexate: → leucovorin rescue; CNS toxicity with cranial RT.

Antitumor antibiotics

Anthracyclines & antibiotics

Doxorubicin, Mitomycin-C, Bleomycin

Doxorubicin: DNA intercalation + topoisomerase II inhibition. Mitomycin: alkylator-like. Bleomycin: free-radical DNA strand breaks.

Doxorubicin: cumulative cardiotoxicity + radiation recall. Mitomycin: radiosensitizer (anal cancer CRT). Bleomycin: pulmonary fibrosis — a key caution with lung RT.

Topoisomerase inhibitors

Topo I / II inhibitors

Etoposide, Topotecan, Irinotecan

Block topoisomerase I/II, trapping cleaved DNA complexes (S phase).

Myelosuppression. Etoposide: paired with cisplatin in lung CRT. Irinotecan: acute + delayed diarrhea (atropine / loperamide).

Vinca alkaloids

Vincas

Vincristine, Vinblastine

Bind tubulin and prevent microtubule spindle formation (M-phase arrest).

Vincristine: peripheral neuropathy, constipation — never intrathecal (fatal). Vinblastine: myelosuppression predominant.

Taxanes

Taxanes

Paclitaxel, Docetaxel

Stabilize microtubules, blocking mitosis (M-phase arrest) — also radiosensitizers.

Peripheral neuropathy, myelosuppression, hypersensitivity → premedicate (dexamethasone + antihistamine).

Immunotherapy

Checkpoint inhibitors

Pembrolizumab, Nivolumab, Atezolizumab

Block PD-1/PD-L1 (or CTLA-4) to release T-cell inhibition against tumor cells.

Immune-related adverse events: pneumonitis, colitis, hepatitis, thyroiditis, rash — managed with corticosteroids. Increasingly paired with RT.

Targeted therapy

Targeted agents

Trastuzumab, Bevacizumab, Erlotinib, Imatinib

Monoclonal antibodies or TKIs against specific drivers: HER2, VEGF, EGFR, BCR-ABL.

Trastuzumab: cardiotoxicity (avoid concurrent anthracycline). Bevacizumab: bleeding, hypertension, impaired wound healing. EGFR TKIs: rash, diarrhea.

Hormonal therapy

Endocrine therapy

Tamoxifen, Anastrozole, ADT (leuprolide)

ER modulation (tamoxifen), aromatase inhibition (AIs), or androgen deprivation (ADT) for hormone-driven cancers.

Tamoxifen: VTE, endometrial cancer risk. AIs: arthralgia, bone loss. ADT: hot flashes, bone-density loss, fatigue — commonly combined with prostate RT.

Quick lookups

Common concurrent chemo–RT regimens

Site
Regimen
Notes
Glioblastoma
Temozolomide 75 mg/m² daily
Stupp: + 60 Gy/30 fx, then adjuvant TMZ 5/28
Head & neck
Cisplatin 100 mg/m² q3wk (or 40 mg/m² weekly)
With 70 Gy/35 fx definitive IMRT
Cervical
Cisplatin 40 mg/m² weekly
With pelvic EBRT + brachytherapy
Rectal
Capecitabine or 5-FU
Long-course 50.4 Gy/28 fx neoadjuvant
Anal
5-FU + mitomycin-C
With 50.4–55.8 Gy definitive CRT
NSCLC (stage III)
Cisplatin/etoposide or carboplatin/paclitaxel
With 60 Gy/30 fx concurrent RT, then durvalumab
Esophageal
Carboplatin + paclitaxel
CROSS protocol: 41.4 Gy/23 fx pre-op
Bladder
Cisplatin-based
Bladder-preserving CRT 64 Gy/32 fx (or 55 Gy/20)
Breast
Chemo before RT (sequential)
Concurrent chemo–RT generally avoided

Emetogenicity & antiemetic control

Risk
Agents
Typical control
High
Cisplatin ≥50 mg/m², cyclophosphamide >1500 mg/m², dacarbazine, BCNU
NK1 + 5-HT3 + dexamethasone
Moderate
Carboplatin, doxorubicin, oxaliplatin, ifosfamide
5-HT3 + dexamethasone ± NK1
Low
Paclitaxel, 5-FU, gemcitabine, etoposide, vincristine, methotrexate
5-HT3 ± dexamethasone
Minimal
Bleomycin, vinblastine, bevacizumab
As needed

Chemo–RT interaction cautions

Drug
Interaction
Action
Bleomycin
Synergistic pulmonary toxicity with lung RT
Monitor PFTs; minimize lung dose
Doxorubicin
Radiation recall; enhanced cardiotoxicity
Deliver sequentially, not concurrently
Gemcitabine
Potent radiosensitizer
Severe toxicity with thoracic RT — reduce dose/field
Methotrexate
Neurotoxicity with cranial RT
Monitor CNS effects closely
Trastuzumab + anthracycline
Additive cardiac toxicity
Avoid concurrent use
Cisplatin, 5-FU, capecitabine, paclitaxel, mitomycin-C
Intentional radiosensitizers
Schedule concurrently by design

Supportive care quick look

Agent
Toxicity managed
Intervention
Cisplatin
Nephrotoxicity
IV hydration + magnesium ± amifostine
Cyclophosphamide / ifosfamide
Hemorrhagic cystitis
Mesna
Methotrexate
Folate antagonism
Leucovorin rescue
Paclitaxel / docetaxel
Hypersensitivity
Premedicate: dexamethasone + antihistamine
Irinotecan
Acute / delayed diarrhea
Atropine (acute), loperamide (delayed)
High-emetogenic chemo
CINV
NK1 + 5-HT3 + dexamethasone
Myelosuppression
Febrile neutropenia risk
G-CSF (filgrastim) support