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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1208348 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
& b) E% B( B. u( D1 XNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 {) l$ T) P6 C7 k  U/ ?
+ Author Affiliations( s$ E$ T# c+ T& |7 I3 z

2 X0 m8 M4 S! [; `  G. `& V1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan * n; }& l1 b2 {+ N& z1 ]
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
) o8 l2 q4 ?" f4 K, e/ x5 e3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * @1 u* k( ~+ S" z
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 6 X: K5 V% t& q3 i& U6 s
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
" _5 u, ~$ L3 T6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
# B* S5 `+ k0 R9 o+ x* A2 d7 r% d7Kinki University School of Medicine, Osaka 589-8511, Japan
: h+ m  A. l' W0 J; G# Z, Y" x8Izumi Municipal Hospital, Osaka 594-0071, Japan # U3 D. j/ V3 l
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
+ {" \8 q+ ^, {$ A+ o: ICorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp   j1 C, g4 Q/ E0 \
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. 5 L) `2 T4 D/ P+ m8 Z+ S6 F$ }
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
0 C3 ^8 @$ a4 Q# u, i6 \! u
; }; P9 W# j6 J7 p9 w( lAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
! ?1 z' e7 C5 ^  d
! m: @4 |, v. ]5 ?6 o, pAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
3 r/ B/ j% F0 ~6 f) P: O! f7 ?; w! T5 g0 S* \6 O! A
Published online on: Thursday, December 1, 2011
- {( l* Y" `' j' b( s2 `9 K# j4 B) U" T  T2 \, k' t* y
Doi: 10.3892/ol.2011.507 0 R" ~0 Y( e! ~: ]# v

5 S+ z  K2 U4 c/ x5 k4 V- JPages: 405-410 3 C4 `* |1 f! i- `
  P% ^2 L$ D- A% O: f* X
Abstract:) {, d9 g1 y1 l% H
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population! q# k; O& D4 I4 _0 k9 Q
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
& G6 G) `  ], ?; Z# L+ x+ Author Affiliations
5 g, w, I% s1 {% e- m% H& X( ]1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ; ^, |  x0 D  q& \
2Department of Thoracic Surgery, Kyoto University, Kyoto
. `- ^/ B- r; ~  U+ Q" Z6 H3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan % P5 K+ q  f7 u; |. G) n
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp ) P4 ~0 E; p$ ^0 c' A
Received September 3, 2010. - H5 E) w# n. y
Revision received November 11, 2010.
: ~6 f& X. V2 p1 h! H" i4 qAccepted November 17, 2010. 1 j6 L: s) R. H" Q' N7 g
Abstract
' l2 z& J- |! yBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. * M0 h" M' {0 a) s9 M" V+ Y/ K* _2 M7 Y  S
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 1 N8 f1 L& n- U  y& k: K
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
* a' \6 w3 v" H% G: ]Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
  M0 |: t+ y: G& M3 T今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?' P+ z  |& i7 q4 d
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy4 p( f/ Y7 h) {- Q2 C' W( h
http://clinicaltrials.gov/ct2/show/NCT01523587
4 _- l& C8 {# u8 @5 T' `
' R0 }7 w# z: k/ A1 F1 pBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC* ?: z! j; p+ y$ y1 M. I
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
7 C$ S$ e8 j7 D( |6 S$ H4 L2 I0 `" }& b; |
从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
+ K9 n" r3 P# Y- w5 d7 o至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
) I1 M) b6 I) p$ `0 b- Q. [7 z从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
7 s2 k. n* L, Q9 \% }) \至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
# q8 H" p( K1 c+ J4 b不错。

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